Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6045 |
| ensemblid | ENSG00000121481.11 |
| hgncid | 10061 |
| symbol | RNF2 |
| name | ring finger protein 2 |
| refseq_nuc | NM_007212.4 |
| refseq_prot | NP_009143.1 |
| ensembl_nuc | ENST00000367510.8 |
| ensembl_prot | ENSP00000356480.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 185045558 |
| end | 185102603 |
| strand | + |
| ver | v1.2 |
| region | chr1:185045558-185102603 |
| region5000 | chr1:185040558-185107603 |
| regionname0 | RNF2_chr1_185045558_185102603 |
| regionname5000 | RNF2_chr1_185040558_185107603 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 336 | 349 | 90 | 74 | 148 | 7 | 28 | 114 | RNF2_chr1_185040558_185107603 | RNF2 | MSQAV others(331): Show |
chr1 | 185040558 | 185107603 |
| a0002 | 0/0 | 336 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | MSQAV others(331): Show |
chr1 | 185040558 | 185107603 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1008 | 348 | 89 | 74 | 148 | 7 | 28 | RNF2_chr1_185040558_185107603 | RNF2 | ATGTC others(1003): Show |
chr1 | 185040558 | 185107603 | ||
| a0001c0003 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATGTC others(1003): Show |
chr1 | 185040558 | 185107603 | ||
| a0002c0002 | 0/0 | 1008 | 1 | 0 | 0 | 0 | 1 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATGTC others(1003): Show |
chr1 | 185040558 | 185107603 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3406 | 55 | 8 | 20 | 17 | 1 | 8 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3401): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0002 | 0/0 | 3406 | 55 | 12 | 10 | 30 | 1 | 2 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3401): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0003 | 0/0 | 3411 | 54 | 12 | 17 | 13 | 3 | 9 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3406): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0004 | 1/0 | 3407 | 50 | 3 | 7 | 33 | 0 | 6 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3402): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0005 | 0/0 | 3407 | 23 | 2 | 4 | 16 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3402): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0006 | 0/0 | 3412 | 18 | 9 | 5 | 3 | 1 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3407): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0007 | 0/0 | 3407 | 11 | 0 | 2 | 9 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3402): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0008 | 0/0 | 3409 | 10 | 10 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3404): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0009 | 0/0 | 3410 | 8 | 0 | 0 | 7 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3405): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0010 | 0/0 | 3410 | 7 | 4 | 3 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3405): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0011 | 0/0 | 3406 | 7 | 0 | 0 | 7 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3401): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0012 | 0/0 | 3408 | 5 | 4 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3403): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0013 | 0/0 | 3408 | 4 | 1 | 1 | 1 | 1 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3403): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0014 | 0/0 | 3413 | 4 | 4 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3408): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0015 | 0/0 | 3407 | 4 | 0 | 0 | 4 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3402): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0016 | 0/0 | 3406 | 3 | 3 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3401): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0017 | 0/0 | 3408 | 3 | 0 | 3 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3403): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0018 | 0/0 | 3411 | 2 | 2 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3406): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0019 | 0/0 | 3408 | 2 | 0 | 0 | 2 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3403): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0020 | 0/0 | 3408 | 2 | 1 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3403): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0021 | 0/0 | 3411 | 2 | 0 | 0 | 2 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3406): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0022 | 0/0 | 3409 | 2 | 2 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3404): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0023 | 0/0 | 3410 | 2 | 2 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3405): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0024 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3401): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0025 | 0/0 | 3407 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3402): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0026 | 0/0 | 3410 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3405): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0027 | 0/0 | 3407 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3402): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0028 | 0/0 | 3407 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3402): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0029 | 0/0 | 3403 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3398): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0030 | 0/0 | 3405 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3400): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0031 | 0/0 | 3408 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3403): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0032 | 0/0 | 3409 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3404): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0033 | 0/0 | 3409 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3404): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0034 | 0/0 | 3412 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3407): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0035 | 0/0 | 3409 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3404): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0036 | 0/0 | 3409 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3404): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0037 | 0/0 | 3410 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3405): Show |
chr1 | 185040558 | 185107603 |
| a0001c0001t0038 | 0/0 | 3410 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3405): Show |
chr1 | 185040558 | 185107603 |
| a0001c0003t0004 | 0/0 | 3407 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3402): Show |
chr1 | 185040558 | 185107603 |
| a0002c0002t0001 | 0/0 | 3406 | 1 | 0 | 0 | 0 | 1 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | ATATT others(3401): Show |
chr1 | 185040558 | 185107603 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0229 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0007g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0007g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0008g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0008g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0009g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0009g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0010g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0010g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0010g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0010g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0011g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0011g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0011g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0011g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0011g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0011g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0011g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0012g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0012g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0013g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0013g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0013g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0013g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0014g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0014g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0014g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0014g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0015g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0015g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0015g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0015g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0016g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0016g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0016g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0017g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0017g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0017g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0018g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0018g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0019g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0019g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0020g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0020g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0021g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0021g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0022g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0022g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0023g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0023g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0024g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0025g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0026g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0027g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0028g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0029g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0030g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0031g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0032g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0033g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0034g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0035g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0036g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0037g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0001t0038g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0001c0003t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0170 | EUR | FIN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | FIN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | CHS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00438 | hp1 | a0001 | c0001 | t0015 | g0230 | EAS | CHS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00438 | hp2 | a0001 | c0001 | t0011 | g0296 | EAS | CHS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | CHS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | CHS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | CHS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01070 | hp2 | a0001 | c0001 | t0010 | g0263 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0239 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0172 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0109 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01081 | hp2 | a0001 | c0001 | t0010 | g0262 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01168 | hp2 | a0001 | c0001 | t0017 | g0222 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0169 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0151 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01243 | hp1 | a0001 | c0001 | t0012 | g0154 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01243 | hp2 | a0001 | c0001 | t0017 | g0223 | AMR | PUR | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0266 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0268 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01261 | hp1 | a0001 | c0001 | t0013 | g0237 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0269 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0238 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0192 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0235 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0282 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0060 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01515 | hp1 | a0001 | c0001 | t0013 | g0194 | EUR | IBS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0177 | EUR | IBS | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01884 | hp1 | a0001 | c0001 | t0036 | g0257 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01884 | hp2 | a0001 | c0003 | t0004 | g0247 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01891 | hp1 | a0001 | c0001 | t0012 | g0189 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01891 | hp2 | a0001 | c0001 | t0038 | g0259 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0316 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0271 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0293 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0311 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01975 | hp2 | a0001 | c0001 | t0007 | g0225 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0100 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01981 | hp1 | a0001 | c0001 | t0007 | g0224 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01981 | hp2 | a0001 | c0001 | t0029 | g0292 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0139 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02056 | hp1 | a0001 | c0001 | t0015 | g0236 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0290 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0220 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02071 | hp2 | a0001 | c0001 | t0009 | g0070 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02080 | hp1 | a0001 | c0001 | t0013 | g0240 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02145 | hp1 | a0001 | c0001 | t0018 | g0284 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02145 | hp2 | a0001 | c0001 | t0016 | g0278 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0168 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0267 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | CDX | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | CDX | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | CDX | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | CDX | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02257 | hp2 | a0001 | c0001 | t0025 | g0280 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0182 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02258 | hp2 | a0001 | c0001 | t0018 | g0046 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02280 | hp1 | a0001 | c0001 | t0016 | g0281 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0286 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02300 | hp1 | a0001 | c0001 | t0017 | g0217 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02523 | hp2 | a0001 | c0001 | t0027 | g0219 | EAS | KHV | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02572 | hp1 | a0001 | c0001 | t0023 | g0056 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0329 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02615 | hp2 | a0001 | c0001 | t0031 | g0260 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02622 | hp2 | a0001 | c0001 | t0014 | g0180 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0090 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0086 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02723 | hp1 | a0001 | c0001 | t0022 | g0055 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02738 | hp2 | a0001 | c0001 | t0020 | g0058 | SAS | PJL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02886 | hp1 | a0001 | c0001 | t0037 | g0258 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0085 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0285 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0305 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | ESN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0005 | AFR | ESN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0287 | AFR | ESN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02970 | hp2 | a0001 | c0001 | t0023 | g0054 | AFR | ESN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0178 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0186 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03098 | hp2 | a0001 | c0001 | t0016 | g0279 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | ESN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03130 | hp2 | a0001 | c0001 | t0012 | g0153 | AFR | ESN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03139 | hp1 | a0001 | c0001 | t0014 | g0183 | AFR | ESN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03139 | hp2 | a0001 | c0001 | t0020 | g0256 | AFR | ESN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03195 | hp1 | a0001 | c0001 | t0012 | g0191 | AFR | ESN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0181 | AFR | ESN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0088 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0152 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0304 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0087 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0146 | SAS | PJL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0081 | SAS | PJL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0188 | AFR | ESN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03540 | hp1 | a0001 | c0001 | t0022 | g0057 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | GWD | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03579 | hp1 | a0001 | c0001 | t0026 | g0082 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0205 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03654 | hp1 | a0001 | c0001 | t0009 | g0067 | SAS | PJL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0264 | SAS | PJL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | STU | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0171 | SAS | BEB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0211 | SAS | BEB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0014 | SAS | BEB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0116 | SAS | BEB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | BEB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0099 | SAS | STU | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0147 | SAS | STU | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0097 | SAS | BEB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0198 | SAS | BEB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0309 | SAS | STU | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | YRI | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | CHB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | CHB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0330 | AFR | YRI | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | YRI | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18941 | hp2 | a0001 | c0001 | t0011 | g0297 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18946 | hp1 | a0001 | c0001 | t0015 | g0233 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18949 | hp1 | a0001 | c0001 | t0021 | g0076 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18960 | hp2 | a0001 | c0001 | t0011 | g0300 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18962 | hp1 | a0001 | c0001 | t0011 | g0315 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18962 | hp2 | a0001 | c0001 | t0007 | g0213 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18963 | hp1 | a0001 | c0001 | t0015 | g0197 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18964 | hp1 | a0001 | c0001 | t0021 | g0068 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0324 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0319 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18967 | hp2 | a0001 | c0001 | t0009 | g0074 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18969 | hp1 | a0001 | c0001 | t0030 | g0027 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18969 | hp2 | a0001 | c0001 | t0032 | g0073 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18970 | hp2 | a0001 | c0001 | t0011 | g0294 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18973 | hp2 | a0001 | c0001 | t0009 | g0077 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18974 | hp1 | a0001 | c0001 | t0033 | g0071 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0323 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18985 | hp2 | a0001 | c0001 | t0006 | g0136 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18998 | hp1 | a0001 | c0001 | t0007 | g0216 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19001 | hp1 | a0001 | c0001 | t0009 | g0078 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19002 | hp1 | a0001 | c0001 | t0007 | g0214 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19006 | hp2 | a0001 | c0001 | t0019 | g0327 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19009 | hp2 | a0001 | c0001 | t0009 | g0072 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19011 | hp2 | a0001 | c0001 | t0009 | g0075 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | LWK | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0277 | AFR | LWK | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0306 | AFR | LWK | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | LWK | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19056 | hp2 | a0001 | c0001 | t0007 | g0212 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19057 | hp1 | a0001 | c0001 | t0011 | g0295 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19066 | hp2 | a0001 | c0001 | t0019 | g0317 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19068 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19074 | hp1 | a0001 | c0001 | t0009 | g0069 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0314 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19079 | hp2 | a0001 | c0001 | t0007 | g0215 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19081 | hp1 | a0001 | c0001 | t0011 | g0301 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19082 | hp1 | a0001 | c0001 | t0007 | g0252 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19083 | hp2 | a0001 | c0001 | t0007 | g0199 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0325 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19086 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0318 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA19091 | hp2 | a0001 | c0001 | t0007 | g0218 | EAS | JPT | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0176 | EUR | TSI | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0126 | EUR | TSI | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0164 | EUR | TSI | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | TSI | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | GIH | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0166 | SAS | GIH | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0206 | AMR | CLM | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02109 | hp2 | a0001 | c0001 | t0034 | g0187 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02486 | hp1 | a0001 | c0001 | t0013 | g0135 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02486 | hp2 | a0001 | c0001 | t0014 | g0149 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0190 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG02559 | hp2 | a0001 | c0001 | t0010 | g0289 | AFR | ACB | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0089 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG03471 | hp2 | a0001 | c0001 | t0035 | g0255 | AFR | MSL | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG06807 | hp1 | a0001 | c0001 | t0028 | g0061 | AFR | USA | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| HG06807 | hp2 | a0001 | c0001 | t0024 | g0110 | AFR | USA | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | USA | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | USA | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0185 | AFR | LWK | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0245 | AFR | LWK | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0283 | REF | REF | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0229 | REF | REF | RNF2_chr1_185040558_185107603 | RNF2 | chr1 | 185040558 | 185107603 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:185098317 | T | C | 1 | a0002 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.710T>C | p.Met237Thr | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 5/7 | 804/3407 | 710/1011 | 237/336 | chr1 | 185098317 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:185100256 | C | T | 1 | a0001c0003 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.966C>T | p.Asn322Asn | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1060/3407 | 966/1011 | 322/336 | chr1 | 185100256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:185045564 | T | TGCG | 2 | a0001c0001t0022 a0001c0001t0023 |
4 | HG02572.hp1 HG02723.hp1 HG02970.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-81_-79dupGCG | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/7 | 41980 | INFO_REALIGN_3_PRIME | chr1 | 185045564 | |||||
| chr1:185045588 | A | G | 1 | a0001c0001t0015 | 4 | HG00438.hp1 HG02056.hp1 NA18946.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-64A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/7 | 41966 | chr1 | 185045588 | ||||||
| chr1:185100429 | A | G | 17 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(14): Show |
109 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*128A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 128 | chr1 | 185100429 | ||||||
| chr1:185100525 | A | G | 1 | a0001c0001t0028 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*224A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 224 | chr1 | 185100525 | ||||||
| chr1:185100543 | G | GT | 6 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0010 others(3): Show |
89 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*253dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 254 | INFO_REALIGN_3_PRIME | chr1 | 185100543 | |||||
| chr1:185100543 | GTTTT | G | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 others(3): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*250_*253delTTTT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 250 | INFO_REALIGN_3_PRIME | chr1 | 185100543 | |||||
| chr1:185100554 | T | C | 1 | a0001c0001t0031 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*253T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 253 | chr1 | 185100554 | ||||||
| chr1:185100691 | T | C | 1 | a0001c0001t0028 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*390T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 390 | chr1 | 185100691 | ||||||
| chr1:185100711 | T | A | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 others(3): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*410T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 410 | chr1 | 185100711 | ||||||
| chr1:185100715 | T | C | 1 | a0001c0001t0032 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*414T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 414 | chr1 | 185100715 | ||||||
| chr1:185101697 | A | G | 4 | a0001c0001t0031 a0001c0001t0036 a0001c0001t0037 others(1): Show |
4 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1396A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1396 | chr1 | 185101697 | ||||||
| chr1:185101757 | C | T | 1 | a0001c0001t0035 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1456C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1456 | chr1 | 185101757 | ||||||
| chr1:185101831 | G | GT | 1 | a0001c0001t0017 | 3 | HG01168.hp2 HG01243.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1530_*1531insT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1531 | chr1 | 185101831 | ||||||
| chr1:185101832 | G | GT | 3 | a0001c0001t0013 a0001c0001t0020 a0001c0001t0031 |
7 | HG01261.hp1 HG01515.hp1 HG02080.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1553dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1554 | INFO_REALIGN_3_PRIME | chr1 | 185101832 | |||||
| chr1:185101832 | G | GTT | 8 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0030 others(5): Show |
23 | HG01070.hp2 HG01081.hp2 HG01175.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1552_*1553dupTT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1554 | INFO_REALIGN_3_PRIME | chr1 | 185101832 | |||||
| chr1:185101832 | G | GTTT | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(3): Show |
126 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1551_*1553dupTTT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1554 | INFO_REALIGN_3_PRIME | chr1 | 185101832 | |||||
| chr1:185101832 | G | GTTTT | 4 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0018 others(1): Show |
45 | HG01074.hp2 HG01192.hp2 HG01361.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1550_*1553dupTTTT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1554 | INFO_REALIGN_3_PRIME | chr1 | 185101832 | |||||
| chr1:185101832 | G | GTTTTT | 3 | a0001c0001t0014 a0001c0001t0019 a0001c0001t0034 |
7 | HG02109.hp2 HG02486.hp2 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1549_*1553dupTTTT others(1): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1554 | INFO_REALIGN_3_PRIME | chr1 | 185101832 | |||||
| chr1:185101832 | G | T | 3 | a0001c0001t0007 a0001c0001t0017 a0001c0001t0027 |
15 | HG01168.hp2 HG01243.hp2 HG01975.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1531G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1531 | chr1 | 185101832 | ||||||
| chr1:185101832 | GT | G | 5 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0022 others(2): Show |
61 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1553delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1553 | INFO_REALIGN_3_PRIME | chr1 | 185101832 | |||||
| chr1:185101866 | C | T | 2 | a0001c0001t0016 a0001c0001t0025 |
4 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1565C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1565 | chr1 | 185101866 | ||||||
| chr1:185101978 | C | T | 1 | a0001c0001t0011 | 7 | HG00438.hp2 NA18941.hp2 NA18960.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1677C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1677 | chr1 | 185101978 | ||||||
| chr1:185102156 | A | G | 1 | a0001c0001t0028 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1855A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 1855 | chr1 | 185102156 | ||||||
| chr1:185102314 | T | A | 1 | a0001c0001t0024 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2013T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 2013 | chr1 | 185102314 | ||||||
| chr1:185102378 | C | T | 1 | a0001c0001t0034 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2077C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 2077 | chr1 | 185102378 | ||||||
| chr1:185102579 | A | G | 1 | a0001c0001t0027 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2278A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 7/7 | 2278 | chr1 | 185102579 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:185045667 | G | C | 1 | a0001c0001t0003g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-3+18G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185045667 | |||||||
| chr1:185045676 | G | A | 34 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(31): Show |
42 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.-3+27G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185045676 | |||||||
| chr1:185045694 | C | T | 2 | a0001c0001t0003g0330 a0001c0001t0006g0329 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-3+45C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185045694 | |||||||
| chr1:185045750 | T | TG | 21 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(18): Show |
21 | HG00544.hp1 HG00609.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.-3+109dupG | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185045750 | ||||||
| chr1:185046148 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-3+499C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185046148 | |||||||
| chr1:185046162 | G | T | 1 | a0001c0001t0001g0012 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-3+513G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185046162 | |||||||
| chr1:185046384 | G | A | 1 | a0001c0001t0028g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-3+735G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185046384 | |||||||
| chr1:185046402 | A | C | 82 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(79): Show |
93 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-3+753A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185046402 | |||||||
| chr1:185046439 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0004g0044 |
2 | HG00609.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.-3+790G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185046439 | |||||||
| chr1:185046497 | T | C | 1 | a0001c0001t0002g0288 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-3+848T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185046497 | |||||||
| chr1:185046501 | A | C | 1 | a0001c0001t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-3+852A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185046501 | |||||||
| chr1:185046607 | A | G | 2 | a0001c0001t0002g0042 a0001c0001t0005g0016 |
2 | HG00408.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.-3+958A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185046607 | |||||||
| chr1:185046637 | A | G | 1 | a0001c0001t0020g0058 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-3+988A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185046637 | |||||||
| chr1:185047324 | C | T | 1 | a0001c0001t0003g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-3+1675C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185047324 | |||||||
| chr1:185048040 | G | T | 3 | a0001c0001t0004g0287 a0001c0001t0008g0285 a0001c0001t0018g0284 |
3 | HG02145.hp1 HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-3+2391G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185048040 | |||||||
| chr1:185048081 | A | G | 1 | a0001c0001t0004g0282 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-3+2432A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185048081 | |||||||
| chr1:185048439 | A | G | 5 | a0001c0001t0004g0277 a0001c0001t0016g0278 a0001c0001t0016g0279 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+2790A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185048439 | |||||||
| chr1:185048440 | T | C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
6 | HG02572.hp2 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3+2791T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185048440 | |||||||
| chr1:185048449 | C | T | 5 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(2): Show |
5 | NA18971.hp1 NA18977.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+2800C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185048449 | |||||||
| chr1:185048475 | T | G | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+2826T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185048475 | |||||||
| chr1:185048567 | T | C | 1 | a0001c0001t0003g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-3+2918T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185048567 | |||||||
| chr1:185048695 | A | G | 1 | a0001c0001t0004g0272 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-3+3046A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185048695 | |||||||
| chr1:185048936 | G | C | 1 | a0001c0001t0003g0080 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-3+3287G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185048936 | |||||||
| chr1:185049318 | G | C | 1 | a0001c0001t0004g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3+3669G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185049318 | |||||||
| chr1:185049337 | G | A | 1 | a0001c0001t0004g0081 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-3+3688G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185049337 | |||||||
| chr1:185049554 | C | G | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-3+3905C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185049554 | |||||||
| chr1:185049670 | T | TA | 11 | a0001c0001t0003g0083 a0001c0001t0003g0084 a0001c0001t0008g0005 others(8): Show |
12 | HG01123.hp1 HG02258.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+4033dupA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185049670 | ||||||
| chr1:185049670 | T | TAAA | 9 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(6): Show |
9 | HG02071.hp2 HG03654.hp1 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3+4031_-3+4033dup others(3): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185049670 | ||||||
| chr1:185049670 | TA | T | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-3+4033delA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185049670 | ||||||
| chr1:185049711 | C | G | 5 | a0001c0001t0002g0326 a0001c0001t0005g0323 a0001c0001t0005g0324 others(2): Show |
5 | NA18965.hp1 NA18983.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+4062C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185049711 | |||||||
| chr1:185049748 | C | T | 2 | a0001c0001t0008g0285 a0001c0001t0018g0284 |
2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-3+4099C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185049748 | |||||||
| chr1:185049753 | C | T | 1 | a0001c0001t0004g0272 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-3+4104C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185049753 | |||||||
| chr1:185050099 | G | A | 3 | a0001c0001t0004g0287 a0001c0001t0008g0285 a0001c0001t0018g0284 |
3 | HG02145.hp1 HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-3+4450G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185050099 | |||||||
| chr1:185050338 | C | G | 10 | a0001c0001t0003g0264 a0001c0001t0003g0265 a0001c0001t0003g0266 others(7): Show |
10 | HG00738.hp1 HG01070.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+4689C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185050338 | |||||||
| chr1:185050391 | C | T | 1 | a0001c0001t0002g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-3+4742C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185050391 | |||||||
| chr1:185050649 | C | G | 10 | a0001c0001t0003g0264 a0001c0001t0003g0265 a0001c0001t0003g0266 others(7): Show |
10 | HG00738.hp1 HG01070.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+5000C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185050649 | |||||||
| chr1:185051271 | A | G | 1 | a0001c0001t0004g0261 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-3+5622A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185051271 | |||||||
| chr1:185051734 | CT | C | 54 | a0001c0001t0001g0012 a0001c0001t0001g0043 a0001c0001t0001g0047 others(51): Show |
55 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.-3+6097delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185051734 | ||||||
| chr1:185051766 | T | C | 5 | a0001c0001t0004g0130 a0001c0001t0004g0131 a0001c0001t0004g0132 others(2): Show |
5 | HG02165.hp2 NA18951.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+6117T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185051766 | |||||||
| chr1:185051831 | GTA | G | 6 | a0001c0001t0020g0256 a0001c0001t0031g0260 a0001c0001t0035g0255 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+6188_-3+6189del others(2): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185051831 | ||||||
| chr1:185051863 | CAT | C | 11 | a0001c0001t0009g0069 a0001c0001t0009g0070 a0001c0001t0009g0072 others(8): Show |
11 | HG02071.hp2 NA18949.hp1 NA18964.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3+6223_-3+6224del others(2): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185051863 | ||||||
| chr1:185051953 | C | CAT | 59 | a0001c0001t0001g0091 a0001c0001t0002g0009 a0001c0001t0002g0010 others(56): Show |
61 | HG00438.hp2 HG00733.hp2 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.-3+6319_-3+6320dup others(2): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185051953 | ||||||
| chr1:185051953 | C | CATAT | 36 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(33): Show |
44 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.-3+6317_-3+6320dup others(4): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185051953 | ||||||
| chr1:185051953 | C | CATATAT | 3 | a0001c0001t0002g0017 a0001c0001t0002g0019 a0001c0001t0005g0018 |
3 | HG01257.hp1 HG02165.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-3+6315_-3+6320dup others(6): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185051953 | ||||||
| chr1:185052278 | G | A | 184 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(181): Show |
197 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.-3+6629G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185052278 | |||||||
| chr1:185052295 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-3+6646T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185052295 | |||||||
| chr1:185052302 | A | C | 1 | a0001c0001t0002g0041 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-3+6653A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185052302 | |||||||
| chr1:185052372 | G | A | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+6723G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185052372 | |||||||
| chr1:185052442 | T | C | 1 | a0001c0001t0005g0293 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-3+6793T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185052442 | |||||||
| chr1:185053277 | T | C | 1 | a0001c0001t0028g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-3+7628T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185053277 | |||||||
| chr1:185053337 | T | C | 1 | a0001c0001t0026g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-3+7688T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185053337 | |||||||
| chr1:185053446 | C | T | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+7797C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185053446 | |||||||
| chr1:185053783 | G | A | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+8134G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185053783 | |||||||
| chr1:185053819 | G | A | 2 | a0001c0001t0005g0323 a0001c0001t0005g0324 |
2 | NA18965.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-3+8170G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185053819 | |||||||
| chr1:185053889 | T | TA | 34 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(31): Show |
42 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.-3+8250dupA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185053889 | ||||||
| chr1:185053946 | G | A | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+8297G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185053946 | |||||||
| chr1:185054081 | C | G | 6 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0320 others(3): Show |
7 | HG02451.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+8432C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054081 | |||||||
| chr1:185054107 | A | G | 1 | a0001c0001t0006g0192 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-3+8458A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054107 | |||||||
| chr1:185054214 | A | G | 5 | a0001c0001t0003g0286 a0001c0001t0006g0188 a0001c0001t0010g0190 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+8565A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054214 | |||||||
| chr1:185054282 | C | T | 1 | a0001c0001t0009g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-3+8633C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054282 | |||||||
| chr1:185054400 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3+8751T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054400 | |||||||
| chr1:185054462 | A | G | 1 | a0001c0001t0034g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-3+8813A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054462 | |||||||
| chr1:185054470 | T | G | 1 | a0001c0001t0005g0323 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-3+8821T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054470 | |||||||
| chr1:185054471 | T | C | 1 | a0001c0001t0005g0323 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-3+8822T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054471 | |||||||
| chr1:185054536 | C | T | 9 | a0001c0001t0003g0179 a0001c0001t0003g0184 a0001c0001t0006g0178 others(6): Show |
9 | HG01099.hp2 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+8887C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054536 | |||||||
| chr1:185054783 | C | T | 3 | a0001c0001t0005g0318 a0001c0001t0005g0319 a0001c0001t0019g0317 |
3 | NA18967.hp1 NA19066.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-3+9134C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054783 | |||||||
| chr1:185054793 | G | C | 2 | a0001c0001t0003g0137 a0001c0001t0003g0138 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-3+9144G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054793 | |||||||
| chr1:185054845 | G | A | 1 | a0001c0001t0009g0070 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-3+9196G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054845 | |||||||
| chr1:185054915 | G | A | 2 | a0001c0001t0008g0285 a0001c0001t0018g0284 |
2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-3+9266G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054915 | |||||||
| chr1:185054993 | C | T | 2 | a0001c0001t0001g0254 a0001c0001t0004g0253 |
2 | HG01934.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-3+9344C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185054993 | |||||||
| chr1:185055047 | C | T | 1 | a0001c0001t0007g0252 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-3+9398C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185055047 | |||||||
| chr1:185055309 | T | C | 4 | a0001c0001t0004g0287 a0001c0001t0008g0285 a0001c0001t0018g0284 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+9660T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185055309 | |||||||
| chr1:185055374 | C | T | 1 | a0001c0001t0005g0316 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-3+9725C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185055374 | |||||||
| chr1:185055502 | C | T | 8 | a0001c0001t0008g0005 a0001c0001t0008g0085 a0001c0001t0008g0086 others(5): Show |
9 | HG02647.hp2 HG02717.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3+9853C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185055502 | |||||||
| chr1:185055573 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-3+9924C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185055573 | |||||||
| chr1:185055621 | G | A | 1 | a0001c0001t0013g0194 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-3+9972G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185055621 | |||||||
| chr1:185055850 | A | C | 11 | a0001c0001t0009g0069 a0001c0001t0009g0070 a0001c0001t0009g0072 others(8): Show |
11 | HG02071.hp2 NA18949.hp1 NA18964.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3+10201A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185055850 | |||||||
| chr1:185055855 | TTTAG | T | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-3+10211_-3+10214d others(6): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185055855 | ||||||
| chr1:185055917 | T | A | 1 | a0001c0001t0004g0195 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-3+10268T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185055917 | |||||||
| chr1:185055976 | T | C | 3 | a0001c0001t0003g0002 a0001c0001t0010g0002 a0001c0001t0010g0289 |
4 | HG02559.hp2 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+10327T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185055976 | |||||||
| chr1:185056533 | T | A | 2 | a0001c0001t0003g0140 a0001c0001t0006g0139 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-3+10884T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185056533 | |||||||
| chr1:185056620 | C | T | 4 | a0001c0001t0031g0260 a0001c0001t0036g0257 a0001c0001t0037g0258 others(1): Show |
4 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+10971C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185056620 | |||||||
| chr1:185057015 | T | C | 4 | a0001c0001t0004g0287 a0001c0001t0008g0285 a0001c0001t0018g0284 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+11366T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185057015 | |||||||
| chr1:185057032 | G | C | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+11383G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185057032 | |||||||
| chr1:185057065 | T | C | 1 | a0001c0001t0004g0081 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-3+11416T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185057065 | |||||||
| chr1:185057303 | AAAAT | A | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+11674_-3+11677d others(6): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185057303 | ||||||
| chr1:185057323 | T | C | 6 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0320 others(3): Show |
7 | HG02451.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+11674T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185057323 | |||||||
| chr1:185057396 | G | T | 1 | a0001c0001t0002g0019 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-3+11747G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185057396 | |||||||
| chr1:185057548 | T | C | 19 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0013 others(16): Show |
19 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-3+11899T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185057548 | |||||||
| chr1:185057681 | A | G | 71 | a0001c0001t0001g0012 a0001c0001t0001g0043 a0001c0001t0001g0047 others(68): Show |
72 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.-3+12032A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185057681 | |||||||
| chr1:185057805 | G | GA | 12 | a0001c0001t0001g0093 a0001c0001t0001g0248 a0001c0001t0003g0179 others(9): Show |
12 | HG01081.hp2 HG01099.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+12170dupA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185057805 | ||||||
| chr1:185057805 | GA | G | 84 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0002g0001 others(81): Show |
94 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.-3+12170delA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185057805 | ||||||
| chr1:185057805 | GAA | G | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+12169_-3+12170d others(4): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185057805 | ||||||
| chr1:185057806 | A | G | 3 | a0001c0001t0036g0257 a0001c0001t0037g0258 a0001c0001t0038g0259 |
3 | HG01884.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-3+12157A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185057806 | |||||||
| chr1:185058032 | G | A | 1 | a0001c0001t0015g0197 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-3+12383G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185058032 | |||||||
| chr1:185058067 | A | C | 4 | a0001c0001t0006g0150 a0001c0001t0006g0151 a0001c0001t0006g0152 others(1): Show |
4 | HG01192.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+12418A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185058067 | |||||||
| chr1:185058115 | T | C | 1 | a0001c0001t0002g0288 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-3+12466T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185058115 | |||||||
| chr1:185058189 | T | G | 3 | a0001c0001t0003g0264 a0001c0001t0010g0262 a0001c0001t0010g0263 |
3 | HG01070.hp2 HG01081.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-3+12540T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185058189 | |||||||
| chr1:185058195 | TA | T | 11 | a0001c0001t0009g0069 a0001c0001t0009g0070 a0001c0001t0009g0072 others(8): Show |
11 | HG02071.hp2 NA18949.hp1 NA18964.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3+12547delA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185058195 | |||||||
| chr1:185058344 | TG | T | 3 | a0001c0001t0004g0287 a0001c0001t0008g0285 a0001c0001t0018g0284 |
3 | HG02145.hp1 HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-3+12697delG | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185058344 | ||||||
| chr1:185058381 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-3+12732T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185058381 | |||||||
| chr1:185058602 | T | G | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+12953T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185058602 | |||||||
| chr1:185058648 | A | G | 9 | a0001c0001t0003g0179 a0001c0001t0003g0184 a0001c0001t0006g0178 others(6): Show |
9 | HG01099.hp2 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+12999A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185058648 | |||||||
| chr1:185058663 | T | C | 5 | a0001c0001t0004g0277 a0001c0001t0016g0278 a0001c0001t0016g0279 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+13014T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185058663 | |||||||
| chr1:185058979 | T | G | 1 | a0001c0001t0002g0041 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-3+13330T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185058979 | |||||||
| chr1:185059220 | G | A | 1 | a0001c0001t0003g0196 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-3+13571G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185059220 | |||||||
| chr1:185059227 | T | TA | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+13578_-3+13579i others(3): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185059227 | |||||||
| chr1:185059228 | T | A | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+13579T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185059228 | |||||||
| chr1:185059228 | T | TA | 187 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(184): Show |
200 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.-3+13591dupA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185059228 | ||||||
| chr1:185059510 | C | T | 1 | a0002c0002t0001g0126 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-3+13861C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185059510 | |||||||
| chr1:185059639 | C | T | 1 | a0001c0001t0035g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-3+13990C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185059639 | |||||||
| chr1:185059670 | C | G | 9 | a0001c0001t0002g0326 a0001c0001t0005g0314 a0001c0001t0005g0318 others(6): Show |
9 | NA18965.hp1 NA18967.hp1 NA18983.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3+14021C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185059670 | |||||||
| chr1:185059700 | C | G | 1 | a0001c0001t0034g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-3+14051C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185059700 | |||||||
| chr1:185059721 | C | A | 2 | a0001c0001t0012g0153 a0001c0001t0012g0154 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-3+14072C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185059721 | |||||||
| chr1:185059933 | A | G | 6 | a0001c0001t0020g0256 a0001c0001t0031g0260 a0001c0001t0035g0255 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+14284A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185059933 | |||||||
| chr1:185059944 | T | G | 9 | a0001c0001t0003g0140 a0001c0001t0003g0155 a0001c0001t0003g0156 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+14295T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185059944 | |||||||
| chr1:185060064 | A | G | 1 | a0001c0001t0035g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-3+14415A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185060064 | |||||||
| chr1:185060214 | A | G | 8 | a0001c0001t0002g0310 a0001c0001t0002g0312 a0001c0001t0002g0313 others(5): Show |
8 | HG01255.hp1 HG01496.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3+14565A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185060214 | |||||||
| chr1:185060380 | C | A | 1 | a0001c0001t0034g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-3+14731C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185060380 | |||||||
| chr1:185060594 | A | C | 1 | a0001c0001t0034g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-3+14945A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185060594 | |||||||
| chr1:185060674 | T | C | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG01099.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-3+15025T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185060674 | |||||||
| chr1:185060845 | A | G | 1 | a0001c0001t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-3+15196A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185060845 | |||||||
| chr1:185060891 | G | C | 1 | a0001c0001t0001g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-3+15242G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185060891 | |||||||
| chr1:185060901 | T | C | 2 | a0001c0001t0003g0140 a0001c0001t0003g0155 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-3+15252T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185060901 | |||||||
| chr1:185061003 | G | C | 1 | a0001c0001t0003g0196 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-3+15354G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185061003 | |||||||
| chr1:185061102 | T | C | 94 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(91): Show |
104 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.-3+15453T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185061102 | |||||||
| chr1:185061128 | CT | C | 197 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0053 others(194): Show |
209 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.-3+15496delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185061128 | ||||||
| chr1:185061130 | T | C | 6 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0023 others(3): Show |
7 | NA18944.hp1 NA18971.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+15481T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185061130 | |||||||
| chr1:185061192 | A | G | 8 | a0001c0001t0008g0005 a0001c0001t0008g0085 a0001c0001t0008g0086 others(5): Show |
9 | HG02647.hp2 HG02717.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3+15543A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185061192 | |||||||
| chr1:185061253 | G | A | 83 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
93 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-3+15604G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185061253 | |||||||
| chr1:185061253 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-3+15604G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185061253 | |||||||
| chr1:185061372 | A | G | 8 | a0001c0001t0004g0277 a0001c0001t0004g0287 a0001c0001t0008g0285 others(5): Show |
8 | HG02145.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+15723A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185061372 | |||||||
| chr1:185061415 | G | A | 23 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0095 others(20): Show |
24 | HG00621.hp1 HG00639.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.-3+15766G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185061415 | |||||||
| chr1:185061610 | G | T | 1 | a0001c0001t0003g0173 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-3+15961G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185061610 | |||||||
| chr1:185062277 | T | C | 1 | a0001c0001t0034g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-3+16628T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185062277 | |||||||
| chr1:185062438 | T | A | 9 | a0001c0001t0003g0179 a0001c0001t0003g0184 a0001c0001t0006g0178 others(6): Show |
9 | HG01099.hp2 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+16789T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185062438 | |||||||
| chr1:185062453 | T | C | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+16804T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185062453 | |||||||
| chr1:185062476 | CAA | C | 5 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0040 others(2): Show |
5 | HG02132.hp1 NA18972.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+16828_-3+16829d others(4): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185062476 | |||||||
| chr1:185062597 | C | CTTCCAAA others(4): Show |
1 | a0001c0001t0006g0136 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-3+16949_-3+16959d others(13): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185062597 | ||||||
| chr1:185062628 | T | A | 1 | a0001c0001t0002g0308 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-3+16979T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185062628 | |||||||
| chr1:185062765 | T | TA | 9 | a0001c0001t0003g0264 a0001c0001t0003g0265 a0001c0001t0003g0266 others(6): Show |
9 | HG00738.hp1 HG01070.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+17126dupA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185062765 | ||||||
| chr1:185062818 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3+17169C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185062818 | |||||||
| chr1:185062820 | C | A | 151 | a0001c0001t0001g0012 a0001c0001t0001g0043 a0001c0001t0001g0047 others(148): Show |
162 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.-3+17171C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185062820 | |||||||
| chr1:185062881 | T | G | 2 | a0001c0001t0003g0142 a0001c0001t0003g0143 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-3+17232T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185062881 | |||||||
| chr1:185063177 | C | A | 1 | a0001c0001t0004g0210 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-3+17528C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185063177 | |||||||
| chr1:185063296 | G | A | 1 | a0001c0001t0020g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-3+17647G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185063296 | |||||||
| chr1:185063330 | G | A | 1 | a0001c0001t0031g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-3+17681G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185063330 | |||||||
| chr1:185063438 | CT | C | 6 | a0001c0001t0003g0157 a0001c0001t0003g0158 a0001c0001t0003g0159 others(3): Show |
6 | NA18961.hp1 NA18982.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+17793delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185063438 | ||||||
| chr1:185063636 | A | G | 1 | a0001c0001t0006g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-3+17987A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185063636 | |||||||
| chr1:185063649 | G | A | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+18000G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185063649 | |||||||
| chr1:185063771 | C | T | 8 | a0001c0001t0003g0179 a0001c0001t0003g0184 a0001c0001t0006g0178 others(5): Show |
8 | HG01099.hp2 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+18122C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185063771 | |||||||
| chr1:185063975 | T | C | 1 | a0001c0001t0012g0153 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-3+18326T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185063975 | |||||||
| chr1:185063997 | A | G | 1 | a0001c0001t0003g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-3+18348A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185063997 | |||||||
| chr1:185064324 | A | G | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+18675A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185064324 | |||||||
| chr1:185064348 | A | C | 94 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
97 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.-3+18699A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185064348 | |||||||
| chr1:185064457 | A | G | 4 | a0001c0001t0004g0287 a0001c0001t0008g0285 a0001c0001t0018g0284 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+18808A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185064457 | |||||||
| chr1:185064468 | G | A | 4 | a0001c0001t0003g0006 a0001c0001t0003g0144 a0001c0001t0003g0145 others(1): Show |
4 | NA18939.hp1 NA19002.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+18819G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185064468 | |||||||
| chr1:185064491 | C | T | 1 | a0001c0001t0005g0016 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-3+18842C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185064491 | |||||||
| chr1:185064684 | TTAA | T | 83 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
93 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-3+19041_-3+19043d others(5): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185064684 | ||||||
| chr1:185064766 | G | T | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+19117G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185064766 | |||||||
| chr1:185064774 | C | T | 1 | a0001c0001t0005g0306 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-3+19125C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185064774 | |||||||
| chr1:185064873 | T | G | 1 | a0001c0001t0001g0128 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-3+19224T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185064873 | |||||||
| chr1:185064927 | A | G | 4 | a0001c0001t0003g0286 a0001c0001t0010g0190 a0001c0001t0012g0189 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+19278A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185064927 | |||||||
| chr1:185065163 | A | G | 13 | a0001c0001t0003g0330 a0001c0001t0009g0067 a0001c0001t0009g0069 others(10): Show |
13 | HG02071.hp2 HG03654.hp1 NA18906.hp1 others(10): Show |
intron_variant | MODIFIER | c.-3+19514A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185065163 | |||||||
| chr1:185065184 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-3+19535A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185065184 | |||||||
| chr1:185065370 | G | C | 95 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(92): Show |
105 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-3+19721G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185065370 | |||||||
| chr1:185065479 | T | C | 6 | a0001c0001t0020g0256 a0001c0001t0031g0260 a0001c0001t0035g0255 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+19830T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185065479 | |||||||
| chr1:185065561 | A | G | 1 | a0001c0001t0003g0249 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-3+19912A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185065561 | |||||||
| chr1:185065636 | C | T | 1 | a0001c0001t0034g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-3+19987C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185065636 | |||||||
| chr1:185065741 | C | T | 1 | a0001c0003t0004g0247 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-3+20092C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185065741 | |||||||
| chr1:185065876 | C | T | 3 | a0001c0001t0036g0257 a0001c0001t0037g0258 a0001c0001t0038g0259 |
3 | HG01884.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-3+20227C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185065876 | |||||||
| chr1:185065941 | CT | C | 49 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(46): Show |
51 | HG00438.hp2 HG00733.hp2 HG01167.hp2 others(48): Show |
intron_variant | MODIFIER | c.-3+20293delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185065941 | |||||||
| chr1:185065956 | A | AT | 39 | a0001c0001t0001g0208 a0001c0001t0002g0001 a0001c0001t0002g0003 others(36): Show |
47 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-3+20320dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185065956 | ||||||
| chr1:185065978 | C | T | 4 | a0001c0001t0002g0009 a0001c0001t0002g0303 a0001c0001t0002g0304 others(1): Show |
5 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+20329C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185065978 | |||||||
| chr1:185066124 | T | C | 8 | a0001c0001t0008g0005 a0001c0001t0008g0085 a0001c0001t0008g0086 others(5): Show |
9 | HG02647.hp2 HG02717.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3+20475T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185066124 | |||||||
| chr1:185066193 | G | A | 1 | a0001c0001t0028g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-3+20544G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185066193 | |||||||
| chr1:185066203 | T | C | 3 | a0001c0001t0003g0002 a0001c0001t0010g0002 a0001c0001t0010g0289 |
4 | HG02559.hp2 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+20554T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185066203 | |||||||
| chr1:185066237 | T | C | 1 | a0001c0001t0006g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-3+20588T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185066237 | |||||||
| chr1:185066403 | T | C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0303 a0001c0001t0002g0304 others(1): Show |
5 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+20754T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185066403 | |||||||
| chr1:185066607 | T | G | 1 | a0001c0001t0003g0008 | 2 | HG00639.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-2-20945T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185066607 | |||||||
| chr1:185066626 | A | G | 1 | a0001c0001t0004g0081 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-2-20926A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185066626 | |||||||
| chr1:185066848 | G | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-2-20704G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185066848 | |||||||
| chr1:185067130 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-2-20422A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185067130 | |||||||
| chr1:185067251 | G | A | 2 | a0001c0001t0003g0162 a0001c0001t0006g0192 |
2 | HG01361.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-2-20301G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185067251 | |||||||
| chr1:185067294 | C | T | 1 | a0001c0001t0006g0172 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-2-20258C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185067294 | |||||||
| chr1:185067375 | C | G | 81 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0007 others(78): Show |
84 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-2-20177C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185067375 | |||||||
| chr1:185067444 | G | T | 2 | a0001c0001t0001g0246 a0001c0001t0008g0245 |
2 | HG00738.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-20108G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185067444 | |||||||
| chr1:185067600 | A | G | 9 | a0001c0001t0001g0104 a0001c0001t0001g0273 a0001c0001t0001g0275 others(6): Show |
9 | HG00621.hp1 HG02129.hp1 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2-19952A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185067600 | |||||||
| chr1:185067601 | G | A | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-2-19951G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185067601 | |||||||
| chr1:185067708 | C | CT | 21 | a0001c0001t0002g0038 a0001c0001t0003g0140 a0001c0001t0003g0148 others(18): Show |
21 | HG00408.hp2 HG00544.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.-2-19824dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185067708 | ||||||
| chr1:185067708 | CT | C | 80 | a0001c0001t0001g0053 a0001c0001t0001g0107 a0001c0001t0001g0193 others(77): Show |
82 | HG00438.hp2 HG00733.hp2 HG01099.hp1 others(79): Show |
intron_variant | MODIFIER | c.-2-19824delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185067708 | ||||||
| chr1:185067708 | CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0008g0005 a0001c0001t0008g0085 a0001c0001t0008g0086 others(4): Show |
8 | HG02647.hp2 HG02717.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-19833_-2-19824d others(12): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185067708 | ||||||
| chr1:185067744 | T | C | 3 | a0001c0001t0036g0257 a0001c0001t0037g0258 a0001c0001t0038g0259 |
3 | HG01884.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2-19808T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185067744 | |||||||
| chr1:185067831 | C | T | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-19721C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185067831 | |||||||
| chr1:185067833 | C | T | 3 | a0001c0001t0004g0287 a0001c0001t0008g0285 a0001c0001t0018g0284 |
3 | HG02145.hp1 HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-2-19719C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185067833 | |||||||
| chr1:185067898 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-2-19654A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185067898 | |||||||
| chr1:185068008 | CT | C | 301 | a0001c0001t0001g0012 a0001c0001t0001g0043 a0001c0001t0001g0045 others(298): Show |
315 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.-2-19532delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185068008 | ||||||
| chr1:185068048 | C | T | 1 | a0001c0001t0004g0123 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-2-19504C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185068048 | |||||||
| chr1:185068078 | G | A | 1 | a0001c0001t0003g0269 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-2-19474G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185068078 | |||||||
| chr1:185068113 | C | T | 3 | a0001c0001t0004g0287 a0001c0001t0008g0285 a0001c0001t0018g0284 |
3 | HG02145.hp1 HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-2-19439C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185068113 | |||||||
| chr1:185068515 | G | A | 1 | a0001c0001t0003g0141 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-2-19037G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185068515 | |||||||
| chr1:185068592 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-2-18960C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185068592 | |||||||
| chr1:185068654 | T | TATTG | 5 | a0001c0001t0001g0250 a0001c0001t0004g0241 a0001c0001t0004g0242 others(2): Show |
5 | HG02027.hp1 NA18612.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-18896_-2-18893d others(6): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185068654 | ||||||
| chr1:185068783 | A | G | 4 | a0001c0001t0004g0287 a0001c0001t0008g0285 a0001c0001t0018g0284 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-18769A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185068783 | |||||||
| chr1:185068828 | T | C | 1 | a0001c0001t0004g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-2-18724T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185068828 | |||||||
| chr1:185068962 | C | A | 1 | a0001c0001t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-2-18590C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185068962 | |||||||
| chr1:185068972 | C | T | 190 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(187): Show |
203 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-2-18580C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185068972 | |||||||
| chr1:185069092 | A | G | 1 | a0001c0001t0002g0021 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-2-18460A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185069092 | |||||||
| chr1:185069118 | T | C | 3 | a0001c0001t0004g0287 a0001c0001t0008g0285 a0001c0001t0018g0284 |
3 | HG02145.hp1 HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-2-18434T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185069118 | |||||||
| chr1:185069165 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-2-18387T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185069165 | |||||||
| chr1:185069223 | T | G | 1 | a0001c0001t0034g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-2-18329T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185069223 | |||||||
| chr1:185069456 | T | TA | 21 | a0001c0001t0001g0047 a0001c0001t0001g0091 a0001c0001t0001g0108 others(18): Show |
21 | HG01081.hp1 HG02071.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.-2-18077dupA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185069456 | ||||||
| chr1:185069456 | TA | T | 6 | a0001c0001t0001g0129 a0001c0001t0002g0033 a0001c0001t0002g0305 others(3): Show |
6 | HG01255.hp1 HG01256.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-18077delA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185069456 | ||||||
| chr1:185069469 | A | C | 1 | a0001c0001t0020g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-2-18083A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185069469 | |||||||
| chr1:185069475 | A | G | 2 | a0001c0001t0003g0052 a0001c0001t0003g0147 |
2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-2-18077A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185069475 | |||||||
| chr1:185069476 | GAA | G | 4 | a0001c0001t0003g0140 a0001c0001t0003g0155 a0001c0001t0003g0156 others(1): Show |
4 | HG02055.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-18074_-2-18073d others(4): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185069476 | ||||||
| chr1:185069524 | A | G | 1 | a0002c0002t0001g0126 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-2-18028A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185069524 | |||||||
| chr1:185069537 | G | A | 1 | a0002c0002t0001g0126 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-2-18015G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185069537 | |||||||
| chr1:185069705 | G | T | 1 | a0001c0001t0020g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-2-17847G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185069705 | |||||||
| chr1:185069751 | C | T | 1 | a0001c0001t0020g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-2-17801C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185069751 | |||||||
| chr1:185070065 | C | A | 1 | a0001c0001t0035g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-17487C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185070065 | |||||||
| chr1:185070091 | A | G | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-2-17461A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185070091 | |||||||
| chr1:185070638 | C | CT | 9 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0001g0122 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2-16896dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185070638 | ||||||
| chr1:185070638 | C | CTT | 10 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(7): Show |
10 | HG02071.hp2 HG03654.hp1 NA18964.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-16897_-2-16896d others(4): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185070638 | ||||||
| chr1:185070638 | CT | C | 39 | a0001c0001t0001g0201 a0001c0001t0002g0001 a0001c0001t0002g0003 others(36): Show |
47 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-2-16896delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185070638 | ||||||
| chr1:185070669 | T | C | 1 | a0001c0001t0024g0110 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-2-16883T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185070669 | |||||||
| chr1:185070675 | G | A | 1 | a0001c0001t0028g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2-16877G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185070675 | |||||||
| chr1:185070697 | G | T | 3 | a0001c0001t0004g0287 a0001c0001t0008g0285 a0001c0001t0018g0284 |
3 | HG02145.hp1 HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-2-16855G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185070697 | |||||||
| chr1:185070785 | C | T | 4 | a0001c0001t0022g0055 a0001c0001t0022g0057 a0001c0001t0023g0054 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-16767C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185070785 | |||||||
| chr1:185070786 | C | G | 4 | a0001c0001t0022g0055 a0001c0001t0022g0057 a0001c0001t0023g0054 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-16766C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185070786 | |||||||
| chr1:185070787 | C | T | 5 | a0001c0001t0004g0097 a0001c0001t0022g0055 a0001c0001t0022g0057 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-16765C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185070787 | |||||||
| chr1:185070798 | C | T | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-2-16754C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185070798 | |||||||
| chr1:185070838 | G | A | 7 | a0001c0001t0007g0199 a0001c0001t0007g0212 a0001c0001t0007g0213 others(4): Show |
7 | NA18962.hp2 NA18998.hp1 NA19002.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-16714G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185070838 | |||||||
| chr1:185070872 | G | T | 3 | a0001c0001t0003g0140 a0001c0001t0003g0155 a0001c0001t0006g0139 |
3 | HG02055.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-2-16680G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185070872 | |||||||
| chr1:185070879 | G | A | 2 | a0001c0001t0004g0241 a0001c0001t0004g0242 |
2 | NA18612.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-2-16673G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185070879 | |||||||
| chr1:185070933 | G | A | 80 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0007 others(77): Show |
83 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-2-16619G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185070933 | |||||||
| chr1:185071162 | A | T | 1 | a0001c0001t0003g0196 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-2-16390A>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185071162 | |||||||
| chr1:185071314 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-2-16238C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185071314 | |||||||
| chr1:185071326 | T | C | 4 | a0001c0001t0004g0198 a0001c0001t0004g0282 a0001c0001t0013g0135 others(1): Show |
4 | HG01433.hp2 HG01515.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-16226T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185071326 | |||||||
| chr1:185071392 | ATTG | A | 3 | a0001c0001t0004g0287 a0001c0001t0008g0285 a0001c0001t0018g0284 |
3 | HG02145.hp1 HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-2-16155_-2-16153d others(5): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185071392 | ||||||
| chr1:185071462 | G | A | 1 | a0001c0001t0030g0027 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-2-16090G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185071462 | |||||||
| chr1:185071529 | G | A | 1 | a0001c0001t0009g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-2-16023G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185071529 | |||||||
| chr1:185071529 | G | C | 1 | a0001c0001t0002g0028 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-2-16023G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185071529 | |||||||
| chr1:185071657 | G | A | 6 | a0001c0001t0020g0256 a0001c0001t0031g0260 a0001c0001t0035g0255 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-15895G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185071657 | |||||||
| chr1:185071895 | C | G | 3 | a0001c0001t0003g0002 a0001c0001t0010g0002 a0001c0001t0010g0289 |
4 | HG02559.hp2 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-15657C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185071895 | |||||||
| chr1:185071920 | C | T | 5 | a0001c0001t0020g0256 a0001c0001t0031g0260 a0001c0001t0036g0257 others(2): Show |
5 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-15632C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185071920 | |||||||
| chr1:185071978 | A | C | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-15574A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185071978 | |||||||
| chr1:185072061 | A | C | 1 | a0001c0001t0003g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-2-15491A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185072061 | |||||||
| chr1:185072064 | A | T | 1 | a0001c0001t0034g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-2-15488A>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185072064 | |||||||
| chr1:185072065 | T | G | 1 | a0001c0001t0034g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-2-15487T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185072065 | |||||||
| chr1:185072149 | G | A | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-15403G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185072149 | |||||||
| chr1:185072207 | C | T | 1 | a0001c0001t0002g0040 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-2-15345C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185072207 | |||||||
| chr1:185072240 | G | T | 8 | a0001c0001t0001g0053 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG01099.hp1 HG01123.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-15312G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185072240 | |||||||
| chr1:185072343 | T | G | 1 | a0001c0001t0005g0306 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-2-15209T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185072343 | |||||||
| chr1:185072498 | A | G | 83 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
93 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-2-15054A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185072498 | |||||||
| chr1:185072685 | A | G | 34 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(31): Show |
42 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.-2-14867A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185072685 | |||||||
| chr1:185072711 | C | T | 1 | a0001c0001t0004g0125 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-2-14841C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185072711 | |||||||
| chr1:185072933 | C | G | 1 | a0001c0001t0035g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-14619C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185072933 | |||||||
| chr1:185073059 | CT | C | 176 | a0001c0001t0001g0091 a0001c0001t0002g0001 a0001c0001t0002g0003 others(173): Show |
189 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.-2-14477delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185073059 | ||||||
| chr1:185073091 | T | G | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-14461T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185073091 | |||||||
| chr1:185073151 | A | G | 1 | a0001c0001t0003g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-2-14401A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185073151 | |||||||
| chr1:185073197 | T | C | 1 | a0001c0001t0008g0086 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-2-14355T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185073197 | |||||||
| chr1:185073268 | T | G | 83 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
93 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-2-14284T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185073268 | |||||||
| chr1:185073303 | T | A | 1 | a0001c0001t0003g0271 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-2-14249T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185073303 | |||||||
| chr1:185073437 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0111 |
2 | HG01361.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-2-14115T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185073437 | |||||||
| chr1:185073579 | C | T | 96 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(93): Show |
106 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-2-13973C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185073579 | |||||||
| chr1:185073636 | A | G | 1 | a0001c0001t0034g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-2-13916A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185073636 | |||||||
| chr1:185073768 | A | G | 1 | a0001c0001t0034g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-2-13784A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185073768 | |||||||
| chr1:185073823 | A | G | 83 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
93 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-2-13729A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185073823 | |||||||
| chr1:185073923 | G | A | 9 | a0001c0001t0008g0005 a0001c0001t0008g0085 a0001c0001t0008g0086 others(6): Show |
10 | HG02258.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-13629G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185073923 | |||||||
| chr1:185073959 | G | A | 1 | a0001c0001t0002g0308 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-2-13593G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185073959 | |||||||
| chr1:185073978 | A | T | 1 | a0001c0001t0034g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-2-13574A>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185073978 | |||||||
| chr1:185074000 | A | G | 2 | a0001c0001t0012g0153 a0001c0001t0012g0154 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-2-13552A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185074000 | |||||||
| chr1:185074020 | A | T | 2 | a0001c0001t0003g0330 a0001c0001t0006g0329 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-2-13532A>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185074020 | |||||||
| chr1:185074459 | A | G | 1 | a0001c0001t0004g0130 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-2-13093A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185074459 | |||||||
| chr1:185074690 | T | C | 4 | a0001c0001t0031g0260 a0001c0001t0036g0257 a0001c0001t0037g0258 others(1): Show |
4 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-12862T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185074690 | |||||||
| chr1:185074815 | G | T | 1 | a0001c0001t0001g0012 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-2-12737G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185074815 | |||||||
| chr1:185074817 | T | C | 1 | a0001c0001t0001g0012 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-2-12735T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185074817 | |||||||
| chr1:185074982 | C | T | 3 | a0001c0001t0003g0002 a0001c0001t0010g0002 a0001c0001t0010g0289 |
4 | HG02559.hp2 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-12570C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185074982 | |||||||
| chr1:185075046 | A | G | 1 | a0001c0001t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-2-12506A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185075046 | |||||||
| chr1:185075078 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-2-12474T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185075078 | |||||||
| chr1:185075517 | G | A | 1 | a0001c0001t0005g0014 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-2-12035G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185075517 | |||||||
| chr1:185075572 | A | G | 2 | a0001c0001t0012g0153 a0001c0001t0012g0154 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-2-11980A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185075572 | |||||||
| chr1:185075646 | A | G | 2 | a0001c0001t0003g0079 a0001c0001t0003g0083 |
2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-2-11906A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185075646 | |||||||
| chr1:185075656 | A | C | 1 | a0001c0001t0026g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-2-11896A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185075656 | |||||||
| chr1:185075741 | AG | A | 6 | a0001c0001t0020g0256 a0001c0001t0031g0260 a0001c0001t0035g0255 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-11806delG | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185075741 | ||||||
| chr1:185075803 | A | T | 3 | a0001c0001t0004g0130 a0001c0001t0004g0133 a0001c0001t0004g0134 |
3 | NA18951.hp1 NA18990.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-2-11749A>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185075803 | |||||||
| chr1:185075871 | C | T | 4 | a0001c0001t0003g0008 a0001c0001t0003g0170 a0001c0001t0003g0171 others(1): Show |
5 | HG00323.hp1 HG00639.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-11681C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185075871 | |||||||
| chr1:185076197 | C | G | 1 | a0001c0001t0004g0251 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-2-11355C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076197 | |||||||
| chr1:185076268 | G | GT | 26 | a0001c0001t0001g0047 a0001c0001t0001g0094 a0001c0001t0001g0108 others(23): Show |
26 | HG00738.hp2 HG01123.hp2 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.-2-11244dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTT | 21 | a0001c0001t0001g0012 a0001c0001t0001g0101 a0001c0001t0001g0112 others(18): Show |
22 | HG00438.hp2 HG00639.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-2-11245_-2-11244d others(4): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTT | 20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0003g0008 others(17): Show |
21 | HG00639.hp1 HG00741.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-2-11246_-2-11244d others(5): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTT | 7 | a0001c0001t0001g0118 a0001c0001t0001g0276 a0001c0001t0003g0176 others(4): Show |
7 | HG01433.hp1 HG01952.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-11247_-2-11244d others(6): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTT | 12 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0207 others(9): Show |
12 | HG01891.hp1 HG01928.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-11248_-2-11244d others(7): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT | 7 | a0001c0001t0001g0102 a0001c0001t0003g0165 a0001c0001t0004g0130 others(4): Show |
7 | HG00558.hp2 HG01255.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-11250_-2-11244d others(9): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(2): Show |
8 | a0001c0001t0001g0107 a0001c0001t0003g0166 a0001c0001t0004g0097 others(5): Show |
8 | HG00621.hp2 HG01168.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-11252_-2-11244d others(11): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(3): Show |
6 | a0001c0001t0002g0298 a0001c0001t0003g0167 a0001c0001t0003g0173 others(3): Show |
6 | HG00733.hp1 HG01169.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-11253_-2-11244d others(12): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(4): Show |
6 | a0001c0001t0002g0299 a0001c0001t0002g0309 a0001c0001t0006g0139 others(3): Show |
6 | HG01167.hp2 HG01361.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-11254_-2-11244d others(13): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(5): Show |
6 | a0001c0001t0003g0286 a0001c0001t0004g0133 a0001c0001t0004g0200 others(3): Show |
6 | HG02280.hp2 HG02622.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-11255_-2-11244d others(14): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(6): Show |
3 | a0001c0001t0005g0293 a0001c0001t0006g0182 a0001c0001t0011g0301 |
3 | HG01952.hp2 HG02258.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-2-11256_-2-11244d others(15): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(7): Show |
4 | a0001c0001t0001g0043 a0001c0001t0003g0161 a0001c0001t0004g0044 others(1): Show |
4 | HG00609.hp2 HG01081.hp1 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-11257_-2-11244d others(16): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(8): Show |
3 | a0001c0001t0005g0311 a0001c0001t0005g0324 a0001c0001t0007g0225 |
3 | HG01975.hp1 HG01975.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.-2-11258_-2-11244d others(17): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(9): Show |
2 | a0001c0001t0003g0083 a0001c0001t0005g0325 |
2 | HG02717.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-2-11259_-2-11244d others(18): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(10): Show |
4 | a0001c0001t0003g0140 a0001c0001t0003g0155 a0001c0001t0004g0238 others(1): Show |
4 | HG01261.hp1 HG01346.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-11260_-2-11244d others(19): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(12): Show |
3 | a0001c0001t0002g0313 a0001c0001t0004g0134 a0001c0001t0005g0034 |
3 | HG01943.hp2 NA18990.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-2-11262_-2-11244d others(21): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(13): Show |
3 | a0001c0001t0003g0196 a0001c0001t0004g0132 a0001c0001t0005g0323 |
3 | HG02523.hp1 NA18964.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-2-11263_-2-11244d others(22): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(14): Show |
3 | a0001c0001t0002g0312 a0001c0001t0010g0190 a0002c0002t0001g0126 |
3 | HG01255.hp1 HG02559.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-2-11264_-2-11244d others(23): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(16): Show |
2 | a0001c0001t0002g0302 a0001c0001t0012g0191 |
2 | HG00733.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-2-11266_-2-11244d others(25): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(17): Show |
1 | a0001c0001t0006g0168 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-2-11267_-2-11244d others(26): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(18): Show |
1 | a0001c0001t0004g0239 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-2-11268_-2-11244d others(27): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(28): Show |
1 | a0001c0001t0010g0169 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-2-11278_-2-11244d others(37): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | GTTTTTTT others(34): Show |
2 | a0001c0001t0003g0330 a0001c0001t0014g0183 |
2 | HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-2-11244_-2-11243i others(43): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | G | T | 1 | a0001c0001t0015g0197 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-2-11284G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076268 | |||||||
| chr1:185076268 | GT | G | 18 | a0001c0001t0001g0128 a0001c0001t0001g0201 a0001c0001t0001g0202 others(15): Show |
18 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2-11244delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTT | G | 5 | a0001c0001t0002g0009 a0001c0001t0003g0148 a0001c0001t0004g0092 others(2): Show |
6 | HG02615.hp2 HG02886.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-11245_-2-11244d others(4): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(3): Show |
G | 4 | a0001c0001t0004g0198 a0001c0001t0009g0067 a0001c0001t0009g0078 others(1): Show |
4 | HG02258.hp2 HG03654.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-11253_-2-11244d others(12): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(4): Show |
G | 13 | a0001c0001t0004g0282 a0001c0001t0009g0069 a0001c0001t0009g0070 others(10): Show |
13 | HG01433.hp2 HG01515.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-2-11254_-2-11244d others(13): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(5): Show |
G | 5 | a0001c0001t0008g0090 a0001c0001t0008g0285 a0001c0001t0018g0284 others(2): Show |
5 | HG02145.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-11255_-2-11244d others(14): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(6): Show |
G | 11 | a0001c0001t0001g0091 a0001c0001t0003g0052 a0001c0001t0003g0147 others(8): Show |
12 | HG00544.hp1 HG02717.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-11256_-2-11244d others(15): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(7): Show |
G | 2 | a0001c0001t0004g0124 a0001c0001t0004g0125 |
2 | HG00408.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-2-11257_-2-11244d others(16): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(8): Show |
G | 9 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0129 others(6): Show |
9 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-11258_-2-11244d others(17): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(9): Show |
G | 6 | a0001c0001t0001g0045 a0001c0001t0001g0063 a0001c0001t0001g0064 others(3): Show |
6 | HG02572.hp2 HG02738.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-11259_-2-11244d others(18): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(11): Show |
G | 3 | a0001c0001t0002g0025 a0001c0001t0002g0042 a0001c0001t0017g0217 |
3 | HG00408.hp1 HG02300.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.-2-11261_-2-11244d others(20): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(12): Show |
G | 32 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(29): Show |
40 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.-2-11262_-2-11244d others(21): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(13): Show |
G | 1 | a0001c0001t0004g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-2-11263_-2-11244d others(22): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(14): Show |
G | 1 | a0001c0001t0010g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-2-11264_-2-11244d others(23): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(15): Show |
G | 6 | a0001c0001t0002g0010 a0001c0001t0002g0308 a0001c0001t0002g0320 others(3): Show |
8 | HG01258.hp1 HG02723.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-11265_-2-11244d others(24): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(16): Show |
G | 20 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0141 others(17): Show |
20 | HG00738.hp1 HG01070.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-2-11266_-2-11244d others(25): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076268 | GTTTTTTT others(18): Show |
G | 1 | a0001c0001t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-2-11268_-2-11244d others(27): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076268 | ||||||
| chr1:185076279 | T | G | 1 | a0001c0001t0028g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2-11273T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076279 | |||||||
| chr1:185076280 | T | G | 1 | a0001c0001t0013g0240 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-2-11272T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076280 | |||||||
| chr1:185076285 | T | G | 2 | a0001c0001t0009g0067 a0001c0001t0009g0078 |
2 | HG03654.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-2-11267T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076285 | |||||||
| chr1:185076286 | T | G | 10 | a0001c0001t0009g0069 a0001c0001t0009g0070 a0001c0001t0009g0072 others(7): Show |
10 | HG02071.hp2 NA18949.hp1 NA18964.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-11266T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076286 | |||||||
| chr1:185076297 | T | G | 1 | a0001c0001t0028g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2-11255T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076297 | |||||||
| chr1:185076556 | G | A | 1 | a0001c0001t0011g0296 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-2-10996G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076556 | |||||||
| chr1:185076581 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-2-10971C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076581 | |||||||
| chr1:185076596 | G | GT | 9 | a0001c0001t0001g0096 a0001c0001t0004g0092 a0001c0001t0004g0242 others(6): Show |
9 | HG00438.hp1 HG01175.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-10945dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076596 | ||||||
| chr1:185076596 | GT | G | 8 | a0001c0001t0003g0052 a0001c0001t0003g0147 a0001c0001t0020g0256 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-10945delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185076596 | ||||||
| chr1:185076597 | T | G | 2 | a0001c0001t0003g0079 a0001c0001t0003g0083 |
2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-2-10955T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076597 | |||||||
| chr1:185076622 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-2-10930A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076622 | |||||||
| chr1:185076676 | T | A | 83 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
93 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-2-10876T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076676 | |||||||
| chr1:185076725 | A | G | 1 | a0001c0001t0028g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2-10827A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076725 | |||||||
| chr1:185076729 | G | A | 1 | a0001c0001t0003g0146 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-2-10823G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076729 | |||||||
| chr1:185076987 | A | G | 1 | a0001c0001t0021g0076 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-2-10565A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185076987 | |||||||
| chr1:185077068 | C | T | 1 | a0001c0001t0012g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2-10484C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185077068 | |||||||
| chr1:185077144 | AT | A | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-10400delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185077144 | ||||||
| chr1:185077152 | T | A | 1 | a0001c0001t0018g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-2-10400T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185077152 | |||||||
| chr1:185077396 | G | T | 1 | a0001c0001t0003g0163 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-2-10156G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185077396 | |||||||
| chr1:185077442 | T | G | 82 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(79): Show |
92 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.-2-10110T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185077442 | |||||||
| chr1:185077452 | G | A | 3 | a0001c0001t0036g0257 a0001c0001t0037g0258 a0001c0001t0038g0259 |
3 | HG01884.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2-10100G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185077452 | |||||||
| chr1:185077625 | G | GT | 16 | a0001c0001t0001g0047 a0001c0001t0003g0146 a0001c0001t0004g0130 others(13): Show |
17 | HG02056.hp1 HG02647.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.-2-9914dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185077625 | ||||||
| chr1:185077625 | G | GTTTTTTT | 68 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(65): Show |
77 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-2-9920_-2-9914dup others(7): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185077625 | ||||||
| chr1:185077625 | G | GTTTTTTT others(1): Show |
13 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0024 others(10): Show |
14 | HG00408.hp1 HG01192.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-2-9921_-2-9914dup others(8): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185077625 | ||||||
| chr1:185077625 | G | GTTTTTTT others(9): Show |
3 | a0001c0001t0036g0257 a0001c0001t0037g0258 a0001c0001t0038g0259 |
3 | HG01884.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2-9915_-2-9914ins others(16): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185077625 | ||||||
| chr1:185077625 | G | GTTTTTTT others(8): Show |
2 | a0001c0001t0034g0187 a0001c0001t0035g0255 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-2-9914_-2-9913ins others(15): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185077625 | ||||||
| chr1:185077625 | G | GTTTTTTT others(10): Show |
2 | a0001c0001t0004g0287 a0001c0001t0018g0284 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-2-9914_-2-9913ins others(17): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185077625 | ||||||
| chr1:185077625 | G | GTTTTTTT others(12): Show |
1 | a0001c0001t0008g0285 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-2-9914_-2-9913ins others(19): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185077625 | ||||||
| chr1:185077641 | C | T | 2 | a0001c0001t0008g0088 a0001c0001t0008g0089 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-2-9911C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185077641 | |||||||
| chr1:185077715 | G | GT | 13 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(10): Show |
13 | HG02071.hp2 HG02109.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2-9825dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185077715 | ||||||
| chr1:185077720 | T | G | 1 | a0001c0001t0002g0036 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-2-9832T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185077720 | |||||||
| chr1:185077727 | T | G | 1 | a0001c0001t0002g0309 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-2-9825T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185077727 | |||||||
| chr1:185077817 | T | G | 1 | a0001c0001t0003g0144 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-2-9735T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185077817 | |||||||
| chr1:185077968 | G | A | 2 | a0001c0001t0009g0077 a0001c0001t0009g0078 |
2 | NA18973.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.-2-9584G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185077968 | |||||||
| chr1:185078108 | G | A | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-2-9444G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185078108 | |||||||
| chr1:185078161 | C | T | 4 | a0001c0001t0022g0055 a0001c0001t0022g0057 a0001c0001t0023g0054 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-9391C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185078161 | |||||||
| chr1:185078544 | A | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG03688.hp1 HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-2-9008A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185078544 | |||||||
| chr1:185078720 | G | A | 1 | a0001c0001t0006g0172 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-2-8832G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185078720 | |||||||
| chr1:185078958 | C | T | 4 | a0001c0001t0004g0287 a0001c0001t0008g0285 a0001c0001t0018g0284 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-8594C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185078958 | |||||||
| chr1:185079079 | C | CT | 24 | a0001c0001t0002g0030 a0001c0001t0002g0039 a0001c0001t0003g0080 others(21): Show |
24 | HG00323.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.-2-8458dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185079079 | ||||||
| chr1:185079079 | C | CTT | 78 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(75): Show |
88 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-2-8459_-2-8458dup others(2): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185079079 | ||||||
| chr1:185079132 | T | G | 3 | a0001c0001t0007g0214 a0001c0001t0007g0215 a0001c0001t0007g0216 |
3 | NA18998.hp1 NA19002.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-2-8420T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185079132 | |||||||
| chr1:185079594 | T | C | 1 | a0001c0001t0004g0228 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-2-7958T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185079594 | |||||||
| chr1:185079623 | G | A | 61 | a0001c0001t0001g0012 a0001c0001t0001g0043 a0001c0001t0001g0047 others(58): Show |
62 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-2-7929G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185079623 | |||||||
| chr1:185079665 | C | A | 3 | a0001c0001t0003g0002 a0001c0001t0010g0002 a0001c0001t0010g0289 |
4 | HG02559.hp2 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-7887C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185079665 | |||||||
| chr1:185079684 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-2-7868C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185079684 | |||||||
| chr1:185079704 | C | T | 1 | a0001c0001t0003g0174 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-2-7848C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185079704 | |||||||
| chr1:185079757 | C | T | 1 | a0001c0001t0006g0267 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-2-7795C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185079757 | |||||||
| chr1:185079782 | A | G | 1 | a0001c0001t0002g0019 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-2-7770A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185079782 | |||||||
| chr1:185079943 | G | A | 79 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
82 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-2-7609G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185079943 | |||||||
| chr1:185080000 | C | T | 4 | a0001c0001t0002g0009 a0001c0001t0002g0303 a0001c0001t0002g0304 others(1): Show |
5 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-7552C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185080000 | |||||||
| chr1:185080211 | G | A | 4 | a0001c0001t0006g0150 a0001c0001t0006g0151 a0001c0001t0006g0152 others(1): Show |
4 | HG01192.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-7341G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185080211 | |||||||
| chr1:185080225 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-2-7327A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185080225 | |||||||
| chr1:185080242 | A | G | 1 | a0001c0001t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-2-7310A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185080242 | |||||||
| chr1:185080392 | T | G | 1 | a0001c0001t0002g0030 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-2-7160T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185080392 | |||||||
| chr1:185080662 | A | G | 2 | a0001c0001t0002g0291 a0001c0001t0005g0290 |
2 | HG02056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-2-6890A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185080662 | |||||||
| chr1:185080823 | A | G | 1 | a0001c0001t0004g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-2-6729A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185080823 | |||||||
| chr1:185080867 | A | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0320 |
3 | HG02723.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-2-6685A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185080867 | |||||||
| chr1:185080901 | G | A | 8 | a0001c0001t0008g0005 a0001c0001t0008g0085 a0001c0001t0008g0086 others(5): Show |
9 | HG02647.hp2 HG02717.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2-6651G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185080901 | |||||||
| chr1:185081039 | G | A | 1 | a0001c0001t0031g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-2-6513G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081039 | |||||||
| chr1:185081041 | A | G | 1 | a0001c0001t0005g0293 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-2-6511A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081041 | |||||||
| chr1:185081113 | A | C | 1 | a0001c0001t0015g0197 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-2-6439A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081113 | |||||||
| chr1:185081122 | A | C | 1 | a0001c0001t0016g0281 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2-6430A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081122 | |||||||
| chr1:185081184 | G | A | 1 | a0001c0001t0005g0014 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-2-6368G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081184 | |||||||
| chr1:185081315 | T | C | 1 | a0001c0001t0020g0058 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-2-6237T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081315 | |||||||
| chr1:185081358 | A | G | 1 | a0001c0001t0004g0227 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-2-6194A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081358 | |||||||
| chr1:185081395 | AT | A | 151 | a0001c0001t0001g0012 a0001c0001t0001g0043 a0001c0001t0001g0045 others(148): Show |
152 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.-2-6142delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185081395 | ||||||
| chr1:185081396 | T | A | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-2-6156T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081396 | |||||||
| chr1:185081423 | C | T | 6 | a0001c0001t0020g0256 a0001c0001t0031g0260 a0001c0001t0035g0255 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-6129C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081423 | |||||||
| chr1:185081552 | C | T | 1 | a0001c0001t0035g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-6000C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081552 | |||||||
| chr1:185081591 | T | TG | 35 | a0001c0001t0001g0043 a0001c0001t0001g0108 a0001c0001t0001g0209 others(32): Show |
35 | HG00609.hp2 HG00738.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.-2-5952dupG | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185081591 | ||||||
| chr1:185081591 | TG | T | 37 | a0001c0001t0003g0008 a0001c0001t0003g0079 a0001c0001t0003g0080 others(34): Show |
39 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.-2-5952delG | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185081591 | ||||||
| chr1:185081703 | C | T | 4 | a0001c0001t0003g0179 a0001c0001t0006g0181 a0001c0001t0006g0182 others(1): Show |
4 | HG01099.hp2 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-5849C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081703 | |||||||
| chr1:185081823 | C | G | 5 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(2): Show |
5 | NA18971.hp1 NA18977.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-5729C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081823 | |||||||
| chr1:185081829 | G | A | 34 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(31): Show |
42 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.-2-5723G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081829 | |||||||
| chr1:185081985 | G | A | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-2-5567G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185081985 | |||||||
| chr1:185082007 | C | T | 1 | a0001c0001t0007g0199 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-2-5545C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185082007 | |||||||
| chr1:185082114 | T | C | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-5438T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185082114 | |||||||
| chr1:185082345 | C | CTT | 63 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(60): Show |
71 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-2-5186_-2-5185dup others(2): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTT | 22 | a0001c0001t0001g0094 a0001c0001t0002g0009 a0001c0001t0002g0010 others(19): Show |
24 | HG01928.hp1 HG02055.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.-2-5187_-2-5185dup others(3): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTT | 6 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0226 others(3): Show |
6 | HG01069.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-5189_-2-5185dup others(5): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTT | 13 | a0001c0001t0001g0012 a0001c0001t0004g0050 a0001c0001t0009g0069 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-5190_-2-5185dup others(6): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0001g0111 a0001c0001t0007g0212 a0001c0001t0007g0218 others(2): Show |
5 | HG03098.hp2 HG03486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-5194_-2-5185dup others(10): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0015g0233 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-2-5195_-2-5185dup others(11): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0273 a0001c0001t0004g0274 a0001c0001t0007g0220 |
3 | HG02071.hp1 NA19011.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-2-5196_-2-5185dup others(12): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0328 a0001c0001t0004g0211 a0001c0001t0027g0219 others(1): Show |
4 | HG02109.hp2 HG02523.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-5197_-2-5185dup others(13): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0004g0243 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-2-5198_-2-5185dup others(14): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0118 a0001c0001t0007g0225 |
2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-2-5199_-2-5185dup others(15): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(9): Show |
3 | a0001c0001t0004g0131 a0001c0001t0004g0244 a0001c0001t0013g0240 |
3 | HG02080.hp1 HG02165.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.-2-5200_-2-5185dup others(16): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0004g0210 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-2-5201_-2-5185dup others(17): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(12): Show |
8 | a0001c0001t0001g0049 a0001c0001t0001g0091 a0001c0001t0001g0101 others(5): Show |
8 | HG00639.hp2 HG01106.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-5203_-2-5185dup others(19): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(13): Show |
11 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0114 others(8): Show |
11 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-5204_-2-5185dup others(20): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(14): Show |
5 | a0001c0001t0004g0100 a0001c0001t0004g0105 a0001c0001t0004g0106 others(2): Show |
5 | HG01978.hp1 HG02040.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-5205_-2-5185dup others(21): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(15): Show |
5 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0093 others(2): Show |
5 | HG00609.hp2 HG01361.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-5206_-2-5185dup others(22): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0193 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(23): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(17): Show |
5 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0004g0200 others(2): Show |
5 | HG01433.hp2 HG02056.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(24): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(18): Show |
8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0084 others(5): Show |
8 | HG00438.hp1 HG01081.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(25): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(19): Show |
5 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0001t0001g0120 others(2): Show |
5 | HG02293.hp1 NA18998.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(26): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(20): Show |
2 | a0001c0001t0004g0092 a0001c0001t0007g0215 |
2 | NA18942.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(27): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(21): Show |
4 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0209 others(1): Show |
4 | HG01175.hp1 HG02132.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(28): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(23): Show |
5 | a0001c0001t0001g0098 a0001c0001t0004g0132 a0001c0001t0004g0134 others(2): Show |
5 | HG01168.hp2 HG03239.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(30): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(24): Show |
2 | a0001c0001t0004g0044 a0001c0001t0007g0213 |
2 | HG02027.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(31): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(25): Show |
2 | a0001c0001t0007g0252 a0001c0001t0013g0135 |
2 | HG02486.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(32): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0017g0223 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(33): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(27): Show |
2 | a0001c0001t0001g0095 a0001c0001t0004g0195 |
2 | HG00741.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(34): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(28): Show |
1 | a0001c0001t0004g0133 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(35): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(29): Show |
2 | a0001c0001t0004g0277 a0001c0001t0016g0281 |
2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(36): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(30): Show |
2 | a0001c0001t0008g0245 a0001c0001t0025g0280 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(37): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(31): Show |
1 | a0001c0001t0016g0278 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(38): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(32): Show |
1 | a0001c0001t0001g0064 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(39): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(33): Show |
1 | a0001c0001t0004g0272 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(40): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(34): Show |
2 | a0001c0001t0001g0112 a0001c0001t0004g0238 |
2 | HG01346.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(41): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(35): Show |
1 | a0001c0001t0013g0237 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(42): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(36): Show |
1 | a0001c0001t0004g0241 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(43): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(37): Show |
1 | a0001c0001t0015g0197 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(44): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(40): Show |
1 | a0001c0001t0001g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(47): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(42): Show |
1 | a0001c0001t0001g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(49): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(45): Show |
1 | a0001c0001t0020g0058 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(52): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | C | CTTTTTTT others(48): Show |
1 | a0001c0001t0004g0242 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(55): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | CT | C | 12 | a0001c0001t0001g0053 a0001c0001t0001g0201 a0001c0001t0001g0202 others(9): Show |
12 | HG01074.hp1 HG01099.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-5185delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | CTTT | C | 6 | a0001c0001t0003g0140 a0001c0001t0003g0160 a0001c0001t0003g0249 others(3): Show |
6 | HG01192.hp2 HG02055.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-5187_-2-5185del others(3): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082345 | CTTTT | C | 85 | a0001c0001t0001g0107 a0001c0001t0003g0002 a0001c0001t0003g0006 others(82): Show |
88 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.-2-5188_-2-5185del others(4): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082345 | ||||||
| chr1:185082364 | T | TTTTTTTT others(38): Show |
1 | a0001c0001t0001g0246 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(45): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082364 | ||||||
| chr1:185082366 | T | TTTTTTTT others(17): Show |
1 | a0001c0001t0001g0276 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(24): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082366 | ||||||
| chr1:185082367 | T | G | 2 | a0001c0001t0008g0285 a0001c0001t0018g0284 |
2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-2-5185T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185082367 | |||||||
| chr1:185082367 | T | TTTTTTTT others(4): Show |
1 | a0001c0001t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-2-5185_-2-5184ins others(11): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185082367 | |||||||
| chr1:185082414 | G | A | 1 | a0001c0001t0009g0072 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-2-5138G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185082414 | |||||||
| chr1:185082454 | G | A | 1 | a0001c0001t0003g0184 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-2-5098G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185082454 | |||||||
| chr1:185082524 | A | AT | 9 | a0001c0001t0003g0179 a0001c0001t0003g0184 a0001c0001t0006g0178 others(6): Show |
9 | HG01099.hp2 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-5018dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082524 | ||||||
| chr1:185082524 | AT | A | 78 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(75): Show |
88 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-2-5018delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185082524 | ||||||
| chr1:185082583 | G | T | 2 | a0001c0001t0001g0043 a0001c0001t0004g0044 |
2 | HG00609.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.-2-4969G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185082583 | |||||||
| chr1:185082645 | G | T | 1 | a0001c0001t0001g0012 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-2-4907G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185082645 | |||||||
| chr1:185082695 | C | T | 1 | a0001c0001t0037g0258 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-2-4857C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185082695 | |||||||
| chr1:185082807 | T | C | 18 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(15): Show |
18 | HG01884.hp1 HG01891.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-2-4745T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185082807 | |||||||
| chr1:185082822 | C | A | 1 | a0001c0001t0006g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-2-4730C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185082822 | |||||||
| chr1:185082873 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-2-4679A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185082873 | |||||||
| chr1:185082971 | A | C | 3 | a0001c0001t0005g0318 a0001c0001t0005g0319 a0001c0001t0019g0317 |
3 | NA18967.hp1 NA19066.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-2-4581A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185082971 | |||||||
| chr1:185083295 | C | T | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-2-4257C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185083295 | |||||||
| chr1:185083510 | T | C | 1 | a0001c0001t0020g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-2-4042T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185083510 | |||||||
| chr1:185083525 | G | T | 1 | a0001c0001t0003g0083 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-2-4027G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185083525 | |||||||
| chr1:185083663 | G | A | 1 | a0001c0001t0035g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-3889G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185083663 | |||||||
| chr1:185083858 | C | T | 2 | a0001c0001t0003g0052 a0001c0001t0003g0147 |
2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-2-3694C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185083858 | |||||||
| chr1:185083910 | C | CT | 6 | a0001c0001t0002g0039 a0001c0001t0002g0307 a0001c0001t0005g0016 others(3): Show |
6 | HG00323.hp2 HG01361.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-3626dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185083910 | ||||||
| chr1:185083910 | C | CTT | 11 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(8): Show |
11 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-3627_-2-3626dup others(2): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185083910 | ||||||
| chr1:185083939 | T | TA | 7 | a0001c0001t0004g0092 a0001c0001t0020g0256 a0001c0001t0024g0110 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-3596dupA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185083939 | ||||||
| chr1:185083939 | TA | T | 15 | a0001c0001t0002g0024 a0001c0001t0002g0039 a0001c0001t0003g0143 others(12): Show |
15 | HG00323.hp2 HG01169.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2-3596delA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185083939 | ||||||
| chr1:185084144 | A | G | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-3408A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185084144 | |||||||
| chr1:185084217 | G | GTCT | 19 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(16): Show |
19 | HG01884.hp1 HG01891.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-2-3331_-2-3329dup others(3): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185084217 | ||||||
| chr1:185084231 | T | C | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-3321T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185084231 | |||||||
| chr1:185084559 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0004g0116 |
2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-2-2993A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185084559 | |||||||
| chr1:185084812 | CAA | C | 6 | a0001c0001t0020g0256 a0001c0001t0031g0260 a0001c0001t0035g0255 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-2739_-2-2738del others(2): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185084812 | |||||||
| chr1:185084942 | A | T | 1 | a0001c0001t0003g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-2-2610A>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185084942 | |||||||
| chr1:185085013 | G | T | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-2539G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085013 | |||||||
| chr1:185085031 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-2-2521C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085031 | |||||||
| chr1:185085058 | C | T | 1 | a0001c0001t0005g0324 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-2-2494C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085058 | |||||||
| chr1:185085103 | T | A | 1 | a0001c0001t0009g0078 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-2-2449T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085103 | |||||||
| chr1:185085145 | C | CT | 24 | a0001c0001t0001g0045 a0001c0001t0001g0098 a0001c0001t0001g0113 others(21): Show |
24 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.-2-2386dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185085145 | ||||||
| chr1:185085145 | C | CTT | 49 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0079 others(46): Show |
52 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.-2-2387_-2-2386dup others(2): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185085145 | ||||||
| chr1:185085145 | C | CTTT | 15 | a0001c0001t0003g0007 a0001c0001t0003g0147 a0001c0001t0003g0158 others(12): Show |
15 | HG01070.hp2 HG01099.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2-2388_-2-2386dup others(3): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185085145 | ||||||
| chr1:185085145 | C | CTTTT | 22 | a0001c0001t0003g0006 a0001c0001t0003g0013 a0001c0001t0003g0052 others(19): Show |
22 | HG01081.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.-2-2389_-2-2386dup others(4): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185085145 | ||||||
| chr1:185085145 | CT | C | 87 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0002g0001 others(84): Show |
97 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-2-2386delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185085145 | ||||||
| chr1:185085209 | C | T | 1 | a0001c0001t0015g0233 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-2-2343C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085209 | |||||||
| chr1:185085258 | C | A | 2 | a0001c0001t0003g0013 a0001c0001t0003g0148 |
2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-2-2294C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085258 | |||||||
| chr1:185085308 | C | A | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-2244C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085308 | |||||||
| chr1:185085334 | G | C | 1 | a0001c0001t0004g0123 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-2-2218G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085334 | |||||||
| chr1:185085452 | T | C | 2 | a0001c0001t0008g0285 a0001c0001t0018g0284 |
2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-2-2100T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085452 | |||||||
| chr1:185085539 | A | G | 1 | a0001c0003t0004g0247 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-2-2013A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085539 | |||||||
| chr1:185085546 | TTTTTAAC others(3): Show |
T | 1 | a0001c0001t0005g0306 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-2-2002_-2-1993del others(10): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 185085546 | ||||||
| chr1:185085555 | A | G | 85 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0007 others(82): Show |
87 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.-2-1997A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085555 | |||||||
| chr1:185085570 | T | C | 2 | a0001c0001t0008g0285 a0001c0001t0018g0284 |
2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-2-1982T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085570 | |||||||
| chr1:185085592 | G | T | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-1960G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085592 | |||||||
| chr1:185085680 | G | A | 1 | a0001c0001t0006g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-2-1872G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085680 | |||||||
| chr1:185085764 | C | A | 3 | a0001c0001t0036g0257 a0001c0001t0037g0258 a0001c0001t0038g0259 |
3 | HG01884.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2-1788C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085764 | |||||||
| chr1:185085779 | G | C | 1 | a0001c0001t0015g0233 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-2-1773G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085779 | |||||||
| chr1:185085798 | C | T | 1 | a0001c0001t0031g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-2-1754C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085798 | |||||||
| chr1:185085911 | C | G | 5 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0040 others(2): Show |
5 | HG02132.hp1 NA18972.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-1641C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185085911 | |||||||
| chr1:185086134 | C | A | 75 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(72): Show |
85 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-2-1418C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185086134 | |||||||
| chr1:185086516 | A | G | 1 | a0001c0001t0015g0233 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-2-1036A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185086516 | |||||||
| chr1:185086912 | G | A | 1 | a0001c0001t0028g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2-640G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185086912 | |||||||
| chr1:185087035 | T | C | 3 | a0001c0001t0007g0199 a0001c0001t0007g0213 a0001c0001t0007g0252 |
3 | NA18962.hp2 NA19082.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-2-517T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185087035 | |||||||
| chr1:185087165 | T | C | 1 | a0001c0001t0034g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-2-387T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185087165 | |||||||
| chr1:185087180 | A | G | 4 | a0001c0001t0022g0055 a0001c0001t0022g0057 a0001c0001t0023g0054 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-372A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185087180 | |||||||
| chr1:185087418 | A | G | 1 | a0001c0001t0006g0192 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-2-134A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 1/6 | chr1 | 185087418 | |||||||
| chr1:185087677 | C | T | 1 | a0001c0001t0004g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.87+37C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185087677 | |||||||
| chr1:185087726 | A | G | 2 | a0001c0001t0003g0052 a0001c0001t0003g0147 |
2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.87+86A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185087726 | |||||||
| chr1:185087813 | A | G | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(73): Show |
86 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.87+173A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185087813 | |||||||
| chr1:185087868 | T | C | 1 | a0001c0001t0013g0240 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.87+228T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185087868 | |||||||
| chr1:185087914 | T | C | 2 | a0001c0001t0003g0330 a0001c0001t0006g0329 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.87+274T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185087914 | |||||||
| chr1:185088107 | A | G | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | NA18961.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.87+467A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185088107 | |||||||
| chr1:185088261 | A | G | 1 | a0001c0001t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.87+621A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185088261 | |||||||
| chr1:185088382 | C | A | 2 | a0001c0001t0005g0323 a0001c0001t0005g0324 |
2 | NA18965.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.87+742C>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185088382 | |||||||
| chr1:185088556 | C | CA | 60 | a0001c0001t0001g0012 a0001c0001t0001g0043 a0001c0001t0001g0047 others(57): Show |
61 | HG00408.hp2 HG00609.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.87+929dupA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 185088556 | ||||||
| chr1:185088586 | C | G | 2 | a0001c0001t0012g0153 a0001c0001t0012g0154 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.87+946C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185088586 | |||||||
| chr1:185088674 | G | A | 1 | a0001c0001t0004g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.87+1034G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185088674 | |||||||
| chr1:185088703 | A | C | 2 | a0001c0001t0012g0153 a0001c0001t0012g0154 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.87+1063A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185088703 | |||||||
| chr1:185088759 | A | C | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.87+1119A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185088759 | |||||||
| chr1:185089147 | G | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(191): Show |
207 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.87+1507G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185089147 | |||||||
| chr1:185089639 | G | A | 3 | a0001c0001t0011g0294 a0001c0001t0011g0295 a0001c0001t0011g0300 |
3 | NA18960.hp2 NA18970.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.88-1940G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185089639 | |||||||
| chr1:185089693 | A | G | 1 | a0001c0001t0018g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.88-1886A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185089693 | |||||||
| chr1:185089856 | C | T | 3 | a0001c0001t0006g0150 a0001c0001t0006g0151 a0001c0001t0014g0149 |
3 | HG01192.hp2 HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.88-1723C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185089856 | |||||||
| chr1:185089950 | A | C | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.88-1629A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185089950 | |||||||
| chr1:185089988 | C | G | 1 | a0001c0001t0018g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.88-1591C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185089988 | |||||||
| chr1:185089989 | G | T | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.88-1590G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185089989 | |||||||
| chr1:185090065 | G | T | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.88-1514G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185090065 | |||||||
| chr1:185090186 | C | T | 2 | a0001c0001t0012g0153 a0001c0001t0012g0154 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.88-1393C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185090186 | |||||||
| chr1:185090275 | T | C | 9 | a0001c0001t0003g0140 a0001c0001t0003g0155 a0001c0001t0003g0156 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.88-1304T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185090275 | |||||||
| chr1:185090652 | G | A | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.88-927G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185090652 | |||||||
| chr1:185090658 | G | A | 2 | a0001c0001t0004g0243 a0001c0001t0004g0244 |
2 | HG02027.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.88-921G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185090658 | |||||||
| chr1:185090692 | C | G | 3 | a0001c0001t0003g0265 a0001c0001t0003g0269 a0001c0001t0003g0270 |
3 | HG00738.hp1 HG01346.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.88-887C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185090692 | |||||||
| chr1:185091424 | A | C | 1 | a0001c0001t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.88-155A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 2/6 | chr1 | 185091424 | |||||||
| chr1:185091809 | A | G | 5 | a0001c0001t0007g0224 a0001c0001t0007g0225 a0001c0001t0017g0217 others(2): Show |
5 | HG01168.hp2 HG01243.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.248+70A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 3/6 | chr1 | 185091809 | |||||||
| chr1:185091818 | CT | C | 80 | a0001c0001t0001g0128 a0001c0001t0002g0001 a0001c0001t0002g0003 others(77): Show |
90 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.248+93delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 185091818 | ||||||
| chr1:185091848 | T | G | 1 | a0001c0001t0008g0087 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.248+109T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 3/6 | chr1 | 185091848 | |||||||
| chr1:185091886 | G | A | 81 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0007 others(78): Show |
83 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.248+147G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 3/6 | chr1 | 185091886 | |||||||
| chr1:185091976 | G | A | 1 | a0001c0001t0027g0219 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.248+237G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 3/6 | chr1 | 185091976 | |||||||
| chr1:185091981 | G | GT | 16 | a0001c0001t0001g0098 a0001c0001t0001g0114 a0001c0001t0001g0120 others(13): Show |
16 | HG02071.hp2 HG02145.hp2 HG03239.hp2 others(13): Show |
intron_variant | MODIFIER | c.248+257dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 185091981 | ||||||
| chr1:185092013 | C | T | 89 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0007 others(86): Show |
92 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.248+274C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 3/6 | chr1 | 185092013 | |||||||
| chr1:185092164 | C | T | 1 | a0001c0001t0003g0145 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.248+425C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 3/6 | chr1 | 185092164 | |||||||
| chr1:185092326 | A | G | 18 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(15): Show |
18 | HG01884.hp1 HG01891.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.248+587A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 3/6 | chr1 | 185092326 | |||||||
| chr1:185092370 | T | G | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.248+631T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 3/6 | chr1 | 185092370 | |||||||
| chr1:185092386 | A | C | 9 | a0001c0001t0003g0179 a0001c0001t0003g0184 a0001c0001t0006g0178 others(6): Show |
9 | HG01099.hp2 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.248+647A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 3/6 | chr1 | 185092386 | |||||||
| chr1:185092465 | G | A | 1 | a0001c0001t0004g0123 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.249-596G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 3/6 | chr1 | 185092465 | |||||||
| chr1:185093399 | G | A | 1 | a0001c0001t0004g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.464+123G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185093399 | |||||||
| chr1:185093435 | T | C | 10 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(7): Show |
12 | HG02055.hp2 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.464+159T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185093435 | |||||||
| chr1:185093492 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | NA18972.hp1 NA19006.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.464+216A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185093492 | |||||||
| chr1:185093537 | AATTCTTT others(4): Show |
A | 1 | a0001c0001t0001g0208 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.464+270_464+280del others(11): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 185093537 | ||||||
| chr1:185093737 | C | G | 1 | a0001c0001t0003g0157 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.464+461C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185093737 | |||||||
| chr1:185093871 | T | G | 1 | a0001c0001t0003g0157 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.464+595T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185093871 | |||||||
| chr1:185094059 | C | G | 1 | a0001c0001t0018g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.464+783C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185094059 | |||||||
| chr1:185094131 | G | GT | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.464+867dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 185094131 | ||||||
| chr1:185094181 | A | G | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.464+905A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185094181 | |||||||
| chr1:185094417 | A | G | 1 | a0001c0001t0002g0020 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.464+1141A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185094417 | |||||||
| chr1:185094601 | A | T | 2 | a0001c0001t0003g0137 a0001c0001t0003g0138 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.464+1325A>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185094601 | |||||||
| chr1:185094757 | C | T | 1 | a0001c0001t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.464+1481C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185094757 | |||||||
| chr1:185095023 | G | A | 1 | a0001c0001t0008g0088 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.464+1747G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185095023 | |||||||
| chr1:185095111 | A | C | 1 | a0001c0001t0002g0032 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.464+1835A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185095111 | |||||||
| chr1:185095119 | T | C | 1 | a0001c0001t0004g0228 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.464+1843T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185095119 | |||||||
| chr1:185095241 | T | C | 1 | a0001c0001t0003g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.464+1965T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185095241 | |||||||
| chr1:185095276 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.464+2000G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185095276 | |||||||
| chr1:185095411 | A | G | 1 | a0001c0001t0009g0074 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.464+2135A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185095411 | |||||||
| chr1:185095417 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.464+2141A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185095417 | |||||||
| chr1:185095462 | C | T | 6 | a0001c0001t0020g0256 a0001c0001t0031g0260 a0001c0001t0035g0255 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.464+2186C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185095462 | |||||||
| chr1:185095481 | CTG | C | 3 | a0001c0001t0036g0257 a0001c0001t0037g0258 a0001c0001t0038g0259 |
3 | HG01884.hp1 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.464+2207_464+2208d others(4): Show |
RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 185095481 | ||||||
| chr1:185095517 | C | G | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.464+2241C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185095517 | |||||||
| chr1:185095518 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.464+2242A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185095518 | |||||||
| chr1:185095599 | T | C | 3 | a0001c0001t0006g0150 a0001c0001t0006g0151 a0001c0001t0014g0149 |
3 | HG01192.hp2 HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.464+2323T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185095599 | |||||||
| chr1:185095815 | TA | T | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.465-2256delA | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185095815 | |||||||
| chr1:185096031 | A | T | 2 | a0001c0001t0012g0153 a0001c0001t0012g0154 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.465-2041A>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185096031 | |||||||
| chr1:185096042 | G | A | 69 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(66): Show |
70 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.465-2030G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185096042 | |||||||
| chr1:185096199 | A | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG03688.hp1 HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.465-1873A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185096199 | |||||||
| chr1:185096368 | C | G | 7 | a0001c0001t0011g0294 a0001c0001t0011g0295 a0001c0001t0011g0296 others(4): Show |
7 | HG00438.hp2 NA18941.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.465-1704C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185096368 | |||||||
| chr1:185096376 | G | A | 1 | a0001c0001t0035g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.465-1696G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185096376 | |||||||
| chr1:185096520 | A | C | 1 | a0001c0001t0012g0191 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.465-1552A>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185096520 | |||||||
| chr1:185096561 | G | GT | 12 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0002g0038 others(9): Show |
12 | HG00741.hp2 HG01175.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.465-1501dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 185096561 | ||||||
| chr1:185096561 | G | T | 1 | a0001c0001t0004g0195 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.465-1511G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185096561 | |||||||
| chr1:185096569 | T | G | 1 | a0001c0001t0028g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.465-1503T>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185096569 | |||||||
| chr1:185096604 | T | C | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.465-1468T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185096604 | |||||||
| chr1:185096806 | G | A | 1 | a0001c0001t0028g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.465-1266G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185096806 | |||||||
| chr1:185096834 | A | AT | 10 | a0001c0001t0001g0094 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
10 | HG00733.hp2 HG03195.hp2 HG03579.hp1 others(7): Show |
intron_variant | MODIFIER | c.465-1219dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 185096834 | ||||||
| chr1:185096834 | AT | A | 9 | a0001c0001t0002g0033 a0001c0001t0002g0307 a0001c0001t0002g0312 others(6): Show |
9 | HG01168.hp1 HG01255.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.465-1219delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 185096834 | ||||||
| chr1:185096914 | G | A | 12 | a0001c0001t0009g0067 a0001c0001t0009g0069 a0001c0001t0009g0070 others(9): Show |
12 | HG02071.hp2 HG03654.hp1 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.465-1158G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185096914 | |||||||
| chr1:185097075 | G | A | 5 | a0001c0001t0001g0091 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG00621.hp2 HG01934.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.465-997G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185097075 | |||||||
| chr1:185097216 | C | T | 1 | a0001c0001t0035g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.465-856C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185097216 | |||||||
| chr1:185097321 | C | G | 2 | a0001c0001t0008g0285 a0001c0001t0018g0284 |
2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.465-751C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185097321 | |||||||
| chr1:185097326 | T | C | 35 | a0001c0001t0002g0059 a0001c0001t0002g0288 a0001c0001t0002g0291 others(32): Show |
35 | HG00438.hp2 HG00733.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.465-746T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185097326 | |||||||
| chr1:185097520 | T | A | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.465-552T>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185097520 | |||||||
| chr1:185097527 | T | C | 2 | a0001c0001t0008g0285 a0001c0001t0018g0284 |
2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.465-545T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185097527 | |||||||
| chr1:185097640 | C | T | 1 | a0001c0001t0009g0075 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.465-432C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185097640 | |||||||
| chr1:185097688 | C | T | 4 | a0001c0001t0020g0256 a0001c0001t0036g0257 a0001c0001t0037g0258 others(1): Show |
4 | HG01884.hp1 HG01891.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.465-384C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185097688 | |||||||
| chr1:185097702 | A | G | 4 | a0001c0001t0003g0163 a0001c0001t0003g0175 a0001c0001t0006g0172 others(1): Show |
4 | HG00741.hp1 HG01074.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.465-370A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 4/6 | chr1 | 185097702 | |||||||
| chr1:185098429 | G | A | 1 | a0001c0001t0020g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.737+85G>A | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 5/6 | chr1 | 185098429 | |||||||
| chr1:185098673 | T | C | 191 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(188): Show |
204 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.737+329T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 5/6 | chr1 | 185098673 | |||||||
| chr1:185098823 | C | T | 1 | a0001c0001t0004g0274 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.737+479C>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 5/6 | chr1 | 185098823 | |||||||
| chr1:185099051 | C | CT | 7 | a0001c0001t0003g0161 a0001c0001t0004g0227 a0001c0001t0004g0287 others(4): Show |
7 | HG00438.hp2 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.738-723dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 185099051 | ||||||
| chr1:185099051 | CT | C | 6 | a0001c0001t0001g0226 a0001c0001t0002g0023 a0001c0001t0003g0137 others(3): Show |
6 | HG01069.hp1 HG01069.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.738-723delT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 185099051 | ||||||
| chr1:185099111 | G | C | 1 | a0001c0001t0023g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.738-680G>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 5/6 | chr1 | 185099111 | |||||||
| chr1:185099120 | T | C | 80 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(77): Show |
90 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.738-671T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 5/6 | chr1 | 185099120 | |||||||
| chr1:185099252 | T | C | 3 | a0001c0001t0003g0079 a0001c0001t0003g0083 a0001c0001t0003g0173 |
3 | HG02622.hp1 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.738-539T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 5/6 | chr1 | 185099252 | |||||||
| chr1:185099530 | G | T | 1 | a0001c0001t0003g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.738-261G>T | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 5/6 | chr1 | 185099530 | |||||||
| chr1:185099672 | A | G | 1 | a0001c0001t0003g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.738-119A>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 5/6 | chr1 | 185099672 | |||||||
| chr1:185099742 | C | G | 2 | a0001c0001t0004g0243 a0001c0001t0004g0244 |
2 | HG02027.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.738-49C>G | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 5/6 | chr1 | 185099742 | |||||||
| chr1:185099987 | T | C | 2 | a0001c0001t0037g0258 a0001c0001t0038g0259 |
2 | HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.909+25T>C | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 6/6 | chr1 | 185099987 | |||||||
| chr1:185100182 | C | CT | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.910-15dupT | RNF2 | ENSG00000121481.11 | transcript | ENST00000367510.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 185100182 |