Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 91869 |
| ensemblid | ENSG00000163933.10 |
| hgncid | 30220 |
| symbol | RFT1 |
| name | RFT1 homolog |
| refseq_nuc | NM_052859.4 |
| refseq_prot | NP_443091.1 |
| ensembl_nuc | ENST00000296292.8 |
| ensembl_prot | ENSP00000296292.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 53088483 |
| end | 53130435 |
| strand | - |
| ver | v1.2 |
| region | chr3:53088483-53130435 |
| region5000 | chr3:53083483-53135435 |
| regionname0 | RFT1_chr3_53088483_53130435 |
| regionname5000 | RFT1_chr3_53083483_53135435 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 541 | 301 | 72 | 66 | 108 | 12 | 41 | 73 | RFT1_chr3_53083483_53135435 | RFT1 | MGSQE others(536): Show |
chr3 | 53083483 | 53135435 |
| a0002 | 0/0 | 541 | 19 | 18 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | MGSQE others(536): Show |
chr3 | 53083483 | 53135435 |
| a0003 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | MGSQE others(536): Show |
chr3 | 53083483 | 53135435 |
| a0004 | 0/0 | 541 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | MGSQE others(536): Show |
chr3 | 53083483 | 53135435 |
| a0005 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | MGSQE others(536): Show |
chr3 | 53083483 | 53135435 |
| a0006 | 0/0 | 371 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | MGSQE others(366): Show |
chr3 | 53083483 | 53135435 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1623 | 168 | 62 | 29 | 43 | 7 | 25 | RFT1_chr3_53083483_53135435 | RFT1 | ATGGG others(1618): Show |
chr3 | 53083483 | 53135435 | ||
| a0001c0002 | 0/0 | 1623 | 132 | 10 | 36 | 65 | 5 | 16 | RFT1_chr3_53083483_53135435 | RFT1 | ATGGG others(1618): Show |
chr3 | 53083483 | 53135435 | ||
| a0001c0008 | 0/0 | 1623 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | ATGGG others(1618): Show |
chr3 | 53083483 | 53135435 | ||
| a0002c0003 | 0/0 | 1623 | 19 | 18 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | ATGGG others(1618): Show |
chr3 | 53083483 | 53135435 | ||
| a0003c0007 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | ATGGG others(1618): Show |
chr3 | 53083483 | 53135435 | ||
| a0004c0005 | 0/0 | 1623 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | ATGGG others(1618): Show |
chr3 | 53083483 | 53135435 | ||
| a0005c0004 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | ATGGG others(1618): Show |
chr3 | 53083483 | 53135435 | ||
| a0006c0006 | 0/0 | 1517 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | ATGGG others(1512): Show |
chr3 | 53083483 | 53135435 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 5081 | 52 | 23 | 8 | 16 | 1 | 4 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0003 | 0/1 | 5081 | 49 | 1 | 12 | 23 | 6 | 6 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0004 | 0/0 | 5081 | 20 | 0 | 5 | 2 | 0 | 13 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0005 | 1/0 | 5081 | 13 | 9 | 3 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0006 | 0/0 | 5081 | 3 | 3 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0007 | 0/0 | 5081 | 14 | 14 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0008 | 0/0 | 5081 | 5 | 4 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0009 | 0/0 | 5081 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0011 | 0/0 | 5081 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0012 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0013 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0014 | 0/0 | 5081 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0015 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0016 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0017 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0018 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0019 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0001t0020 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0002t0001 | 0/0 | 5081 | 126 | 9 | 32 | 64 | 5 | 16 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0002t0010 | 0/0 | 5081 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0002t0021 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0002t0022 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0002t0023 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0002t0024 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0001c0008t0001 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0002c0003t0005 | 0/0 | 5081 | 7 | 6 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0002c0003t0006 | 0/0 | 5081 | 12 | 12 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0003c0007t0001 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0004c0005t0001 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0005c0004t0001 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(5076): Show |
chr3 | 53083483 | 53135435 |
| a0006c0006t0004 | 0/0 | 4975 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | GGCAT others(4970): Show |
chr3 | 53083483 | 53135435 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0003 | 0/0 | 9 | 0 | 1 | 6 | 1 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0004 | 0/0 | 7 | 0 | 3 | 2 | 0 | 2 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0005 | 0/0 | 5 | 0 | 2 | 2 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0004g0007 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0004g0013 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0005g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0005g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0005g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0007g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0007g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0008g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0008g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0011g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0013g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0014g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0015g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0016g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0017g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0018g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0019g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0001t0020g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0001 | 0/0 | 14 | 0 | 2 | 11 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0002 | 0/0 | 10 | 1 | 3 | 6 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0008 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0010g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0010g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0021g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0022g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0023g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0002t0024g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0001c0008t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0005g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0005g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0006g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0002c0003t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0003c0007t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0004c0005t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0005c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| a0006c0006t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0020 | EUR | GBR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0044 | EUR | GBR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0172 | EUR | FIN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0052 | EUR | FIN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0044 | EUR | FIN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0012 | EUR | FIN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00438 | hp2 | a0003 | c0007 | t0001 | g0083 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00558 | hp2 | a0001 | c0001 | t0013 | g0068 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | CHS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01074 | hp2 | a0001 | c0001 | t0008 | g0211 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01109 | hp1 | a0002 | c0003 | t0005 | g0042 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01167 | hp1 | a0001 | c0002 | t0010 | g0105 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01168 | hp1 | a0001 | c0002 | t0021 | g0150 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01169 | hp2 | a0001 | c0002 | t0010 | g0106 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01175 | hp2 | a0001 | c0002 | t0024 | g0166 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0031 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PUR | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0152 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01346 | hp2 | a0001 | c0008 | t0001 | g0191 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0174 | AMR | CLM | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0183 | EUR | IBS | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01884 | hp2 | a0002 | c0003 | t0005 | g0088 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01891 | hp2 | a0001 | c0001 | t0017 | g0138 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0013 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0216 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0089 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02129 | hp1 | a0001 | c0001 | t0019 | g0159 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02145 | hp1 | a0001 | c0002 | t0023 | g0154 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0064 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | CDX | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | CDX | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0073 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02258 | hp2 | a0001 | c0001 | t0020 | g0224 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0062 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02300 | hp2 | a0004 | c0005 | t0001 | g0108 | AMR | PEL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02572 | hp2 | a0001 | c0001 | t0016 | g0056 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02622 | hp1 | a0002 | c0003 | t0006 | g0041 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0085 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02630 | hp2 | a0002 | c0003 | t0006 | g0197 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02647 | hp1 | a0001 | c0001 | t0018 | g0079 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0135 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0013 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0134 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0213 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02809 | hp1 | a0001 | c0001 | t0012 | g0151 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02818 | hp2 | a0002 | c0003 | t0006 | g0206 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02922 | hp1 | a0002 | c0003 | t0005 | g0043 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0139 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02976 | hp1 | a0002 | c0003 | t0006 | g0103 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0084 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03041 | hp1 | a0002 | c0003 | t0006 | g0196 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0087 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03139 | hp1 | a0002 | c0003 | t0006 | g0201 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0017 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0228 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0069 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03225 | hp1 | a0001 | c0001 | t0015 | g0136 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0070 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0013 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0143 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0096 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0023 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03516 | hp2 | a0002 | c0003 | t0006 | g0203 | AFR | ESN | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0208 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0221 | AFR | GWD | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0207 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0095 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03704 | hp1 | a0001 | c0001 | t0014 | g0190 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0120 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0115 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0020 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0182 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0092 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG03942 | hp2 | a0001 | c0001 | t0011 | g0104 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0093 | SAS | BEB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0094 | SAS | STU | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0059 | SAS | STU | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | STU | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0023 | SAS | STU | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | STU | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | STU | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0140 | AFR | YRI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | CHB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0067 | AFR | YRI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | YRI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18941 | hp1 | a0001 | c0002 | t0022 | g0176 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18961 | hp2 | a0005 | c0004 | t0001 | g0045 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19030 | hp1 | a0002 | c0003 | t0006 | g0198 | AFR | LWK | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | LWK | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | LWK | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | LWK | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19240 | hp1 | a0002 | c0003 | t0005 | g0204 | AFR | YRI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA19240 | hp2 | a0002 | c0003 | t0006 | g0199 | AFR | YRI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA20129 | hp1 | a0002 | c0003 | t0006 | g0202 | AFR | ASW | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | ASW | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | TSI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0178 | EUR | TSI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0121 | EUR | TSI | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA20905 | hp1 | a0006 | c0006 | t0004 | g0097 | SAS | GIH | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | GIH | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0061 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0171 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02486 | hp1 | a0002 | c0003 | t0005 | g0205 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02486 | hp2 | a0002 | c0003 | t0006 | g0200 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG02559 | hp2 | a0002 | c0003 | t0005 | g0043 | AFR | ACB | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | USA | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| HG06807 | hp2 | a0002 | c0003 | t0005 | g0042 | AFR | USA | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | LWK | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| NA21309 | hp2 | a0002 | c0003 | t0006 | g0041 | AFR | LWK | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0048 | REF | REF | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0210 | REF | REF | RFT1_chr3_53083483_53135435 | RFT1 | chr3 | 53083483 | 53135435 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:53098541 | GCCTGTAA others(1177): Show |
G | 1 | a0006 | 1 | NA20905.hp1 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1103-239_1208+839d others(2): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/13 | chr3 | 53098541 | |||||||
| chr3:53099456 | T | C | 1 | a0001 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.1133A>G | p.Tyr378Cys | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/13 | 1168/5081 | 1133/1626 | 378/541 | chr3 | 53099456 | |||
| chr3:53099471 | C | T | 1 | a0002 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1118G>A | p.Arg373His | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/13 | 1153/5081 | 1118/1626 | 373/541 | chr3 | 53099471 | |||
| chr3:53119948 | G | A | 1 | a0003 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.632C>T | p.Thr211Ile | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/13 | 667/5081 | 632/1626 | 211/541 | chr3 | 53119948 | |||
| chr3:53121704 | C | T | 1 | a0002 | 19 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(16): Show |
missense_variant | MODERATE | c.553G>A | p.Ala185Thr | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/13 | 588/5081 | 553/1626 | 185/541 | chr3 | 53121704 | |||
| chr3:53122390 | A | T | 1 | a0004 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.440T>A | p.Met147Lys | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 4/13 | 475/5081 | 440/1626 | 147/541 | chr3 | 53122390 | |||
| chr3:53130378 | C | T | 1 | a0005 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.23G>A | p.Gly8Asp | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/13 | 58/5081 | 23/1626 | 8/541 | chr3 | 53130378 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:53091906 | T | C | 5 | a0001c0002 a0001c0008 a0003c0007 others(2): Show |
136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
synonymous_variant | LOW | c.1623A>G | p.Thr541Thr | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1658/5081 | 1623/1626 | 541/541 | chr3 | 53091906 | |||
| chr3:53122527 | G | C | 1 | a0001c0008 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.303C>G | p.Gly101Gly | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 4/13 | 338/5081 | 303/1626 | 101/541 | chr3 | 53122527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:53088550 | A | G | 1 | a0001c0001t0018 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3353T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 3353 | chr3 | 53088550 | ||||||
| chr3:53088664 | T | C | 1 | a0001c0002t0023 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3239A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 3239 | chr3 | 53088664 | ||||||
| chr3:53088708 | C | G | 1 | a0001c0002t0022 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3195G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 3195 | chr3 | 53088708 | ||||||
| chr3:53088953 | G | A | 10 | a0001c0002t0001 a0001c0002t0010 a0001c0002t0021 others(7): Show |
136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*2950C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2950 | chr3 | 53088953 | ||||||
| chr3:53089016 | C | T | 22 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(19): Show |
223 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*2887G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2887 | chr3 | 53089016 | ||||||
| chr3:53089063 | A | T | 9 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(6): Show |
65 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2840T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2840 | chr3 | 53089063 | ||||||
| chr3:53089083 | C | T | 1 | a0001c0002t0010 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2820G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2820 | chr3 | 53089083 | ||||||
| chr3:53089197 | G | A | 1 | a0001c0002t0021 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2706C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2706 | chr3 | 53089197 | ||||||
| chr3:53089248 | A | G | 3 | a0001c0001t0004 a0001c0001t0011 a0006c0006t0004 |
22 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2655T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2655 | chr3 | 53089248 | ||||||
| chr3:53089257 | A | G | 10 | a0001c0002t0001 a0001c0002t0010 a0001c0002t0021 others(7): Show |
136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*2646T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2646 | chr3 | 53089257 | ||||||
| chr3:53089446 | T | C | 1 | a0001c0002t0024 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2457A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2457 | chr3 | 53089446 | ||||||
| chr3:53089470 | G | A | 10 | a0001c0002t0001 a0001c0002t0010 a0001c0002t0021 others(7): Show |
136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*2433C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2433 | chr3 | 53089470 | ||||||
| chr3:53089537 | A | T | 1 | a0001c0001t0014 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2366T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2366 | chr3 | 53089537 | ||||||
| chr3:53089623 | A | T | 1 | a0001c0001t0013 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2280T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2280 | chr3 | 53089623 | ||||||
| chr3:53089738 | A | G | 1 | a0001c0002t0021 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2165T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 2165 | chr3 | 53089738 | ||||||
| chr3:53089928 | G | A | 1 | a0001c0001t0007 | 14 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1975C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1975 | chr3 | 53089928 | ||||||
| chr3:53090099 | G | A | 2 | a0001c0001t0006 a0002c0003t0006 |
15 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1804C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1804 | chr3 | 53090099 | ||||||
| chr3:53090100 | A | T | 2 | a0001c0001t0006 a0002c0003t0006 |
15 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1803T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1803 | chr3 | 53090100 | ||||||
| chr3:53090210 | C | T | 1 | a0001c0001t0016 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1693G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1693 | chr3 | 53090210 | ||||||
| chr3:53090217 | G | A | 1 | a0001c0001t0019 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1686C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1686 | chr3 | 53090217 | ||||||
| chr3:53090370 | C | T | 2 | a0001c0001t0004 a0006c0006t0004 |
21 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1533G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1533 | chr3 | 53090370 | ||||||
| chr3:53090771 | A | G | 1 | a0001c0001t0017 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1132T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1132 | chr3 | 53090771 | ||||||
| chr3:53090894 | C | T | 1 | a0001c0001t0008 | 5 | HG01074.hp2 HG01891.hp1 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1009G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 1009 | chr3 | 53090894 | ||||||
| chr3:53091023 | G | C | 1 | a0001c0001t0020 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*880C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 880 | chr3 | 53091023 | ||||||
| chr3:53091104 | A | T | 1 | a0001c0001t0016 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 799 | chr3 | 53091104 | ||||||
| chr3:53091281 | G | C | 10 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(7): Show |
65 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*622C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 622 | chr3 | 53091281 | ||||||
| chr3:53091413 | A | T | 2 | a0001c0001t0003 a0001c0001t0013 |
49 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*490T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 490 | chr3 | 53091413 | ||||||
| chr3:53091453 | G | A | 17 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0016 others(14): Show |
198 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*450C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 450 | chr3 | 53091453 | ||||||
| chr3:53091552 | A | G | 1 | a0001c0001t0012 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*351T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 351 | chr3 | 53091552 | ||||||
| chr3:53091569 | T | C | 10 | a0001c0002t0001 a0001c0002t0010 a0001c0002t0021 others(7): Show |
136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*334A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 334 | chr3 | 53091569 | ||||||
| chr3:53091663 | A | G | 1 | a0001c0001t0011 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*240T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 240 | chr3 | 53091663 | ||||||
| chr3:53091757 | G | A | 2 | a0001c0001t0006 a0002c0003t0006 |
15 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*146C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 13/13 | 146 | chr3 | 53091757 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:53092127 | G | A | 94 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(91): Show |
136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1459-57C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 12/12 | chr3 | 53092127 | |||||||
| chr3:53092210 | C | T | 1 | a0001c0002t0001g0127 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1459-140G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 12/12 | chr3 | 53092210 | |||||||
| chr3:53092656 | TTGCCCTG others(8): Show |
T | 44 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0011 others(41): Show |
66 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1209-53_1209-39del others(15): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53092656 | |||||||
| chr3:53092704 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1209-86G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53092704 | |||||||
| chr3:53092731 | C | G | 1 | a0001c0002t0001g0112 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1209-113G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53092731 | |||||||
| chr3:53092778 | C | T | 1 | a0001c0002t0001g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1209-160G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53092778 | |||||||
| chr3:53092900 | A | C | 1 | a0001c0002t0001g0102 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1209-282T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53092900 | |||||||
| chr3:53093006 | C | A | 4 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0085 others(1): Show |
6 | HG01243.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-388G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093006 | |||||||
| chr3:53093119 | AC | A | 94 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(91): Show |
136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1209-502delG | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093119 | |||||||
| chr3:53093189 | C | A | 1 | a0001c0001t0007g0070 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1209-571G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093189 | |||||||
| chr3:53093268 | A | C | 5 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0085 others(2): Show |
7 | HG01243.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1209-650T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093268 | |||||||
| chr3:53093280 | A | G | 1 | a0001c0002t0001g0164 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1209-662T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093280 | |||||||
| chr3:53093499 | C | A | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1209-881G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093499 | |||||||
| chr3:53093524 | G | A | 1 | a0001c0001t0016g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1209-906C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093524 | |||||||
| chr3:53093599 | C | A | 1 | a0001c0002t0001g0177 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1209-981G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093599 | |||||||
| chr3:53093657 | G | C | 19 | a0001c0001t0002g0015 a0001c0001t0002g0034 a0001c0001t0002g0057 others(16): Show |
22 | HG01891.hp2 HG01934.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.1209-1039C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093657 | |||||||
| chr3:53093661 | G | T | 91 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(88): Show |
132 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1209-1043C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093661 | |||||||
| chr3:53093751 | T | C | 44 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0011 others(41): Show |
66 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1209-1133A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093751 | |||||||
| chr3:53093759 | A | T | 1 | a0001c0001t0005g0134 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1209-1141T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093759 | |||||||
| chr3:53093860 | A | G | 19 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0036 others(16): Show |
32 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1209-1242T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53093860 | |||||||
| chr3:53094184 | G | C | 1 | a0001c0001t0020g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1209-1566C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094184 | |||||||
| chr3:53094264 | C | G | 1 | a0001c0001t0002g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1209-1646G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094264 | |||||||
| chr3:53094269 | A | G | 1 | a0001c0001t0003g0078 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1209-1651T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094269 | |||||||
| chr3:53094304 | T | C | 1 | a0001c0001t0003g0021 | 2 | HG00733.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1209-1686A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094304 | |||||||
| chr3:53094335 | G | A | 44 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0011 others(41): Show |
66 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1209-1717C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094335 | |||||||
| chr3:53094349 | A | ACG | 3 | a0001c0001t0004g0007 a0001c0001t0004g0089 a0006c0006t0004g0097 |
6 | HG01993.hp2 HG02004.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-1733_1209-173 others(6): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094349 | |||||||
| chr3:53094351 | G | GCA | 4 | a0001c0001t0005g0031 a0001c0001t0005g0085 a0001c0001t0005g0134 others(1): Show |
5 | HG01243.hp1 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1209-1735_1209-173 others(6): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094351 | |||||||
| chr3:53094351 | GCA | G | 6 | a0001c0001t0003g0011 a0001c0001t0003g0052 a0001c0001t0003g0063 others(3): Show |
10 | HG00280.hp2 HG00673.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1209-1735_1209-173 others(6): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094351 | |||||||
| chr3:53094351 | GCACA | G | 50 | a0001c0001t0002g0015 a0001c0001t0002g0132 a0001c0001t0002g0144 others(47): Show |
72 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.1209-1737_1209-173 others(8): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094351 | |||||||
| chr3:53094351 | GCACACA | G | 51 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0024 others(48): Show |
68 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1209-1739_1209-173 others(10): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094351 | |||||||
| chr3:53094351 | GCACACAC others(1): Show |
G | 7 | a0001c0001t0003g0051 a0001c0002t0001g0027 a0001c0002t0001g0113 others(4): Show |
8 | HG01243.hp2 HG01256.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1209-1741_1209-173 others(12): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094351 | |||||||
| chr3:53094351 | GCACACAC others(3): Show |
G | 87 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(84): Show |
128 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1209-1743_1209-173 others(14): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094351 | |||||||
| chr3:53094353 | A | G | 11 | a0001c0001t0004g0013 a0001c0001t0004g0023 a0001c0001t0004g0032 others(8): Show |
14 | HG00673.hp1 HG02698.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1209-1735T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094353 | |||||||
| chr3:53094355 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1209-1737T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094355 | |||||||
| chr3:53094357 | A | G | 2 | a0001c0001t0005g0035 a0001c0001t0012g0151 |
3 | HG02809.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1209-1739T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094357 | |||||||
| chr3:53094359 | A | G | 9 | a0001c0001t0002g0015 a0001c0001t0002g0132 a0001c0001t0002g0144 others(6): Show |
11 | HG01934.hp1 HG02451.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1209-1741T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094359 | |||||||
| chr3:53094361 | A | G | 46 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(43): Show |
65 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1209-1743T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094361 | |||||||
| chr3:53094363 | A | G | 6 | a0001c0001t0002g0034 a0001c0001t0002g0133 a0001c0001t0002g0142 others(3): Show |
7 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1209-1745T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094363 | |||||||
| chr3:53094412 | C | A | 1 | a0001c0002t0001g0164 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1209-1794G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094412 | |||||||
| chr3:53094790 | G | A | 1 | a0001c0001t0002g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1209-2172C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53094790 | |||||||
| chr3:53095024 | TTGGGAGG others(99): Show |
T | 1 | a0001c0002t0001g0221 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1209-2512_1209-240 others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095024 | |||||||
| chr3:53095050 | G | A | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1209-2432C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095050 | |||||||
| chr3:53095167 | G | A | 46 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(43): Show |
64 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1209-2549C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095167 | |||||||
| chr3:53095508 | T | TG | 14 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0023 others(11): Show |
21 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.1209-2891dupC | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095508 | |||||||
| chr3:53095514 | C | G | 4 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0085 others(1): Show |
6 | HG01243.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-2896G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095514 | |||||||
| chr3:53095519 | C | T | 1 | a0001c0001t0020g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1209-2901G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095519 | |||||||
| chr3:53095695 | G | A | 14 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0023 others(11): Show |
21 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.1209-3077C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095695 | |||||||
| chr3:53095725 | TA | T | 198 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(195): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1209-3108delT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095725 | |||||||
| chr3:53095876 | C | A | 2 | a0001c0001t0005g0035 a0001c0001t0012g0151 |
3 | HG02809.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1209-3258G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53095876 | |||||||
| chr3:53096383 | T | TA | 19 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0036 others(16): Show |
32 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1208+2997dupT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096383 | |||||||
| chr3:53096419 | C | T | 44 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0011 others(41): Show |
66 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1208+2962G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096419 | |||||||
| chr3:53096422 | C | T | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1208+2959G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096422 | |||||||
| chr3:53096424 | A | G | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1208+2957T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096424 | |||||||
| chr3:53096450 | G | A | 44 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0011 others(41): Show |
66 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1208+2931C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096450 | |||||||
| chr3:53096461 | C | T | 1 | a0001c0002t0001g0222 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1208+2920G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096461 | |||||||
| chr3:53096701 | A | G | 1 | a0001c0002t0001g0175 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1208+2680T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096701 | |||||||
| chr3:53096729 | T | C | 48 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(45): Show |
67 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1208+2652A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096729 | |||||||
| chr3:53096754 | A | C | 2 | a0001c0001t0005g0035 a0001c0001t0012g0151 |
3 | HG02809.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1208+2627T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096754 | |||||||
| chr3:53096889 | C | T | 46 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(43): Show |
65 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1208+2492G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096889 | |||||||
| chr3:53096897 | C | A | 94 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(91): Show |
136 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1208+2484G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096897 | |||||||
| chr3:53096908 | C | A | 19 | a0001c0001t0002g0015 a0001c0001t0002g0034 a0001c0001t0002g0057 others(16): Show |
22 | HG01891.hp2 HG01934.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.1208+2473G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53096908 | |||||||
| chr3:53097027 | G | C | 19 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0036 others(16): Show |
32 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1208+2354C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097027 | |||||||
| chr3:53097035 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1208+2346C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097035 | |||||||
| chr3:53097040 | C | T | 1 | a0001c0001t0017g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1208+2341G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097040 | |||||||
| chr3:53097252 | A | G | 1 | a0001c0001t0005g0134 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1208+2129T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097252 | |||||||
| chr3:53097257 | C | T | 1 | a0001c0001t0002g0038 | 2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1208+2124G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097257 | |||||||
| chr3:53097261 | G | A | 3 | a0001c0002t0001g0008 a0001c0002t0001g0033 a0001c0008t0001g0191 |
7 | HG01069.hp2 HG01071.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1208+2120C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097261 | |||||||
| chr3:53097427 | T | C | 1 | a0001c0001t0003g0080 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1208+1954A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097427 | |||||||
| chr3:53097458 | A | G | 1 | a0001c0001t0020g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1208+1923T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097458 | |||||||
| chr3:53097505 | T | C | 1 | a0001c0002t0001g0186 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1208+1876A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097505 | |||||||
| chr3:53097725 | T | C | 1 | a0001c0002t0001g0122 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1208+1656A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097725 | |||||||
| chr3:53097756 | T | C | 92 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(89): Show |
134 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1208+1625A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097756 | |||||||
| chr3:53097813 | T | C | 92 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(89): Show |
134 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1208+1568A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097813 | |||||||
| chr3:53097814 | G | A | 92 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(89): Show |
134 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1208+1567C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097814 | |||||||
| chr3:53097932 | A | G | 44 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0011 others(41): Show |
66 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1208+1449T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097932 | |||||||
| chr3:53097933 | G | A | 1 | a0001c0002t0001g0164 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1208+1448C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53097933 | |||||||
| chr3:53098080 | G | A | 2 | a0001c0001t0005g0085 a0001c0001t0005g0143 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1208+1301C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098080 | |||||||
| chr3:53098355 | C | G | 49 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(46): Show |
69 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1208+1026G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098355 | |||||||
| chr3:53098356 | A | T | 49 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(46): Show |
69 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1208+1025T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098356 | |||||||
| chr3:53098357 | A | C | 49 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(46): Show |
69 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1208+1024T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098357 | |||||||
| chr3:53098409 | G | A | 2 | a0001c0002t0001g0222 a0001c0002t0001g0223 |
2 | NA19066.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1208+972C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098409 | |||||||
| chr3:53098427 | T | TGAGACAC others(13): Show |
23 | a0001c0001t0002g0015 a0001c0001t0002g0024 a0001c0001t0002g0034 others(20): Show |
27 | HG01891.hp2 HG01934.hp1 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.1208+934_1208+953d others(22): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098427 | |||||||
| chr3:53098524 | T | C | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1208+857A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098524 | |||||||
| chr3:53098530 | C | T | 1 | a0001c0002t0001g0126 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1208+851G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098530 | |||||||
| chr3:53098540 | T | C | 14 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0172 others(11): Show |
20 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1208+841A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098540 | |||||||
| chr3:53098573 | C | T | 1 | a0001c0002t0001g0152 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1208+808G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098573 | |||||||
| chr3:53098587 | G | A | 1 | a0001c0002t0001g0001 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1208+794C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098587 | |||||||
| chr3:53098598 | C | G | 1 | a0001c0002t0001g0117 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1208+783G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098598 | |||||||
| chr3:53098598 | C | T | 1 | a0001c0002t0001g0131 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1208+783G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098598 | |||||||
| chr3:53098606 | A | T | 111 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0053 others(108): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1208+775T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098606 | |||||||
| chr3:53098614 | G | A | 5 | a0001c0001t0002g0003 a0001c0002t0001g0001 a0001c0002t0001g0002 others(2): Show |
5 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208+767C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098614 | |||||||
| chr3:53098703 | G | A | 1 | a0002c0003t0005g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1208+678C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098703 | |||||||
| chr3:53098799 | C | T | 2 | a0001c0001t0002g0147 a0001c0001t0002g0149 |
2 | HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1208+582G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098799 | |||||||
| chr3:53098801 | C | CA | 41 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0036 others(38): Show |
60 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1208+579dupT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098801 | |||||||
| chr3:53098801 | C | CAA | 122 | a0001c0001t0002g0003 a0001c0001t0002g0024 a0001c0001t0002g0098 others(119): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1208+578_1208+579d others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098801 | |||||||
| chr3:53098801 | C | CAAA | 20 | a0001c0001t0002g0024 a0001c0001t0002g0170 a0001c0001t0003g0005 others(17): Show |
21 | HG00423.hp2 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.1208+577_1208+579d others(5): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098801 | |||||||
| chr3:53098801 | CA | C | 12 | a0001c0001t0006g0139 a0001c0001t0006g0207 a0001c0001t0006g0208 others(9): Show |
13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1208+579delT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098801 | |||||||
| chr3:53098823 | A | G | 13 | a0001c0001t0002g0015 a0001c0001t0002g0132 a0001c0001t0002g0133 others(10): Show |
16 | HG01934.hp1 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1208+558T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098823 | |||||||
| chr3:53098863 | A | C | 1 | a0001c0002t0001g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1208+518T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53098863 | |||||||
| chr3:53099052 | G | A | 1 | a0002c0003t0006g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1208+329C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53099052 | |||||||
| chr3:53099133 | C | G | 96 | a0001c0001t0002g0170 a0001c0001t0003g0172 a0001c0001t0004g0032 others(93): Show |
140 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1208+248G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53099133 | |||||||
| chr3:53099362 | T | C | 2 | a0001c0001t0004g0023 a0001c0001t0004g0096 |
3 | HG03491.hp2 HG03492.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1208+19A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 11/12 | chr3 | 53099362 | |||||||
| chr3:53099510 | A | G | 96 | a0001c0001t0002g0170 a0001c0001t0003g0172 a0001c0001t0004g0032 others(93): Show |
140 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1103-24T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099510 | |||||||
| chr3:53099527 | G | C | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1103-41C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099527 | |||||||
| chr3:53099576 | C | A | 1 | a0001c0001t0002g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1103-90G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099576 | |||||||
| chr3:53099653 | T | C | 1 | a0001c0001t0020g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1103-167A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099653 | |||||||
| chr3:53099672 | T | C | 3 | a0001c0001t0005g0035 a0001c0001t0012g0151 a0001c0001t0014g0190 |
4 | HG02809.hp1 HG03486.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-186A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099672 | |||||||
| chr3:53099816 | C | T | 1 | a0001c0002t0001g0187 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1103-330G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099816 | |||||||
| chr3:53099955 | T | C | 1 | a0001c0001t0014g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1103-469A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53099955 | |||||||
| chr3:53100063 | G | A | 2 | a0001c0002t0001g0194 a0001c0002t0001g0195 |
2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1103-577C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100063 | |||||||
| chr3:53100082 | T | C | 96 | a0001c0001t0002g0170 a0001c0001t0003g0172 a0001c0001t0004g0032 others(93): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1103-596A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100082 | |||||||
| chr3:53100184 | C | T | 1 | a0001c0002t0001g0116 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1103-698G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100184 | |||||||
| chr3:53100294 | A | C | 1 | a0001c0001t0003g0063 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1103-808T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100294 | |||||||
| chr3:53100353 | C | T | 2 | a0001c0001t0002g0037 a0001c0001t0002g0086 |
3 | HG00597.hp2 HG02132.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.1103-867G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100353 | |||||||
| chr3:53100440 | C | G | 1 | a0001c0001t0003g0063 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1103-954G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100440 | |||||||
| chr3:53100682 | G | A | 13 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0023 others(10): Show |
19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.1103-1196C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100682 | |||||||
| chr3:53100847 | T | C | 96 | a0001c0001t0002g0170 a0001c0001t0003g0172 a0001c0001t0004g0032 others(93): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1103-1361A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100847 | |||||||
| chr3:53100955 | A | G | 96 | a0001c0001t0002g0170 a0001c0001t0003g0172 a0001c0001t0004g0032 others(93): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1103-1469T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100955 | |||||||
| chr3:53100969 | C | CA | 79 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0011 others(76): Show |
109 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1103-1484dupT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53100969 | |||||||
| chr3:53101150 | C | T | 1 | a0001c0001t0004g0032 | 2 | HG02738.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1103-1664G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53101150 | |||||||
| chr3:53101439 | C | G | 1 | a0001c0002t0001g0126 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1103-1953G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53101439 | |||||||
| chr3:53101623 | C | T | 1 | a0001c0002t0001g0174 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1103-2137G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53101623 | |||||||
| chr3:53101682 | C | T | 1 | a0001c0002t0001g0124 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1103-2196G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53101682 | |||||||
| chr3:53101922 | T | C | 96 | a0001c0001t0002g0170 a0001c0001t0003g0172 a0001c0001t0004g0032 others(93): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1102+2031A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53101922 | |||||||
| chr3:53101925 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1102+2028C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53101925 | |||||||
| chr3:53102000 | G | C | 1 | a0001c0002t0001g0218 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1102+1953C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102000 | |||||||
| chr3:53102014 | G | A | 2 | a0001c0001t0005g0030 a0001c0001t0005g0031 |
4 | HG01243.hp1 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1102+1939C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102014 | |||||||
| chr3:53102108 | G | A | 1 | a0001c0001t0003g0081 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1102+1845C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102108 | |||||||
| chr3:53102414 | G | A | 1 | a0001c0002t0001g0129 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1102+1539C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102414 | |||||||
| chr3:53102445 | G | A | 96 | a0001c0001t0002g0170 a0001c0001t0003g0172 a0001c0001t0004g0032 others(93): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1102+1508C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102445 | |||||||
| chr3:53102535 | G | A | 45 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0011 others(42): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1102+1418C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102535 | |||||||
| chr3:53102538 | A | G | 1 | a0001c0001t0020g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1102+1415T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102538 | |||||||
| chr3:53102606 | C | T | 14 | a0001c0001t0006g0139 a0001c0001t0006g0207 a0001c0001t0006g0208 others(11): Show |
15 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1102+1347G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102606 | |||||||
| chr3:53102687 | T | G | 1 | a0001c0001t0003g0072 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1102+1266A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102687 | |||||||
| chr3:53102792 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1102+1161C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102792 | |||||||
| chr3:53102917 | G | A | 2 | a0001c0001t0005g0085 a0001c0001t0005g0143 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1102+1036C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102917 | |||||||
| chr3:53102941 | C | T | 3 | a0001c0001t0002g0024 a0001c0001t0002g0098 a0001c0001t0016g0056 |
4 | HG02572.hp2 HG03516.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1102+1012G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53102941 | |||||||
| chr3:53103295 | C | G | 96 | a0001c0001t0002g0170 a0001c0001t0003g0172 a0001c0001t0004g0032 others(93): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1102+658G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53103295 | |||||||
| chr3:53103354 | A | G | 221 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(218): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1102+599T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53103354 | |||||||
| chr3:53103798 | T | C | 1 | a0001c0002t0001g0033 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1102+155A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53103798 | |||||||
| chr3:53103949 | G | A | 2 | a0001c0001t0005g0085 a0001c0001t0005g0143 |
2 | HG02622.hp2 HG03486.hp1 |
splice_region_variant&intron_variant | LOW | c.1102+4C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 10/12 | chr3 | 53103949 | |||||||
| chr3:53104211 | G | A | 14 | a0001c0001t0006g0139 a0001c0001t0006g0207 a0001c0001t0006g0208 others(11): Show |
15 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.958-114C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53104211 | |||||||
| chr3:53104238 | T | C | 158 | a0001c0001t0002g0170 a0001c0001t0003g0004 a0001c0001t0003g0005 others(155): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.958-141A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53104238 | |||||||
| chr3:53104279 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.958-182C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53104279 | |||||||
| chr3:53104329 | G | T | 1 | a0001c0002t0001g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.958-232C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53104329 | |||||||
| chr3:53104386 | C | CT | 8 | a0001c0001t0002g0132 a0001c0002t0001g0010 a0001c0002t0001g0044 others(5): Show |
12 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.958-290dupA | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53104386 | |||||||
| chr3:53105042 | C | T | 221 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(218): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.957+631G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105042 | |||||||
| chr3:53105093 | T | C | 1 | a0001c0001t0007g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.957+580A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105093 | |||||||
| chr3:53105200 | A | G | 221 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(218): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.957+473T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105200 | |||||||
| chr3:53105319 | C | T | 2 | a0001c0001t0004g0093 a0001c0001t0004g0095 |
2 | HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.957+354G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105319 | |||||||
| chr3:53105362 | C | A | 1 | a0001c0001t0014g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.957+311G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105362 | |||||||
| chr3:53105364 | A | G | 1 | a0001c0001t0014g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.957+309T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105364 | |||||||
| chr3:53105410 | TCCCCG | T | 95 | a0001c0001t0002g0170 a0001c0001t0003g0046 a0001c0001t0003g0054 others(92): Show |
137 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.957+258_957+262del others(5): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105410 | |||||||
| chr3:53105411 | CCCCG | C | 43 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0011 others(40): Show |
66 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.957+258_957+261del others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105411 | |||||||
| chr3:53105412 | CCCG | C | 17 | a0001c0001t0003g0005 a0001c0001t0003g0066 a0001c0001t0003g0074 others(14): Show |
19 | HG01175.hp1 HG02486.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.957+258_957+260del others(3): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105412 | |||||||
| chr3:53105415 | G | C | 2 | a0001c0001t0005g0085 a0001c0001t0005g0143 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.957+258C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105415 | |||||||
| chr3:53105415 | G | GC | 15 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0024 others(12): Show |
21 | HG00544.hp1 HG00621.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.957+257dupG | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105415 | |||||||
| chr3:53105415 | GC | G | 15 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 others(12): Show |
20 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.957+257delG | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105415 | |||||||
| chr3:53105417 | C | G | 3 | a0001c0001t0002g0137 a0001c0001t0002g0141 a0001c0001t0002g0220 |
3 | HG03098.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.957+256G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105417 | |||||||
| chr3:53105417 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.957+256G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105417 | |||||||
| chr3:53105424 | C | A | 1 | a0001c0001t0007g0087 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.957+249G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105424 | |||||||
| chr3:53105424 | C | G | 1 | a0001c0001t0014g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.957+249G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105424 | |||||||
| chr3:53105425 | C | G | 96 | a0001c0001t0002g0170 a0001c0001t0003g0172 a0001c0001t0004g0032 others(93): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.957+248G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105425 | |||||||
| chr3:53105426 | C | A | 3 | a0001c0001t0003g0012 a0001c0001t0003g0065 a0001c0001t0003g0081 |
5 | HG00323.hp2 HG00438.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.957+247G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105426 | |||||||
| chr3:53105490 | C | T | 96 | a0001c0001t0002g0170 a0001c0001t0003g0172 a0001c0001t0004g0032 others(93): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.957+183G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105490 | |||||||
| chr3:53105491 | A | G | 96 | a0001c0001t0002g0170 a0001c0001t0003g0172 a0001c0001t0004g0032 others(93): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.957+182T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105491 | |||||||
| chr3:53105628 | T | C | 5 | a0001c0002t0001g0025 a0001c0002t0001g0155 a0001c0002t0001g0168 others(2): Show |
6 | HG00642.hp2 HG01099.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.957+45A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 9/12 | chr3 | 53105628 | |||||||
| chr3:53105961 | G | A | 96 | a0001c0001t0002g0170 a0001c0001t0003g0172 a0001c0001t0004g0032 others(93): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.827-158C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53105961 | |||||||
| chr3:53105997 | C | A | 1 | a0001c0001t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.827-194G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53105997 | |||||||
| chr3:53106187 | G | A | 12 | a0001c0001t0002g0015 a0001c0001t0002g0034 a0001c0001t0002g0133 others(9): Show |
15 | HG01891.hp2 HG01934.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.827-384C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106187 | |||||||
| chr3:53106224 | C | A | 2 | a0001c0001t0003g0066 a0001c0001t0003g0074 |
2 | NA19064.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.827-421G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106224 | |||||||
| chr3:53106277 | T | C | 1 | a0001c0002t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.827-474A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106277 | |||||||
| chr3:53106294 | T | C | 6 | a0001c0001t0005g0035 a0001c0001t0009g0135 a0001c0001t0009g0228 others(3): Show |
7 | HG02647.hp2 HG02809.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-491A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106294 | |||||||
| chr3:53106315 | A | G | 1 | a0002c0003t0006g0199 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.826+504T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106315 | |||||||
| chr3:53106319 | T | G | 15 | a0001c0001t0006g0139 a0001c0001t0006g0207 a0001c0001t0008g0213 others(12): Show |
16 | HG02486.hp1 HG02486.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.826+500A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106319 | |||||||
| chr3:53106391 | AACAGTAC others(8): Show |
A | 1 | a0001c0001t0002g0024 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.826+413_826+427del others(15): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106391 | |||||||
| chr3:53106456 | T | C | 1 | a0001c0001t0003g0075 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.826+363A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106456 | |||||||
| chr3:53106529 | T | C | 1 | a0001c0002t0001g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.826+290A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106529 | |||||||
| chr3:53106546 | G | A | 3 | a0001c0002t0001g0040 a0001c0002t0001g0129 a0001c0002t0001g0182 |
4 | HG03491.hp1 HG03669.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+273C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106546 | |||||||
| chr3:53106587 | T | C | 150 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(147): Show |
217 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.826+232A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106587 | |||||||
| chr3:53106604 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.826+215T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106604 | |||||||
| chr3:53106614 | A | C | 87 | a0001c0001t0002g0036 a0001c0001t0002g0053 a0001c0001t0002g0132 others(84): Show |
123 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.826+205T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106614 | |||||||
| chr3:53106747 | A | C | 1 | a0001c0001t0003g0059 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.826+72T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106747 | |||||||
| chr3:53106812 | A | G | 1 | a0001c0001t0014g0190 | 1 | HG03704.hp1 | splice_region_variant&intron_variant | LOW | c.826+7T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 8/12 | chr3 | 53106812 | |||||||
| chr3:53107093 | A | C | 2 | a0001c0002t0001g0222 a0001c0002t0001g0223 |
2 | NA19066.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.776-224T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107093 | |||||||
| chr3:53107136 | G | GT | 44 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0012 others(41): Show |
63 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.776-268dupA | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107136 | |||||||
| chr3:53107136 | G | GTT | 11 | a0001c0001t0002g0053 a0001c0001t0003g0005 a0001c0001t0003g0051 others(8): Show |
15 | HG00423.hp1 HG00438.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.776-269_776-268dup others(2): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107136 | |||||||
| chr3:53107136 | GTTTT | G | 148 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(145): Show |
213 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.776-271_776-268del others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107136 | |||||||
| chr3:53107177 | C | T | 3 | a0001c0001t0002g0034 a0001c0001t0002g0142 a0001c0001t0005g0143 |
4 | HG02559.hp1 HG02572.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.776-308G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107177 | |||||||
| chr3:53107204 | C | T | 3 | a0001c0002t0001g0027 a0001c0002t0001g0113 a0001c0002t0001g0116 |
4 | HG01243.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.776-335G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107204 | |||||||
| chr3:53107235 | A | G | 1 | a0001c0002t0001g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.776-366T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107235 | |||||||
| chr3:53107236 | T | C | 1 | a0002c0003t0005g0205 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.776-367A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107236 | |||||||
| chr3:53107290 | C | T | 17 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0036 others(14): Show |
30 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.776-421G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107290 | |||||||
| chr3:53107291 | G | A | 13 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0023 others(10): Show |
19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.776-422C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107291 | |||||||
| chr3:53107359 | G | A | 1 | a0001c0001t0002g0038 | 2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.776-490C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107359 | |||||||
| chr3:53107500 | C | G | 47 | a0001c0001t0002g0053 a0001c0001t0003g0004 a0001c0001t0003g0005 others(44): Show |
69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.776-631G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107500 | |||||||
| chr3:53107533 | C | T | 47 | a0001c0001t0002g0053 a0001c0001t0003g0004 a0001c0001t0003g0005 others(44): Show |
69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.776-664G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107533 | |||||||
| chr3:53107708 | A | G | 1 | a0001c0001t0007g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.776-839T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107708 | |||||||
| chr3:53107821 | G | C | 13 | a0001c0001t0006g0207 a0001c0001t0006g0208 a0002c0003t0006g0041 others(10): Show |
14 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.776-952C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107821 | |||||||
| chr3:53107896 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.776-1027G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107896 | |||||||
| chr3:53107911 | C | T | 1 | a0001c0001t0005g0134 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.776-1042G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107911 | |||||||
| chr3:53107913 | C | G | 1 | a0001c0002t0001g0122 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.776-1044G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107913 | |||||||
| chr3:53107949 | G | C | 46 | a0001c0001t0002g0053 a0001c0001t0003g0004 a0001c0001t0003g0005 others(43): Show |
68 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.776-1080C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53107949 | |||||||
| chr3:53108055 | G | A | 17 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0036 others(14): Show |
30 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.776-1186C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108055 | |||||||
| chr3:53108058 | T | G | 1 | a0001c0001t0003g0077 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.776-1189A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108058 | |||||||
| chr3:53108071 | CAG | C | 3 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 |
3 | HG02040.hp1 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.776-1204_776-1203d others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108071 | |||||||
| chr3:53108072 | A | T | 13 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0023 others(10): Show |
19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.776-1203T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108072 | |||||||
| chr3:53108080 | A | T | 1 | a0001c0002t0001g0121 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.776-1211T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108080 | |||||||
| chr3:53108205 | A | T | 46 | a0001c0001t0002g0053 a0001c0001t0003g0004 a0001c0001t0003g0005 others(43): Show |
68 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.776-1336T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108205 | |||||||
| chr3:53108240 | A | G | 46 | a0001c0001t0002g0053 a0001c0001t0003g0004 a0001c0001t0003g0005 others(43): Show |
68 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.776-1371T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108240 | |||||||
| chr3:53108341 | T | G | 2 | a0001c0001t0002g0133 a0001c0001t0006g0139 |
2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.776-1472A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108341 | |||||||
| chr3:53108357 | C | T | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.776-1488G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108357 | |||||||
| chr3:53108389 | CT | C | 135 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0024 others(132): Show |
202 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.776-1521delA | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108389 | |||||||
| chr3:53108389 | CTT | C | 18 | a0001c0001t0005g0085 a0001c0001t0006g0207 a0001c0001t0006g0208 others(15): Show |
21 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.776-1522_776-1521d others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108389 | |||||||
| chr3:53108585 | G | C | 1 | a0002c0003t0006g0201 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.776-1716C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108585 | |||||||
| chr3:53108693 | T | A | 2 | a0001c0001t0002g0057 a0001c0001t0016g0056 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.776-1824A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108693 | |||||||
| chr3:53108703 | G | GT | 34 | a0001c0001t0002g0158 a0001c0001t0002g0163 a0001c0001t0002g0170 others(31): Show |
38 | HG00621.hp1 HG01109.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.776-1835dupA | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108703 | |||||||
| chr3:53108825 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.776-1956G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108825 | |||||||
| chr3:53108946 | G | C | 1 | a0001c0001t0007g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.776-2077C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108946 | |||||||
| chr3:53108964 | G | A | 58 | a0001c0001t0004g0032 a0001c0001t0005g0030 a0001c0001t0005g0031 others(55): Show |
91 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.776-2095C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53108964 | |||||||
| chr3:53109143 | A | T | 1 | a0001c0002t0001g0100 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.776-2274T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109143 | |||||||
| chr3:53109362 | A | G | 19 | a0001c0001t0005g0085 a0001c0001t0006g0207 a0001c0001t0006g0208 others(16): Show |
22 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.775+2468T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109362 | |||||||
| chr3:53109459 | T | C | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.775+2371A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109459 | |||||||
| chr3:53109568 | G | C | 19 | a0001c0001t0005g0085 a0001c0001t0006g0207 a0001c0001t0006g0208 others(16): Show |
22 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.775+2262C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109568 | |||||||
| chr3:53109710 | G | A | 1 | a0001c0002t0024g0166 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.775+2120C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109710 | |||||||
| chr3:53109760 | G | A | 19 | a0001c0001t0005g0085 a0001c0001t0006g0207 a0001c0001t0006g0208 others(16): Show |
22 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.775+2070C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109760 | |||||||
| chr3:53109844 | A | C | 2 | a0001c0001t0008g0017 a0001c0001t0008g0211 |
4 | HG01074.hp2 HG01891.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.775+1986T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109844 | |||||||
| chr3:53109885 | A | G | 47 | a0001c0001t0002g0053 a0001c0001t0003g0004 a0001c0001t0003g0005 others(44): Show |
69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.775+1945T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53109885 | |||||||
| chr3:53110032 | A | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0098 |
3 | HG03516.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.775+1798T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110032 | |||||||
| chr3:53110071 | T | C | 1 | a0001c0002t0001g0130 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.775+1759A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110071 | |||||||
| chr3:53110224 | C | T | 1 | a0001c0002t0001g0119 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.775+1606G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110224 | |||||||
| chr3:53110347 | T | C | 47 | a0001c0001t0002g0053 a0001c0001t0003g0004 a0001c0001t0003g0005 others(44): Show |
69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.775+1483A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110347 | |||||||
| chr3:53110386 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.775+1444G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110386 | |||||||
| chr3:53110518 | G | A | 1 | a0001c0002t0001g0116 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.775+1312C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110518 | |||||||
| chr3:53110913 | T | C | 1 | a0002c0003t0006g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.775+917A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110913 | |||||||
| chr3:53110934 | C | T | 1 | a0001c0002t0001g0169 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.775+896G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53110934 | |||||||
| chr3:53111181 | G | A | 3 | a0001c0001t0002g0034 a0001c0001t0002g0142 a0001c0001t0005g0143 |
4 | HG02559.hp1 HG02572.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.775+649C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53111181 | |||||||
| chr3:53111226 | A | G | 1 | a0001c0002t0001g0111 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.775+604T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 7/12 | chr3 | 53111226 | |||||||
| chr3:53112177 | C | T | 1 | a0003c0007t0001g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.697-269G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53112177 | |||||||
| chr3:53112542 | G | A | 1 | a0001c0001t0005g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.697-634C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53112542 | |||||||
| chr3:53112716 | C | A | 18 | a0001c0001t0002g0015 a0001c0001t0002g0034 a0001c0001t0002g0132 others(15): Show |
21 | HG01891.hp2 HG01934.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.697-808G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53112716 | |||||||
| chr3:53112866 | C | G | 1 | a0002c0003t0006g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.697-958G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53112866 | |||||||
| chr3:53113222 | G | A | 1 | a0001c0001t0005g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.697-1314C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113222 | |||||||
| chr3:53113222 | G | T | 1 | a0001c0001t0003g0055 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.697-1314C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113222 | |||||||
| chr3:53113237 | A | T | 1 | a0001c0002t0001g0168 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.697-1329T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113237 | |||||||
| chr3:53113246 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1338C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113246 | |||||||
| chr3:53113251 | A | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1343T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113251 | |||||||
| chr3:53113254 | A | G | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1346T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113254 | |||||||
| chr3:53113257 | C | G | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1349G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113257 | |||||||
| chr3:53113258 | C | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1350G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113258 | |||||||
| chr3:53113260 | C | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1352G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113260 | |||||||
| chr3:53113267 | C | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1359G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113267 | |||||||
| chr3:53113268 | G | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1360C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113268 | |||||||
| chr3:53113269 | G | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1361C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113269 | |||||||
| chr3:53113270 | C | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1362G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113270 | |||||||
| chr3:53113272 | C | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1364G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113272 | |||||||
| chr3:53113276 | A | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1368T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113276 | |||||||
| chr3:53113277 | A | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1369T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113277 | |||||||
| chr3:53113278 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1370C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113278 | |||||||
| chr3:53113279 | T | G | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1371A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113279 | |||||||
| chr3:53113281 | C | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1373G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113281 | |||||||
| chr3:53113282 | T | G | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1374A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113282 | |||||||
| chr3:53113283 | G | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1375C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113283 | |||||||
| chr3:53113284 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1376C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113284 | |||||||
| chr3:53113292 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1384C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113292 | |||||||
| chr3:53113293 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1385C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113293 | |||||||
| chr3:53113311 | G | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1403C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113311 | |||||||
| chr3:53113313 | T | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1405A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113313 | |||||||
| chr3:53113321 | A | G | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1413T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113321 | |||||||
| chr3:53113322 | G | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1414C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113322 | |||||||
| chr3:53113323 | G | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1415C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113323 | |||||||
| chr3:53113329 | A | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1421T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113329 | |||||||
| chr3:53113332 | C | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1424G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113332 | |||||||
| chr3:53113334 | T | G | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1426A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113334 | |||||||
| chr3:53113336 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1428C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113336 | |||||||
| chr3:53113338 | G | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1430C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113338 | |||||||
| chr3:53113339 | T | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1431A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113339 | |||||||
| chr3:53113340 | A | G | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1432T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113340 | |||||||
| chr3:53113341 | C | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1433G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113341 | |||||||
| chr3:53113344 | G | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1436C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113344 | |||||||
| chr3:53113352 | A | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1444T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113352 | |||||||
| chr3:53113356 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1448C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113356 | |||||||
| chr3:53113357 | T | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1449A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113357 | |||||||
| chr3:53113358 | A | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1450T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113358 | |||||||
| chr3:53113361 | G | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1453C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113361 | |||||||
| chr3:53113364 | T | G | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1456A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113364 | |||||||
| chr3:53113367 | C | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1459G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113367 | |||||||
| chr3:53113369 | A | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1461T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113369 | |||||||
| chr3:53113371 | A | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1463T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113371 | |||||||
| chr3:53113372 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1464C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113372 | |||||||
| chr3:53113374 | G | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1466C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113374 | |||||||
| chr3:53113378 | A | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1470T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113378 | |||||||
| chr3:53113380 | T | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1472A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113380 | |||||||
| chr3:53113384 | C | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1476G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113384 | |||||||
| chr3:53113385 | A | G | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1477T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113385 | |||||||
| chr3:53113389 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1481C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113389 | |||||||
| chr3:53113390 | TAGGATTT others(3): Show |
T | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.697-1492_697-1483d others(12): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113390 | |||||||
| chr3:53113397 | T | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1489A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113397 | |||||||
| chr3:53113402 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1494C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113402 | |||||||
| chr3:53113403 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1495C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113403 | |||||||
| chr3:53113404 | G | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1496C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113404 | |||||||
| chr3:53113406 | T | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1498A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113406 | |||||||
| chr3:53113413 | G | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1505C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113413 | |||||||
| chr3:53113414 | A | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1506T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113414 | |||||||
| chr3:53113416 | G | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1508C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113416 | |||||||
| chr3:53113417 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1509C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113417 | |||||||
| chr3:53113420 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1512C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113420 | |||||||
| chr3:53113421 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1513C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113421 | |||||||
| chr3:53113422 | G | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1514C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113422 | |||||||
| chr3:53113430 | A | C | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1522T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113430 | |||||||
| chr3:53113433 | A | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1525T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113433 | |||||||
| chr3:53113434 | A | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1526T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113434 | |||||||
| chr3:53113435 | G | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1527C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113435 | |||||||
| chr3:53113437 | C | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1529G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113437 | |||||||
| chr3:53113438 | C | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1530G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113438 | |||||||
| chr3:53113439 | A | G | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1531T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113439 | |||||||
| chr3:53113441 | G | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1533C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113441 | |||||||
| chr3:53113442 | C | G | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1534G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113442 | |||||||
| chr3:53113443 | C | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1535G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113443 | |||||||
| chr3:53113445 | A | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1537T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113445 | |||||||
| chr3:53113448 | C | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1540G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113448 | |||||||
| chr3:53113450 | A | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1542T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113450 | |||||||
| chr3:53113452 | C | A | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1544G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113452 | |||||||
| chr3:53113454 | C | T | 1 | a0001c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.697-1546G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113454 | |||||||
| chr3:53113463 | G | A | 1 | a0001c0002t0001g0130 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.697-1555C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113463 | |||||||
| chr3:53113560 | C | A | 16 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0036 others(13): Show |
29 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.697-1652G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113560 | |||||||
| chr3:53113635 | T | C | 1 | a0001c0002t0001g0152 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.697-1727A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113635 | |||||||
| chr3:53113796 | A | C | 1 | a0001c0001t0002g0157 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.697-1888T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113796 | |||||||
| chr3:53113808 | T | C | 1 | a0001c0001t0005g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.697-1900A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113808 | |||||||
| chr3:53113870 | C | T | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.697-1962G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113870 | |||||||
| chr3:53113923 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.697-2015G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53113923 | |||||||
| chr3:53114014 | T | C | 1 | a0001c0001t0002g0148 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.697-2106A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114014 | |||||||
| chr3:53114105 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.697-2197G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114105 | |||||||
| chr3:53114126 | G | A | 1 | a0001c0001t0005g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.697-2218C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114126 | |||||||
| chr3:53114158 | G | A | 1 | a0001c0001t0002g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.697-2250C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114158 | |||||||
| chr3:53114292 | G | A | 3 | a0001c0002t0001g0152 a0001c0002t0001g0194 a0001c0002t0001g0195 |
3 | HG00639.hp1 HG01069.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.697-2384C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114292 | |||||||
| chr3:53114439 | G | C | 146 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(143): Show |
211 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.697-2531C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114439 | |||||||
| chr3:53114573 | G | A | 6 | a0001c0001t0003g0080 a0002c0003t0005g0042 a0002c0003t0005g0043 others(3): Show |
8 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.697-2665C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114573 | |||||||
| chr3:53114579 | T | C | 13 | a0001c0001t0006g0207 a0001c0001t0006g0208 a0002c0003t0006g0041 others(10): Show |
14 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.697-2671A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114579 | |||||||
| chr3:53114794 | C | A | 5 | a0002c0003t0005g0042 a0002c0003t0005g0043 a0002c0003t0005g0088 others(2): Show |
7 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.697-2886G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114794 | |||||||
| chr3:53114817 | T | A | 1 | a0001c0001t0002g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.697-2909A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114817 | |||||||
| chr3:53114817 | T | G | 194 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(191): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.697-2909A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114817 | |||||||
| chr3:53114942 | A | G | 1 | a0001c0002t0001g0117 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.697-3034T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114942 | |||||||
| chr3:53114952 | C | T | 1 | a0001c0001t0002g0016 | 3 | HG01070.hp1 HG01071.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.697-3044G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53114952 | |||||||
| chr3:53115099 | A | G | 1 | a0001c0002t0001g0111 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.697-3191T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53115099 | |||||||
| chr3:53115205 | T | C | 3 | a0001c0001t0004g0023 a0001c0001t0004g0096 a0001c0001t0011g0104 |
4 | HG03491.hp2 HG03492.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.697-3297A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53115205 | |||||||
| chr3:53115248 | C | G | 13 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0023 others(10): Show |
19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.697-3340G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53115248 | |||||||
| chr3:53115248 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.697-3340G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53115248 | |||||||
| chr3:53115252 | G | A | 16 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0023 others(13): Show |
22 | HG00673.hp1 HG01346.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.697-3344C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53115252 | |||||||
| chr3:53115614 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.697-3706A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53115614 | |||||||
| chr3:53116101 | G | A | 4 | a0001c0002t0001g0165 a0001c0002t0001g0185 a0001c0002t0001g0186 others(1): Show |
4 | NA18961.hp2 NA18971.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+3783C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116101 | |||||||
| chr3:53116291 | CT | C | 70 | a0001c0001t0002g0053 a0001c0001t0002g0170 a0001c0001t0003g0054 others(67): Show |
87 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.696+3592delA | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116291 | |||||||
| chr3:53116291 | CTT | C | 153 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(150): Show |
232 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.696+3591_696+3592d others(4): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116291 | |||||||
| chr3:53116329 | T | C | 2 | a0001c0001t0005g0035 a0001c0001t0012g0151 |
3 | HG02809.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.696+3555A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116329 | |||||||
| chr3:53116333 | G | A | 5 | a0001c0001t0002g0024 a0001c0001t0002g0098 a0001c0001t0005g0035 others(2): Show |
7 | HG02258.hp2 HG02809.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.696+3551C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116333 | |||||||
| chr3:53116418 | A | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0098 |
3 | HG03516.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.696+3466T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116418 | |||||||
| chr3:53116578 | G | A | 1 | a0001c0002t0001g0131 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.696+3306C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116578 | |||||||
| chr3:53116984 | G | T | 18 | a0001c0001t0006g0207 a0001c0001t0006g0208 a0002c0003t0005g0042 others(15): Show |
21 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.696+2900C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53116984 | |||||||
| chr3:53117330 | C | T | 1 | a0001c0002t0001g0194 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.696+2554G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53117330 | |||||||
| chr3:53117648 | A | C | 49 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(46): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.696+2236T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53117648 | |||||||
| chr3:53117703 | G | A | 2 | a0001c0001t0005g0035 a0001c0001t0012g0151 |
3 | HG02809.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.696+2181C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53117703 | |||||||
| chr3:53117754 | C | T | 1 | a0001c0002t0001g0026 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.696+2130G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53117754 | |||||||
| chr3:53118042 | A | G | 1 | a0001c0001t0002g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.696+1842T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118042 | |||||||
| chr3:53118046 | T | C | 212 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(209): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.696+1838A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118046 | |||||||
| chr3:53118066 | T | A | 225 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(222): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.696+1818A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118066 | |||||||
| chr3:53118091 | C | T | 13 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0023 others(10): Show |
19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.696+1793G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118091 | |||||||
| chr3:53118435 | G | C | 1 | a0001c0001t0002g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.696+1449C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118435 | |||||||
| chr3:53118587 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.696+1297T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118587 | |||||||
| chr3:53118706 | T | C | 3 | a0001c0001t0002g0034 a0001c0001t0002g0142 a0001c0001t0005g0143 |
4 | HG02559.hp1 HG02572.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+1178A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118706 | |||||||
| chr3:53118755 | G | A | 1 | a0001c0001t0003g0081 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.696+1129C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118755 | |||||||
| chr3:53118906 | A | G | 1 | a0001c0001t0003g0051 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.696+978T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53118906 | |||||||
| chr3:53119047 | CA | C | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.696+836delT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119047 | |||||||
| chr3:53119056 | A | T | 2 | a0001c0001t0004g0090 a0001c0001t0004g0091 |
2 | HG00673.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.696+828T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119056 | |||||||
| chr3:53119122 | G | C | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.696+762C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119122 | |||||||
| chr3:53119333 | T | C | 3 | a0001c0001t0008g0017 a0001c0001t0008g0211 a0001c0001t0008g0213 |
5 | HG01074.hp2 HG01891.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.696+551A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119333 | |||||||
| chr3:53119415 | A | T | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.696+469T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119415 | |||||||
| chr3:53119649 | C | A | 1 | a0001c0001t0002g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.696+235G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 6/12 | chr3 | 53119649 | |||||||
| chr3:53120116 | ATTAACTG others(3): Show |
A | 49 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(46): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.559-105_559-96delG others(9): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120116 | |||||||
| chr3:53120127 | T | G | 49 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(46): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.559-106A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120127 | |||||||
| chr3:53120133 | T | G | 1 | a0001c0001t0005g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.559-112A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120133 | |||||||
| chr3:53120251 | C | G | 4 | a0001c0002t0001g0010 a0001c0002t0001g0216 a0001c0002t0001g0217 others(1): Show |
7 | HG00639.hp2 HG01074.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.559-230G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120251 | |||||||
| chr3:53120300 | C | G | 2 | a0001c0002t0001g0165 a0005c0004t0001g0045 |
2 | NA18961.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.559-279G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120300 | |||||||
| chr3:53120350 | C | T | 1 | a0001c0002t0001g0164 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.559-329G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120350 | |||||||
| chr3:53120445 | T | C | 2 | a0001c0002t0001g0102 a0001c0002t0001g0189 |
2 | NA19003.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.559-424A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120445 | |||||||
| chr3:53120448 | A | T | 1 | a0001c0001t0003g0050 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.559-427T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120448 | |||||||
| chr3:53120489 | T | C | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.559-468A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120489 | |||||||
| chr3:53120663 | A | G | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.559-642T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120663 | |||||||
| chr3:53120852 | C | T | 1 | a0001c0001t0004g0089 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.559-831G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120852 | |||||||
| chr3:53120884 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.558+815T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120884 | |||||||
| chr3:53120972 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.558+727G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53120972 | |||||||
| chr3:53121002 | A | T | 1 | a0001c0001t0008g0211 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.558+697T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53121002 | |||||||
| chr3:53121056 | C | T | 16 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0036 others(13): Show |
29 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.558+643G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53121056 | |||||||
| chr3:53121142 | C | T | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.558+557G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53121142 | |||||||
| chr3:53121157 | G | C | 3 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0146 |
3 | HG01934.hp1 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.558+542C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 5/12 | chr3 | 53121157 | |||||||
| chr3:53121944 | T | C | 1 | a0001c0001t0014g0190 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.457-144A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 4/12 | chr3 | 53121944 | |||||||
| chr3:53122004 | A | G | 1 | a0001c0001t0020g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.457-204T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 4/12 | chr3 | 53122004 | |||||||
| chr3:53122049 | G | C | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.457-249C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 4/12 | chr3 | 53122049 | |||||||
| chr3:53122276 | T | A | 3 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0149 |
3 | HG02922.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.456+98A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 4/12 | chr3 | 53122276 | |||||||
| chr3:53122583 | T | A | 22 | a0001c0001t0002g0015 a0001c0001t0002g0034 a0001c0001t0002g0132 others(19): Show |
25 | HG01891.hp2 HG01934.hp1 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.267-20A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53122583 | |||||||
| chr3:53122676 | T | A | 1 | a0001c0002t0001g0192 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.267-113A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53122676 | |||||||
| chr3:53122851 | T | C | 49 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(46): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.267-288A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53122851 | |||||||
| chr3:53123040 | TGGGGCAC others(22): Show |
T | 1 | a0003c0007t0001g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.267-506_267-478del others(29): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123040 | |||||||
| chr3:53123286 | A | T | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.266+438T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123286 | |||||||
| chr3:53123419 | C | T | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.266+305G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123419 | |||||||
| chr3:53123453 | C | T | 16 | a0002c0003t0005g0042 a0002c0003t0005g0043 a0002c0003t0005g0088 others(13): Show |
19 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.266+271G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123453 | |||||||
| chr3:53123530 | T | C | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.266+194A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123530 | |||||||
| chr3:53123544 | G | A | 2 | a0001c0002t0001g0194 a0001c0002t0001g0195 |
2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.266+180C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123544 | |||||||
| chr3:53123587 | T | C | 5 | a0001c0001t0002g0024 a0001c0001t0002g0098 a0001c0001t0005g0035 others(2): Show |
7 | HG02258.hp2 HG02809.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.266+137A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 3/12 | chr3 | 53123587 | |||||||
| chr3:53123888 | AGAGAACT others(5): Show |
A | 1 | a0001c0002t0001g0009 | 4 | HG00621.hp2 NA18941.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-60_150-49delCC others(10): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53123888 | |||||||
| chr3:53123955 | G | A | 1 | a0006c0006t0004g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.150-115C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53123955 | |||||||
| chr3:53124064 | G | A | 1 | a0001c0002t0021g0150 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.150-224C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124064 | |||||||
| chr3:53124142 | T | C | 212 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(209): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.150-302A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124142 | |||||||
| chr3:53124382 | G | A | 1 | a0001c0001t0005g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.150-542C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124382 | |||||||
| chr3:53124752 | A | G | 212 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(209): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.150-912T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124752 | |||||||
| chr3:53124815 | T | A | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.150-975A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124815 | |||||||
| chr3:53124819 | A | G | 2 | a0001c0002t0001g0155 a0001c0002t0023g0154 |
2 | HG01255.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.150-979T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124819 | |||||||
| chr3:53124877 | C | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0098 |
3 | HG03516.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.149+1032G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124877 | |||||||
| chr3:53124878 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.149+1031C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124878 | |||||||
| chr3:53124937 | A | C | 1 | a0001c0002t0001g0099 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.149+972T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124937 | |||||||
| chr3:53124970 | G | A | 1 | a0001c0002t0001g0009 | 4 | HG00621.hp2 NA18941.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+939C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124970 | |||||||
| chr3:53124973 | T | A | 1 | a0001c0002t0001g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.149+936A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53124973 | |||||||
| chr3:53125208 | G | C | 13 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0023 others(10): Show |
19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.149+701C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53125208 | |||||||
| chr3:53125302 | C | G | 1 | a0001c0002t0001g0153 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.149+607G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53125302 | |||||||
| chr3:53125438 | C | A | 1 | a0001c0002t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.149+471G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53125438 | |||||||
| chr3:53125444 | C | G | 1 | a0001c0001t0002g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.149+465G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53125444 | |||||||
| chr3:53125493 | A | C | 1 | a0001c0002t0001g0107 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.149+416T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53125493 | |||||||
| chr3:53125494 | AG | A | 7 | a0001c0002t0001g0010 a0001c0002t0001g0044 a0001c0002t0001g0216 others(4): Show |
11 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.149+414delC | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 2/12 | chr3 | 53125494 | |||||||
| chr3:53126008 | G | A | 5 | a0001c0001t0002g0024 a0001c0001t0002g0098 a0001c0001t0005g0035 others(2): Show |
7 | HG02258.hp2 HG02809.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-14C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126008 | |||||||
| chr3:53126067 | T | C | 1 | a0001c0002t0001g0152 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.64-73A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126067 | |||||||
| chr3:53126116 | T | C | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-122A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126116 | |||||||
| chr3:53126177 | G | T | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-183C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126177 | |||||||
| chr3:53126200 | T | C | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-206A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126200 | |||||||
| chr3:53126227 | G | A | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-233C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126227 | |||||||
| chr3:53126253 | A | T | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-259T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126253 | |||||||
| chr3:53126254 | C | T | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-260G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126254 | |||||||
| chr3:53126255 | C | T | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-261G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126255 | |||||||
| chr3:53126344 | G | A | 55 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0036 others(52): Show |
80 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.64-350C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126344 | |||||||
| chr3:53126364 | C | G | 1 | a0001c0001t0011g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.64-370G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126364 | |||||||
| chr3:53126389 | T | C | 212 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(209): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.64-395A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126389 | |||||||
| chr3:53126446 | C | CTAATTTC others(321): Show |
1 | a0001c0002t0010g0106 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.64-453_64-452insCT others(326): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126446 | |||||||
| chr3:53126446 | C | CTAATTTC others(322): Show |
1 | a0001c0002t0010g0105 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.64-453_64-452insCT others(327): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126446 | |||||||
| chr3:53126905 | T | C | 1 | a0001c0001t0005g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.64-911A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53126905 | |||||||
| chr3:53127015 | A | G | 213 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(210): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.64-1021T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127015 | |||||||
| chr3:53127092 | C | T | 1 | a0001c0002t0001g0025 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.64-1098G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127092 | |||||||
| chr3:53127292 | T | A | 2 | a0001c0002t0001g0194 a0001c0002t0001g0195 |
2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.64-1298A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127292 | |||||||
| chr3:53127468 | G | A | 13 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0023 others(10): Show |
19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-1474C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127468 | |||||||
| chr3:53127492 | G | C | 19 | a0001c0001t0002g0214 a0001c0001t0006g0207 a0001c0001t0006g0208 others(16): Show |
22 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.64-1498C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127492 | |||||||
| chr3:53127557 | T | C | 212 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(209): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.64-1563A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127557 | |||||||
| chr3:53127619 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.64-1625C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127619 | |||||||
| chr3:53127652 | TA | T | 169 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(166): Show |
242 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.64-1659delT | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127652 | |||||||
| chr3:53127652 | TAA | T | 6 | a0001c0001t0009g0228 a0001c0002t0001g0099 a0001c0002t0001g0100 others(3): Show |
6 | HG01167.hp2 HG02735.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-1660_64-1659del others(2): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127652 | |||||||
| chr3:53127884 | C | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0098 |
3 | HG03516.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.64-1890G>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127884 | |||||||
| chr3:53127929 | C | A | 1 | a0001c0001t0002g0214 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.64-1935G>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53127929 | |||||||
| chr3:53128024 | G | A | 1 | a0001c0002t0001g0215 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.64-2030C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128024 | |||||||
| chr3:53128263 | A | C | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+2075T>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128263 | |||||||
| chr3:53128322 | T | A | 6 | a0001c0002t0001g0010 a0001c0002t0001g0044 a0001c0002t0001g0216 others(3): Show |
10 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+2016A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128322 | |||||||
| chr3:53128390 | G | A | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+1948C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128390 | |||||||
| chr3:53128429 | A | G | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+1909T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128429 | |||||||
| chr3:53128443 | C | T | 13 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0023 others(10): Show |
19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.63+1895G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128443 | |||||||
| chr3:53128444 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63+1894C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128444 | |||||||
| chr3:53128644 | G | C | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+1694C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128644 | |||||||
| chr3:53128656 | G | T | 13 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0023 others(10): Show |
19 | HG00673.hp1 HG01943.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.63+1682C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128656 | |||||||
| chr3:53128731 | C | T | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+1607G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128731 | |||||||
| chr3:53128802 | C | T | 1 | a0002c0003t0005g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.63+1536G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128802 | |||||||
| chr3:53128942 | G | C | 1 | a0001c0002t0001g0221 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63+1396C>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53128942 | |||||||
| chr3:53129041 | A | T | 48 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(45): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+1297T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129041 | |||||||
| chr3:53129200 | A | G | 1 | a0001c0001t0002g0086 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.63+1138T>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129200 | |||||||
| chr3:53129308 | G | T | 1 | a0001c0001t0005g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.63+1030C>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129308 | |||||||
| chr3:53129359 | C | T | 1 | a0001c0001t0004g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.63+979G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129359 | |||||||
| chr3:53129671 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.63+667C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129671 | |||||||
| chr3:53129676 | G | A | 2 | a0001c0002t0001g0222 a0001c0002t0001g0223 |
2 | NA19066.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.63+662C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129676 | |||||||
| chr3:53129685 | T | C | 1 | a0001c0001t0020g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.63+653A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129685 | |||||||
| chr3:53129814 | G | A | 1 | a0001c0002t0001g0225 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.63+524C>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129814 | |||||||
| chr3:53129873 | T | C | 1 | a0001c0002t0001g0226 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.63+465A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129873 | |||||||
| chr3:53129922 | A | T | 1 | a0003c0007t0001g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+416T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129922 | |||||||
| chr3:53129926 | A | T | 1 | a0003c0007t0001g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+412T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129926 | |||||||
| chr3:53129927 | T | A | 1 | a0003c0007t0001g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+411A>T | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129927 | |||||||
| chr3:53129931 | A | T | 1 | a0003c0007t0001g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+407T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129931 | |||||||
| chr3:53129933 | A | T | 1 | a0003c0007t0001g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+405T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129933 | |||||||
| chr3:53129934 | T | TCTTTTCT others(9): Show |
1 | a0003c0007t0001g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+403_63+404insGA others(14): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129934 | |||||||
| chr3:53129937 | A | T | 47 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(44): Show |
69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.63+401T>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129937 | |||||||
| chr3:53129939 | T | TTAGCACT others(4): Show |
1 | a0003c0007t0001g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+398_63+399insCA others(9): Show |
RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129939 | |||||||
| chr3:53129940 | C | T | 1 | a0003c0007t0001g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+398G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53129940 | |||||||
| chr3:53130078 | C | T | 47 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(44): Show |
69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.63+260G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53130078 | |||||||
| chr3:53130177 | C | T | 47 | a0001c0001t0002g0053 a0001c0001t0002g0057 a0001c0001t0003g0004 others(44): Show |
69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.63+161G>A | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53130177 | |||||||
| chr3:53130200 | T | C | 1 | a0001c0001t0003g0227 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.63+138A>G | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53130200 | |||||||
| chr3:53130222 | T | G | 1 | a0001c0001t0009g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+116A>C | RFT1 | ENSG00000163933.10 | transcript | ENST00000296292.8 | protein_coding | 1/12 | chr3 | 53130222 |