Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79657 |
| ensemblid | ENSG00000005175.10 |
| hgncid | 26151 |
| symbol | RPAP3 |
| name | RNA polymerase II associated protein 3 |
| refseq_nuc | NM_024604.3 |
| refseq_prot | NP_078880.2 |
| ensembl_nuc | ENST00000005386.8 |
| ensembl_prot | ENSP00000005386.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 47661249 |
| end | 47706030 |
| strand | - |
| ver | v1.2 |
| region | chr12:47661249-47706030 |
| region5000 | chr12:47656249-47711030 |
| regionname0 | RPAP3_chr12_47661249_47706030 |
| regionname5000 | RPAP3_chr12_47656249_47711030 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 665 | 407 | 91 | 72 | 187 | 13 | 42 | 153 | RPAP3_chr12_47656249_47711030 | RPAP3 | MTSAN others(660): Show |
chr12 | 47656249 | 47711030 |
| a0002 | 0/0 | 665 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | MTSAN others(660): Show |
chr12 | 47656249 | 47711030 |
| a0003 | 0/0 | 524 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | MTSAN others(519): Show |
chr12 | 47656249 | 47711030 |
| a0004 | 0/0 | 665 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | MTSAN others(660): Show |
chr12 | 47656249 | 47711030 |
| a0005 | 0/0 | 665 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | MTSAN others(660): Show |
chr12 | 47656249 | 47711030 |
| a0006 | 0/0 | 665 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | MTSAN others(660): Show |
chr12 | 47656249 | 47711030 |
| a0007 | 0/0 | 665 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | MTSAN others(660): Show |
chr12 | 47656249 | 47711030 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1995 | 386 | 77 | 67 | 187 | 12 | 41 | RPAP3_chr12_47656249_47711030 | RPAP3 | ATGAC others(1990): Show |
chr12 | 47656249 | 47711030 | ||
| a0001c0002 | 0/0 | 1995 | 17 | 13 | 4 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | ATGAC others(1990): Show |
chr12 | 47656249 | 47711030 | ||
| a0001c0003 | 0/0 | 1995 | 3 | 0 | 1 | 0 | 1 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | ATGAC others(1990): Show |
chr12 | 47656249 | 47711030 | ||
| a0001c0005 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | ATGAC others(1990): Show |
chr12 | 47656249 | 47711030 | ||
| a0002c0004 | 0/0 | 1995 | 2 | 0 | 0 | 0 | 2 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | ATGAC others(1990): Show |
chr12 | 47656249 | 47711030 | ||
| a0003c0009 | 0/0 | 2240 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | ATGAC others(2235): Show |
chr12 | 47656249 | 47711030 | ||
| a0004c0007 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | ATGAC others(1990): Show |
chr12 | 47656249 | 47711030 | ||
| a0005c0008 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | ATGAC others(1990): Show |
chr12 | 47656249 | 47711030 | ||
| a0006c0006 | 0/0 | 1995 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | ATGAC others(1990): Show |
chr12 | 47656249 | 47711030 | ||
| a0007c0010 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | ATGAC others(1990): Show |
chr12 | 47656249 | 47711030 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4342 | 168 | 38 | 29 | 82 | 5 | 13 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0002 | 0/0 | 4339 | 69 | 16 | 23 | 22 | 0 | 8 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4334): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0003 | 0/0 | 4342 | 67 | 1 | 3 | 48 | 4 | 11 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0004 | 1/0 | 4339 | 24 | 8 | 0 | 10 | 0 | 5 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4334): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0005 | 0/0 | 4339 | 13 | 0 | 0 | 13 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4334): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0006 | 0/0 | 4342 | 11 | 1 | 6 | 0 | 1 | 3 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0009 | 0/0 | 4342 | 7 | 7 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0010 | 0/0 | 4339 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4334): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0011 | 0/0 | 4342 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0012 | 0/0 | 4342 | 2 | 0 | 2 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0013 | 0/0 | 4342 | 2 | 0 | 1 | 0 | 1 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0014 | 0/0 | 4339 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4334): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0015 | 0/0 | 10410 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(10405): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0016 | 0/0 | 4339 | 2 | 0 | 1 | 0 | 1 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4334): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0017 | 0/0 | 4342 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0019 | 0/0 | 4342 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0020 | 0/0 | 4339 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4334): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0021 | 0/0 | 4331 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4326): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0022 | 0/0 | 4342 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0023 | 0/0 | 4342 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0024 | 0/0 | 4342 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0025 | 0/0 | 4342 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0026 | 0/0 | 4342 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0028 | 0/0 | 4339 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4334): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0029 | 0/0 | 4339 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4334): Show |
chr12 | 47656249 | 47711030 |
| a0001c0001t0030 | 0/0 | 4342 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0002t0007 | 0/0 | 4342 | 9 | 6 | 3 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0002t0008 | 0/0 | 4342 | 8 | 7 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0003t0001 | 0/0 | 4342 | 3 | 0 | 1 | 0 | 1 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0001c0005t0010 | 0/0 | 4339 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4334): Show |
chr12 | 47656249 | 47711030 |
| a0002c0004t0018 | 0/0 | 4342 | 2 | 0 | 0 | 0 | 2 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0003c0009t0001 | 0/0 | 4587 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4582): Show |
chr12 | 47656249 | 47711030 |
| a0004c0007t0027 | 0/0 | 4342 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| a0005c0008t0010 | 0/0 | 4339 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4334): Show |
chr12 | 47656249 | 47711030 |
| a0006c0006t0004 | 0/0 | 4339 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4334): Show |
chr12 | 47656249 | 47711030 |
| a0007c0010t0001 | 0/0 | 4342 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | GCGTG others(4337): Show |
chr12 | 47656249 | 47711030 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 1 | 7 | 13 | 1 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0056 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0005 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0006 | 0/0 | 7 | 3 | 1 | 0 | 0 | 3 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0025 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0055 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0002 | 0/0 | 12 | 0 | 0 | 7 | 1 | 4 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0008 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0009 | 0/0 | 6 | 4 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0020 | 1/0 | 3 | 0 | 0 | 0 | 0 | 2 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0045 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0005g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0005g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0006g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0006g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0009g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0009g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0009g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0009g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0010g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0011g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0011g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0012g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0012g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0013g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0013g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0014g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0014g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0015g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0016g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0017g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0019g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0020g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0021g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0022g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0023g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0024g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0025g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0026g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0028g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0029g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0001t0030g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0002t0007g0013 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0002t0007g0028 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0002t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0002t0008g0010 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0002t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0002t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0003t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0001c0005t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0002c0004t0018g0061 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0003c0009t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0004c0007t0027g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0005c0008t0010g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0006c0006t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| a0007c0010t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0013 | g0203 | EUR | GBR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0019 | EUR | GBR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | FIN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0066 | EUR | FIN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0108 | EUR | FIN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | CHS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | CHS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | CHS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | CHS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | CHS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00738 | hp1 | a0001 | c0002 | t0007 | g0028 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0029 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01070 | hp2 | a0001 | c0001 | t0022 | g0123 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01081 | hp1 | a0001 | c0001 | t0016 | g0044 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0019 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01106 | hp2 | a0001 | c0001 | t0021 | g0116 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01109 | hp1 | a0001 | c0002 | t0007 | g0013 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01167 | hp1 | a0001 | c0002 | t0008 | g0010 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01167 | hp2 | a0001 | c0001 | t0012 | g0168 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01169 | hp1 | a0001 | c0001 | t0012 | g0169 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01175 | hp1 | a0001 | c0001 | t0013 | g0236 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0070 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0068 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01192 | hp2 | a0001 | c0002 | t0007 | g0028 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0254 | AMR | PUR | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0069 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01515 | hp1 | a0002 | c0004 | t0018 | g0061 | EUR | IBS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01515 | hp2 | a0003 | c0009 | t0001 | g0127 | EUR | IBS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0035 | EUR | IBS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | IBS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01517 | hp1 | a0002 | c0004 | t0018 | g0061 | EUR | IBS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0035 | EUR | IBS | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01891 | hp2 | a0001 | c0002 | t0007 | g0013 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0067 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0165 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0185 | EAS | CDX | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0113 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02630 | hp1 | a0004 | c0007 | t0027 | g0246 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0037 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0163 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0072 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02717 | hp2 | a0001 | c0001 | t0026 | g0245 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02723 | hp1 | a0005 | c0008 | t0010 | g0170 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02723 | hp2 | a0001 | c0002 | t0007 | g0253 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0037 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02922 | hp1 | a0001 | c0002 | t0008 | g0010 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02922 | hp2 | a0001 | c0001 | t0010 | g0048 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02965 | hp2 | a0001 | c0002 | t0008 | g0251 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02970 | hp2 | a0001 | c0002 | t0007 | g0028 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02976 | hp1 | a0001 | c0002 | t0008 | g0010 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0048 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03130 | hp2 | a0001 | c0002 | t0008 | g0010 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0016 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03139 | hp2 | a0001 | c0002 | t0007 | g0013 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0016 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0114 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03486 | hp2 | a0001 | c0002 | t0008 | g0010 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0019 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03579 | hp1 | a0001 | c0002 | t0007 | g0013 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03579 | hp2 | a0001 | c0002 | t0008 | g0252 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0075 | SAS | STU | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0096 | SAS | BEB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0158 | SAS | BEB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0073 | SAS | STU | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0071 | SAS | STU | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | STU | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | STU | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | STU | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG04228 | hp1 | a0001 | c0001 | t0028 | g0183 | SAS | STU | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0157 | SAS | STU | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | YRI | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | CHB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | CHB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | YRI | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0016 | AFR | YRI | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18961 | hp1 | a0001 | c0001 | t0030 | g0081 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18963 | hp1 | a0001 | c0001 | t0011 | g0101 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0173 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18966 | hp2 | a0001 | c0001 | t0017 | g0059 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18970 | hp2 | a0001 | c0001 | t0015 | g0032 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18977 | hp2 | a0001 | c0001 | t0025 | g0091 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18979 | hp1 | a0006 | c0006 | t0004 | g0152 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18985 | hp2 | a0001 | c0001 | t0023 | g0155 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18987 | hp1 | a0001 | c0001 | t0029 | g0193 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18989 | hp2 | a0001 | c0001 | t0020 | g0159 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | LWK | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19030 | hp2 | a0001 | c0005 | t0010 | g0248 | AFR | LWK | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19043 | hp2 | a0007 | c0010 | t0001 | g0247 | AFR | LWK | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19058 | hp2 | a0001 | c0001 | t0024 | g0090 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19060 | hp1 | a0001 | c0001 | t0015 | g0032 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19078 | hp1 | a0001 | c0001 | t0011 | g0100 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19090 | hp1 | a0001 | c0001 | t0017 | g0059 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19240 | hp1 | a0001 | c0002 | t0008 | g0010 | AFR | YRI | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ASW | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | ASW | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA20752 | hp2 | a0001 | c0001 | t0016 | g0044 | EUR | TSI | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | TSI | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | GIH | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | GIH | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02109 | hp2 | a0001 | c0002 | t0007 | g0013 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG02559 | hp2 | a0001 | c0001 | t0014 | g0166 | AFR | ACB | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | USA | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | USA | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | USA | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | USA | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA21309 | hp1 | a0001 | c0001 | t0019 | g0153 | AFR | LWK | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0029 | AFR | LWK | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0135 | REF | REF | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0020 | REF | REF | RPAP3_chr12_47656249_47711030 | RPAP3 | chr12 | 47656249 | 47711030 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47670329 | A | C | 1 | a0003 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.1304T>G | p.Val435Gly | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 13/17 | 1389/4339 | 1304/1998 | 435/665 | chr12 | 47670329 | |||
| chr12:47670330 | C | CCTCGCCC others(238): Show |
1 | a0003 | 1 | HG01515.hp2 | frameshift_variant | HIGH | c.1302_1303insAGGGGG others(239): Show |
p.Val435fs | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 13/17 | 1387/4339 | 1302/1998 | 434/665 | chr12 | 47670330 | |||
| chr12:47670333 | T | C | 2 | a0003 a0007 |
2 | HG01515.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.1300A>G | p.Lys434Glu | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 13/17 | 1385/4339 | 1300/1998 | 434/665 | chr12 | 47670333 | |||
| chr12:47679500 | C | T | 1 | a0005 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1280G>A | p.Gly427Glu | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/17 | 1365/4339 | 1280/1998 | 427/665 | chr12 | 47679500 | |||
| chr12:47687877 | C | T | 1 | a0004 | 1 | HG02630.hp1 | missense_variant&splice_region_variant | MODERATE | c.863G>A | p.Arg288Gln | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 8/17 | 948/4339 | 863/1998 | 288/665 | chr12 | 47687877 | |||
| chr12:47696352 | T | C | 1 | a0002 | 2 | HG01515.hp1 HG01517.hp1 |
missense_variant | MODERATE | c.469A>G | p.Thr157Ala | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/17 | 554/4339 | 469/1998 | 157/665 | chr12 | 47696352 | |||
| chr12:47697647 | C | T | 1 | a0006 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.367G>A | p.Glu123Lys | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/17 | 452/4339 | 367/1998 | 123/665 | chr12 | 47697647 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47681814 | A | G | 1 | a0001c0002 | 17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
synonymous_variant | LOW | c.996T>C | p.Tyr332Tyr | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/17 | 1081/4339 | 996/1998 | 332/665 | chr12 | 47681814 | |||
| chr12:47696335 | G | A | 1 | a0001c0003 | 3 | HG00140.hp2 HG01106.hp1 HG03492.hp2 |
synonymous_variant | LOW | c.486C>T | p.Ala162Ala | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/17 | 571/4339 | 486/1998 | 162/665 | chr12 | 47696335 | |||
| chr12:47701551 | A | T | 1 | a0001c0005 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.207T>A | p.Ala69Ala | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/17 | 292/4339 | 207/1998 | 69/665 | chr12 | 47701551 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47661278 | C | T | 1 | a0001c0001t0023 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2227G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 2227 | chr12 | 47661278 | ||||||
| chr12:47661283 | T | C | 1 | a0001c0002t0008 | 8 | HG01167.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2222A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 2222 | chr12 | 47661283 | ||||||
| chr12:47661379 | T | TAAC | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(21): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*2123_*2125dupGTT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 2125 | chr12 | 47661379 | ||||||
| chr12:47661449 | T | C | 8 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0015 others(5): Show |
76 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2056A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 2056 | chr12 | 47661449 | ||||||
| chr12:47661620 | T | TTAAAATT others(6061): Show |
1 | a0001c0001t0015 | 2 | NA18970.hp2 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1884_*1885insGAGG others(6064): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1884 | chr12 | 47661620 | ||||||
| chr12:47661621 | T | A | 1 | a0001c0001t0024 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1884A>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1884 | chr12 | 47661621 | ||||||
| chr12:47661644 | T | C | 1 | a0001c0001t0029 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1861A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1861 | chr12 | 47661644 | ||||||
| chr12:47661666 | G | A | 1 | a0001c0001t0025 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1839C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1839 | chr12 | 47661666 | ||||||
| chr12:47661837 | G | A | 1 | a0001c0001t0005 | 13 | HG00558.hp1 HG02132.hp1 HG02165.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1668C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1668 | chr12 | 47661837 | ||||||
| chr12:47661902 | C | T | 1 | a0001c0001t0026 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1603G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1603 | chr12 | 47661902 | ||||||
| chr12:47661903 | G | A | 1 | a0001c0001t0014 | 2 | HG02145.hp2 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1602C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1602 | chr12 | 47661903 | ||||||
| chr12:47661922 | T | A | 10 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0011 others(7): Show |
89 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1583A>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1583 | chr12 | 47661922 | ||||||
| chr12:47661943 | A | C | 1 | a0001c0001t0028 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1562T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1562 | chr12 | 47661943 | ||||||
| chr12:47661958 | T | C | 1 | a0001c0001t0016 | 2 | HG01081.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1547A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1547 | chr12 | 47661958 | ||||||
| chr12:47662244 | T | C | 2 | a0001c0002t0007 a0001c0002t0008 |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1261A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1261 | chr12 | 47662244 | ||||||
| chr12:47662382 | T | C | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(29): Show |
385 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(382): Show |
3_prime_UTR_variant | MODIFIER | c.*1123A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1123 | chr12 | 47662382 | ||||||
| chr12:47662412 | T | C | 1 | a0001c0001t0016 | 2 | HG01081.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1093A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1093 | chr12 | 47662412 | ||||||
| chr12:47662434 | T | C | 1 | a0001c0001t0017 | 2 | NA18966.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1071A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 1071 | chr12 | 47662434 | ||||||
| chr12:47662597 | C | A | 2 | a0001c0001t0026 a0004c0007t0027 |
2 | HG02630.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*908G>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 908 | chr12 | 47662597 | ||||||
| chr12:47662610 | A | G | 2 | a0001c0002t0007 a0001c0002t0008 |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*895T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 895 | chr12 | 47662610 | ||||||
| chr12:47662671 | A | C | 1 | a0001c0001t0022 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*834T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 834 | chr12 | 47662671 | ||||||
| chr12:47662776 | T | C | 5 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0028 others(2): Show |
85 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*729A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 729 | chr12 | 47662776 | ||||||
| chr12:47662782 | C | T | 1 | a0001c0001t0013 | 2 | HG00140.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*723G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 723 | chr12 | 47662782 | ||||||
| chr12:47662787 | C | T | 3 | a0001c0001t0010 a0001c0005t0010 a0005c0008t0010 |
4 | HG02723.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*718G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 718 | chr12 | 47662787 | ||||||
| chr12:47662885 | TTAACTGG others(4): Show |
T | 1 | a0001c0001t0021 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*609_*619delCATACC others(5): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 609 | chr12 | 47662885 | ||||||
| chr12:47662905 | A | C | 1 | a0001c0001t0012 | 2 | HG01167.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*600T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 600 | chr12 | 47662905 | ||||||
| chr12:47662930 | G | T | 1 | a0001c0001t0009 | 7 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*575C>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 575 | chr12 | 47662930 | ||||||
| chr12:47662993 | C | T | 2 | a0001c0001t0006 a0002c0004t0018 |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*512G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 512 | chr12 | 47662993 | ||||||
| chr12:47663010 | A | C | 2 | a0001c0001t0011 a0001c0001t0020 |
3 | NA18963.hp1 NA18989.hp2 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*495T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 495 | chr12 | 47663010 | ||||||
| chr12:47663284 | A | G | 1 | a0001c0001t0019 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*221T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 17/17 | 221 | chr12 | 47663284 | ||||||
| chr12:47706010 | G | A | 1 | a0002c0004t0018 | 2 | HG01515.hp1 HG01517.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-65C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/17 | chr12 | 47706010 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47663945 | A | C | 48 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0011 others(45): Show |
75 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1913-355T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47663945 | |||||||
| chr12:47663948 | CTG | C | 18 | a0001c0001t0001g0026 a0001c0001t0001g0057 a0001c0001t0001g0060 others(15): Show |
22 | HG00140.hp1 HG01099.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.1913-360_1913-359d others(4): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47663948 | |||||||
| chr12:47664008 | G | A | 51 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(48): Show |
85 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.1913-418C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47664008 | |||||||
| chr12:47664127 | C | A | 1 | a0001c0001t0026g0245 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1913-537G>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47664127 | |||||||
| chr12:47664132 | G | A | 1 | a0001c0001t0001g0056 | 2 | HG01346.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1913-542C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47664132 | |||||||
| chr12:47664164 | C | T | 5 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0008g0010 others(2): Show |
16 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1913-574G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47664164 | |||||||
| chr12:47664617 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1913-1027G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47664617 | |||||||
| chr12:47664971 | G | A | 1 | a0001c0001t0003g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1913-1381C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47664971 | |||||||
| chr12:47664996 | T | G | 34 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0018 others(31): Show |
54 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1913-1406A>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47664996 | |||||||
| chr12:47665016 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1913-1426C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665016 | |||||||
| chr12:47665022 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1913-1432A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665022 | |||||||
| chr12:47665068 | A | C | 1 | a0001c0001t0002g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1913-1478T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665068 | |||||||
| chr12:47665091 | A | AT | 10 | a0001c0001t0001g0205 a0001c0001t0002g0198 a0001c0001t0003g0074 others(7): Show |
21 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1913-1502dupA | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665091 | |||||||
| chr12:47665091 | AT | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(51): Show |
103 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1913-1502delA | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665091 | |||||||
| chr12:47665091 | ATT | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0006g0066 others(8): Show |
14 | HG00280.hp2 HG00733.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1913-1503_1913-150 others(6): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665091 | |||||||
| chr12:47665141 | G | A | 1 | a0001c0005t0010g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1913-1551C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665141 | |||||||
| chr12:47665161 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0125 |
3 | HG01069.hp1 HG01255.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1913-1571G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665161 | |||||||
| chr12:47665195 | C | T | 2 | a0001c0001t0012g0168 a0001c0001t0012g0169 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1913-1605G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665195 | |||||||
| chr12:47665394 | G | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02895.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1912+1586C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665394 | |||||||
| chr12:47665418 | A | T | 1 | a0007c0010t0001g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1912+1562T>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665418 | |||||||
| chr12:47665501 | A | G | 16 | a0001c0001t0001g0003 a0001c0001t0001g0065 a0001c0001t0001g0204 others(13): Show |
26 | HG00639.hp1 HG00673.hp2 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.1912+1479T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665501 | |||||||
| chr12:47665589 | C | A | 4 | a0001c0001t0009g0016 a0001c0001t0009g0037 a0001c0001t0009g0113 others(1): Show |
7 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1912+1391G>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665589 | |||||||
| chr12:47665629 | A | AT | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1912+1350dupA | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665629 | |||||||
| chr12:47665734 | G | A | 47 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0011 others(44): Show |
74 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1912+1246C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665734 | |||||||
| chr12:47665829 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1912+1151G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665829 | |||||||
| chr12:47665891 | G | A | 3 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 |
3 | HG02698.hp2 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1912+1089C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47665891 | |||||||
| chr12:47666143 | A | AT | 2 | a0001c0001t0001g0041 a0001c0003t0001g0019 |
5 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1912+836dupA | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47666143 | |||||||
| chr12:47666239 | A | C | 1 | a0001c0001t0001g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1912+741T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47666239 | |||||||
| chr12:47666309 | C | T | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1912+671G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47666309 | |||||||
| chr12:47666689 | A | G | 1 | a0001c0001t0003g0086 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1912+291T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47666689 | |||||||
| chr12:47666875 | T | C | 1 | a0001c0001t0017g0059 | 2 | NA18966.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1912+105A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 16/16 | chr12 | 47666875 | |||||||
| chr12:47667198 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1812-118C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 15/16 | chr12 | 47667198 | |||||||
| chr12:47667282 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1812-202G>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 15/16 | chr12 | 47667282 | |||||||
| chr12:47667309 | G | A | 1 | a0001c0001t0014g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1812-229C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 15/16 | chr12 | 47667309 | |||||||
| chr12:47667516 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1811+238T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 15/16 | chr12 | 47667516 | |||||||
| chr12:47667542 | C | T | 4 | a0001c0001t0009g0016 a0001c0001t0009g0037 a0001c0001t0009g0113 others(1): Show |
7 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1811+212G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 15/16 | chr12 | 47667542 | |||||||
| chr12:47667568 | G | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(69): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1811+186C>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 15/16 | chr12 | 47667568 | |||||||
| chr12:47667652 | G | A | 5 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0008g0010 others(2): Show |
16 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1811+102C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 15/16 | chr12 | 47667652 | |||||||
| chr12:47667696 | A | G | 2 | a0001c0001t0026g0245 a0004c0007t0027g0246 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1811+58T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 15/16 | chr12 | 47667696 | |||||||
| chr12:47667731 | T | C | 1 | a0001c0001t0028g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1811+23A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 15/16 | chr12 | 47667731 | |||||||
| chr12:47668020 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1714-169G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 14/16 | chr12 | 47668020 | |||||||
| chr12:47668036 | A | C | 1 | a0001c0001t0003g0087 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1714-185T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 14/16 | chr12 | 47668036 | |||||||
| chr12:47668053 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0233 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1714-202C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 14/16 | chr12 | 47668053 | |||||||
| chr12:47668141 | G | C | 5 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0008g0010 others(2): Show |
16 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1714-290C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 14/16 | chr12 | 47668141 | |||||||
| chr12:47668392 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1713+524T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 14/16 | chr12 | 47668392 | |||||||
| chr12:47668427 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1713+489A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 14/16 | chr12 | 47668427 | |||||||
| chr12:47669185 | A | T | 2 | a0001c0001t0003g0086 a0001c0001t0003g0088 |
2 | NA18998.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1527-83T>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 13/16 | chr12 | 47669185 | |||||||
| chr12:47669269 | G | A | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1527-167C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 13/16 | chr12 | 47669269 | |||||||
| chr12:47669496 | A | G | 1 | a0001c0002t0007g0253 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1527-394T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 13/16 | chr12 | 47669496 | |||||||
| chr12:47669604 | A | G | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1527-502T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 13/16 | chr12 | 47669604 | |||||||
| chr12:47669808 | T | C | 1 | a0005c0008t0010g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1526+299A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 13/16 | chr12 | 47669808 | |||||||
| chr12:47669958 | G | A | 2 | a0001c0001t0003g0085 a0001c0001t0003g0154 |
2 | NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1526+149C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 13/16 | chr12 | 47669958 | |||||||
| chr12:47670562 | T | C | 2 | a0001c0001t0002g0025 a0001c0001t0002g0197 |
4 | HG01081.hp2 HG01099.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288-217A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47670562 | |||||||
| chr12:47670602 | G | A | 1 | a0001c0001t0005g0185 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1288-257C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47670602 | |||||||
| chr12:47670701 | T | C | 1 | a0001c0001t0001g0039 | 2 | NA18957.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1288-356A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47670701 | |||||||
| chr12:47670754 | G | A | 1 | a0001c0001t0002g0186 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1288-409C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47670754 | |||||||
| chr12:47670970 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0232 others(4): Show |
7 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1288-625A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47670970 | |||||||
| chr12:47670990 | T | C | 1 | a0001c0001t0006g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1288-645A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47670990 | |||||||
| chr12:47671114 | G | A | 1 | a0001c0001t0004g0164 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1288-769C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47671114 | |||||||
| chr12:47671528 | A | G | 1 | a0007c0010t0001g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1288-1183T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47671528 | |||||||
| chr12:47671543 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1288-1198G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47671543 | |||||||
| chr12:47671587 | A | G | 1 | a0001c0002t0007g0013 | 5 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288-1242T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47671587 | |||||||
| chr12:47671781 | G | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0235 |
3 | HG02451.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1288-1436C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47671781 | |||||||
| chr12:47671950 | C | T | 1 | a0001c0005t0010g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1288-1605G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47671950 | |||||||
| chr12:47671986 | C | T | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1288-1641G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47671986 | |||||||
| chr12:47672087 | G | GA | 51 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(48): Show |
85 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.1288-1743dupT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47672087 | |||||||
| chr12:47672088 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02895.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1288-1743T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47672088 | |||||||
| chr12:47672129 | G | C | 2 | a0001c0001t0003g0036 a0001c0001t0003g0097 |
3 | NA18941.hp2 NA18944.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1288-1784C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47672129 | |||||||
| chr12:47672253 | C | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0188 |
4 | NA18957.hp1 NA18971.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288-1908G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47672253 | |||||||
| chr12:47672277 | C | A | 3 | a0001c0001t0026g0245 a0001c0002t0007g0253 a0004c0007t0027g0246 |
3 | HG02630.hp1 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1288-1932G>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47672277 | |||||||
| chr12:47672285 | G | C | 1 | a0004c0007t0027g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1288-1940C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47672285 | |||||||
| chr12:47672377 | G | A | 1 | a0004c0007t0027g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1288-2032C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47672377 | |||||||
| chr12:47672433 | T | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(53): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1288-2088A>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47672433 | |||||||
| chr12:47672629 | A | AT | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(45): Show |
95 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1288-2285dupA | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47672629 | |||||||
| chr12:47672880 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1288-2535C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47672880 | |||||||
| chr12:47673002 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1288-2657C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673002 | |||||||
| chr12:47673071 | G | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02895.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1288-2726C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673071 | |||||||
| chr12:47673262 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1288-2917C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673262 | |||||||
| chr12:47673392 | G | A | 3 | a0001c0001t0010g0048 a0001c0005t0010g0248 a0005c0008t0010g0170 |
4 | HG02723.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288-3047C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673392 | |||||||
| chr12:47673440 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1288-3095C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673440 | |||||||
| chr12:47673444 | C | CA | 29 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0042 others(26): Show |
42 | HG00423.hp1 HG00597.hp2 HG01515.hp2 others(39): Show |
intron_variant | MODIFIER | c.1288-3100dupT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673444 | |||||||
| chr12:47673444 | C | CAA | 8 | a0001c0001t0001g0138 a0001c0001t0001g0249 a0001c0001t0009g0016 others(5): Show |
11 | HG02145.hp2 HG02257.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1288-3101_1288-310 others(6): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673444 | |||||||
| chr12:47673444 | CA | C | 24 | a0001c0001t0001g0040 a0001c0001t0001g0063 a0001c0001t0001g0119 others(21): Show |
29 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1288-3100delT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673444 | |||||||
| chr12:47673444 | CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0002g0005 a0001c0001t0002g0049 a0001c0001t0002g0076 others(3): Show |
14 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1288-3110_1288-310 others(15): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673444 | |||||||
| chr12:47673444 | CAAAAAAA others(5): Show |
C | 44 | a0001c0001t0002g0006 a0001c0001t0002g0022 a0001c0001t0002g0023 others(41): Show |
70 | HG00558.hp1 HG00642.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.1288-3111_1288-310 others(16): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673444 | |||||||
| chr12:47673484 | T | G | 1 | a0001c0001t0001g0043 | 2 | NA18972.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1288-3139A>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673484 | |||||||
| chr12:47673634 | G | C | 1 | a0001c0001t0004g0161 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1288-3289C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673634 | |||||||
| chr12:47673813 | G | A | 1 | a0001c0001t0010g0048 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1288-3468C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673813 | |||||||
| chr12:47673941 | TTTAATA | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0077 others(6): Show |
17 | NA18747.hp1 NA18954.hp2 NA18956.hp2 others(14): Show |
intron_variant | MODIFIER | c.1288-3602_1288-359 others(10): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673941 | |||||||
| chr12:47673994 | A | G | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1288-3649T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47673994 | |||||||
| chr12:47674084 | T | TA | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(109): Show |
205 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.1288-3740dupT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674084 | |||||||
| chr12:47674084 | T | TAA | 100 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0026 others(97): Show |
153 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1288-3741_1288-374 others(6): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674084 | |||||||
| chr12:47674084 | T | TAAA | 6 | a0001c0001t0001g0210 a0001c0001t0003g0080 a0001c0001t0003g0083 others(3): Show |
7 | HG02135.hp2 NA18967.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1288-3742_1288-374 others(7): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674084 | |||||||
| chr12:47674207 | C | T | 1 | a0001c0001t0003g0086 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1288-3862G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674207 | |||||||
| chr12:47674350 | G | C | 1 | a0007c0010t0001g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1288-4005C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674350 | |||||||
| chr12:47674374 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1288-4029C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674374 | |||||||
| chr12:47674417 | T | A | 1 | a0001c0001t0002g0178 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1288-4072A>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674417 | |||||||
| chr12:47674477 | T | C | 1 | a0001c0001t0006g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1288-4132A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674477 | |||||||
| chr12:47674529 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1288-4184T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674529 | |||||||
| chr12:47674562 | T | A | 6 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(3): Show |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1288-4217A>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674562 | |||||||
| chr12:47674711 | GAAAC | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(51): Show |
104 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1288-4370_1288-436 others(8): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674711 | |||||||
| chr12:47674745 | T | C | 1 | a0001c0001t0014g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1288-4400A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674745 | |||||||
| chr12:47674809 | T | C | 3 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 |
3 | HG02698.hp2 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1288-4464A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674809 | |||||||
| chr12:47674946 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1287+4547G>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47674946 | |||||||
| chr12:47675005 | G | A | 1 | a0001c0001t0003g0095 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1287+4488C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47675005 | |||||||
| chr12:47675046 | C | A | 2 | a0001c0001t0003g0035 a0001c0001t0003g0108 |
3 | HG00323.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1287+4447G>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47675046 | |||||||
| chr12:47675112 | A | G | 1 | a0001c0001t0026g0245 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1287+4381T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47675112 | |||||||
| chr12:47675227 | T | C | 1 | a0001c0001t0002g0053 | 2 | HG03239.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1287+4266A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47675227 | |||||||
| chr12:47675673 | T | A | 48 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0011 others(45): Show |
75 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1287+3820A>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47675673 | |||||||
| chr12:47675753 | T | C | 5 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0008g0010 others(2): Show |
16 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1287+3740A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47675753 | |||||||
| chr12:47675977 | T | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0026 others(50): Show |
77 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.1287+3516A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47675977 | |||||||
| chr12:47675994 | A | C | 2 | a0001c0001t0026g0245 a0004c0007t0027g0246 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1287+3499T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47675994 | |||||||
| chr12:47676168 | G | C | 1 | a0001c0001t0002g0198 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1287+3325C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47676168 | |||||||
| chr12:47676338 | T | C | 1 | a0001c0001t0004g0162 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1287+3155A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47676338 | |||||||
| chr12:47676424 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1287+3069T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47676424 | |||||||
| chr12:47676586 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1287+2907T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47676586 | |||||||
| chr12:47676926 | A | G | 61 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0011 others(58): Show |
90 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1287+2567T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47676926 | |||||||
| chr12:47676970 | G | A | 2 | a0001c0001t0012g0168 a0001c0001t0012g0169 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1287+2523C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47676970 | |||||||
| chr12:47677105 | C | T | 1 | a0007c0010t0001g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1287+2388G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47677105 | |||||||
| chr12:47677224 | G | A | 9 | a0001c0001t0002g0023 a0001c0001t0002g0186 a0001c0001t0005g0012 others(6): Show |
17 | HG00558.hp1 HG02132.hp1 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.1287+2269C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47677224 | |||||||
| chr12:47677249 | A | G | 2 | a0001c0001t0002g0182 a0001c0001t0002g0189 |
2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1287+2244T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47677249 | |||||||
| chr12:47677304 | C | G | 1 | a0001c0001t0001g0239 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1287+2189G>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47677304 | |||||||
| chr12:47677328 | A | T | 1 | a0001c0001t0001g0118 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1287+2165T>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47677328 | |||||||
| chr12:47677580 | C | T | 1 | a0001c0001t0002g0049 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1287+1913G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47677580 | |||||||
| chr12:47677678 | G | C | 1 | a0001c0001t0002g0053 | 2 | HG03239.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1287+1815C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47677678 | |||||||
| chr12:47677685 | A | G | 4 | a0001c0001t0009g0016 a0001c0001t0009g0037 a0001c0001t0009g0113 others(1): Show |
7 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1287+1808T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47677685 | |||||||
| chr12:47677781 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1287+1712A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47677781 | |||||||
| chr12:47677797 | A | G | 5 | a0001c0001t0002g0050 a0001c0001t0002g0052 a0001c0001t0002g0149 others(2): Show |
7 | HG02615.hp1 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1287+1696T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47677797 | |||||||
| chr12:47677831 | T | C | 1 | a0001c0001t0006g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1287+1662A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47677831 | |||||||
| chr12:47678274 | T | A | 2 | a0001c0001t0010g0048 a0005c0008t0010g0170 |
3 | HG02723.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1287+1219A>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47678274 | |||||||
| chr12:47678288 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1287+1205A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47678288 | |||||||
| chr12:47678321 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0117 |
4 | HG01168.hp2 HG01243.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1287+1172A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47678321 | |||||||
| chr12:47678564 | C | T | 2 | a0001c0001t0002g0180 a0001c0001t0002g0190 |
2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1287+929G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47678564 | |||||||
| chr12:47678691 | A | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(45): Show |
95 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1287+802T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47678691 | |||||||
| chr12:47678977 | T | C | 4 | a0001c0001t0002g0005 a0001c0001t0002g0049 a0001c0001t0002g0076 others(1): Show |
12 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1287+516A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47678977 | |||||||
| chr12:47679142 | C | T | 2 | a0001c0001t0012g0168 a0001c0001t0012g0169 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1287+351G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47679142 | |||||||
| chr12:47679165 | G | A | 1 | a0001c0001t0003g0036 | 2 | NA18941.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.1287+328C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47679165 | |||||||
| chr12:47679171 | T | C | 1 | a0001c0005t0010g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1287+322A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47679171 | |||||||
| chr12:47679374 | T | A | 1 | a0001c0001t0003g0093 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1287+119A>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 12/16 | chr12 | 47679374 | |||||||
| chr12:47679833 | G | A | 12 | a0001c0001t0004g0009 a0001c0001t0004g0045 a0001c0001t0004g0150 others(9): Show |
18 | HG02080.hp2 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1115-59C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47679833 | |||||||
| chr12:47679940 | A | G | 1 | a0004c0007t0027g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1115-166T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47679940 | |||||||
| chr12:47680178 | T | C | 1 | a0001c0001t0003g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1115-404A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680178 | |||||||
| chr12:47680223 | T | G | 50 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0011 others(47): Show |
77 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1115-449A>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680223 | |||||||
| chr12:47680277 | G | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02895.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1115-503C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680277 | |||||||
| chr12:47680325 | T | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA18980.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1115-551A>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680325 | |||||||
| chr12:47680388 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1115-614G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680388 | |||||||
| chr12:47680725 | A | G | 2 | a0001c0001t0002g0051 a0001c0001t0002g0191 |
3 | NA18940.hp1 NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1115-951T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680725 | |||||||
| chr12:47680806 | C | T | 51 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(48): Show |
85 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.1114+890G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680806 | |||||||
| chr12:47680836 | G | A | 47 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0011 others(44): Show |
74 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1114+860C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680836 | |||||||
| chr12:47680841 | T | TA | 2 | a0001c0001t0001g0065 a0001c0001t0017g0059 |
3 | NA18966.hp2 NA19064.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1114+854_1114+855i others(3): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680841 | |||||||
| chr12:47680842 | T | A | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
8 | HG00741.hp2 HG01358.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114+854A>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680842 | |||||||
| chr12:47680842 | T | TA | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0026 others(48): Show |
74 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.1114+853dupT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680842 | |||||||
| chr12:47680843 | A | T | 5 | a0001c0001t0003g0086 a0001c0001t0010g0048 a0001c0001t0014g0165 others(2): Show |
6 | HG02145.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114+853T>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680843 | |||||||
| chr12:47680906 | T | C | 1 | a0001c0001t0011g0101 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1114+790A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680906 | |||||||
| chr12:47680968 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1114+728G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680968 | |||||||
| chr12:47680969 | G | A | 17 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(14): Show |
30 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1114+727C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680969 | |||||||
| chr12:47680973 | C | CA | 8 | a0001c0001t0001g0133 a0001c0001t0001g0228 a0001c0001t0002g0194 others(5): Show |
14 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1114+722dupT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680973 | |||||||
| chr12:47680986 | A | C | 1 | a0001c0001t0001g0220 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1114+710T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47680986 | |||||||
| chr12:47681029 | G | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | NA18968.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1114+667C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47681029 | |||||||
| chr12:47681107 | TC | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(69): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1114+588delG | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47681107 | |||||||
| chr12:47681374 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1114+322T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47681374 | |||||||
| chr12:47681532 | G | A | 3 | a0001c0001t0010g0048 a0001c0005t0010g0248 a0005c0008t0010g0170 |
4 | HG02723.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+164C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 10/16 | chr12 | 47681532 | |||||||
| chr12:47681821 | T | C | 1 | a0001c0001t0003g0098 | 1 | HG02735.hp2 | splice_region_variant&intron_variant | LOW | c.993-4A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47681821 | |||||||
| chr12:47682519 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.993-702T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47682519 | |||||||
| chr12:47682680 | T | TA | 13 | a0001c0001t0002g0195 a0001c0001t0005g0174 a0001c0001t0006g0029 others(10): Show |
15 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.993-864dupT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47682680 | |||||||
| chr12:47682889 | A | G | 3 | a0001c0001t0010g0048 a0001c0005t0010g0248 a0005c0008t0010g0170 |
4 | HG02723.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.993-1072T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47682889 | |||||||
| chr12:47682914 | C | T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
5 | HG01261.hp2 HG01934.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.993-1097G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47682914 | |||||||
| chr12:47682943 | C | A | 50 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(47): Show |
84 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.993-1126G>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47682943 | |||||||
| chr12:47683283 | T | C | 1 | a0001c0001t0010g0048 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.993-1466A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47683283 | |||||||
| chr12:47683290 | A | G | 17 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(14): Show |
30 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.993-1473T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47683290 | |||||||
| chr12:47683583 | C | T | 1 | a0001c0001t0021g0116 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.993-1766G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47683583 | |||||||
| chr12:47683658 | G | C | 17 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(14): Show |
30 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.993-1841C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47683658 | |||||||
| chr12:47683713 | C | T | 1 | a0001c0002t0007g0253 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.993-1896G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47683713 | |||||||
| chr12:47683986 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.993-2169A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47683986 | |||||||
| chr12:47684167 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.993-2350G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47684167 | |||||||
| chr12:47684168 | A | C | 2 | a0001c0001t0003g0085 a0001c0001t0003g0154 |
2 | NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.993-2351T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47684168 | |||||||
| chr12:47684390 | T | G | 2 | a0001c0001t0001g0229 a0001c0001t0001g0238 |
2 | HG01123.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.992+2390A>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47684390 | |||||||
| chr12:47684571 | A | G | 1 | a0001c0001t0009g0016 | 3 | HG03139.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.992+2209T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47684571 | |||||||
| chr12:47684618 | G | C | 2 | a0001c0001t0010g0048 a0005c0008t0010g0170 |
3 | HG02723.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.992+2162C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47684618 | |||||||
| chr12:47684815 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.992+1965T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47684815 | |||||||
| chr12:47684816 | T | C | 55 | a0001c0001t0001g0007 a0001c0001t0001g0214 a0001c0001t0001g0215 others(52): Show |
95 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.992+1964A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47684816 | |||||||
| chr12:47684843 | C | T | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.992+1937G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47684843 | |||||||
| chr12:47685023 | A | G | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.992+1757T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685023 | |||||||
| chr12:47685090 | A | T | 3 | a0001c0001t0010g0048 a0001c0005t0010g0248 a0005c0008t0010g0170 |
4 | HG02723.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.992+1690T>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685090 | |||||||
| chr12:47685120 | T | C | 1 | a0001c0001t0004g0046 | 2 | NA19070.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.992+1660A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685120 | |||||||
| chr12:47685145 | G | A | 48 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0011 others(45): Show |
75 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.992+1635C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685145 | |||||||
| chr12:47685196 | T | C | 1 | a0001c0001t0002g0172 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.992+1584A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685196 | |||||||
| chr12:47685213 | T | C | 1 | a0006c0006t0004g0152 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.992+1567A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685213 | |||||||
| chr12:47685255 | T | C | 1 | a0001c0001t0006g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.992+1525A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685255 | |||||||
| chr12:47685361 | A | G | 6 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(3): Show |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.992+1419T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685361 | |||||||
| chr12:47685378 | C | CA | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(51): Show |
104 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.992+1401dupT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685378 | |||||||
| chr12:47685378 | C | CAA | 11 | a0001c0001t0001g0134 a0001c0001t0001g0148 a0001c0001t0006g0029 others(8): Show |
13 | HG00280.hp2 HG00621.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.992+1400_992+1401d others(4): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685378 | |||||||
| chr12:47685378 | C | CAAA | 7 | a0001c0001t0006g0072 a0001c0002t0007g0013 a0001c0002t0007g0028 others(4): Show |
18 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.992+1399_992+1401d others(5): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685378 | |||||||
| chr12:47685378 | CA | C | 51 | a0001c0001t0001g0205 a0001c0001t0002g0005 a0001c0001t0002g0006 others(48): Show |
85 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.992+1401delT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685378 | |||||||
| chr12:47685519 | G | A | 1 | a0001c0001t0001g0047 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.992+1261C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685519 | |||||||
| chr12:47685724 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(69): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.992+1056G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685724 | |||||||
| chr12:47685818 | AAGC | A | 6 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(3): Show |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.992+959_992+961del others(3): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47685818 | |||||||
| chr12:47686150 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.992+630T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686150 | |||||||
| chr12:47686339 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.992+441T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686339 | |||||||
| chr12:47686545 | T | C | 2 | a0001c0002t0008g0251 a0001c0002t0008g0252 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.992+235A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686545 | T | TAC | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(53): Show |
81 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.992+233_992+234dup others(2): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686545 | T | TACAC | 31 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0058 others(28): Show |
40 | HG01081.hp1 HG01106.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.992+231_992+234dup others(4): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686545 | T | TACACAC | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(43): Show |
75 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.992+229_992+234dup others(6): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686545 | T | TACACACA others(1): Show |
15 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0047 others(12): Show |
20 | HG00280.hp2 HG00741.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.992+227_992+234dup others(8): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686545 | T | TACACACA others(3): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0077 |
4 | HG00733.hp1 HG00735.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.992+225_992+234dup others(10): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686545 | T | TACACACA others(7): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0022g0123 others(1): Show |
7 | HG00639.hp2 HG00642.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.992+221_992+234dup others(14): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686545 | T | TACACATA others(3): Show |
3 | a0001c0001t0003g0011 a0001c0001t0014g0165 a0001c0001t0019g0153 |
3 | HG02135.hp1 HG02145.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.992+234_992+235ins others(10): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686545 | T | TACACATA others(5): Show |
3 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0106 |
4 | HG00597.hp2 HG02015.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.992+234_992+235ins others(12): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686545 | T | TACACATA others(7): Show |
13 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0035 others(10): Show |
18 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.992+234_992+235ins others(14): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686545 | T | TACACATA others(9): Show |
23 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0011 others(20): Show |
34 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.992+234_992+235ins others(16): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686545 | T | TACACATA others(11): Show |
13 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0033 others(10): Show |
13 | HG00408.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.992+234_992+235ins others(18): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686545 | T | TACACATA others(13): Show |
1 | a0001c0001t0003g0002 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.992+234_992+235ins others(20): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686545 | TAC | T | 38 | a0001c0001t0001g0007 a0001c0001t0001g0214 a0001c0001t0001g0215 others(35): Show |
66 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.992+233_992+234del others(2): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686545 | |||||||
| chr12:47686667 | T | A | 1 | a0001c0001t0001g0047 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.992+113A>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686667 | |||||||
| chr12:47686710 | T | C | 1 | a0001c0001t0014g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.992+70A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 9/16 | chr12 | 47686710 | |||||||
| chr12:47686947 | T | A | 51 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(48): Show |
85 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.865-40A>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 8/16 | chr12 | 47686947 | |||||||
| chr12:47687001 | C | T | 2 | a0001c0001t0026g0245 a0004c0007t0027g0246 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.865-94G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 8/16 | chr12 | 47687001 | |||||||
| chr12:47687359 | T | G | 1 | a0001c0001t0003g0109 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.865-452A>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 8/16 | chr12 | 47687359 | |||||||
| chr12:47687369 | T | G | 1 | a0001c0001t0001g0136 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.865-462A>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 8/16 | chr12 | 47687369 | |||||||
| chr12:47687478 | A | G | 49 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(46): Show |
83 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.864+398T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 8/16 | chr12 | 47687478 | |||||||
| chr12:47687663 | T | G | 4 | a0001c0002t0007g0028 a0001c0002t0008g0010 a0001c0002t0008g0251 others(1): Show |
11 | HG00738.hp1 HG01167.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.864+213A>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 8/16 | chr12 | 47687663 | |||||||
| chr12:47687669 | T | G | 1 | a0001c0001t0003g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.864+207A>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 8/16 | chr12 | 47687669 | |||||||
| chr12:47687756 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(120): Show |
220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.864+120G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 8/16 | chr12 | 47687756 | |||||||
| chr12:47687854 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(45): Show |
95 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.864+22G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 8/16 | chr12 | 47687854 | |||||||
| chr12:47688087 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.739-86T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 7/16 | chr12 | 47688087 | |||||||
| chr12:47688241 | C | G | 51 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(48): Show |
85 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.739-240G>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 7/16 | chr12 | 47688241 | |||||||
| chr12:47688328 | G | A | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG01884.hp1 HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.739-327C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 7/16 | chr12 | 47688328 | |||||||
| chr12:47688340 | T | C | 1 | a0001c0001t0002g0188 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.739-339A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 7/16 | chr12 | 47688340 | |||||||
| chr12:47688349 | G | T | 1 | a0001c0001t0002g0178 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.739-348C>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 7/16 | chr12 | 47688349 | |||||||
| chr12:47688473 | T | A | 3 | a0001c0001t0010g0048 a0001c0005t0010g0248 a0005c0008t0010g0170 |
4 | HG02723.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.739-472A>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 7/16 | chr12 | 47688473 | |||||||
| chr12:47688564 | T | C | 1 | a0001c0001t0006g0073 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.738+561A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 7/16 | chr12 | 47688564 | |||||||
| chr12:47688699 | T | C | 49 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0011 others(46): Show |
76 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.738+426A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 7/16 | chr12 | 47688699 | |||||||
| chr12:47688930 | T | C | 1 | a0001c0001t0026g0245 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.738+195A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 7/16 | chr12 | 47688930 | |||||||
| chr12:47688973 | C | T | 1 | a0001c0002t0007g0253 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.738+152G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 7/16 | chr12 | 47688973 | |||||||
| chr12:47689222 | T | A | 1 | a0001c0001t0004g0163 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.668-27A>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47689222 | |||||||
| chr12:47689523 | G | C | 1 | a0001c0001t0026g0245 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.668-328C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47689523 | |||||||
| chr12:47689651 | T | C | 3 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0001t0015g0032 |
4 | NA18947.hp1 NA18970.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-456A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47689651 | |||||||
| chr12:47689661 | TC | T | 62 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(59): Show |
98 | HG00280.hp2 HG00558.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.668-467delG | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47689661 | |||||||
| chr12:47689686 | T | C | 6 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(3): Show |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.668-491A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47689686 | |||||||
| chr12:47689719 | T | C | 6 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(3): Show |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.668-524A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47689719 | |||||||
| chr12:47689808 | G | A | 1 | a0001c0001t0003g0099 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.668-613C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47689808 | |||||||
| chr12:47689926 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(52): Show |
105 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.667+592C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47689926 | |||||||
| chr12:47689932 | T | C | 52 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(49): Show |
86 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.667+586A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47689932 | |||||||
| chr12:47690048 | A | C | 1 | a0001c0001t0001g0027 | 3 | HG01884.hp2 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.667+470T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47690048 | |||||||
| chr12:47690054 | AAG | A | 10 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0068 others(7): Show |
12 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.667+462_667+463del others(2): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47690054 | |||||||
| chr12:47690060 | A | G | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.667+458T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47690060 | |||||||
| chr12:47690071 | A | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0218 a0001c0001t0001g0219 |
4 | NA18945.hp2 NA19000.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+447T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47690071 | |||||||
| chr12:47690311 | C | T | 1 | a0001c0001t0002g0054 | 2 | HG02040.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.667+207G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 6/16 | chr12 | 47690311 | |||||||
| chr12:47690753 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18978.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.546-114C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47690753 | |||||||
| chr12:47690773 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(229): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.546-134G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47690773 | |||||||
| chr12:47690829 | T | G | 1 | a0001c0001t0001g0249 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.546-190A>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47690829 | |||||||
| chr12:47691344 | G | A | 1 | a0001c0001t0001g0047 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.546-705C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47691344 | |||||||
| chr12:47691352 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.546-713C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47691352 | |||||||
| chr12:47691520 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02895.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.546-881A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47691520 | |||||||
| chr12:47691748 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.546-1109A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47691748 | |||||||
| chr12:47691872 | A | C | 6 | a0001c0001t0002g0025 a0001c0001t0002g0055 a0001c0001t0002g0177 others(3): Show |
9 | HG00738.hp2 HG01081.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.546-1233T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47691872 | |||||||
| chr12:47691980 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(121): Show |
221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.546-1341A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47691980 | |||||||
| chr12:47691997 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.546-1358C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47691997 | |||||||
| chr12:47692065 | G | A | 52 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(49): Show |
86 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.546-1426C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47692065 | |||||||
| chr12:47692157 | TTGGA | T | 45 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0011 others(42): Show |
72 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.546-1522_546-1519d others(6): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47692157 | |||||||
| chr12:47692302 | C | T | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.546-1663G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47692302 | |||||||
| chr12:47692382 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(49): Show |
102 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.546-1743T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47692382 | |||||||
| chr12:47692478 | G | A | 1 | a0001c0005t0010g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.546-1839C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47692478 | |||||||
| chr12:47692499 | T | G | 1 | a0001c0001t0001g0234 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.546-1860A>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47692499 | |||||||
| chr12:47692596 | T | C | 49 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0011 others(46): Show |
76 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.546-1957A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47692596 | |||||||
| chr12:47692672 | T | C | 6 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(3): Show |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.546-2033A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47692672 | |||||||
| chr12:47692854 | C | G | 1 | a0001c0001t0009g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.546-2215G>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47692854 | |||||||
| chr12:47693025 | A | G | 1 | a0001c0001t0019g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.546-2386T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693025 | |||||||
| chr12:47693028 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.546-2389G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693028 | |||||||
| chr12:47693029 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.546-2390C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693029 | |||||||
| chr12:47693049 | G | T | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.546-2410C>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693049 | |||||||
| chr12:47693124 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.546-2485C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693124 | |||||||
| chr12:47693128 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0026 others(50): Show |
77 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.546-2489C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693128 | |||||||
| chr12:47693223 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.546-2584C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693223 | |||||||
| chr12:47693266 | G | T | 1 | a0001c0001t0019g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.546-2627C>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693266 | |||||||
| chr12:47693373 | C | G | 1 | a0001c0001t0014g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.546-2734G>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693373 | |||||||
| chr12:47693435 | G | A | 47 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0011 others(44): Show |
74 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.546-2796C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693435 | |||||||
| chr12:47693449 | C | A | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.546-2810G>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693449 | |||||||
| chr12:47693528 | C | T | 5 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0008g0010 others(2): Show |
16 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.545+2748G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693528 | |||||||
| chr12:47693613 | T | C | 2 | a0001c0001t0012g0168 a0001c0001t0012g0169 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.545+2663A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693613 | |||||||
| chr12:47693815 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.545+2461A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47693815 | |||||||
| chr12:47694093 | T | G | 2 | a0001c0001t0026g0245 a0004c0007t0027g0246 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.545+2183A>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47694093 | |||||||
| chr12:47694147 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.545+2129C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47694147 | |||||||
| chr12:47694147 | G | C | 1 | a0001c0001t0001g0047 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.545+2129C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47694147 | |||||||
| chr12:47694189 | T | C | 1 | a0001c0001t0009g0114 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.545+2087A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47694189 | |||||||
| chr12:47694315 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.545+1961C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47694315 | |||||||
| chr12:47694390 | G | T | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.545+1886C>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47694390 | |||||||
| chr12:47694500 | C | G | 5 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0008g0010 others(2): Show |
16 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.545+1776G>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47694500 | |||||||
| chr12:47694766 | T | C | 1 | a0001c0001t0010g0048 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.545+1510A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47694766 | |||||||
| chr12:47694860 | A | C | 50 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(47): Show |
84 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.545+1416T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47694860 | |||||||
| chr12:47695094 | A | AGAAAGAA others(16): Show |
1 | a0001c0001t0001g0047 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.545+1159_545+1181d others(25): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47695094 | |||||||
| chr12:47695148 | G | T | 1 | a0001c0001t0004g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.545+1128C>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47695148 | |||||||
| chr12:47695228 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.545+1048G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47695228 | |||||||
| chr12:47695274 | CAAGA | C | 48 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0011 others(45): Show |
75 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.545+998_545+1001de others(5): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47695274 | |||||||
| chr12:47695376 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.545+900A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47695376 | |||||||
| chr12:47695523 | G | A | 1 | a0001c0001t0002g0191 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.545+753C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47695523 | |||||||
| chr12:47695921 | G | A | 50 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(47): Show |
84 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.545+355C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 5/16 | chr12 | 47695921 | |||||||
| chr12:47696494 | G | A | 1 | a0001c0001t0004g0163 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.418-91C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47696494 | |||||||
| chr12:47696511 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0214 a0001c0001t0001g0215 others(4): Show |
13 | HG02622.hp2 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.418-108A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47696511 | |||||||
| chr12:47696732 | A | G | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.418-329T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47696732 | |||||||
| chr12:47696802 | T | C | 3 | a0001c0001t0010g0048 a0001c0005t0010g0248 a0005c0008t0010g0170 |
4 | HG02723.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.418-399A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47696802 | |||||||
| chr12:47696841 | G | A | 1 | a0001c0001t0003g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.418-438C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47696841 | |||||||
| chr12:47696888 | T | C | 2 | a0001c0001t0013g0203 a0001c0001t0013g0236 |
2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.418-485A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47696888 | |||||||
| chr12:47696967 | A | G | 6 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(3): Show |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.418-564T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47696967 | |||||||
| chr12:47697128 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.417+469C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47697128 | |||||||
| chr12:47697297 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(45): Show |
95 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.417+300A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47697297 | |||||||
| chr12:47697330 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.417+267A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47697330 | |||||||
| chr12:47697348 | T | C | 1 | a0001c0001t0002g0199 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.417+249A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47697348 | |||||||
| chr12:47697364 | A | G | 6 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(3): Show |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.417+233T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47697364 | |||||||
| chr12:47697428 | A | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0214 a0001c0001t0001g0215 others(2): Show |
11 | HG02622.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.417+169T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47697428 | |||||||
| chr12:47697574 | A | C | 1 | a0001c0001t0006g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.417+23T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 4/16 | chr12 | 47697574 | |||||||
| chr12:47697735 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.295-16C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47697735 | |||||||
| chr12:47697739 | AACAGGG | A | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.295-26_295-21delCC others(4): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47697739 | |||||||
| chr12:47697741 | CAG | C | 5 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(2): Show |
16 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.295-24_295-23delCT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47697741 | |||||||
| chr12:47697743 | G | A | 1 | a0001c0002t0008g0251 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.295-24C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47697743 | |||||||
| chr12:47697765 | GA | G | 16 | a0001c0001t0001g0003 a0001c0001t0001g0065 a0001c0001t0001g0204 others(13): Show |
26 | HG00639.hp1 HG00673.hp2 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.295-47delT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47697765 | |||||||
| chr12:47697774 | GA | G | 6 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(3): Show |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.295-56delT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47697774 | |||||||
| chr12:47697777 | A | G | 1 | a0001c0001t0002g0050 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.295-58T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47697777 | |||||||
| chr12:47697803 | CAAAT | C | 6 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(3): Show |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.295-88_295-85delAT others(2): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47697803 | |||||||
| chr12:47698087 | A | T | 1 | a0001c0001t0004g0151 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.295-368T>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47698087 | |||||||
| chr12:47698194 | G | A | 13 | a0001c0001t0002g0005 a0001c0001t0002g0024 a0001c0001t0002g0049 others(10): Show |
24 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.295-475C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47698194 | |||||||
| chr12:47698274 | C | G | 6 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(3): Show |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.295-555G>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47698274 | |||||||
| chr12:47698322 | T | C | 3 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 |
3 | HG02698.hp2 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.295-603A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47698322 | |||||||
| chr12:47698631 | G | A | 3 | a0001c0001t0003g0103 a0001c0001t0003g0104 a0001c0001t0003g0105 |
3 | HG01070.hp1 HG01071.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.295-912C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47698631 | |||||||
| chr12:47698755 | G | T | 1 | a0001c0001t0003g0084 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.295-1036C>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47698755 | |||||||
| chr12:47698758 | C | T | 1 | a0001c0001t0013g0203 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.295-1039G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47698758 | |||||||
| chr12:47698905 | A | G | 1 | a0001c0001t0001g0058 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.295-1186T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47698905 | |||||||
| chr12:47698940 | T | C | 5 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0008g0010 others(2): Show |
16 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.295-1221A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47698940 | |||||||
| chr12:47698948 | T | C | 1 | a0001c0001t0003g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.295-1229A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47698948 | |||||||
| chr12:47699091 | A | C | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.295-1372T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47699091 | |||||||
| chr12:47699229 | C | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(52): Show |
105 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.295-1510G>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47699229 | |||||||
| chr12:47699235 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.295-1516T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47699235 | |||||||
| chr12:47699426 | AAAG | A | 6 | a0001c0001t0002g0025 a0001c0001t0002g0055 a0001c0001t0002g0177 others(3): Show |
9 | HG00738.hp2 HG01081.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.295-1710_295-1708d others(5): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47699426 | |||||||
| chr12:47699769 | C | T | 1 | a0001c0001t0001g0057 | 2 | HG03831.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.294+1695G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47699769 | |||||||
| chr12:47699779 | A | T | 2 | a0001c0001t0006g0029 a0001c0001t0006g0254 |
3 | HG00741.hp1 HG01243.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.294+1685T>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47699779 | |||||||
| chr12:47699782 | G | A | 1 | a0001c0001t0002g0049 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.294+1682C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47699782 | |||||||
| chr12:47699900 | C | G | 2 | a0001c0001t0026g0245 a0004c0007t0027g0246 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.294+1564G>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47699900 | |||||||
| chr12:47699943 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.294+1521A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47699943 | |||||||
| chr12:47699944 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.294+1520G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47699944 | |||||||
| chr12:47699975 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.294+1489G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47699975 | |||||||
| chr12:47699991 | C | CT | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0026 others(63): Show |
102 | HG00140.hp1 HG00408.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.294+1472dupA | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47699991 | |||||||
| chr12:47699991 | CT | C | 16 | a0001c0001t0001g0047 a0001c0001t0001g0145 a0001c0001t0001g0146 others(13): Show |
18 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.294+1472delA | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47699991 | |||||||
| chr12:47700087 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | NA18968.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.294+1377C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47700087 | |||||||
| chr12:47700129 | G | GTTTCTT | 4 | a0001c0001t0005g0021 a0001c0001t0005g0173 a0001c0001t0005g0174 others(1): Show |
6 | NA18965.hp1 NA18982.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+1334_294+1335i others(8): Show |
RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47700129 | |||||||
| chr12:47700189 | C | T | 3 | a0001c0001t0010g0048 a0001c0005t0010g0248 a0005c0008t0010g0170 |
4 | HG02723.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+1275G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47700189 | |||||||
| chr12:47700625 | C | G | 1 | a0001c0001t0001g0146 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.294+839G>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47700625 | |||||||
| chr12:47700626 | G | C | 1 | a0001c0001t0001g0146 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.294+838C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47700626 | |||||||
| chr12:47700702 | T | C | 1 | a0001c0001t0014g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.294+762A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47700702 | |||||||
| chr12:47700709 | T | C | 1 | a0001c0001t0001g0047 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.294+755A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47700709 | |||||||
| chr12:47700790 | T | C | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.294+674A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47700790 | |||||||
| chr12:47700931 | T | C | 1 | a0001c0001t0002g0200 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.294+533A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47700931 | |||||||
| chr12:47700951 | G | A | 1 | a0001c0001t0001g0060 | 2 | NA18945.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.294+513C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 3/16 | chr12 | 47700951 | |||||||
| chr12:47701732 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.154-128C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 2/16 | chr12 | 47701732 | |||||||
| chr12:47701779 | A | G | 2 | a0001c0001t0026g0245 a0004c0007t0027g0246 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.154-175T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 2/16 | chr12 | 47701779 | |||||||
| chr12:47701871 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.154-267T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 2/16 | chr12 | 47701871 | |||||||
| chr12:47702126 | C | T | 5 | a0001c0001t0002g0005 a0001c0001t0002g0049 a0001c0001t0002g0076 others(2): Show |
13 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.154-522G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 2/16 | chr12 | 47702126 | |||||||
| chr12:47702130 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.154-526A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 2/16 | chr12 | 47702130 | |||||||
| chr12:47702273 | C | T | 1 | a0001c0001t0014g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.153+415G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 2/16 | chr12 | 47702273 | |||||||
| chr12:47702312 | G | A | 1 | a0001c0001t0003g0110 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.153+376C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 2/16 | chr12 | 47702312 | |||||||
| chr12:47702383 | T | TA | 5 | a0001c0001t0001g0027 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
7 | HG01884.hp2 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+304dupT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 2/16 | chr12 | 47702383 | |||||||
| chr12:47702426 | C | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0026 others(50): Show |
77 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.153+262G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 2/16 | chr12 | 47702426 | |||||||
| chr12:47702452 | G | A | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.153+236C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 2/16 | chr12 | 47702452 | |||||||
| chr12:47702503 | G | A | 1 | a0001c0001t0004g0046 | 2 | NA19070.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.153+185C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 2/16 | chr12 | 47702503 | |||||||
| chr12:47702889 | A | G | 1 | a0001c0001t0014g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-6-43T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47702889 | |||||||
| chr12:47702947 | A | C | 50 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(47): Show |
84 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.-6-101T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47702947 | |||||||
| chr12:47702958 | C | G | 1 | a0001c0002t0007g0013 | 5 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-112G>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47702958 | |||||||
| chr12:47702973 | T | A | 1 | a0001c0001t0014g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-6-127A>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47702973 | |||||||
| chr12:47702992 | A | T | 1 | a0001c0001t0026g0245 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-6-146T>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47702992 | |||||||
| chr12:47703091 | G | A | 1 | a0001c0001t0014g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-6-245C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47703091 | |||||||
| chr12:47703255 | G | C | 1 | a0001c0001t0014g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-6-409C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47703255 | |||||||
| chr12:47703264 | G | A | 1 | a0001c0005t0010g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-6-418C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47703264 | |||||||
| chr12:47703286 | A | C | 1 | a0001c0005t0010g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-6-440T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47703286 | |||||||
| chr12:47703297 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-6-451C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47703297 | |||||||
| chr12:47703451 | C | T | 1 | a0001c0002t0007g0013 | 5 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-605G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47703451 | |||||||
| chr12:47703485 | C | T | 5 | a0001c0001t0003g0011 a0001c0001t0003g0078 a0001c0001t0003g0079 others(2): Show |
10 | HG02135.hp1 NA18947.hp1 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.-6-639G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47703485 | |||||||
| chr12:47703531 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(69): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-6-685G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47703531 | |||||||
| chr12:47703872 | A | G | 1 | a0001c0001t0001g0056 | 2 | HG01346.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-6-1026T>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47703872 | |||||||
| chr12:47703901 | C | T | 1 | a0001c0001t0001g0014 | 4 | HG00597.hp1 NA18983.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-1055G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47703901 | |||||||
| chr12:47704135 | G | A | 1 | a0001c0001t0004g0167 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-6-1289C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47704135 | |||||||
| chr12:47704393 | G | A | 1 | a0001c0001t0003g0111 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-6-1547C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47704393 | |||||||
| chr12:47704407 | C | A | 2 | a0001c0001t0012g0168 a0001c0001t0012g0169 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-7+1545G>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47704407 | |||||||
| chr12:47704543 | A | AT | 49 | a0001c0001t0001g0077 a0001c0001t0003g0002 a0001c0001t0003g0008 others(46): Show |
76 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.-7+1408dupA | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47704543 | |||||||
| chr12:47704557 | T | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
5 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+1395A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47704557 | |||||||
| chr12:47704581 | T | C | 3 | a0001c0001t0010g0048 a0001c0005t0010g0248 a0005c0008t0010g0170 |
4 | HG02723.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+1371A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47704581 | |||||||
| chr12:47704586 | C | A | 49 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0022 others(46): Show |
83 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.-7+1366G>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47704586 | |||||||
| chr12:47704649 | A | C | 1 | a0001c0001t0002g0076 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-7+1303T>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47704649 | |||||||
| chr12:47704777 | G | T | 1 | a0001c0002t0008g0251 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-7+1175C>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47704777 | |||||||
| chr12:47704779 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0026 others(50): Show |
77 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.-7+1173C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47704779 | |||||||
| chr12:47704930 | G | C | 1 | a0004c0007t0027g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-7+1022C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47704930 | |||||||
| chr12:47705034 | T | C | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7+918A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47705034 | |||||||
| chr12:47705036 | G | A | 1 | a0001c0001t0002g0244 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7+916C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47705036 | |||||||
| chr12:47705093 | G | A | 6 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(3): Show |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-7+859C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47705093 | |||||||
| chr12:47705188 | G | A | 2 | a0001c0001t0026g0245 a0004c0007t0027g0246 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-7+764C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47705188 | |||||||
| chr12:47705289 | T | C | 3 | a0001c0001t0001g0249 a0001c0005t0010g0248 a0007c0010t0001g0247 |
3 | HG04204.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-7+663A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47705289 | |||||||
| chr12:47705342 | G | C | 1 | a0001c0001t0002g0250 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-7+610C>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47705342 | |||||||
| chr12:47705572 | C | G | 4 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0074 others(1): Show |
6 | HG00558.hp2 HG00673.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+380G>C | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47705572 | |||||||
| chr12:47705592 | T | C | 6 | a0001c0002t0007g0013 a0001c0002t0007g0028 a0001c0002t0007g0253 others(3): Show |
17 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-7+360A>G | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47705592 | |||||||
| chr12:47705693 | CA | C | 11 | a0001c0001t0006g0029 a0001c0001t0006g0066 a0001c0001t0006g0067 others(8): Show |
13 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7+258delT | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47705693 | |||||||
| chr12:47705796 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-7+156G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47705796 | |||||||
| chr12:47705849 | G | A | 1 | a0001c0001t0006g0254 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-7+103C>T | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47705849 | |||||||
| chr12:47705921 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02895.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-7+31G>A | RPAP3 | ENSG00000005175.10 | transcript | ENST00000005386.8 | protein_coding | 1/16 | chr12 | 47705921 |