Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5983 |
| ensemblid | ENSG00000133119.13 |
| hgncid | 9971 |
| symbol | RFC3 |
| name | replication factor C subunit 3 |
| refseq_nuc | NM_002915.4 |
| refseq_prot | NP_002906.1 |
| ensembl_nuc | ENST00000380071.8 |
| ensembl_prot | ENSP00000369411.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 33818149 |
| end | 33837500 |
| strand | + |
| ver | v1.2 |
| region | chr13:33818149-33837500 |
| region5000 | chr13:33813149-33842500 |
| regionname0 | RFC3_chr13_33818149_33837500 |
| regionname5000 | RFC3_chr13_33813149_33842500 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 356 | 413 | 90 | 70 | 205 | 10 | 36 | 157 | RFC3_chr13_33813149_33842500 | RFC3 | MSLWV others(351): Show |
chr13 | 33813149 | 33842500 |
| a0002 | 0/0 | 356 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | RFC3_chr13_33813149_33842500 | RFC3 | MSLWV others(351): Show |
chr13 | 33813149 | 33842500 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1068 | 406 | 86 | 70 | 203 | 10 | 35 | RFC3_chr13_33813149_33842500 | RFC3 | ATGAG others(1063): Show |
chr13 | 33813149 | 33842500 | ||
| a0001c0002 | 0/0 | 1068 | 5 | 3 | 0 | 1 | 0 | 1 | RFC3_chr13_33813149_33842500 | RFC3 | ATGAG others(1063): Show |
chr13 | 33813149 | 33842500 | ||
| a0001c0004 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | ATGAG others(1063): Show |
chr13 | 33813149 | 33842500 | ||
| a0001c0005 | 0/0 | 1068 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | ATGAG others(1063): Show |
chr13 | 33813149 | 33842500 | ||
| a0002c0003 | 0/0 | 1068 | 3 | 0 | 0 | 3 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | ATGAG others(1063): Show |
chr13 | 33813149 | 33842500 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2306 | 241 | 34 | 37 | 133 | 10 | 25 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2301): Show |
chr13 | 33813149 | 33842500 |
| a0001c0001t0002 | 0/0 | 2306 | 145 | 36 | 29 | 70 | 0 | 10 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2301): Show |
chr13 | 33813149 | 33842500 |
| a0001c0001t0003 | 0/0 | 2306 | 6 | 5 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2301): Show |
chr13 | 33813149 | 33842500 |
| a0001c0001t0004 | 0/0 | 2292 | 5 | 3 | 2 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2287): Show |
chr13 | 33813149 | 33842500 |
| a0001c0001t0005 | 0/0 | 2306 | 3 | 3 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2301): Show |
chr13 | 33813149 | 33842500 |
| a0001c0001t0006 | 0/0 | 2292 | 2 | 2 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2287): Show |
chr13 | 33813149 | 33842500 |
| a0001c0001t0007 | 0/0 | 2306 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2301): Show |
chr13 | 33813149 | 33842500 |
| a0001c0001t0008 | 0/0 | 2306 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2301): Show |
chr13 | 33813149 | 33842500 |
| a0001c0001t0009 | 0/0 | 2306 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2301): Show |
chr13 | 33813149 | 33842500 |
| a0001c0001t0010 | 0/0 | 2306 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2301): Show |
chr13 | 33813149 | 33842500 |
| a0001c0002t0001 | 0/0 | 2306 | 5 | 3 | 0 | 1 | 0 | 1 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2301): Show |
chr13 | 33813149 | 33842500 |
| a0001c0004t0001 | 0/0 | 2306 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2301): Show |
chr13 | 33813149 | 33842500 |
| a0001c0005t0001 | 0/0 | 2306 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2301): Show |
chr13 | 33813149 | 33842500 |
| a0002c0003t0001 | 0/0 | 2306 | 3 | 0 | 0 | 3 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | AAGCG others(2301): Show |
chr13 | 33813149 | 33842500 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 51 | 7 | 11 | 23 | 3 | 7 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0002 | 0/0 | 35 | 0 | 0 | 26 | 1 | 8 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0004 | 0/0 | 26 | 14 | 4 | 5 | 0 | 3 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0006 | 0/0 | 13 | 0 | 2 | 9 | 0 | 2 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0009 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0010 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0012 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0014 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0025 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0003 | 0/0 | 33 | 4 | 4 | 19 | 0 | 6 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0005 | 0/0 | 24 | 0 | 10 | 13 | 0 | 1 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0007 | 0/0 | 12 | 0 | 1 | 11 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0008 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0011 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0013 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0004g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0005g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0006g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0001t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0004t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0001c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0002c0003t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0078 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0125 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0003 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0076 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | BEB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | BEB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | STU | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | CHB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | YRI | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18960 | hp2 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18995 | hp2 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19005 | hp1 | a0001 | c0005 | t0001 | g0036 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19067 | hp2 | a0002 | c0003 | t0001 | g0117 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ASW | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | GIH | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | MSL | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | USA | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | USA | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0112 | REF | REF | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0088 | REF | REF | RFC3_chr13_33813149_33842500 | RFC3 | chr13 | 33813149 | 33842500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:33830728 | G | A | 1 | a0002 | 3 | NA18960.hp2 NA18995.hp2 NA19067.hp2 |
missense_variant | MODERATE | c.583G>A | p.Val195Met | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 6/9 | 613/2306 | 583/1071 | 195/356 | chr13 | 33830728 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:33830775 | A | G | 2 | a0001c0002 a0001c0005 |
6 | HG02109.hp2 HG03225.hp1 HG03453.hp2 others(3): Show |
synonymous_variant | LOW | c.630A>G | p.Gln210Gln | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 6/9 | 660/2306 | 630/1071 | 210/356 | chr13 | 33830775 | |||
| chr13:33836190 | A | G | 1 | a0001c0005 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.966A>G | p.Leu322Leu | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 9/9 | 996/2306 | 966/1071 | 322/356 | chr13 | 33836190 | |||
| chr13:33836190 | A | T | 1 | a0001c0004 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.966A>T | p.Leu322Leu | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 9/9 | 996/2306 | 966/1071 | 322/356 | chr13 | 33836190 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:33836394 | C | T | 3 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0010 |
149 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*99C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 9/9 | 99 | chr13 | 33836394 | ||||||
| chr13:33836403 | G | A | 1 | a0001c0001t0007 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*108G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 9/9 | 108 | chr13 | 33836403 | ||||||
| chr13:33836459 | T | C | 1 | a0001c0001t0005 | 3 | HG02145.hp2 HG03139.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*164T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 9/9 | 164 | chr13 | 33836459 | ||||||
| chr13:33836493 | A | G | 1 | a0001c0001t0006 | 2 | HG02572.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*198A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 9/9 | 198 | chr13 | 33836493 | ||||||
| chr13:33836690 | G | A | 1 | a0001c0001t0010 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*395G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 9/9 | 395 | chr13 | 33836690 | ||||||
| chr13:33836868 | A | G | 2 | a0001c0001t0003 a0001c0001t0009 |
7 | HG01175.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*573A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 9/9 | 573 | chr13 | 33836868 | ||||||
| chr13:33836948 | TATGTTAC others(7): Show |
T | 2 | a0001c0001t0004 a0001c0001t0006 |
7 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*656_*669delGTTACT others(8): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 9/9 | 656 | INFO_REALIGN_3_PRIME | chr13 | 33836948 | |||||
| chr13:33836966 | A | T | 2 | a0001c0001t0004 a0001c0001t0006 |
7 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*671A>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 9/9 | 671 | chr13 | 33836966 | ||||||
| chr13:33837027 | T | C | 1 | a0001c0001t0008 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*732T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 9/9 | 732 | chr13 | 33837027 | ||||||
| chr13:33837056 | T | C | 1 | a0001c0001t0009 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*761T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 9/9 | 761 | chr13 | 33837056 | ||||||
| chr13:33837258 | C | A | 1 | a0001c0001t0006 | 2 | HG02572.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*963C>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 9/9 | 963 | chr13 | 33837258 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:33818330 | C | G | 1 | a0001c0001t0001g0126 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.87+65C>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33818330 | |||||||
| chr13:33818383 | G | A | 1 | a0001c0001t0006g0030 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.87+118G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33818383 | |||||||
| chr13:33818772 | G | A | 41 | a0001c0001t0001g0051 a0001c0001t0002g0003 a0001c0001t0002g0005 others(38): Show |
148 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(145): Show |
intron_variant | MODIFIER | c.87+507G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33818772 | |||||||
| chr13:33818881 | G | GT | 21 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0028 others(18): Show |
57 | HG00639.hp1 HG00642.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.87+642dupT | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 33818881 | ||||||
| chr13:33818881 | GT | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0074 a0001c0001t0001g0075 others(15): Show |
25 | HG00733.hp2 HG01070.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.87+642delT | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 33818881 | ||||||
| chr13:33818881 | GTT | G | 42 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0002g0003 others(39): Show |
149 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.87+641_87+642delTT | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 33818881 | ||||||
| chr13:33818895 | T | G | 6 | a0001c0001t0002g0071 a0001c0002t0001g0035 a0001c0002t0001g0036 others(3): Show |
7 | HG02109.hp2 HG02630.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.87+630T>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33818895 | |||||||
| chr13:33818896 | T | G | 41 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0002g0003 others(38): Show |
148 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(145): Show |
intron_variant | MODIFIER | c.87+631T>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33818896 | |||||||
| chr13:33818897 | T | G | 1 | a0001c0001t0002g0067 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.87+632T>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33818897 | |||||||
| chr13:33819011 | C | G | 1 | a0001c0001t0002g0065 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.87+746C>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33819011 | |||||||
| chr13:33819027 | A | T | 1 | a0001c0001t0003g0081 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.87+762A>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33819027 | |||||||
| chr13:33819126 | A | G | 2 | a0001c0001t0001g0019 a0001c0004t0001g0125 |
5 | HG02055.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+861A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33819126 | |||||||
| chr13:33819158 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.87+893C>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33819158 | |||||||
| chr13:33819276 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.87+1011A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33819276 | |||||||
| chr13:33819381 | A | C | 48 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0002g0003 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.87+1116A>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33819381 | |||||||
| chr13:33819437 | C | T | 4 | a0001c0001t0003g0079 a0001c0001t0003g0110 a0001c0001t0003g0111 others(1): Show |
4 | HG01175.hp1 HG02615.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+1172C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33819437 | |||||||
| chr13:33819481 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.87+1216C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33819481 | |||||||
| chr13:33819714 | G | A | 48 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0002g0003 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.88-1418G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33819714 | |||||||
| chr13:33819727 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.88-1405G>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33819727 | |||||||
| chr13:33819745 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.88-1387A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33819745 | |||||||
| chr13:33819864 | C | A | 1 | a0001c0001t0002g0046 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.88-1268C>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33819864 | |||||||
| chr13:33819890 | G | T | 48 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0002g0003 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.88-1242G>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33819890 | |||||||
| chr13:33820017 | C | T | 6 | a0001c0001t0002g0071 a0001c0002t0001g0035 a0001c0002t0001g0036 others(3): Show |
7 | HG02109.hp2 HG02630.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.88-1115C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820017 | |||||||
| chr13:33820041 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.88-1091G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820041 | |||||||
| chr13:33820042 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.88-1090A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820042 | |||||||
| chr13:33820095 | A | G | 1 | a0001c0001t0002g0017 | 4 | HG02886.hp2 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-1037A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820095 | |||||||
| chr13:33820096 | C | T | 48 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0002g0003 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.88-1036C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820096 | |||||||
| chr13:33820146 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.88-986C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820146 | |||||||
| chr13:33820217 | C | T | 18 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(15): Show |
75 | HG00408.hp2 HG00609.hp1 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.88-915C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820217 | |||||||
| chr13:33820338 | T | C | 48 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0002g0003 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.88-794T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820338 | |||||||
| chr13:33820339 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.88-793A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820339 | |||||||
| chr13:33820377 | C | G | 1 | a0001c0001t0003g0081 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.88-755C>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820377 | |||||||
| chr13:33820573 | C | T | 3 | a0001c0001t0003g0079 a0001c0001t0003g0111 a0001c0001t0009g0080 |
3 | HG02615.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.88-559C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820573 | |||||||
| chr13:33820579 | C | T | 51 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0051 others(48): Show |
162 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.88-553C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820579 | |||||||
| chr13:33820587 | C | G | 2 | a0001c0001t0002g0023 a0001c0001t0002g0066 |
4 | HG02647.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.88-545C>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820587 | |||||||
| chr13:33820811 | C | T | 18 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(15): Show |
75 | HG00408.hp2 HG00609.hp1 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.88-321C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820811 | |||||||
| chr13:33820883 | C | T | 4 | a0001c0001t0002g0021 a0001c0001t0002g0033 a0001c0001t0002g0054 others(1): Show |
7 | HG01884.hp2 HG01891.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.88-249C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820883 | |||||||
| chr13:33820902 | CATATATA others(5): Show |
C | 33 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0002g0003 others(30): Show |
130 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.88-219_88-208delTT others(10): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 33820902 | ||||||
| chr13:33820903 | ATATATAT others(3): Show |
A | 14 | a0001c0001t0001g0019 a0001c0001t0002g0013 a0001c0001t0002g0015 others(11): Show |
25 | HG00735.hp2 HG01109.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.88-219_88-210delTT others(8): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 33820903 | ||||||
| chr13:33820905 | ATATATAT others(1): Show |
A | 3 | a0001c0001t0002g0023 a0001c0001t0002g0066 a0001c0002t0001g0035 |
6 | HG02647.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-219_88-212delTT others(6): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 33820905 | ||||||
| chr13:33820913 | TTA | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
246 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.88-198_88-197delTA | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 33820913 | ||||||
| chr13:33820917 | A | T | 3 | a0001c0001t0003g0079 a0001c0001t0003g0111 a0001c0001t0009g0080 |
3 | HG02615.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.88-215A>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820917 | |||||||
| chr13:33820945 | C | G | 1 | a0001c0001t0002g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.88-187C>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820945 | |||||||
| chr13:33820982 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.88-150T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820982 | |||||||
| chr13:33820991 | A | G | 1 | a0001c0004t0001g0125 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.88-141A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33820991 | |||||||
| chr13:33821052 | T | G | 3 | a0001c0001t0003g0079 a0001c0001t0003g0111 a0001c0001t0009g0080 |
3 | HG02615.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.88-80T>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 1/8 | chr13 | 33821052 | |||||||
| chr13:33821309 | CG | C | 4 | a0001c0001t0002g0013 a0001c0001t0002g0020 a0001c0001t0002g0047 others(1): Show |
12 | HG00642.hp2 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.225+44delG | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 33821309 | ||||||
| chr13:33821391 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.225+122A>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33821391 | |||||||
| chr13:33821425 | T | C | 4 | a0001c0001t0002g0011 a0001c0001t0002g0056 a0001c0001t0002g0061 others(1): Show |
11 | NA18957.hp2 NA18961.hp1 NA18967.hp2 others(8): Show |
intron_variant | MODIFIER | c.225+156T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33821425 | |||||||
| chr13:33821477 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.225+208C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33821477 | |||||||
| chr13:33821589 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.225+320A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33821589 | |||||||
| chr13:33821608 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.225+339A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33821608 | |||||||
| chr13:33821710 | A | G | 1 | a0001c0001t0001g0014 | 7 | HG02135.hp1 NA18941.hp2 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+441A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33821710 | |||||||
| chr13:33821763 | G | A | 50 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0068 others(47): Show |
161 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(158): Show |
intron_variant | MODIFIER | c.225+494G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33821763 | |||||||
| chr13:33821838 | C | A | 2 | a0001c0001t0001g0019 a0001c0004t0001g0125 |
5 | HG02055.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+569C>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33821838 | |||||||
| chr13:33822062 | T | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0025 others(9): Show |
37 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.225+793T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33822062 | |||||||
| chr13:33822122 | G | A | 6 | a0001c0001t0002g0071 a0001c0002t0001g0035 a0001c0002t0001g0036 others(3): Show |
7 | HG02109.hp2 HG02630.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.225+853G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33822122 | |||||||
| chr13:33822297 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.225+1028G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33822297 | |||||||
| chr13:33822351 | T | C | 1 | a0001c0001t0002g0049 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.225+1082T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33822351 | |||||||
| chr13:33822463 | A | G | 2 | a0001c0001t0001g0019 a0001c0004t0001g0125 |
5 | HG02055.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+1194A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33822463 | |||||||
| chr13:33822491 | G | A | 50 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0068 others(47): Show |
161 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(158): Show |
intron_variant | MODIFIER | c.225+1222G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33822491 | |||||||
| chr13:33822506 | G | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0054 a0001c0001t0002g0055 |
5 | HG01884.hp2 HG02976.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+1237G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33822506 | |||||||
| chr13:33822529 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.225+1260G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33822529 | |||||||
| chr13:33822635 | C | G | 1 | a0001c0001t0009g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.226-1282C>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33822635 | |||||||
| chr13:33822961 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.226-956G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33822961 | |||||||
| chr13:33823152 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0043 |
4 | NA18970.hp2 NA19063.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-765G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33823152 | |||||||
| chr13:33823286 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.226-631A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33823286 | |||||||
| chr13:33823382 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.226-535A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33823382 | |||||||
| chr13:33823425 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.226-492T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33823425 | |||||||
| chr13:33823452 | A | G | 48 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0002g0003 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.226-465A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33823452 | |||||||
| chr13:33823492 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.226-425A>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33823492 | |||||||
| chr13:33823581 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.226-336T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33823581 | |||||||
| chr13:33823633 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0121 |
2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.226-284A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 2/8 | chr13 | 33823633 | |||||||
| chr13:33824013 | A | G | 23 | a0001c0001t0001g0051 a0001c0001t0002g0003 a0001c0001t0002g0013 others(20): Show |
73 | HG00423.hp2 HG00621.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.293+29A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33824013 | |||||||
| chr13:33824405 | G | T | 4 | a0001c0001t0002g0021 a0001c0001t0002g0033 a0001c0001t0002g0054 others(1): Show |
7 | HG01884.hp2 HG01891.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.293+421G>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33824405 | |||||||
| chr13:33824443 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.293+459A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33824443 | |||||||
| chr13:33824483 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(51): Show |
201 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.293+499C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33824483 | |||||||
| chr13:33824512 | C | T | 48 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0002g0003 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.293+528C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33824512 | |||||||
| chr13:33824642 | T | C | 50 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0068 others(47): Show |
161 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(158): Show |
intron_variant | MODIFIER | c.293+658T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33824642 | |||||||
| chr13:33824757 | G | A | 18 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(15): Show |
75 | HG00408.hp2 HG00609.hp1 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.293+773G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33824757 | |||||||
| chr13:33824775 | C | T | 41 | a0001c0001t0001g0051 a0001c0001t0002g0003 a0001c0001t0002g0005 others(38): Show |
148 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(145): Show |
intron_variant | MODIFIER | c.293+791C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33824775 | |||||||
| chr13:33824792 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.293+808A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33824792 | |||||||
| chr13:33824967 | G | T | 18 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(15): Show |
75 | HG00408.hp2 HG00609.hp1 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.294-822G>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33824967 | |||||||
| chr13:33825009 | G | A | 1 | a0001c0001t0006g0030 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.294-780G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33825009 | |||||||
| chr13:33825126 | T | G | 19 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(16): Show |
71 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.294-663T>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33825126 | |||||||
| chr13:33825163 | G | C | 1 | a0001c0001t0001g0038 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.294-626G>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33825163 | |||||||
| chr13:33825187 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.294-602A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33825187 | |||||||
| chr13:33825243 | C | T | 23 | a0001c0001t0001g0051 a0001c0001t0002g0003 a0001c0001t0002g0013 others(20): Show |
73 | HG00423.hp2 HG00621.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.294-546C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33825243 | |||||||
| chr13:33825287 | C | T | 1 | a0001c0001t0002g0034 | 2 | NA18962.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.294-502C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33825287 | |||||||
| chr13:33825340 | CTTTG | C | 6 | a0001c0001t0002g0071 a0001c0002t0001g0035 a0001c0002t0001g0036 others(3): Show |
7 | HG02109.hp2 HG02630.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.294-442_294-439del others(4): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 33825340 | ||||||
| chr13:33825357 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.294-432T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33825357 | |||||||
| chr13:33825488 | A | G | 18 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(15): Show |
75 | HG00408.hp2 HG00609.hp1 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.294-301A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33825488 | |||||||
| chr13:33825491 | C | A | 6 | a0001c0001t0002g0071 a0001c0002t0001g0035 a0001c0002t0001g0036 others(3): Show |
7 | HG02109.hp2 HG02630.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.294-298C>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33825491 | |||||||
| chr13:33825746 | A | G | 1 | a0001c0001t0009g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.294-43A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 3/8 | chr13 | 33825746 | |||||||
| chr13:33825912 | A | G | 1 | a0001c0001t0003g0081 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.391+26A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33825912 | |||||||
| chr13:33826060 | A | G | 1 | a0001c0001t0003g0073 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.391+174A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33826060 | |||||||
| chr13:33826152 | T | C | 3 | a0001c0001t0001g0039 a0002c0003t0001g0040 a0002c0003t0001g0117 |
5 | HG00408.hp1 NA18960.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+266T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33826152 | |||||||
| chr13:33826162 | T | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0029 others(2): Show |
17 | HG01346.hp2 HG01993.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.391+276T>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33826162 | |||||||
| chr13:33826394 | G | A | 1 | a0001c0001t0002g0031 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.391+508G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33826394 | |||||||
| chr13:33826493 | G | A | 2 | a0001c0001t0001g0019 a0001c0004t0001g0125 |
5 | HG02055.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+607G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33826493 | |||||||
| chr13:33826663 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0003g0073 |
2 | HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.391+777T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33826663 | |||||||
| chr13:33826685 | C | CT | 42 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0002g0003 others(39): Show |
149 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.391+803dupT | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr13 | 33826685 | ||||||
| chr13:33826738 | G | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0025 others(15): Show |
44 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.391+852G>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33826738 | |||||||
| chr13:33826739 | G | A | 60 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0025 others(57): Show |
193 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.391+853G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33826739 | |||||||
| chr13:33826758 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.391+872A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33826758 | |||||||
| chr13:33826875 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | NA18943.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.391+989G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33826875 | |||||||
| chr13:33826983 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.391+1097A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33826983 | |||||||
| chr13:33827118 | T | A | 1 | a0001c0001t0008g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.391+1232T>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33827118 | |||||||
| chr13:33827322 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.391+1436C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33827322 | |||||||
| chr13:33827335 | G | C | 63 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0019 others(60): Show |
160 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.391+1449G>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33827335 | |||||||
| chr13:33827541 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0002g0031 a0001c0004t0001g0125 |
7 | HG02055.hp2 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.391+1655A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33827541 | |||||||
| chr13:33827626 | A | G | 1 | a0001c0001t0008g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.391+1740A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33827626 | |||||||
| chr13:33827632 | A | T | 1 | a0001c0001t0002g0056 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.391+1746A>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33827632 | |||||||
| chr13:33827846 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0028 others(9): Show |
37 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.391+1960C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33827846 | |||||||
| chr13:33828016 | G | C | 1 | a0001c0001t0008g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.392-1820G>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33828016 | |||||||
| chr13:33828020 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.392-1816A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33828020 | |||||||
| chr13:33828244 | C | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0066 |
4 | HG02647.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-1592C>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33828244 | |||||||
| chr13:33828256 | T | C | 48 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.392-1580T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33828256 | |||||||
| chr13:33828360 | G | A | 1 | a0001c0002t0001g0035 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.392-1476G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33828360 | |||||||
| chr13:33828409 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.392-1427A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33828409 | |||||||
| chr13:33828793 | T | A | 5 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0069 others(2): Show |
6 | HG02109.hp2 HG03225.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-1043T>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33828793 | |||||||
| chr13:33828850 | A | C | 1 | a0001c0001t0002g0032 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.392-986A>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33828850 | |||||||
| chr13:33829167 | T | C | 48 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.392-669T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33829167 | |||||||
| chr13:33829313 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.392-523A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33829313 | |||||||
| chr13:33829385 | A | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(17): Show |
72 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.392-451A>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33829385 | |||||||
| chr13:33829394 | A | G | 18 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(15): Show |
75 | HG00408.hp2 HG00609.hp1 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.392-442A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33829394 | |||||||
| chr13:33829647 | T | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0099 |
2 | NA18997.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.392-189T>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33829647 | |||||||
| chr13:33829757 | A | T | 2 | a0001c0001t0001g0019 a0001c0004t0001g0125 |
5 | HG02055.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-79A>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33829757 | |||||||
| chr13:33829809 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.392-27A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 4/8 | chr13 | 33829809 | |||||||
| chr13:33830112 | T | C | 50 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0002g0003 others(47): Show |
158 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(155): Show |
intron_variant | MODIFIER | c.573+95T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 5/8 | chr13 | 33830112 | |||||||
| chr13:33830148 | A | C | 1 | a0001c0001t0002g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.573+131A>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 5/8 | chr13 | 33830148 | |||||||
| chr13:33830265 | G | C | 18 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(15): Show |
75 | HG00408.hp2 HG00609.hp1 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.573+248G>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 5/8 | chr13 | 33830265 | |||||||
| chr13:33830333 | T | C | 24 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0015 others(21): Show |
74 | HG00423.hp2 HG00621.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.573+316T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 5/8 | chr13 | 33830333 | |||||||
| chr13:33830356 | A | G | 1 | a0001c0001t0002g0059 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.573+339A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 5/8 | chr13 | 33830356 | |||||||
| chr13:33830371 | A | T | 1 | a0001c0001t0002g0058 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.574-348A>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 5/8 | chr13 | 33830371 | |||||||
| chr13:33830388 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.574-331A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 5/8 | chr13 | 33830388 | |||||||
| chr13:33830427 | A | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0045 others(3): Show |
17 | HG00609.hp2 HG02055.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.574-292A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 5/8 | chr13 | 33830427 | |||||||
| chr13:33830631 | A | T | 5 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0069 others(2): Show |
6 | HG02109.hp2 HG03225.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-88A>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 5/8 | chr13 | 33830631 | |||||||
| chr13:33831025 | C | T | 2 | a0001c0001t0001g0019 a0001c0004t0001g0125 |
5 | HG02055.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.710+170C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 6/8 | chr13 | 33831025 | |||||||
| chr13:33831057 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.711-199G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 6/8 | chr13 | 33831057 | |||||||
| chr13:33831064 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0122 |
4 | HG01257.hp2 HG01952.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-192G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 6/8 | chr13 | 33831064 | |||||||
| chr13:33831106 | T | C | 48 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.711-150T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 6/8 | chr13 | 33831106 | |||||||
| chr13:33831175 | C | T | 1 | a0001c0001t0004g0078 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.711-81C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 6/8 | chr13 | 33831175 | |||||||
| chr13:33831229 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.711-27T>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 6/8 | chr13 | 33831229 | |||||||
| chr13:33831241 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.711-15C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 6/8 | chr13 | 33831241 | |||||||
| chr13:33831404 | A | C | 1 | a0001c0001t0002g0047 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.809+50A>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33831404 | |||||||
| chr13:33831465 | A | G | 2 | a0001c0001t0002g0052 a0001c0001t0002g0109 |
2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.809+111A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33831465 | |||||||
| chr13:33831491 | A | G | 4 | a0001c0001t0002g0021 a0001c0001t0002g0033 a0001c0001t0002g0054 others(1): Show |
7 | HG01884.hp2 HG01891.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.809+137A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33831491 | |||||||
| chr13:33831514 | TG | T | 42 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(39): Show |
149 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.809+162delG | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33831514 | ||||||
| chr13:33831569 | GGC | G | 48 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.809+216_809+217del others(2): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33831569 | |||||||
| chr13:33831572 | T | TAATGATA others(43): Show |
43 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(40): Show |
150 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(147): Show |
intron_variant | MODIFIER | c.809+218_809+219ins others(50): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33831572 | |||||||
| chr13:33831572 | T | TAATGATA others(75): Show |
5 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0069 others(2): Show |
6 | HG02109.hp2 HG03225.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.809+218_809+219ins others(82): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33831572 | |||||||
| chr13:33831811 | T | C | 2 | a0001c0001t0001g0019 a0001c0004t0001g0125 |
5 | HG02055.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.809+457T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33831811 | |||||||
| chr13:33831906 | A | G | 24 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0015 others(21): Show |
74 | HG00423.hp2 HG00621.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.809+552A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33831906 | |||||||
| chr13:33832051 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.809+697A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832051 | |||||||
| chr13:33832057 | T | C | 48 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.809+703T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832057 | |||||||
| chr13:33832239 | G | C | 48 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.809+885G>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832239 | |||||||
| chr13:33832277 | G | C | 24 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0015 others(21): Show |
74 | HG00423.hp2 HG00621.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.809+923G>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832277 | |||||||
| chr13:33832359 | C | T | 1 | a0001c0001t0008g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.809+1005C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832359 | |||||||
| chr13:33832432 | T | G | 1 | a0001c0002t0001g0069 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.809+1078T>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832432 | |||||||
| chr13:33832507 | G | A | 48 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.809+1153G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832507 | |||||||
| chr13:33832619 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.809+1265A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832619 | |||||||
| chr13:33832724 | T | G | 4 | a0001c0001t0003g0073 a0001c0001t0003g0077 a0001c0001t0003g0081 others(1): Show |
4 | HG01175.hp1 HG02572.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.809+1370T>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832724 | |||||||
| chr13:33832744 | T | C | 4 | a0001c0001t0002g0021 a0001c0001t0002g0033 a0001c0001t0002g0054 others(1): Show |
7 | HG01884.hp2 HG01891.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.809+1390T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832744 | |||||||
| chr13:33832760 | CTTTTATA others(6): Show |
C | 1 | a0001c0001t0001g0084 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.809+1409_809+1421d others(15): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33832760 | ||||||
| chr13:33832897 | A | G | 18 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(15): Show |
75 | HG00408.hp2 HG00609.hp1 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.809+1543A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832897 | |||||||
| chr13:33832899 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.809+1545G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832899 | |||||||
| chr13:33832915 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.809+1561A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832915 | |||||||
| chr13:33832989 | G | A | 1 | a0001c0001t0002g0033 | 2 | HG01891.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.809+1635G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33832989 | |||||||
| chr13:33833223 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0025 others(9): Show |
37 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.809+1869C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33833223 | |||||||
| chr13:33833278 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.810-1870G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33833278 | |||||||
| chr13:33833280 | G | T | 48 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.810-1868G>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33833280 | |||||||
| chr13:33833332 | A | G | 5 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0069 others(2): Show |
6 | HG02109.hp2 HG03225.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.810-1816A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33833332 | |||||||
| chr13:33833490 | C | G | 1 | a0001c0001t0002g0062 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.810-1658C>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33833490 | |||||||
| chr13:33833586 | A | C | 2 | a0002c0003t0001g0040 a0002c0003t0001g0117 |
3 | NA18960.hp2 NA18995.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.810-1562A>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33833586 | |||||||
| chr13:33833929 | G | A | 1 | a0001c0001t0002g0022 | 3 | HG02015.hp1 NA19055.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.810-1219G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33833929 | |||||||
| chr13:33834127 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.810-1021A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834127 | |||||||
| chr13:33834165 | T | C | 3 | a0001c0001t0001g0119 a0001c0001t0002g0052 a0001c0001t0002g0109 |
3 | HG00639.hp1 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.810-983T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834165 | |||||||
| chr13:33834187 | A | AATGTG | 18 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(15): Show |
75 | HG00408.hp2 HG00609.hp1 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.810-960_810-956dup others(5): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834187 | ||||||
| chr13:33834192 | G | T | 1 | a0001c0001t0003g0110 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.810-956G>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834192 | |||||||
| chr13:33834284 | CATCTGTA others(38): Show |
C | 1 | a0001c0001t0008g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.810-852_810-808del others(45): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834284 | ||||||
| chr13:33834292 | C | CTGTG | 2 | a0001c0001t0002g0007 a0001c0001t0002g0016 |
5 | HG02056.hp1 HG02129.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.810-852_810-849dup others(4): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834292 | ||||||
| chr13:33834296 | G | A | 4 | a0001c0001t0002g0021 a0001c0001t0002g0033 a0001c0001t0002g0054 others(1): Show |
7 | HG01884.hp2 HG01891.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.810-852G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834296 | |||||||
| chr13:33834298 | G | GTATATAT others(5): Show |
1 | a0001c0001t0009g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.810-828_810-817dup others(12): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTATATAT others(7): Show |
1 | a0001c0001t0003g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.810-830_810-817dup others(14): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTATATAT others(9): Show |
2 | a0001c0001t0001g0019 a0001c0004t0001g0125 |
3 | HG02055.hp2 HG02257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.810-832_810-817dup others(16): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0019 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.810-834_810-817dup others(18): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTATATTA others(6): Show |
1 | a0001c0001t0002g0054 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.810-845_810-844ins others(13): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTGTATAT others(9): Show |
1 | a0001c0001t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.810-849_810-848ins others(16): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTGTGTAT others(5): Show |
4 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0046 others(1): Show |
11 | HG01256.hp2 HG01943.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.810-849_810-848ins others(12): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTGTGTAT others(7): Show |
4 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0016 others(1): Show |
7 | HG01074.hp2 HG01358.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.810-849_810-848ins others(14): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTGTGTAT others(9): Show |
6 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(3): Show |
16 | HG00609.hp1 HG02015.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.810-849_810-848ins others(16): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTGTGTAT others(11): Show |
3 | a0001c0001t0002g0005 a0001c0001t0002g0023 a0001c0001t0002g0066 |
4 | HG02004.hp2 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.810-849_810-848ins others(18): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTGTGTAT others(13): Show |
3 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 |
5 | HG01891.hp2 HG02083.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.810-849_810-848ins others(20): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTGTGTAT others(15): Show |
5 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(2): Show |
10 | HG01106.hp1 HG02258.hp1 HG03516.hp2 others(7): Show |
intron_variant | MODIFIER | c.810-849_810-848ins others(22): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTGTGTAT others(17): Show |
2 | a0001c0001t0002g0005 a0001c0001t0002g0059 |
2 | NA18955.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.810-849_810-848ins others(24): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTGTGTGT others(7): Show |
4 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0061 others(1): Show |
8 | HG03540.hp1 NA18961.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.810-849_810-848ins others(14): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTGTGTGT others(9): Show |
1 | a0001c0001t0002g0011 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.810-849_810-848ins others(16): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTGTGTGT others(15): Show |
1 | a0001c0001t0002g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.810-849_810-848ins others(22): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0002g0011 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.810-849_810-848ins others(14): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | GTA | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(13): Show |
51 | HG00423.hp1 HG00438.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.810-818_810-817del others(2): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | GTATA | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(49): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.810-820_810-817del others(4): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | GTATATA | G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0095 others(7): Show |
16 | HG00408.hp2 HG01074.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.810-822_810-817del others(6): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834298 | GTATATAT others(17): Show |
G | 5 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0069 others(2): Show |
6 | HG02109.hp2 HG03225.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.810-840_810-817del others(24): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834298 | ||||||
| chr13:33834300 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0002g0050 a0001c0001t0005g0015 |
4 | HG03139.hp2 HG03195.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.810-848A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834300 | |||||||
| chr13:33834302 | A | AT | 3 | a0001c0001t0002g0021 a0001c0001t0002g0033 a0001c0001t0002g0055 |
6 | HG01884.hp2 HG01891.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.810-845dupT | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834302 | ||||||
| chr13:33834302 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0068 a0001c0001t0001g0121 |
3 | HG01261.hp1 HG01261.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.810-846A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834302 | |||||||
| chr13:33834304 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0051 |
2 | HG02723.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.810-844A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834304 | |||||||
| chr13:33834306 | A | G | 2 | a0001c0001t0002g0007 a0001c0001t0002g0060 |
4 | HG00408.hp2 HG02165.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.810-842A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834306 | |||||||
| chr13:33834308 | A | G | 2 | a0001c0001t0002g0007 a0001c0001t0002g0060 |
4 | HG00408.hp2 HG02165.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.810-840A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834308 | |||||||
| chr13:33834323 | T | C | 4 | a0001c0001t0002g0003 a0001c0001t0002g0032 a0001c0001t0002g0052 others(1): Show |
6 | HG01243.hp1 HG02109.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.810-825T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834323 | |||||||
| chr13:33834325 | T | C | 4 | a0001c0001t0002g0003 a0001c0001t0002g0032 a0001c0001t0002g0052 others(1): Show |
6 | HG01243.hp1 HG02109.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.810-823T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834325 | |||||||
| chr13:33834325 | T | TACATATA others(29): Show |
1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.810-822_810-821ins others(36): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834325 | ||||||
| chr13:33834329 | T | C | 5 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0032 others(2): Show |
7 | HG01243.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.810-819T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834329 | |||||||
| chr13:33834329 | T | TATACACA others(3): Show |
1 | a0001c0001t0002g0003 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.810-817_810-816ins others(10): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834329 | T | TATATATA others(7): Show |
1 | a0001c0001t0002g0003 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.810-817_810-816ins others(14): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834329 | T | TATATATA others(11): Show |
2 | a0001c0001t0002g0003 a0001c0001t0002g0049 |
2 | HG00621.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.810-817_810-816ins others(18): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834329 | T | TATATATA others(13): Show |
2 | a0001c0001t0002g0003 a0001c0001t0002g0020 |
7 | HG01433.hp1 HG03654.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.810-817_810-816ins others(20): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834329 | T | TATATATA others(15): Show |
5 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0033 others(2): Show |
10 | HG01069.hp1 HG01070.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.810-817_810-816ins others(22): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834329 | T | TATATATA others(17): Show |
4 | a0001c0001t0002g0003 a0001c0001t0002g0048 a0001c0001t0002g0071 others(1): Show |
7 | HG00423.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.810-817_810-816ins others(24): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834329 | T | TATATATA others(19): Show |
9 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0020 others(6): Show |
13 | HG00642.hp2 HG01192.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.810-817_810-816ins others(26): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834329 | T | TATATATA others(23): Show |
1 | a0001c0001t0002g0003 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.810-817_810-816ins others(30): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834329 | T | TATATATA others(21): Show |
5 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0017 others(2): Show |
9 | HG00735.hp2 HG01109.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.810-817_810-816ins others(28): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834329 | T | TATATATA others(25): Show |
1 | a0001c0001t0005g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.810-817_810-816ins others(32): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834329 | T | TATATATA others(23): Show |
1 | a0001c0001t0002g0003 | 5 | HG00673.hp1 HG03834.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.810-817_810-816ins others(30): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834329 | T | TATATATA others(25): Show |
4 | a0001c0001t0002g0003 a0001c0001t0002g0017 a0001c0001t0002g0020 others(1): Show |
5 | HG03041.hp1 HG03834.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.810-817_810-816ins others(32): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834329 | T | TATATATA others(27): Show |
1 | a0001c0001t0002g0003 | 3 | HG03225.hp2 NA18982.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.810-817_810-816ins others(34): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834329 | T | TATATATA others(31): Show |
1 | a0001c0001t0002g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.810-817_810-816ins others(38): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834329 | ||||||
| chr13:33834339 | G | GTAAAAA | 5 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0022 others(2): Show |
22 | HG00408.hp2 HG01934.hp1 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.810-807_810-802dup others(6): Show |
RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834339 | ||||||
| chr13:33834365 | A | G | 48 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.810-783A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834365 | |||||||
| chr13:33834391 | C | CT | 4 | a0001c0001t0001g0019 a0001c0001t0001g0101 a0001c0001t0001g0120 others(1): Show |
7 | HG02055.hp2 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.810-743dupT | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834391 | ||||||
| chr13:33834391 | CT | C | 6 | a0001c0001t0001g0116 a0001c0002t0001g0035 a0001c0002t0001g0036 others(3): Show |
7 | HG02109.hp2 HG03225.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.810-743delT | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 33834391 | ||||||
| chr13:33834499 | A | T | 5 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0069 others(2): Show |
6 | HG02109.hp2 HG03225.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.810-649A>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834499 | |||||||
| chr13:33834512 | G | A | 59 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0068 others(56): Show |
170 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(167): Show |
intron_variant | MODIFIER | c.810-636G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834512 | |||||||
| chr13:33834531 | T | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0075 others(3): Show |
20 | HG00438.hp1 HG01192.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.810-617T>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834531 | |||||||
| chr13:33834629 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.810-519A>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834629 | |||||||
| chr13:33834796 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.810-352C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834796 | |||||||
| chr13:33834797 | G | A | 5 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0069 others(2): Show |
6 | HG02109.hp2 HG03225.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.810-351G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834797 | |||||||
| chr13:33834873 | C | T | 1 | a0001c0001t0008g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.810-275C>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834873 | |||||||
| chr13:33834927 | T | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0118 |
10 | HG01346.hp2 HG01993.hp2 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.810-221T>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33834927 | |||||||
| chr13:33835105 | T | C | 48 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.810-43T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33835105 | |||||||
| chr13:33835114 | C | G | 24 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0015 others(21): Show |
74 | HG00423.hp2 HG00621.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.810-34C>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33835114 | |||||||
| chr13:33835115 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0092 |
2 | NA19067.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.810-33T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 7/8 | chr13 | 33835115 | |||||||
| chr13:33835307 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.879+90T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 8/8 | chr13 | 33835307 | |||||||
| chr13:33835466 | T | G | 48 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(45): Show |
156 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.879+249T>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 8/8 | chr13 | 33835466 | |||||||
| chr13:33835542 | A | C | 2 | a0001c0001t0001g0019 a0001c0004t0001g0125 |
5 | HG02055.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+325A>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 8/8 | chr13 | 33835542 | |||||||
| chr13:33835668 | G | A | 20 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0015 others(17): Show |
67 | HG00423.hp2 HG00621.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.880-436G>A | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 8/8 | chr13 | 33835668 | |||||||
| chr13:33835772 | C | G | 1 | a0001c0001t0008g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.880-332C>G | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 8/8 | chr13 | 33835772 | |||||||
| chr13:33835991 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.880-113T>C | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 8/8 | chr13 | 33835991 | |||||||
| chr13:33836049 | G | T | 1 | a0001c0001t0006g0030 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.880-55G>T | RFC3 | ENSG00000133119.13 | transcript | ENST00000380071.8 | protein_coding | 8/8 | chr13 | 33836049 |