Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5985 |
| ensemblid | ENSG00000111445.14 |
| hgncid | 9973 |
| symbol | RFC5 |
| name | replication factor C subunit 5 |
| refseq_nuc | NM_007370.7 |
| refseq_prot | NP_031396.1 |
| ensembl_nuc | ENST00000454402.7 |
| ensembl_prot | ENSP00000408295.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 118016703 |
| end | 118032234 |
| strand | + |
| ver | v1.2 |
| region | chr12:118016703-118032234 |
| region5000 | chr12:118011703-118037234 |
| regionname0 | RFC5_chr12_118016703_118032234 |
| regionname5000 | RFC5_chr12_118011703_118037234 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 340 | 437 | 98 | 74 | 201 | 18 | 44 | 155 | RFC5_chr12_118011703_118037234 | RFC5 | METSA others(335): Show |
chr12 | 118011703 | 118037234 |
| a0002 | 0/0 | 340 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | METSA others(335): Show |
chr12 | 118011703 | 118037234 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1020 | 400 | 71 | 67 | 200 | 18 | 42 | RFC5_chr12_118011703_118037234 | RFC5 | ATGGA others(1015): Show |
chr12 | 118011703 | 118037234 | ||
| a0001c0002 | 0/0 | 1020 | 35 | 27 | 7 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | ATGGA others(1015): Show |
chr12 | 118011703 | 118037234 | ||
| a0001c0003 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | ATGGA others(1015): Show |
chr12 | 118011703 | 118037234 | ||
| a0001c0005 | 0/0 | 1020 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | ATGGA others(1015): Show |
chr12 | 118011703 | 118037234 | ||
| a0002c0004 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | ATGGA others(1015): Show |
chr12 | 118011703 | 118037234 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2104 | 383 | 61 | 65 | 199 | 16 | 40 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0001t0002 | 0/0 | 2104 | 4 | 4 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0001t0003 | 0/0 | 2104 | 4 | 0 | 1 | 0 | 2 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0001t0004 | 0/0 | 2104 | 3 | 3 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0001t0006 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0001t0007 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0001t0008 | 0/0 | 5605 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(5600): Show |
chr12 | 118011703 | 118037234 |
| a0001c0001t0009 | 0/0 | 2104 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0001t0010 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0001t0011 | 0/0 | 2104 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0002t0001 | 0/0 | 2104 | 31 | 23 | 7 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0002t0005 | 0/0 | 2104 | 2 | 2 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0002t0006 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0002t0012 | 0/0 | 2104 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0003t0001 | 0/0 | 2104 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0001c0005t0001 | 0/0 | 2104 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| a0002c0004t0001 | 0/0 | 2104 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | GAGAG others(2099): Show |
chr12 | 118011703 | 118037234 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 43 | 2 | 9 | 31 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0002 | 1/0 | 33 | 0 | 9 | 18 | 2 | 3 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0003 | 0/0 | 14 | 4 | 3 | 6 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0004 | 0/0 | 14 | 2 | 0 | 12 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0005 | 0/0 | 12 | 1 | 6 | 4 | 1 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0006 | 0/0 | 11 | 0 | 2 | 8 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 6 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0010 | 0/0 | 6 | 2 | 0 | 3 | 1 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0022 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0033 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0134 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0008g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0009g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0001t0011g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0005g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0002t0012g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0001c0005t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| a0002c0004t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | FIN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01168 | hp1 | a0001 | c0001 | t0011 | g0168 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02523 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0202 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02723 | hp1 | a0001 | c0002 | t0005 | g0056 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02735 | hp2 | a0001 | c0005 | t0001 | g0162 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0056 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03486 | hp1 | a0001 | c0002 | t0006 | g0100 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03490 | hp2 | a0001 | c0001 | t0009 | g0069 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | ESN | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0163 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0169 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | STU | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | BEB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | YRI | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18956 | hp2 | a0002 | c0004 | t0001 | g0003 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18984 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0102 | AFR | LWK | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | YRI | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | ASW | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | GIH | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | USA | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | USA | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | USA | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA21309 | hp1 | a0001 | c0002 | t0012 | g0192 | AFR | LWK | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0130 | AFR | LWK | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0134 | REF | REF | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | RFC5_chr12_118011703_118037234 | RFC5 | chr12 | 118011703 | 118037234 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:118020972 | A | T | 1 | a0002 | 1 | NA18956.hp2 | missense_variant | MODERATE | c.334A>T | p.Arg112Trp | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/11 | 459/2104 | 334/1023 | 112/340 | chr12 | 118020972 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:118020953 | C | T | 1 | a0001c0005 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.315C>T | p.Ile105Ile | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/11 | 440/2104 | 315/1023 | 105/340 | chr12 | 118020953 | |||
| chr12:118025768 | A | G | 1 | a0001c0003 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.603A>G | p.Gly201Gly | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/11 | 728/2104 | 603/1023 | 201/340 | chr12 | 118025768 | |||
| chr12:118028015 | T | C | 1 | a0001c0002 | 35 | HG00639.hp1 HG01123.hp1 HG01168.hp2 others(32): Show |
synonymous_variant | LOW | c.856T>C | p.Leu286Leu | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/11 | 981/2104 | 856/1023 | 286/340 | chr12 | 118028015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:118016791 | C | G | 1 | a0001c0002t0012 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-37C>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/11 | 37 | chr12 | 118016791 | ||||||
| chr12:118016805 | C | G | 1 | a0001c0001t0011 | 1 | HG01168.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-23C>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/11 | chr12 | 118016805 | |||||||
| chr12:118031737 | A | G | 1 | a0001c0001t0004 | 3 | HG02257.hp2 HG02572.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*459A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 11/11 | 459 | chr12 | 118031737 | ||||||
| chr12:118031763 | A | G | 1 | a0001c0001t0010 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*485A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 11/11 | 485 | chr12 | 118031763 | ||||||
| chr12:118031769 | A | G | 1 | a0001c0001t0009 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*491A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 11/11 | 491 | chr12 | 118031769 | ||||||
| chr12:118031845 | G | C | 1 | a0001c0002t0005 | 2 | HG02723.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*567G>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 11/11 | 567 | chr12 | 118031845 | ||||||
| chr12:118031964 | G | A | 2 | a0001c0001t0006 a0001c0002t0006 |
2 | HG03486.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*686G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 11/11 | 686 | chr12 | 118031964 | ||||||
| chr12:118032005 | G | A | 2 | a0001c0001t0002 a0001c0001t0010 |
5 | HG02055.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*727G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 11/11 | 727 | chr12 | 118032005 | ||||||
| chr12:118032070 | A | G | 1 | a0001c0001t0003 | 4 | HG01175.hp2 HG03927.hp2 NA20752.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*792A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 11/11 | 792 | chr12 | 118032070 | ||||||
| chr12:118032084 | T | TAAAAAAC others(3494): Show |
1 | a0001c0001t0008 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*815_*816insGCCCTC others(3495): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 11/11 | 816 | INFO_REALIGN_3_PRIME | chr12 | 118032084 | |||||
| chr12:118032139 | A | G | 1 | a0001c0001t0007 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*861A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 11/11 | 861 | chr12 | 118032139 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:118016933 | A | C | 1 | a0001c0001t0001g0205 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.65+41A>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118016933 | |||||||
| chr12:118017028 | C | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
306 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.65+136C>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017028 | |||||||
| chr12:118017190 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.65+298C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017190 | |||||||
| chr12:118017207 | A | T | 1 | a0001c0001t0001g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.65+315A>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017207 | |||||||
| chr12:118017208 | T | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0058 |
3 | HG01099.hp2 HG01934.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.65+316T>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017208 | |||||||
| chr12:118017376 | C | T | 3 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0202 |
3 | HG02647.hp2 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.65+484C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017376 | |||||||
| chr12:118017419 | G | A | 1 | a0001c0002t0001g0095 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.65+527G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017419 | |||||||
| chr12:118017477 | C | G | 4 | a0001c0002t0001g0199 a0001c0002t0001g0200 a0001c0002t0001g0201 others(1): Show |
4 | HG01884.hp2 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.65+585C>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017477 | |||||||
| chr12:118017490 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.65+598T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017490 | |||||||
| chr12:118017521 | A | G | 1 | a0001c0002t0001g0202 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.65+629A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017521 | |||||||
| chr12:118017633 | A | C | 1 | a0001c0002t0001g0198 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65+741A>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017633 | |||||||
| chr12:118017672 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.65+780C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017672 | |||||||
| chr12:118017704 | T | A | 1 | a0001c0001t0001g0042 | 2 | HG02683.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.65+812T>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017704 | |||||||
| chr12:118017736 | T | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | NA19055.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.65+844T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017736 | |||||||
| chr12:118017760 | A | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0093 |
6 | HG00438.hp1 NA18941.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.65+868A>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017760 | |||||||
| chr12:118017811 | T | C | 1 | a0001c0001t0001g0035 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.65+919T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017811 | |||||||
| chr12:118017933 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.65+1041A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017933 | |||||||
| chr12:118017954 | T | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
332 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.65+1062T>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118017954 | |||||||
| chr12:118018026 | ATG | A | 1 | a0001c0001t0001g0021 | 3 | NA18950.hp1 NA18951.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.66-1045_66-1044del others(2): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118018026 | |||||||
| chr12:118018107 | G | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
333 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.66-965G>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118018107 | |||||||
| chr12:118018232 | A | G | 1 | a0001c0001t0001g0024 | 3 | NA18964.hp2 NA18983.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.66-840A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118018232 | |||||||
| chr12:118018357 | T | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0099 |
5 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.66-715T>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118018357 | |||||||
| chr12:118018428 | G | A | 9 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0043 others(6): Show |
16 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.66-644G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118018428 | |||||||
| chr12:118018480 | G | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(27): Show |
59 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.66-592G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118018480 | |||||||
| chr12:118018663 | G | A | 1 | a0001c0001t0010g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.66-409G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118018663 | |||||||
| chr12:118018695 | C | T | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(27): Show |
59 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.66-377C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118018695 | |||||||
| chr12:118018755 | G | T | 1 | a0001c0001t0001g0055 | 2 | HG00544.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.66-317G>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118018755 | |||||||
| chr12:118018848 | A | G | 1 | a0001c0002t0001g0030 | 3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.66-224A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118018848 | |||||||
| chr12:118018958 | C | T | 1 | a0001c0002t0012g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.66-114C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118018958 | |||||||
| chr12:118018981 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | NA19005.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.66-91G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118018981 | |||||||
| chr12:118019012 | T | G | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.66-60T>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118019012 | |||||||
| chr12:118019020 | A | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0053 others(16): Show |
41 | HG00280.hp1 HG00642.hp2 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.66-52A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 1/10 | chr12 | 118019020 | |||||||
| chr12:118019161 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.130+25C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 2/10 | chr12 | 118019161 | |||||||
| chr12:118019568 | A | G | 9 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0043 others(6): Show |
16 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.131-64A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 2/10 | chr12 | 118019568 | |||||||
| chr12:118019627 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02165.hp1 | splice_region_variant&intron_variant | LOW | c.131-5C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 2/10 | chr12 | 118019627 | |||||||
| chr12:118019869 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG02080.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.267+101C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 3/10 | chr12 | 118019869 | |||||||
| chr12:118019881 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.267+113A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 3/10 | chr12 | 118019881 | |||||||
| chr12:118019889 | A | G | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0002t0001g0030 others(1): Show |
6 | HG01243.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.267+121A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 3/10 | chr12 | 118019889 | |||||||
| chr12:118019946 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
7 | HG00639.hp1 HG00639.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.267+178G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 3/10 | chr12 | 118019946 | |||||||
| chr12:118020058 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.267+290C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 3/10 | chr12 | 118020058 | |||||||
| chr12:118020059 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.267+291C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 3/10 | chr12 | 118020059 | |||||||
| chr12:118020148 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.267+380T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 3/10 | chr12 | 118020148 | |||||||
| chr12:118020151 | T | C | 26 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0027 others(23): Show |
42 | HG00558.hp2 HG00597.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.267+383T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 3/10 | chr12 | 118020151 | |||||||
| chr12:118020585 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.268-321G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 3/10 | chr12 | 118020585 | |||||||
| chr12:118020872 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.268-34G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 3/10 | chr12 | 118020872 | |||||||
| chr12:118021009 | G | A | 1 | a0001c0002t0005g0056 | 2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.347+24G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118021009 | |||||||
| chr12:118021067 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.347+82C>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118021067 | |||||||
| chr12:118021228 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.347+243T>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118021228 | |||||||
| chr12:118021241 | G | A | 1 | a0001c0001t0001g0038 | 2 | HG01943.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.347+256G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118021241 | |||||||
| chr12:118021314 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(18): Show |
43 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.347+329C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118021314 | |||||||
| chr12:118021368 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0173 |
3 | HG03490.hp1 HG03492.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.347+383C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118021368 | |||||||
| chr12:118021440 | T | A | 1 | a0001c0001t0001g0062 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.347+455T>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118021440 | |||||||
| chr12:118021459 | C | T | 9 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0043 others(6): Show |
16 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.347+474C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118021459 | |||||||
| chr12:118021464 | C | T | 1 | a0001c0001t0001g0023 | 3 | HG00741.hp2 HG01074.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.347+479C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118021464 | |||||||
| chr12:118021490 | T | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
352 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.347+505T>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118021490 | |||||||
| chr12:118021639 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.348-647C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118021639 | |||||||
| chr12:118021640 | TA | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0087 a0001c0001t0001g0088 others(3): Show |
7 | HG00558.hp2 HG01167.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.348-633delA | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 118021640 | ||||||
| chr12:118021682 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.348-604C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118021682 | |||||||
| chr12:118021830 | G | A | 3 | a0001c0001t0004g0117 a0001c0001t0004g0118 a0001c0001t0004g0119 |
3 | HG02257.hp2 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.348-456G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118021830 | |||||||
| chr12:118022022 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG01975.hp2 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.348-264T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118022022 | |||||||
| chr12:118022036 | G | A | 1 | a0001c0002t0006g0100 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.348-250G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118022036 | |||||||
| chr12:118022097 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.348-189A>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 4/10 | chr12 | 118022097 | |||||||
| chr12:118022381 | C | T | 3 | a0001c0002t0001g0051 a0001c0002t0001g0169 a0001c0002t0001g0175 |
4 | HG01123.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+22C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118022381 | |||||||
| chr12:118022456 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0011g0168 |
2 | HG01168.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.421+97C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118022456 | |||||||
| chr12:118022526 | G | A | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0002t0001g0030 others(1): Show |
6 | HG01243.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+167G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118022526 | |||||||
| chr12:118022532 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.421+173T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118022532 | |||||||
| chr12:118022625 | C | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0072 others(4): Show |
12 | HG02451.hp1 HG02622.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.421+266C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118022625 | |||||||
| chr12:118022707 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.421+348C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118022707 | |||||||
| chr12:118022717 | G | A | 1 | a0001c0002t0001g0046 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.421+358G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118022717 | |||||||
| chr12:118022805 | A | C | 1 | a0001c0001t0001g0150 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.421+446A>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118022805 | |||||||
| chr12:118022824 | G | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0123 a0001c0001t0001g0179 |
7 | HG01109.hp1 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+465G>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118022824 | |||||||
| chr12:118022863 | T | C | 3 | a0001c0002t0001g0051 a0001c0002t0001g0169 a0001c0002t0001g0175 |
4 | HG01123.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+504T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118022863 | |||||||
| chr12:118022886 | C | T | 1 | a0001c0002t0005g0056 | 2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.421+527C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118022886 | |||||||
| chr12:118022943 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.421+584G>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118022943 | |||||||
| chr12:118023031 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.421+672G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023031 | |||||||
| chr12:118023079 | C | CT | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
354 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.421+722dupT | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 118023079 | ||||||
| chr12:118023132 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.421+773T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023132 | |||||||
| chr12:118023214 | C | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
354 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.421+855C>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023214 | |||||||
| chr12:118023233 | C | G | 1 | a0001c0001t0004g0119 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.421+874C>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023233 | |||||||
| chr12:118023322 | T | C | 41 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(38): Show |
78 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.421+963T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023322 | |||||||
| chr12:118023395 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.421+1036A>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023395 | |||||||
| chr12:118023399 | G | GGGA | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(73): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.421+1052_421+1054d others(5): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 118023399 | ||||||
| chr12:118023411 | A | AGGAG | 8 | a0001c0001t0001g0105 a0001c0001t0001g0111 a0001c0001t0001g0112 others(5): Show |
8 | HG00609.hp2 HG02055.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.421+1054_421+1055i others(6): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 118023411 | ||||||
| chr12:118023414 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(42): Show |
108 | HG00544.hp1 HG00597.hp2 HG01071.hp2 others(105): Show |
intron_variant | MODIFIER | c.421+1055G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023414 | |||||||
| chr12:118023415 | G | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0174 a0001c0001t0004g0118 |
3 | HG02572.hp1 HG03710.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.421+1056G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023415 | |||||||
| chr12:118023418 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(42): Show |
108 | HG00544.hp1 HG00597.hp2 HG01071.hp2 others(105): Show |
intron_variant | MODIFIER | c.421+1059A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023418 | |||||||
| chr12:118023421 | A | AG | 1 | a0001c0002t0001g0016 | 4 | HG01243.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+1066dupG | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 118023421 | ||||||
| chr12:118023421 | A | AGG | 5 | a0001c0002t0001g0017 a0001c0002t0001g0043 a0001c0002t0001g0199 others(2): Show |
9 | HG01884.hp2 HG02809.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.421+1065_421+1066d others(4): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 118023421 | ||||||
| chr12:118023421 | A | G | 1 | a0001c0002t0001g0202 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.421+1062A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023421 | |||||||
| chr12:118023422 | G | GGA | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.421+1064_421+1065i others(4): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 118023422 | ||||||
| chr12:118023422 | GGGGAGGA others(1): Show |
G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(42): Show |
108 | HG00544.hp1 HG00597.hp2 HG01071.hp2 others(105): Show |
intron_variant | MODIFIER | c.421+1065_421+1072d others(10): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 118023422 | ||||||
| chr12:118023426 | A | G | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.421+1067A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023426 | |||||||
| chr12:118023430 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0166 |
2 | NA18955.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.421+1071A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023430 | |||||||
| chr12:118023440 | G | T | 1 | a0001c0001t0001g0174 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.421+1081G>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023440 | |||||||
| chr12:118023440 | GT | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(42): Show |
107 | HG00544.hp1 HG01071.hp2 HG01123.hp1 others(104): Show |
intron_variant | MODIFIER | c.421+1082delT | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023440 | |||||||
| chr12:118023441 | T | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0165 |
3 | HG00597.hp2 HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.421+1082T>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023441 | |||||||
| chr12:118023444 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(44): Show |
110 | HG00544.hp1 HG00597.hp2 HG01071.hp2 others(107): Show |
intron_variant | MODIFIER | c.421+1085G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023444 | |||||||
| chr12:118023453 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
351 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.421+1094G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023453 | |||||||
| chr12:118023456 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.421+1097G>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023456 | |||||||
| chr12:118023467 | C | T | 1 | a0001c0001t0007g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.421+1108C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023467 | |||||||
| chr12:118023468 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0072 others(4): Show |
13 | HG02451.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.421+1109G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023468 | |||||||
| chr12:118023469 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.421+1110G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023469 | |||||||
| chr12:118023507 | G | GGGA | 13 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0072 others(10): Show |
26 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.421+1167_421+1169d others(5): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 118023507 | ||||||
| chr12:118023524 | G | A | 1 | a0001c0001t0001g0018 | 4 | NA18944.hp1 NA18980.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+1165G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023524 | |||||||
| chr12:118023533 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.421+1174G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023533 | |||||||
| chr12:118023652 | G | A | 1 | a0001c0001t0001g0032 | 3 | HG02451.hp1 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.422-1199G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023652 | |||||||
| chr12:118023676 | G | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(16): Show |
41 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.422-1175G>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023676 | |||||||
| chr12:118023769 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.422-1082T>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023769 | |||||||
| chr12:118023781 | G | GCCAAATA others(311): Show |
1 | a0001c0001t0001g0022 | 3 | HG01175.hp1 HG06807.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.422-1056_422-1055i others(320): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 118023781 | ||||||
| chr12:118023807 | C | CAAG | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
186 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(183): Show |
intron_variant | MODIFIER | c.422-1040_422-1038d others(5): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 118023807 | ||||||
| chr12:118023826 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.422-1025A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023826 | |||||||
| chr12:118023920 | A | G | 2 | a0001c0001t0006g0130 a0001c0002t0001g0129 |
2 | HG02145.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.422-931A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023920 | |||||||
| chr12:118023955 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.422-896A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118023955 | |||||||
| chr12:118024033 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.422-818C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024033 | |||||||
| chr12:118024083 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.422-768G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024083 | |||||||
| chr12:118024088 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0103 a0001c0001t0004g0117 others(2): Show |
8 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.422-763T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024088 | |||||||
| chr12:118024115 | G | A | 1 | a0001c0001t0001g0019 | 4 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-736G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024115 | |||||||
| chr12:118024117 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.422-734G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024117 | |||||||
| chr12:118024118 | A | G | 1 | a0001c0001t0001g0019 | 4 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-733A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024118 | |||||||
| chr12:118024123 | T | C | 1 | a0001c0001t0001g0019 | 4 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-728T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024123 | |||||||
| chr12:118024137 | C | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0165 |
2 | HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.422-714C>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024137 | |||||||
| chr12:118024144 | A | C | 11 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0123 others(8): Show |
17 | HG01109.hp1 HG01243.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.422-707A>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024144 | |||||||
| chr12:118024145 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0068 |
4 | HG01175.hp1 HG06807.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-706T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024145 | |||||||
| chr12:118024145 | T | G | 1 | a0001c0001t0001g0063 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.422-706T>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024145 | |||||||
| chr12:118024169 | G | A | 23 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0018 others(20): Show |
46 | HG00609.hp1 HG00639.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.422-682G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024169 | |||||||
| chr12:118024197 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.422-654C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024197 | |||||||
| chr12:118024211 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.422-640C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024211 | |||||||
| chr12:118024255 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.422-596C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024255 | |||||||
| chr12:118024290 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.422-561A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024290 | |||||||
| chr12:118024340 | C | CAA | 39 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(36): Show |
102 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.422-506_422-505dup others(2): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 118024340 | ||||||
| chr12:118024347 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
389 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(386): Show |
intron_variant | MODIFIER | c.422-504G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024347 | |||||||
| chr12:118024426 | T | C | 14 | a0001c0001t0002g0125 a0001c0001t0002g0128 a0001c0001t0002g0141 others(11): Show |
18 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.422-425T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024426 | |||||||
| chr12:118024449 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.422-402A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024449 | |||||||
| chr12:118024468 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(51): Show |
121 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.422-383C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024468 | |||||||
| chr12:118024658 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0135 a0001c0001t0001g0136 |
5 | HG01884.hp1 HG02258.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-193G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024658 | |||||||
| chr12:118024687 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.422-164A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024687 | |||||||
| chr12:118024691 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.422-160G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024691 | |||||||
| chr12:118024697 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0093 |
6 | HG00438.hp1 NA18941.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-154C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 5/10 | chr12 | 118024697 | |||||||
| chr12:118025045 | A | G | 1 | a0001c0002t0001g0095 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.581+35A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 6/10 | chr12 | 118025045 | |||||||
| chr12:118025393 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.582-354C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 6/10 | chr12 | 118025393 | |||||||
| chr12:118025478 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG00323.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.582-269A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 6/10 | chr12 | 118025478 | |||||||
| chr12:118025514 | G | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
6 | HG01884.hp1 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.582-233G>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 6/10 | chr12 | 118025514 | |||||||
| chr12:118025524 | T | A | 25 | a0001c0001t0002g0125 a0001c0001t0002g0128 a0001c0001t0002g0141 others(22): Show |
37 | HG00639.hp1 HG01123.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.582-223T>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 6/10 | chr12 | 118025524 | |||||||
| chr12:118025540 | T | C | 21 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0030 others(18): Show |
33 | HG00639.hp1 HG01123.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.582-207T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 6/10 | chr12 | 118025540 | |||||||
| chr12:118025643 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.582-104C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 6/10 | chr12 | 118025643 | |||||||
| chr12:118025848 | C | CT | 35 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(32): Show |
60 | HG00140.hp2 HG00609.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.663+38dupT | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 118025848 | ||||||
| chr12:118025848 | CT | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0074 others(3): Show |
12 | HG00323.hp1 HG00438.hp2 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.663+38delT | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 118025848 | ||||||
| chr12:118025935 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.663+107G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/10 | chr12 | 118025935 | |||||||
| chr12:118026233 | T | C | 3 | a0001c0001t0002g0125 a0001c0001t0002g0141 a0001c0001t0002g0204 |
3 | HG02055.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.663+405T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/10 | chr12 | 118026233 | |||||||
| chr12:118026378 | G | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(35): Show |
99 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.664-511G>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/10 | chr12 | 118026378 | |||||||
| chr12:118026394 | C | G | 22 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0030 others(19): Show |
35 | HG00639.hp1 HG01123.hp1 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.664-495C>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/10 | chr12 | 118026394 | |||||||
| chr12:118026458 | G | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0099 |
5 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.664-431G>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/10 | chr12 | 118026458 | |||||||
| chr12:118026517 | T | A | 1 | a0001c0002t0001g0198 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.664-372T>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/10 | chr12 | 118026517 | |||||||
| chr12:118026590 | C | A | 1 | a0001c0001t0001g0149 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.664-299C>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/10 | chr12 | 118026590 | |||||||
| chr12:118026679 | G | A | 5 | a0001c0001t0002g0125 a0001c0001t0002g0128 a0001c0001t0002g0141 others(2): Show |
5 | HG02055.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-210G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/10 | chr12 | 118026679 | |||||||
| chr12:118026801 | G | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(40): Show |
104 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.664-88G>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/10 | chr12 | 118026801 | |||||||
| chr12:118026845 | G | A | 1 | a0001c0002t0012g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.664-44G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/10 | chr12 | 118026845 | |||||||
| chr12:118026883 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
192 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(189): Show |
splice_region_variant&intron_variant | LOW | c.664-6A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 7/10 | chr12 | 118026883 | |||||||
| chr12:118027067 | A | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(35): Show |
99 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.793+49A>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 8/10 | chr12 | 118027067 | |||||||
| chr12:118027185 | T | G | 1 | a0001c0001t0001g0205 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.793+167T>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 8/10 | chr12 | 118027185 | |||||||
| chr12:118027371 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.793+353C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 8/10 | chr12 | 118027371 | |||||||
| chr12:118027443 | C | CG | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
192 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.793+427dupG | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 118027443 | ||||||
| chr12:118027482 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.793+464G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 8/10 | chr12 | 118027482 | |||||||
| chr12:118027493 | G | A | 1 | a0001c0002t0001g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.794-460G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 8/10 | chr12 | 118027493 | |||||||
| chr12:118027500 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.794-453C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 8/10 | chr12 | 118027500 | |||||||
| chr12:118027517 | C | G | 9 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0043 others(6): Show |
16 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.794-436C>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 8/10 | chr12 | 118027517 | |||||||
| chr12:118027671 | TA | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0059 others(5): Show |
13 | HG00639.hp2 HG03239.hp2 HG03688.hp1 others(10): Show |
intron_variant | MODIFIER | c.794-267delA | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 118027671 | ||||||
| chr12:118027683 | A | AAAAG | 42 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(39): Show |
106 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.794-258_794-255dup others(4): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 118027683 | ||||||
| chr12:118027683 | A | AAAG | 18 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0043 others(15): Show |
28 | HG00639.hp1 HG01123.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.794-268_794-267ins others(3): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 118027683 | ||||||
| chr12:118027706 | C | T | 1 | a0001c0002t0006g0100 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.794-247C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 8/10 | chr12 | 118027706 | |||||||
| chr12:118027854 | G | C | 1 | a0001c0001t0010g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.794-99G>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 8/10 | chr12 | 118027854 | |||||||
| chr12:118028339 | G | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(40): Show |
104 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.871+309G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118028339 | |||||||
| chr12:118028408 | C | T | 1 | a0001c0001t0001g0022 | 3 | HG01175.hp1 HG06807.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.871+378C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118028408 | |||||||
| chr12:118028409 | T | G | 22 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0030 others(19): Show |
35 | HG00639.hp1 HG01123.hp1 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.871+379T>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118028409 | |||||||
| chr12:118028463 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.871+433G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118028463 | |||||||
| chr12:118028483 | C | CA | 12 | a0001c0001t0001g0075 a0001c0001t0001g0092 a0001c0001t0001g0147 others(9): Show |
15 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.871+464dupA | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 118028483 | ||||||
| chr12:118028483 | C | CAA | 28 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0042 others(25): Show |
78 | HG00280.hp1 HG00544.hp1 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.871+463_871+464dup others(2): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 118028483 | ||||||
| chr12:118028483 | C | CAAA | 12 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0096 others(9): Show |
23 | HG00597.hp2 HG01891.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.871+462_871+464dup others(3): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 118028483 | ||||||
| chr12:118028494 | AC | A | 13 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0030 others(10): Show |
23 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.871+465delC | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118028494 | |||||||
| chr12:118028495 | C | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
169 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.871+465C>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118028495 | |||||||
| chr12:118028500 | C | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(37): Show |
102 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.871+470C>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118028500 | |||||||
| chr12:118028544 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.871+514G>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118028544 | |||||||
| chr12:118028642 | T | TA | 23 | a0001c0001t0001g0111 a0001c0001t0001g0150 a0001c0002t0001g0016 others(20): Show |
36 | HG00639.hp1 HG01123.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.871+627dupA | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 118028642 | ||||||
| chr12:118028642 | TA | T | 7 | a0001c0001t0001g0049 a0001c0001t0001g0121 a0001c0001t0001g0136 others(4): Show |
8 | HG01975.hp2 HG02735.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.871+627delA | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 118028642 | ||||||
| chr12:118028657 | AGTCT | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0193 |
4 | HG02109.hp1 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.871+632_871+635del others(4): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 118028657 | ||||||
| chr12:118028674 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
192 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.871+644G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118028674 | |||||||
| chr12:118028745 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.871+715G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118028745 | |||||||
| chr12:118028850 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.871+820C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118028850 | |||||||
| chr12:118028902 | G | A | 1 | a0001c0002t0006g0100 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.872-869G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118028902 | |||||||
| chr12:118028975 | G | A | 1 | a0001c0001t0001g0022 | 3 | HG01175.hp1 HG06807.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.872-796G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118028975 | |||||||
| chr12:118029133 | G | A | 25 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(22): Show |
50 | HG00140.hp2 HG00609.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.872-638G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118029133 | |||||||
| chr12:118029237 | C | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0193 |
4 | HG02109.hp1 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.872-534C>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118029237 | |||||||
| chr12:118029272 | GC | G | 25 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(22): Show |
50 | HG00140.hp2 HG00609.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.872-497delC | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 118029272 | ||||||
| chr12:118029314 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(41): Show |
105 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.872-457G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118029314 | |||||||
| chr12:118029328 | A | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(41): Show |
105 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.872-443A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118029328 | |||||||
| chr12:118029347 | G | T | 1 | a0001c0001t0006g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.872-424G>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118029347 | |||||||
| chr12:118029358 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(41): Show |
105 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.872-413C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118029358 | |||||||
| chr12:118029380 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.872-391G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118029380 | |||||||
| chr12:118029564 | T | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(61): Show |
138 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.872-207T>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118029564 | |||||||
| chr12:118029652 | AG | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(41): Show |
105 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.872-117delG | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 118029652 | ||||||
| chr12:118029748 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(100): Show |
219 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(216): Show |
intron_variant | MODIFIER | c.872-23A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 9/10 | chr12 | 118029748 | |||||||
| chr12:118029840 | C | T | 19 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0030 others(16): Show |
32 | HG00639.hp1 HG01123.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.926+15C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118029840 | |||||||
| chr12:118029876 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.926+51T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118029876 | |||||||
| chr12:118029927 | G | A | 1 | a0001c0001t0001g0022 | 3 | HG01175.hp1 HG06807.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.926+102G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118029927 | |||||||
| chr12:118029937 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
7 | HG00673.hp2 HG02074.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.926+112G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118029937 | |||||||
| chr12:118030191 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.926+366A>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118030191 | |||||||
| chr12:118030266 | A | G | 1 | a0001c0001t0001g0022 | 3 | HG01175.hp1 HG06807.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.926+441A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118030266 | |||||||
| chr12:118030321 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.926+496A>G | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118030321 | |||||||
| chr12:118030369 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.926+544T>C | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118030369 | |||||||
| chr12:118030387 | G | T | 4 | a0001c0001t0002g0125 a0001c0001t0002g0141 a0001c0001t0002g0204 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.926+562G>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118030387 | |||||||
| chr12:118030492 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG00140.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.926+667C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118030492 | |||||||
| chr12:118030503 | C | CTTAA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
203 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.927-678_927-675dup others(4): Show |
RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 118030503 | ||||||
| chr12:118030543 | G | A | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0160 others(1): Show |
4 | HG01515.hp2 HG01517.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.927-639G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118030543 | |||||||
| chr12:118030700 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.927-482G>A | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118030700 | |||||||
| chr12:118030741 | C | T | 1 | a0001c0001t0001g0022 | 3 | HG01175.hp1 HG06807.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.927-441C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118030741 | |||||||
| chr12:118030922 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.927-260C>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118030922 | |||||||
| chr12:118030960 | G | T | 20 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0030 others(17): Show |
33 | HG00639.hp1 HG01123.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.927-222G>T | RFC5 | ENSG00000111445.14 | transcript | ENST00000454402.7 | protein_coding | 10/10 | chr12 | 118030960 |