Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2222 |
| ensemblid | ENSG00000079459.14 |
| hgncid | 3629 |
| symbol | FDFT1 |
| name | farnesyl-diphosphate farnesyltransferase 1 |
| refseq_nuc | NM_004462.5 |
| refseq_prot | NP_004453.3 |
| ensembl_nuc | ENST00000220584.9 |
| ensembl_prot | ENSP00000220584.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 11802741 |
| end | 11839298 |
| strand | + |
| ver | v1.2 |
| region | chr8:11802741-11839298 |
| region5000 | chr8:11797741-11844298 |
| regionname0 | FDFT1_chr8_11802741_11839298 |
| regionname5000 | FDFT1_chr8_11797741_11844298 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 417 | 434 | 97 | 75 | 199 | 15 | 46 | 156 | FDFT1_chr8_11797741_11844298 | FDFT1 | MEFVK others(412): Show |
chr8 | 11797741 | 11844298 |
| a0002 | 0/0 | 417 | 11 | 0 | 5 | 1 | 1 | 4 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | MEFVK others(412): Show |
chr8 | 11797741 | 11844298 |
| a0003 | 0/0 | 417 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | FDFT1_chr8_11797741_11844298 | FDFT1 | MEFVK others(412): Show |
chr8 | 11797741 | 11844298 |
| a0004 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | MEFVK others(412): Show |
chr8 | 11797741 | 11844298 |
| a0005 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | MEFVK others(412): Show |
chr8 | 11797741 | 11844298 |
| a0006 | 0/0 | 417 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | MEFVK others(412): Show |
chr8 | 11797741 | 11844298 |
| a0007 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | MEFVK others(412): Show |
chr8 | 11797741 | 11844298 |
| a0008 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | MEFVK others(412): Show |
chr8 | 11797741 | 11844298 |
| a0009 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | MEFVK others(412): Show |
chr8 | 11797741 | 11844298 |
| a0010 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | MEFVK others(412): Show |
chr8 | 11797741 | 11844298 |
| a0011 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | MEFVK others(412): Show |
chr8 | 11797741 | 11844298 |
| a0012 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | MEFVK others(412): Show |
chr8 | 11797741 | 11844298 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1251 | 166 | 34 | 39 | 55 | 9 | 29 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0002 | 0/0 | 1251 | 112 | 6 | 15 | 77 | 1 | 13 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0003 | 0/0 | 1251 | 67 | 4 | 2 | 60 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0004 | 0/1 | 1251 | 42 | 27 | 11 | 0 | 2 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0005 | 0/0 | 1251 | 12 | 5 | 3 | 0 | 2 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0006 | 0/0 | 1251 | 11 | 2 | 2 | 6 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0008 | 0/0 | 1251 | 5 | 5 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0010 | 1/0 | 1251 | 5 | 4 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0011 | 0/0 | 1251 | 4 | 4 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0013 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0014 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0015 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0016 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0017 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0018 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0021 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0025 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0001c0028 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0002c0007 | 0/0 | 1251 | 6 | 0 | 5 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0002c0009 | 0/0 | 1251 | 5 | 0 | 0 | 1 | 0 | 4 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0003c0012 | 0/0 | 1251 | 4 | 0 | 0 | 4 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0004c0027 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0005c0029 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0006c0023 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0007c0019 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0008c0020 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0009c0022 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0010c0026 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0011c0024 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 | ||
| a0012c0030 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | ATGGA others(1246): Show |
chr8 | 11797741 | 11844298 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2035 | 110 | 16 | 27 | 45 | 5 | 17 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0001t0002 | 0/0 | 2035 | 41 | 11 | 11 | 5 | 4 | 10 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0001t0003 | 0/0 | 2035 | 4 | 0 | 0 | 3 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0001t0004 | 0/0 | 2035 | 2 | 0 | 1 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0001t0006 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0001t0008 | 0/0 | 2035 | 3 | 3 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0001t0009 | 0/0 | 2035 | 2 | 0 | 0 | 1 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0001t0010 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0001t0011 | 0/0 | 2035 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0002t0001 | 0/0 | 2035 | 15 | 2 | 2 | 7 | 0 | 4 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0002t0002 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0002t0003 | 0/0 | 2035 | 80 | 0 | 13 | 58 | 1 | 8 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0002t0004 | 0/0 | 2035 | 6 | 3 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0002t0005 | 0/0 | 2035 | 9 | 0 | 0 | 9 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0002t0015 | 0/0 | 2035 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0003t0001 | 0/0 | 2035 | 50 | 0 | 0 | 50 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0003t0002 | 0/0 | 2035 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0003t0003 | 0/0 | 2035 | 12 | 1 | 1 | 9 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0003t0004 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0003t0013 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0003t0014 | 0/0 | 2035 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0004t0001 | 0/0 | 2035 | 6 | 6 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0004t0002 | 0/1 | 2035 | 26 | 14 | 8 | 0 | 2 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0004t0006 | 0/0 | 2035 | 6 | 6 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0004t0007 | 0/0 | 2035 | 3 | 0 | 3 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0004t0010 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0005t0001 | 0/0 | 2035 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0005t0002 | 0/0 | 2035 | 8 | 1 | 3 | 0 | 2 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0005t0012 | 0/0 | 2035 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0006t0001 | 0/0 | 2035 | 5 | 1 | 1 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0006t0002 | 0/0 | 2035 | 4 | 0 | 1 | 2 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0006t0005 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0006t0006 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0008t0001 | 0/0 | 2035 | 4 | 4 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0008t0002 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0010t0002 | 1/0 | 2035 | 5 | 4 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0011t0002 | 0/0 | 2035 | 4 | 4 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0013t0002 | 0/0 | 2035 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0014t0016 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0015t0002 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0016t0002 | 0/0 | 2035 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0017t0002 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0018t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0021t0001 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0025t0003 | 0/0 | 2035 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0001c0028t0002 | 0/0 | 2035 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0002c0007t0001 | 0/0 | 2035 | 5 | 0 | 4 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0002c0007t0002 | 0/0 | 2035 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0002c0009t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0002c0009t0002 | 0/0 | 2035 | 4 | 0 | 0 | 0 | 0 | 4 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0003c0012t0001 | 0/0 | 2035 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0003c0012t0018 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0004c0027t0003 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0005c0029t0003 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0006c0023t0017 | 0/0 | 2035 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0007c0019t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0008c0020t0002 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0009c0022t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0010c0026t0004 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0011c0024t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| a0012c0030t0001 | 0/0 | 2035 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | GAAGC others(2030): Show |
chr8 | 11797741 | 11844298 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0393 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0395 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0396 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0001g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0002g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0006g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0009g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0011g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0003g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0004g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0005g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0002t0015g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0002g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0003g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0004g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0013g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0003t0014g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0001 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0002g0397 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0007g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0007g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0004t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0005t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0005t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0005t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0005t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0005t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0005t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0005t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0005t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0005t0012g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0005t0012g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0006t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0006t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0006t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0006t0001g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0006t0001g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0006t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0006t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0006t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0006t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0006t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0006t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0008t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0008t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0008t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0008t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0008t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0010t0002g0006 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0010t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0010t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0011t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0011t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0013t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0013t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0014t0016g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0015t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0016t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0017t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0018t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0021t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0025t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0001c0028t0002g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0002c0007t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0002c0007t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0002c0007t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0002c0007t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0002c0007t0002g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0002c0009t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0002c0009t0002g0005 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0002c0009t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0003c0012t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0003c0012t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0003c0012t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0003c0012t0018g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0004c0027t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0005c0029t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0006c0023t0017g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0007c0019t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0008c0020t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0009c0022t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0010c0026t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0011c0024t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| a0012c0030t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0108 | EUR | GBR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0119 | EUR | GBR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00140 | hp1 | a0001 | c0003 | t0003 | g0307 | EUR | GBR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0377 | EUR | GBR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0296 | EUR | FIN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0360 | EUR | FIN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00323 | hp1 | a0002 | c0007 | t0001 | g0035 | EUR | FIN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00323 | hp2 | a0001 | c0005 | t0002 | g0070 | EUR | FIN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0100 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00423 | hp2 | a0004 | c0027 | t0003 | g0275 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0390 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0269 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00597 | hp2 | a0003 | c0012 | t0018 | g0339 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0209 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00609 | hp2 | a0001 | c0002 | t0005 | g0240 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0153 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00639 | hp1 | a0001 | c0003 | t0014 | g0120 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00642 | hp1 | a0001 | c0004 | t0002 | g0001 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00642 | hp2 | a0002 | c0007 | t0001 | g0352 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00673 | hp2 | a0001 | c0002 | t0005 | g0219 | EAS | CHS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0220 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00735 | hp1 | a0001 | c0004 | t0002 | g0001 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0218 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00741 | hp1 | a0001 | c0004 | t0002 | g0397 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG00741 | hp2 | a0001 | c0028 | t0002 | g0373 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0203 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01070 | hp2 | a0001 | c0004 | t0007 | g0025 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01071 | hp1 | a0001 | c0004 | t0007 | g0025 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0376 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01081 | hp2 | a0002 | c0007 | t0001 | g0313 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0366 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01106 | hp1 | a0001 | c0004 | t0002 | g0001 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0374 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01109 | hp2 | a0001 | c0004 | t0002 | g0170 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0224 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01168 | hp2 | a0001 | c0005 | t0002 | g0137 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01169 | hp2 | a0001 | c0005 | t0002 | g0136 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01175 | hp2 | a0001 | c0004 | t0007 | g0176 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0378 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01243 | hp1 | a0001 | c0005 | t0002 | g0151 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01255 | hp1 | a0001 | c0016 | t0002 | g0169 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01255 | hp2 | a0001 | c0006 | t0001 | g0356 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01256 | hp2 | a0002 | c0007 | t0002 | g0348 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01261 | hp1 | a0001 | c0004 | t0002 | g0026 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0239 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0204 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0384 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01361 | hp2 | a0001 | c0006 | t0002 | g0185 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0056 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01496 | hp1 | a0001 | c0004 | t0002 | g0001 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01496 | hp2 | a0001 | c0004 | t0002 | g0172 | AMR | CLM | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0350 | EUR | IBS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0395 | EUR | IBS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0111 | EUR | IBS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0396 | EUR | IBS | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01891 | hp1 | a0001 | c0008 | t0001 | g0157 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01891 | hp2 | a0001 | c0011 | t0002 | g0014 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0362 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01943 | hp1 | a0001 | c0003 | t0003 | g0354 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0364 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0266 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0267 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0358 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0229 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0336 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01993 | hp1 | a0002 | c0007 | t0001 | g0038 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02004 | hp1 | a0002 | c0007 | t0001 | g0035 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02004 | hp2 | a0001 | c0002 | t0003 | g0054 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0088 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02071 | hp2 | a0001 | c0003 | t0003 | g0105 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0265 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0079 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0226 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0106 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0208 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02083 | hp2 | a0005 | c0029 | t0003 | g0264 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02129 | hp1 | a0001 | c0001 | t0009 | g0017 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0252 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0401 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0091 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0398 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02135 | hp2 | a0001 | c0002 | t0005 | g0261 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0368 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02145 | hp2 | a0001 | c0013 | t0002 | g0180 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02165 | hp1 | a0001 | c0006 | t0001 | g0399 | EAS | CDX | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0236 | EAS | CDX | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0367 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0148 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02273 | hp2 | a0001 | c0025 | t0003 | g0055 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02280 | hp1 | a0001 | c0006 | t0001 | g0383 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0053 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02451 | hp1 | a0001 | c0005 | t0012 | g0040 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0147 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0214 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0093 | EAS | KHV | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02602 | hp2 | a0001 | c0002 | t0015 | g0222 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02615 | hp1 | a0001 | c0008 | t0002 | g0132 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02622 | hp1 | a0001 | c0004 | t0006 | g0142 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0043 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02630 | hp1 | a0001 | c0011 | t0002 | g0027 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02630 | hp2 | a0001 | c0021 | t0001 | g0073 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02647 | hp1 | a0001 | c0004 | t0002 | g0171 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02647 | hp2 | a0001 | c0005 | t0012 | g0049 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0237 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0191 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02717 | hp1 | a0001 | c0004 | t0002 | g0131 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0141 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02723 | hp1 | a0001 | c0005 | t0002 | g0149 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02723 | hp2 | a0001 | c0004 | t0002 | g0021 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0189 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02735 | hp2 | a0001 | c0001 | t0009 | g0017 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0161 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02809 | hp2 | a0001 | c0010 | t0002 | g0006 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0274 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02818 | hp2 | a0001 | c0011 | t0002 | g0014 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02886 | hp1 | a0001 | c0015 | t0002 | g0181 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0402 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02895 | hp1 | a0001 | c0004 | t0006 | g0164 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0125 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02896 | hp1 | a0001 | c0010 | t0002 | g0075 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02897 | hp2 | a0001 | c0004 | t0006 | g0165 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02922 | hp2 | a0001 | c0004 | t0006 | g0145 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02965 | hp2 | a0001 | c0010 | t0002 | g0069 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02970 | hp1 | a0001 | c0013 | t0002 | g0177 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0133 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02976 | hp2 | a0001 | c0008 | t0001 | g0134 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0184 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0247 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03041 | hp1 | a0001 | c0003 | t0013 | g0404 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03041 | hp2 | a0001 | c0006 | t0006 | g0193 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03098 | hp1 | a0001 | c0017 | t0002 | g0041 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03098 | hp2 | a0001 | c0004 | t0002 | g0022 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03130 | hp1 | a0001 | c0008 | t0001 | g0155 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03130 | hp2 | a0001 | c0004 | t0002 | g0068 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03139 | hp1 | a0001 | c0014 | t0016 | g0143 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03139 | hp2 | a0001 | c0004 | t0002 | g0024 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03195 | hp2 | a0001 | c0004 | t0002 | g0168 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0403 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0009 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03225 | hp1 | a0001 | c0004 | t0002 | g0021 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03225 | hp2 | a0006 | c0023 | t0017 | g0042 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0382 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0363 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03453 | hp2 | a0001 | c0002 | t0004 | g0009 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0140 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03490 | hp1 | a0002 | c0009 | t0002 | g0005 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03492 | hp1 | a0002 | c0009 | t0002 | g0005 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03540 | hp1 | a0001 | c0004 | t0002 | g0130 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03540 | hp2 | a0001 | c0005 | t0001 | g0138 | AFR | GWD | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03579 | hp1 | a0001 | c0002 | t0004 | g0009 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0271 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0361 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03669 | hp2 | a0002 | c0009 | t0002 | g0005 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0357 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03704 | hp2 | a0001 | c0004 | t0002 | g0173 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0031 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03710 | hp2 | a0001 | c0005 | t0002 | g0023 | SAS | PJL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0342 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0192 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03927 | hp2 | a0001 | c0006 | t0002 | g0233 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0259 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0388 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0385 | SAS | BEB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0221 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG04204 | hp1 | a0001 | c0005 | t0002 | g0023 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0359 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0393 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG04228 | hp2 | a0002 | c0009 | t0002 | g0166 | SAS | STU | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18522 | hp1 | a0001 | c0008 | t0001 | g0156 | AFR | YRI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18522 | hp2 | a0001 | c0011 | t0002 | g0027 | AFR | YRI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0092 | EAS | CHB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0290 | EAS | CHB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0084 | EAS | CHB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18747 | hp2 | a0001 | c0002 | t0003 | g0251 | EAS | CHB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0047 | AFR | YRI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18906 | hp2 | a0001 | c0004 | t0002 | g0135 | AFR | YRI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18940 | hp1 | a0001 | c0003 | t0004 | g0386 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18940 | hp2 | a0001 | c0002 | t0003 | g0400 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0083 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18943 | hp2 | a0001 | c0002 | t0005 | g0244 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0127 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18945 | hp2 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18946 | hp1 | a0001 | c0002 | t0003 | g0355 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18948 | hp1 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18948 | hp2 | a0001 | c0002 | t0005 | g0002 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18949 | hp1 | a0001 | c0006 | t0005 | g0234 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18949 | hp2 | a0001 | c0002 | t0003 | g0227 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0273 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18952 | hp2 | a0001 | c0006 | t0001 | g0241 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18953 | hp1 | a0001 | c0006 | t0001 | g0215 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0250 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18956 | hp2 | a0001 | c0018 | t0001 | g0372 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0308 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0394 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18959 | hp2 | a0001 | c0002 | t0003 | g0217 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18960 | hp2 | a0001 | c0003 | t0003 | g0104 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18962 | hp1 | a0003 | c0012 | t0001 | g0353 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0099 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18963 | hp2 | a0001 | c0002 | t0004 | g0033 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18965 | hp1 | a0003 | c0012 | t0001 | g0329 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18966 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18966 | hp2 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18968 | hp1 | a0001 | c0003 | t0003 | g0102 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0097 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18970 | hp1 | a0001 | c0002 | t0005 | g0248 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18970 | hp2 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18971 | hp1 | a0001 | c0003 | t0003 | g0020 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18972 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18972 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18973 | hp1 | a0002 | c0009 | t0001 | g0174 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18975 | hp1 | a0001 | c0002 | t0003 | g0246 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18979 | hp1 | a0001 | c0003 | t0001 | g0263 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0243 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18981 | hp1 | a0001 | c0002 | t0003 | g0277 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18982 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18982 | hp2 | a0007 | c0019 | t0001 | g0335 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0242 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0272 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18984 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18985 | hp1 | a0001 | c0003 | t0001 | g0087 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18985 | hp2 | a0001 | c0002 | t0003 | g0256 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18986 | hp1 | a0001 | c0002 | t0003 | g0183 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18987 | hp1 | a0001 | c0002 | t0003 | g0052 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18987 | hp2 | a0008 | c0020 | t0002 | g0059 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18988 | hp2 | a0001 | c0002 | t0004 | g0072 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18992 | hp1 | a0001 | c0002 | t0003 | g0228 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18992 | hp2 | a0001 | c0003 | t0001 | g0098 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18994 | hp2 | a0001 | c0003 | t0001 | g0090 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18995 | hp1 | a0001 | c0003 | t0003 | g0270 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18997 | hp1 | a0001 | c0002 | t0003 | g0190 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18997 | hp2 | a0001 | c0003 | t0001 | g0298 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0285 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0254 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0152 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19001 | hp1 | a0009 | c0022 | t0001 | g0381 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0238 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19002 | hp2 | a0001 | c0002 | t0005 | g0002 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19004 | hp2 | a0001 | c0002 | t0005 | g0002 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19005 | hp2 | a0001 | c0002 | t0003 | g0276 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19006 | hp2 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19007 | hp1 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0392 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19010 | hp2 | a0001 | c0002 | t0004 | g0231 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19012 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | LWK | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | LWK | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0380 | AFR | LWK | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19043 | hp2 | a0001 | c0004 | t0002 | g0178 | AFR | LWK | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19055 | hp1 | a0001 | c0003 | t0001 | g0187 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19055 | hp2 | a0010 | c0026 | t0004 | g0262 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0288 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19056 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0096 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0230 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0391 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19062 | hp1 | a0001 | c0003 | t0003 | g0062 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19062 | hp2 | a0011 | c0024 | t0001 | g0089 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19063 | hp1 | a0001 | c0003 | t0001 | g0283 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19063 | hp2 | a0001 | c0002 | t0003 | g0249 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0284 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19066 | hp2 | a0001 | c0006 | t0002 | g0260 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19068 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19075 | hp1 | a0012 | c0030 | t0001 | g0139 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19076 | hp1 | a0001 | c0002 | t0003 | g0253 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19076 | hp2 | a0003 | c0012 | t0001 | g0340 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19077 | hp1 | a0001 | c0003 | t0001 | g0082 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19078 | hp2 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0278 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19079 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19080 | hp1 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19080 | hp2 | a0001 | c0002 | t0003 | g0258 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19081 | hp1 | a0001 | c0002 | t0003 | g0245 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19081 | hp2 | a0001 | c0006 | t0002 | g0235 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19082 | hp1 | a0001 | c0003 | t0003 | g0020 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19082 | hp2 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19085 | hp1 | a0001 | c0003 | t0003 | g0286 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19085 | hp2 | a0001 | c0002 | t0003 | g0287 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19086 | hp1 | a0001 | c0003 | t0001 | g0103 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19086 | hp2 | a0001 | c0003 | t0001 | g0375 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19087 | hp1 | a0001 | c0003 | t0001 | g0205 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19087 | hp2 | a0001 | c0002 | t0003 | g0216 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19088 | hp1 | a0001 | c0003 | t0003 | g0213 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19088 | hp2 | a0001 | c0002 | t0005 | g0002 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19091 | hp1 | a0001 | c0003 | t0001 | g0289 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0210 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0048 | AFR | YRI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA19240 | hp2 | a0001 | c0004 | t0002 | g0022 | AFR | YRI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA20129 | hp1 | a0001 | c0004 | t0002 | g0175 | AFR | ASW | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA20129 | hp2 | a0001 | c0004 | t0006 | g0144 | AFR | ASW | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA20752 | hp1 | a0001 | c0004 | t0002 | g0001 | EUR | TSI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA20752 | hp2 | a0001 | c0005 | t0002 | g0150 | EUR | TSI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA20805 | hp1 | a0001 | c0004 | t0002 | g0026 | EUR | TSI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA20805 | hp2 | a0001 | c0002 | t0003 | g0223 | EUR | TSI | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | GIH | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0031 | SAS | GIH | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02109 | hp2 | a0001 | c0010 | t0002 | g0006 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0045 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02559 | hp1 | a0001 | c0004 | t0002 | g0024 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0154 | AFR | MSL | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | USA | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| HG06807 | hp2 | a0001 | c0004 | t0006 | g0146 | AFR | USA | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0225 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0387 | EAS | JPT | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | USA | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA20300 | hp2 | a0001 | c0001 | t0008 | g0044 | AFR | USA | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA21309 | hp1 | a0001 | c0003 | t0003 | g0039 | AFR | LWK | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| NA21309 | hp2 | a0001 | c0004 | t0010 | g0179 | AFR | LWK | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| homoSapiens | chm13v2 | a0001 | c0004 | t0002 | g0167 | REF | REF | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| homoSapiens | grch38p0 | a0001 | c0010 | t0002 | g0006 | REF | REF | FDFT1_chr8_11797741_11844298 | FDFT1 | chr8 | 11797741 | 11844298 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:11808828 | A | G | 2 | a0002 a0012 |
12 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(9): Show |
missense_variant | MODERATE | c.134A>G | p.Lys45Arg | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/8 | 226/2035 | 134/1254 | 45/417 | chr8 | 11808828 | |||
| chr8:11809729 | C | G | 1 | a0005 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.260C>G | p.Thr87Ser | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/8 | 352/2035 | 260/1254 | 87/417 | chr8 | 11809729 | |||
| chr8:11821790 | C | T | 1 | a0011 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.422C>T | p.Thr141Ile | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/8 | 514/2035 | 422/1254 | 141/417 | chr8 | 11821790 | |||
| chr8:11830287 | C | T | 1 | a0009 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.746C>T | p.Pro249Leu | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/8 | 838/2035 | 746/1254 | 249/417 | chr8 | 11830287 | |||
| chr8:11830330 | A | G | 1 | a0006 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.789A>G | p.Ile263Met | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/8 | 881/2035 | 789/1254 | 263/417 | chr8 | 11830330 | |||
| chr8:11838422 | C | G | 3 | a0003 a0008 a0012 |
6 | HG00597.hp2 NA18962.hp1 NA18965.hp1 others(3): Show |
missense_variant | MODERATE | c.1067C>G | p.Ser356Cys | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 1159/2035 | 1067/1254 | 356/417 | chr8 | 11838422 | |||
| chr8:11838431 | C | G | 1 | a0007 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.1076C>G | p.Thr359Arg | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 1168/2035 | 1076/1254 | 359/417 | chr8 | 11838431 | |||
| chr8:11838526 | A | G | 1 | a0004 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.1171A>G | p.Met391Val | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 1263/2035 | 1171/1254 | 391/417 | chr8 | 11838526 | |||
| chr8:11838606 | C | G | 3 | a0003 a0010 a0012 |
6 | HG00597.hp2 NA18962.hp1 NA18965.hp1 others(3): Show |
missense_variant | MODERATE | c.1251C>G | p.His417Gln | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 1343/2035 | 1251/1254 | 417/417 | chr8 | 11838606 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:11802853 | T | C | 8 | a0001c0004 a0001c0008 a0001c0011 others(5): Show |
60 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(57): Show |
synonymous_variant | LOW | c.21T>C | p.Leu7Leu | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/8 | 113/2035 | 21/1254 | 7/417 | chr8 | 11802853 | |||
| chr8:11808875 | C | T | 1 | a0001c0011 | 4 | HG01891.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
synonymous_variant | LOW | c.181C>T | p.Leu61Leu | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/8 | 273/2035 | 181/1254 | 61/417 | chr8 | 11808875 | |||
| chr8:11809670 | C | T | 7 | a0001c0002 a0001c0006 a0001c0025 others(4): Show |
128 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(125): Show |
synonymous_variant | LOW | c.201C>T | p.Asn67Asn | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/8 | 293/2035 | 201/1254 | 67/417 | chr8 | 11809670 | |||
| chr8:11826113 | T | C | 3 | a0001c0005 a0001c0008 a0001c0014 |
18 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(15): Show |
synonymous_variant | LOW | c.600T>C | p.Asp200Asp | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/8 | 692/2035 | 600/1254 | 200/417 | chr8 | 11826113 | |||
| chr8:11826144 | T | C | 26 | a0001c0001 a0001c0002 a0001c0003 others(23): Show |
448 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(445): Show |
synonymous_variant | LOW | c.631T>C | p.Leu211Leu | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/8 | 723/2035 | 631/1254 | 211/417 | chr8 | 11826144 | |||
| chr8:11830288 | G | A | 1 | a0001c0025 | 1 | HG02273.hp2 | synonymous_variant | LOW | c.747G>A | p.Pro249Pro | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/8 | 839/2035 | 747/1254 | 249/417 | chr8 | 11830288 | |||
| chr8:11831592 | A | G | 1 | a0001c0016 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.954A>G | p.Lys318Lys | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/8 | 1046/2035 | 954/1254 | 318/417 | chr8 | 11831592 | |||
| chr8:11831608 | C | T | 1 | a0001c0021 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.970C>T | p.Leu324Leu | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/8 | 1062/2035 | 970/1254 | 324/417 | chr8 | 11831608 | |||
| chr8:11831610 | G | C | 8 | a0001c0002 a0001c0003 a0001c0025 others(5): Show |
185 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(182): Show |
synonymous_variant | LOW | c.972G>C | p.Leu324Leu | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/8 | 1064/2035 | 972/1254 | 324/417 | chr8 | 11831610 | |||
| chr8:11838504 | C | T | 1 | a0001c0018 | 1 | NA18956.hp2 | synonymous_variant | LOW | c.1149C>T | p.Ser383Ser | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 1241/2035 | 1149/1254 | 383/417 | chr8 | 11838504 | |||
| chr8:11838552 | G | A | 3 | a0001c0014 a0001c0015 a0001c0017 |
3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.1197G>A | p.Gln399Gln | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 1289/2035 | 1197/1254 | 399/417 | chr8 | 11838552 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:11802753 | C | G | 3 | a0001c0001t0008 a0001c0001t0011 a0001c0005t0012 |
7 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-80C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/8 | chr8 | 11802753 | |||||||
| chr8:11802756 | C | G | 1 | a0003c0012t0018 | 1 | HG00597.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/8 | 77 | chr8 | 11802756 | ||||||
| chr8:11802760 | T | C | 1 | a0001c0004t0007 | 3 | HG01070.hp2 HG01071.hp1 HG01175.hp2 |
5_prime_UTR_variant | MODIFIER | c.-73T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/8 | 73 | chr8 | 11802760 | ||||||
| chr8:11802761 | C | T | 1 | a0006c0023t0017 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-72C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/8 | 72 | chr8 | 11802761 | ||||||
| chr8:11838758 | C | T | 2 | a0001c0001t0010 a0001c0004t0010 |
2 | HG02622.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*149C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 149 | chr8 | 11838758 | ||||||
| chr8:11838830 | A | G | 2 | a0001c0001t0010 a0001c0004t0010 |
2 | HG02622.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*221A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 221 | chr8 | 11838830 | ||||||
| chr8:11838843 | T | C | 24 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(21): Show |
225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*234T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 234 | chr8 | 11838843 | ||||||
| chr8:11838885 | C | T | 3 | a0001c0001t0006 a0001c0004t0006 a0001c0006t0006 |
8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*276C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 276 | chr8 | 11838885 | ||||||
| chr8:11838914 | A | C | 2 | a0001c0002t0005 a0001c0006t0005 |
10 | HG00609.hp2 HG00673.hp2 HG02135.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*305A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 305 | chr8 | 11838914 | ||||||
| chr8:11838931 | C | T | 1 | a0001c0014t0016 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*322C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 322 | chr8 | 11838931 | ||||||
| chr8:11838974 | A | G | 1 | a0001c0002t0015 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*365A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 365 | chr8 | 11838974 | ||||||
| chr8:11838983 | A | C | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0002t0003 others(11): Show |
121 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*374A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 374 | chr8 | 11838983 | ||||||
| chr8:11839024 | A | G | 1 | a0001c0003t0014 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 415 | chr8 | 11839024 | ||||||
| chr8:11839056 | G | T | 2 | a0001c0001t0009 a0001c0001t0011 |
4 | HG02109.hp1 HG02129.hp1 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*447G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 447 | chr8 | 11839056 | ||||||
| chr8:11839107 | T | G | 1 | a0001c0003t0013 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*498T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 498 | chr8 | 11839107 | ||||||
| chr8:11839168 | G | C | 3 | a0001c0001t0006 a0001c0004t0006 a0001c0006t0006 |
8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*559G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 8/8 | 559 | chr8 | 11839168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:11802956 | C | T | 2 | a0001c0003t0002g0403 a0001c0003t0013g0404 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.99+25C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11802956 | |||||||
| chr8:11802994 | C | T | 1 | a0001c0001t0001g0402 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.99+63C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11802994 | |||||||
| chr8:11803070 | C | G | 4 | a0001c0002t0003g0398 a0001c0002t0003g0400 a0001c0002t0003g0401 others(1): Show |
4 | HG02132.hp1 HG02135.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+139C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803070 | |||||||
| chr8:11803084 | C | T | 1 | a0001c0004t0002g0397 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.99+153C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803084 | |||||||
| chr8:11803105 | C | T | 238 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(235): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.99+174C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803105 | |||||||
| chr8:11803135 | C | T | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.99+204C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803135 | |||||||
| chr8:11803146 | C | G | 2 | a0001c0001t0001g0395 a0001c0001t0001g0396 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.99+215C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803146 | |||||||
| chr8:11803176 | G | A | 1 | a0001c0003t0003g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.99+245G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803176 | |||||||
| chr8:11803201 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99+270C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803201 | |||||||
| chr8:11803219 | C | T | 3 | a0001c0004t0010g0179 a0001c0013t0002g0180 a0001c0015t0002g0181 |
3 | HG02145.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+288C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803219 | |||||||
| chr8:11803223 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99+292C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803223 | |||||||
| chr8:11803248 | C | T | 1 | a0001c0001t0001g0394 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.99+317C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803248 | |||||||
| chr8:11803255 | G | C | 121 | a0001c0001t0001g0207 a0001c0001t0001g0211 a0001c0001t0001g0212 others(118): Show |
137 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.99+324G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803255 | |||||||
| chr8:11803266 | T | G | 1 | a0001c0005t0012g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+335T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803266 | |||||||
| chr8:11803285 | C | T | 1 | a0001c0001t0001g0393 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.99+354C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803285 | |||||||
| chr8:11803407 | C | T | 239 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(236): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.99+476C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803407 | |||||||
| chr8:11803428 | G | T | 1 | a0001c0002t0003g0278 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.99+497G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803428 | |||||||
| chr8:11803463 | T | G | 1 | a0001c0003t0001g0050 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.99+532T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803463 | |||||||
| chr8:11803567 | A | G | 2 | a0001c0013t0002g0180 a0001c0015t0002g0181 |
2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.99+636A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803567 | |||||||
| chr8:11803582 | G | A | 1 | a0001c0001t0001g0279 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.99+651G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803582 | |||||||
| chr8:11803657 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02056.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.99+726G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803657 | |||||||
| chr8:11803689 | C | G | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.99+758C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803689 | |||||||
| chr8:11803713 | A | T | 1 | a0001c0004t0010g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+782A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803713 | |||||||
| chr8:11803751 | G | A | 1 | a0001c0011t0002g0014 | 2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.99+820G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803751 | |||||||
| chr8:11803784 | T | G | 1 | a0001c0002t0003g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.99+853T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803784 | |||||||
| chr8:11803837 | A | G | 3 | a0001c0002t0003g0276 a0001c0002t0003g0277 a0004c0027t0003g0275 |
3 | HG00423.hp2 NA18981.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.99+906A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803837 | |||||||
| chr8:11803855 | G | A | 3 | a0001c0001t0010g0043 a0001c0017t0002g0041 a0006c0023t0017g0042 |
3 | HG02622.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.99+924G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803855 | |||||||
| chr8:11803855 | G | T | 1 | a0001c0004t0010g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+924G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803855 | |||||||
| chr8:11803958 | T | A | 13 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(10): Show |
13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+1027T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803958 | |||||||
| chr8:11803993 | T | A | 1 | a0001c0001t0001g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.99+1062T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11803993 | |||||||
| chr8:11804057 | G | C | 110 | a0001c0001t0001g0207 a0001c0001t0001g0211 a0001c0001t0001g0212 others(107): Show |
124 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.99+1126G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804057 | |||||||
| chr8:11804138 | C | A | 3 | a0001c0001t0010g0043 a0001c0017t0002g0041 a0006c0023t0017g0042 |
3 | HG02622.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.99+1207C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804138 | |||||||
| chr8:11804165 | G | A | 404 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(401): Show |
454 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(451): Show |
intron_variant | MODIFIER | c.99+1234G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804165 | |||||||
| chr8:11804221 | C | G | 18 | a0001c0004t0002g0001 a0001c0004t0002g0024 a0001c0004t0002g0026 others(15): Show |
29 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.99+1290C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804221 | |||||||
| chr8:11804250 | C | G | 2 | a0001c0004t0006g0164 a0001c0004t0006g0165 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.99+1319C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804250 | |||||||
| chr8:11804258 | G | T | 1 | a0001c0002t0003g0269 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.99+1327G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804258 | |||||||
| chr8:11804312 | G | A | 1 | a0002c0009t0002g0166 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.99+1381G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804312 | |||||||
| chr8:11804411 | G | A | 311 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(308): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.99+1480G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804411 | |||||||
| chr8:11804412 | T | A | 1 | a0001c0003t0001g0283 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99+1481T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804412 | |||||||
| chr8:11804586 | T | A | 4 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(1): Show |
4 | HG02738.hp1 HG03490.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+1655T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804586 | |||||||
| chr8:11804600 | C | CT | 54 | a0001c0001t0001g0394 a0001c0001t0008g0044 a0001c0002t0003g0186 others(51): Show |
67 | HG00621.hp1 HG00642.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.99+1690dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804600 | ||||||
| chr8:11804600 | C | CTT | 240 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(237): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.99+1689_99+1690dup others(2): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804600 | ||||||
| chr8:11804600 | C | CTTT | 20 | a0001c0001t0001g0385 a0001c0001t0001g0387 a0001c0001t0001g0389 others(17): Show |
20 | HG00544.hp2 HG01361.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.99+1688_99+1690dup others(3): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804600 | ||||||
| chr8:11804639 | T | C | 13 | a0001c0004t0001g0133 a0001c0004t0001g0154 a0001c0004t0002g0021 others(10): Show |
15 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+1708T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804639 | |||||||
| chr8:11804647 | A | T | 3 | a0001c0004t0010g0179 a0001c0013t0002g0180 a0001c0015t0002g0181 |
3 | HG02145.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+1716A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804647 | |||||||
| chr8:11804685 | C | T | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.99+1754C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804685 | |||||||
| chr8:11804692 | C | T | 1 | a0001c0001t0001g0382 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.99+1761C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804692 | |||||||
| chr8:11804697 | C | G | 13 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(10): Show |
13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+1766C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804697 | |||||||
| chr8:11804714 | C | T | 1 | a0009c0022t0001g0381 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.99+1783C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804714 | |||||||
| chr8:11804745 | T | C | 4 | a0001c0001t0010g0043 a0001c0004t0010g0179 a0001c0017t0002g0041 others(1): Show |
4 | HG02622.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+1814T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804745 | |||||||
| chr8:11804746 | A | G | 13 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(10): Show |
13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+1815A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804746 | |||||||
| chr8:11804800 | G | C | 2 | a0001c0005t0002g0136 a0001c0005t0002g0137 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.99+1869G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804800 | |||||||
| chr8:11804816 | T | C | 315 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(312): Show |
354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.99+1885T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804816 | |||||||
| chr8:11804840 | C | G | 7 | a0001c0001t0008g0044 a0001c0001t0008g0047 a0001c0001t0008g0048 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+1909C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804840 | |||||||
| chr8:11804867 | C | T | 11 | a0001c0001t0006g0380 a0001c0004t0001g0141 a0001c0004t0001g0147 others(8): Show |
11 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+1936C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804867 | |||||||
| chr8:11804868 | C | A | 2 | a0001c0005t0002g0136 a0001c0005t0002g0137 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.99+1937C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804868 | |||||||
| chr8:11804875 | C | T | 13 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(10): Show |
13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+1944C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804875 | |||||||
| chr8:11804908 | C | CT | 24 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0001t0001g0378 others(21): Show |
28 | HG00140.hp2 HG01074.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.99+1994dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804908 | ||||||
| chr8:11804908 | CT | C | 32 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(29): Show |
33 | HG00323.hp2 HG00733.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.99+1994delT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804908 | ||||||
| chr8:11804908 | CTT | C | 8 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(5): Show |
8 | HG02145.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+1993_99+1994del others(2): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804908 | ||||||
| chr8:11804925 | T | G | 5 | a0001c0002t0003g0191 a0001c0002t0003g0192 a0001c0003t0001g0283 others(2): Show |
6 | HG01891.hp2 HG02698.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+1994T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804925 | |||||||
| chr8:11804926 | G | A | 5 | a0001c0002t0003g0191 a0001c0002t0003g0192 a0001c0003t0001g0283 others(2): Show |
6 | HG01891.hp2 HG02698.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+1995G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804926 | |||||||
| chr8:11804927 | A | AG | 267 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(264): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.99+2004dupG | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11804927 | ||||||
| chr8:11804927 | A | G | 7 | a0001c0001t0001g0374 a0001c0002t0003g0191 a0001c0002t0003g0192 others(4): Show |
8 | HG01109.hp1 HG01891.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+1996A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804927 | |||||||
| chr8:11804930 | G | GT | 7 | a0001c0001t0008g0044 a0001c0001t0008g0047 a0001c0001t0008g0048 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+1999_99+2000ins others(1): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804930 | |||||||
| chr8:11804930 | G | T | 1 | a0001c0002t0001g0063 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.99+1999G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804930 | |||||||
| chr8:11804939 | C | T | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.99+2008C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804939 | |||||||
| chr8:11804974 | A | G | 1 | a0001c0001t0002g0128 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.99+2043A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11804974 | |||||||
| chr8:11805039 | C | T | 313 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(310): Show |
352 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.99+2108C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805039 | |||||||
| chr8:11805054 | C | T | 2 | a0001c0001t0001g0368 a0001c0001t0001g0369 |
2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.99+2123C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805054 | |||||||
| chr8:11805075 | A | C | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.99+2144A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805075 | |||||||
| chr8:11805077 | G | A | 5 | a0001c0001t0003g0010 a0001c0001t0003g0271 a0001c0003t0001g0272 others(2): Show |
7 | HG00438.hp1 HG03654.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+2146G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805077 | |||||||
| chr8:11805090 | A | AT | 289 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(286): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.99+2166dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11805090 | ||||||
| chr8:11805114 | G | C | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.99+2183G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805114 | |||||||
| chr8:11805141 | T | A | 1 | a0001c0001t0001g0291 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.99+2210T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805141 | |||||||
| chr8:11805142 | C | A | 1 | a0001c0001t0001g0291 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.99+2211C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805142 | |||||||
| chr8:11805176 | A | C | 1 | a0001c0003t0001g0127 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.99+2245A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805176 | |||||||
| chr8:11805261 | C | T | 403 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(400): Show |
453 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(450): Show |
intron_variant | MODIFIER | c.99+2330C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805261 | |||||||
| chr8:11805323 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.99+2392T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805323 | |||||||
| chr8:11805356 | T | G | 13 | a0001c0002t0001g0196 a0001c0002t0001g0200 a0001c0002t0001g0201 others(10): Show |
17 | NA18948.hp1 NA18950.hp1 NA18952.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+2425T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805356 | |||||||
| chr8:11805363 | A | G | 5 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0202 others(2): Show |
5 | NA18963.hp2 NA18971.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+2432A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805363 | |||||||
| chr8:11805373 | G | A | 1 | a0001c0003t0001g0071 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.99+2442G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805373 | |||||||
| chr8:11805376 | G | A | 62 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(59): Show |
75 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+2445G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805376 | |||||||
| chr8:11805426 | A | G | 1 | a0001c0003t0003g0020 | 2 | NA18971.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.99+2495A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805426 | |||||||
| chr8:11805453 | C | T | 3 | a0001c0001t0001g0126 a0001c0001t0002g0067 a0001c0005t0001g0125 |
3 | HG02559.hp2 HG02895.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.99+2522C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805453 | |||||||
| chr8:11805455 | C | A | 1 | a0001c0003t0001g0050 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.99+2524C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805455 | |||||||
| chr8:11805482 | G | A | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.99+2551G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805482 | |||||||
| chr8:11805490 | T | C | 1 | a0001c0001t0002g0015 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.99+2559T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805490 | |||||||
| chr8:11805504 | T | C | 7 | a0001c0001t0008g0044 a0001c0001t0008g0047 a0001c0001t0008g0048 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+2573T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805504 | |||||||
| chr8:11805512 | G | C | 1 | a0001c0002t0003g0384 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.99+2581G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805512 | |||||||
| chr8:11805558 | C | G | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+2627C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805558 | |||||||
| chr8:11805566 | C | T | 13 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(10): Show |
13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+2635C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805566 | |||||||
| chr8:11805590 | G | C | 1 | a0001c0001t0002g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99+2659G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805590 | |||||||
| chr8:11805600 | T | C | 1 | a0001c0002t0003g0203 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.99+2669T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805600 | |||||||
| chr8:11805609 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0374 |
2 | HG01099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.99+2678G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805609 | |||||||
| chr8:11805661 | G | C | 236 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(233): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.99+2730G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805661 | |||||||
| chr8:11805662 | A | T | 303 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(300): Show |
342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.99+2731A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805662 | |||||||
| chr8:11805664 | T | A | 303 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(300): Show |
342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.99+2733T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805664 | |||||||
| chr8:11805675 | G | C | 1 | a0001c0001t0001g0279 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.99+2744G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805675 | |||||||
| chr8:11805778 | C | T | 43 | a0001c0001t0006g0380 a0001c0004t0001g0133 a0001c0004t0001g0140 others(40): Show |
56 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.99+2847C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805778 | |||||||
| chr8:11805885 | G | T | 2 | a0001c0001t0001g0182 a0001c0002t0003g0366 |
2 | HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-2909G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11805885 | |||||||
| chr8:11806025 | T | C | 1 | a0001c0005t0001g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.100-2769T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806025 | |||||||
| chr8:11806038 | T | C | 7 | a0001c0001t0008g0044 a0001c0001t0008g0047 a0001c0001t0008g0048 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-2756T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806038 | |||||||
| chr8:11806075 | C | A | 4 | a0001c0001t0010g0043 a0001c0004t0010g0179 a0001c0017t0002g0041 others(1): Show |
4 | HG02622.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-2719C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806075 | |||||||
| chr8:11806141 | C | T | 6 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(3): Show |
6 | HG02896.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-2653C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806141 | |||||||
| chr8:11806160 | G | A | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-2634G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806160 | |||||||
| chr8:11806202 | A | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
8 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-2592A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806202 | |||||||
| chr8:11806224 | C | T | 1 | a0001c0004t0001g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100-2570C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806224 | |||||||
| chr8:11806245 | A | G | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.100-2549A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806245 | |||||||
| chr8:11806254 | C | T | 20 | a0001c0004t0001g0140 a0001c0004t0002g0001 a0001c0004t0002g0024 others(17): Show |
31 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.100-2540C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806254 | |||||||
| chr8:11806392 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.100-2402T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806392 | |||||||
| chr8:11806397 | C | T | 1 | a0001c0002t0003g0269 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.100-2397C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806397 | |||||||
| chr8:11806437 | G | T | 1 | a0001c0001t0001g0365 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.100-2357G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806437 | |||||||
| chr8:11806605 | C | G | 1 | a0001c0002t0003g0384 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.100-2189C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806605 | |||||||
| chr8:11806626 | G | A | 1 | a0001c0013t0002g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-2168G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806626 | |||||||
| chr8:11806767 | A | G | 1 | a0001c0004t0002g0135 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.100-2027A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806767 | |||||||
| chr8:11806779 | G | C | 6 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(3): Show |
6 | HG02896.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-2015G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806779 | |||||||
| chr8:11806790 | A | T | 7 | a0001c0001t0008g0044 a0001c0001t0008g0047 a0001c0001t0008g0048 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-2004A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806790 | |||||||
| chr8:11806938 | A | G | 1 | a0001c0001t0004g0257 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.100-1856A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11806938 | |||||||
| chr8:11807023 | TACAAATA others(3): Show |
T | 244 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(241): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.100-1766_100-1757d others(12): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11807023 | ||||||
| chr8:11807044 | T | G | 1 | a0001c0002t0003g0204 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.100-1750T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807044 | |||||||
| chr8:11807048 | T | A | 2 | a0001c0003t0002g0403 a0001c0003t0013g0404 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.100-1746T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807048 | |||||||
| chr8:11807072 | G | A | 2 | a0001c0001t0011g0045 a0001c0001t0011g0046 |
2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.100-1722G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807072 | |||||||
| chr8:11807078 | T | TGTTACCA others(18): Show |
1 | a0001c0005t0002g0023 | 2 | HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.100-1715_100-1691d others(27): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11807078 | ||||||
| chr8:11807097 | CTA | C | 237 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(234): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.100-1695_100-1694d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11807097 | ||||||
| chr8:11807164 | A | C | 2 | a0001c0013t0002g0180 a0001c0015t0002g0181 |
2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.100-1630A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807164 | |||||||
| chr8:11807228 | C | G | 1 | a0001c0002t0003g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.100-1566C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807228 | |||||||
| chr8:11807229 | C | T | 256 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(253): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.100-1565C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807229 | |||||||
| chr8:11807303 | A | C | 1 | a0001c0003t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.100-1491A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807303 | |||||||
| chr8:11807309 | C | G | 269 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(266): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.100-1485C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807309 | |||||||
| chr8:11807325 | ATTTTTTA others(5): Show |
A | 269 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(266): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.100-1461_100-1450d others(14): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11807325 | ||||||
| chr8:11807355 | G | C | 2 | a0001c0003t0003g0039 a0001c0021t0001g0073 |
2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100-1439G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807355 | |||||||
| chr8:11807359 | C | G | 1 | a0001c0003t0014g0120 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.100-1435C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807359 | |||||||
| chr8:11807386 | T | C | 313 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(310): Show |
352 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.100-1408T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807386 | |||||||
| chr8:11807393 | G | T | 1 | a0001c0001t0001g0364 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.100-1401G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807393 | |||||||
| chr8:11807422 | C | A | 1 | a0001c0001t0001g0294 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.100-1372C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807422 | |||||||
| chr8:11807422 | C | T | 13 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(10): Show |
13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-1372C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807422 | |||||||
| chr8:11807443 | G | A | 1 | a0001c0004t0001g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100-1351G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807443 | |||||||
| chr8:11807507 | A | G | 318 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(315): Show |
357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.100-1287A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807507 | |||||||
| chr8:11807511 | CTG | C | 4 | a0001c0001t0010g0043 a0001c0004t0010g0179 a0001c0017t0002g0041 others(1): Show |
4 | HG02622.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-1280_100-1279d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11807511 | ||||||
| chr8:11807514 | T | G | 44 | a0001c0001t0006g0380 a0001c0004t0001g0133 a0001c0004t0001g0140 others(41): Show |
57 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.100-1280T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807514 | |||||||
| chr8:11807548 | C | T | 1 | a0001c0002t0001g0255 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.100-1246C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807548 | |||||||
| chr8:11807586 | TA | T | 240 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(237): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.100-1202delA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11807586 | ||||||
| chr8:11807638 | A | C | 1 | a0001c0005t0002g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.100-1156A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807638 | |||||||
| chr8:11807708 | G | A | 240 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(237): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.100-1086G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807708 | |||||||
| chr8:11807816 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.100-978T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807816 | |||||||
| chr8:11807818 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.100-976G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807818 | |||||||
| chr8:11807999 | A | G | 1 | a0001c0002t0001g0032 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.100-795A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11807999 | |||||||
| chr8:11808003 | G | T | 2 | a0001c0013t0002g0180 a0001c0015t0002g0181 |
2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.100-791G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808003 | |||||||
| chr8:11808009 | A | G | 314 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(311): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.100-785A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808009 | |||||||
| chr8:11808049 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.100-745G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808049 | |||||||
| chr8:11808152 | C | T | 263 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(260): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.100-642C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808152 | |||||||
| chr8:11808166 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.100-628G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808166 | |||||||
| chr8:11808195 | C | T | 19 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0107 others(16): Show |
21 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-599C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808195 | |||||||
| chr8:11808296 | C | T | 258 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(255): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.100-498C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808296 | |||||||
| chr8:11808350 | T | A | 14 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(11): Show |
14 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-444T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808350 | |||||||
| chr8:11808399 | G | T | 6 | a0001c0003t0001g0103 a0001c0003t0001g0106 a0001c0003t0003g0020 others(3): Show |
7 | HG02071.hp2 HG02080.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-395G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808399 | |||||||
| chr8:11808419 | G | A | 3 | a0001c0004t0002g0001 a0001c0004t0002g0173 a0001c0004t0002g0397 |
7 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-375G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808419 | |||||||
| chr8:11808444 | C | G | 2 | a0001c0001t0002g0101 a0001c0003t0002g0161 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.100-350C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808444 | |||||||
| chr8:11808450 | C | T | 257 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(254): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.100-344C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808450 | |||||||
| chr8:11808474 | G | C | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.100-320G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808474 | |||||||
| chr8:11808493 | A | G | 1 | a0001c0002t0001g0363 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.100-301A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808493 | |||||||
| chr8:11808498 | C | T | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100-296C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808498 | |||||||
| chr8:11808562 | G | C | 1 | a0001c0001t0001g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100-232G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808562 | |||||||
| chr8:11808599 | G | A | 1 | a0001c0005t0001g0125 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.100-195G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808599 | |||||||
| chr8:11808638 | C | T | 1 | a0001c0001t0001g0362 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.100-156C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808638 | |||||||
| chr8:11808647 | G | T | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100-147G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808647 | |||||||
| chr8:11808649 | C | G | 6 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(3): Show |
6 | HG02896.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-145C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808649 | |||||||
| chr8:11808692 | T | G | 1 | a0001c0003t0001g0205 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.100-102T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808692 | |||||||
| chr8:11808709 | G | GTCCCACT others(5): Show |
13 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(10): Show |
13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-57_100-46dupCA others(10): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11808709 | ||||||
| chr8:11808709 | G | GTCCCACT others(11): Show |
5 | a0001c0005t0002g0070 a0001c0005t0002g0136 a0001c0005t0002g0137 others(2): Show |
5 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-63_100-46dupCA others(16): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11808709 | ||||||
| chr8:11808709 | G | GTCCCACT others(17): Show |
1 | a0001c0005t0002g0023 | 2 | HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.100-69_100-46dupCA others(22): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11808709 | ||||||
| chr8:11808709 | GTCCCAC | G | 367 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(364): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.100-51_100-46delCA others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11808709 | ||||||
| chr8:11808709 | GTCCCACT others(5): Show |
G | 8 | a0001c0001t0001g0361 a0001c0001t0001g0392 a0001c0002t0003g0254 others(5): Show |
8 | HG02080.hp2 HG02145.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-57_100-46delCA others(10): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11808709 | ||||||
| chr8:11808709 | GTCCCACT others(11): Show |
G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0123 a0001c0001t0001g0124 |
4 | HG02257.hp1 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-63_100-46delCA others(16): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 11808709 | ||||||
| chr8:11808738 | A | C | 9 | a0001c0004t0001g0141 a0001c0004t0001g0147 a0001c0004t0006g0142 others(6): Show |
9 | HG02451.hp2 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-56A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 1/7 | chr8 | 11808738 | |||||||
| chr8:11808942 | C | T | 243 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(240): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.197+51C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11808942 | |||||||
| chr8:11808991 | C | A | 1 | a0001c0002t0003g0210 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.197+100C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11808991 | |||||||
| chr8:11809015 | A | C | 1 | a0001c0003t0001g0288 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.197+124A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809015 | |||||||
| chr8:11809107 | A | C | 70 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0078 others(67): Show |
82 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.197+216A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809107 | |||||||
| chr8:11809107 | A | G | 254 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(251): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.197+216A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809107 | |||||||
| chr8:11809108 | G | T | 1 | a0001c0002t0003g0384 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.197+217G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809108 | |||||||
| chr8:11809109 | G | T | 2 | a0001c0002t0003g0253 a0001c0003t0001g0100 |
2 | HG00423.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.197+218G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809109 | |||||||
| chr8:11809145 | T | C | 23 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(20): Show |
23 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(20): Show |
intron_variant | MODIFIER | c.197+254T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809145 | |||||||
| chr8:11809205 | T | C | 1 | a0001c0001t0001g0385 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.197+314T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809205 | |||||||
| chr8:11809220 | A | G | 1 | a0001c0002t0001g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.197+329A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809220 | |||||||
| chr8:11809224 | T | C | 13 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(10): Show |
13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.197+333T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809224 | |||||||
| chr8:11809249 | C | T | 17 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(14): Show |
17 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.197+358C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809249 | |||||||
| chr8:11809259 | C | G | 269 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(266): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.197+368C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809259 | |||||||
| chr8:11809261 | T | C | 34 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0078 others(31): Show |
46 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.197+370T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809261 | |||||||
| chr8:11809282 | A | C | 4 | a0001c0001t0001g0357 a0001c0001t0001g0358 a0001c0001t0001g0359 others(1): Show |
4 | HG00280.hp2 HG01975.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-385A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809282 | |||||||
| chr8:11809308 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.198-359A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809308 | |||||||
| chr8:11809343 | T | G | 2 | a0001c0004t0002g0068 a0001c0013t0002g0177 |
2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.198-324T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809343 | |||||||
| chr8:11809466 | A | T | 1 | a0001c0001t0001g0369 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.198-201A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809466 | |||||||
| chr8:11809518 | C | A | 1 | a0001c0001t0001g0370 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.198-149C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809518 | |||||||
| chr8:11809535 | G | T | 6 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(3): Show |
6 | HG02896.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-132G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809535 | |||||||
| chr8:11809540 | A | T | 2 | a0001c0004t0002g0068 a0001c0013t0002g0177 |
2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.198-127A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809540 | |||||||
| chr8:11809594 | G | C | 1 | a0001c0004t0010g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.198-73G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809594 | |||||||
| chr8:11809646 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.198-21A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 2/7 | chr8 | 11809646 | |||||||
| chr8:11809903 | C | T | 9 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG00733.hp2 HG02145.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.381+53C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11809903 | |||||||
| chr8:11809976 | G | A | 1 | a0001c0002t0003g0188 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.381+126G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11809976 | |||||||
| chr8:11809987 | C | T | 141 | a0001c0001t0002g0013 a0001c0001t0002g0051 a0001c0001t0002g0057 others(138): Show |
157 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.381+137C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11809987 | |||||||
| chr8:11810064 | C | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0123 a0001c0001t0001g0124 |
4 | HG02257.hp1 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+214C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810064 | |||||||
| chr8:11810074 | C | G | 1 | a0001c0001t0002g0367 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.381+224C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810074 | |||||||
| chr8:11810105 | G | C | 1 | a0001c0004t0001g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+255G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810105 | |||||||
| chr8:11810107 | GTAA | G | 124 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(121): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.381+264_381+266del others(3): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810107 | ||||||
| chr8:11810114 | T | C | 3 | a0001c0002t0003g0276 a0001c0002t0003g0277 a0004c0027t0003g0275 |
3 | HG00423.hp2 NA18981.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.381+264T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810114 | |||||||
| chr8:11810130 | G | A | 1 | a0001c0005t0002g0150 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.381+280G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810130 | |||||||
| chr8:11810172 | G | C | 1 | a0001c0001t0001g0296 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.381+322G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810172 | |||||||
| chr8:11810191 | TATTATC | T | 15 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(12): Show |
15 | HG00733.hp2 HG02145.hp2 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+343_381+348del others(6): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810191 | ||||||
| chr8:11810193 | T | C | 1 | a0002c0007t0002g0348 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.381+343T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810193 | |||||||
| chr8:11810214 | T | C | 13 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(10): Show |
13 | HG00733.hp2 HG01433.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.381+364T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810214 | |||||||
| chr8:11810230 | A | T | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.381+380A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810230 | |||||||
| chr8:11810234 | C | A | 1 | a0001c0001t0010g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.381+384C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810234 | |||||||
| chr8:11810373 | G | T | 1 | a0001c0002t0003g0188 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.381+523G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810373 | |||||||
| chr8:11810386 | C | T | 9 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(6): Show |
9 | HG00733.hp2 HG02145.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.381+536C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810386 | |||||||
| chr8:11810510 | A | C | 2 | a0001c0013t0002g0180 a0001c0015t0002g0181 |
2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.381+660A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810510 | |||||||
| chr8:11810534 | G | C | 1 | a0001c0002t0003g0191 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.381+684G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810534 | |||||||
| chr8:11810537 | C | T | 1 | a0001c0003t0003g0354 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.381+687C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810537 | |||||||
| chr8:11810563 | G | A | 1 | a0001c0001t0002g0057 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.381+713G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810563 | |||||||
| chr8:11810588 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.381+738T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810588 | |||||||
| chr8:11810644 | T | C | 116 | a0001c0001t0001g0211 a0001c0001t0001g0297 a0001c0002t0001g0032 others(113): Show |
130 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.381+794T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810644 | |||||||
| chr8:11810655 | G | A | 3 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0008c0020t0002g0059 |
3 | NA18939.hp2 NA18987.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.381+805G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810655 | |||||||
| chr8:11810670 | T | C | 7 | a0001c0002t0003g0214 a0001c0002t0003g0216 a0001c0002t0003g0217 others(4): Show |
7 | HG00558.hp2 HG02074.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.381+820T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810670 | |||||||
| chr8:11810693 | A | G | 1 | a0006c0023t0017g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.381+843A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810693 | |||||||
| chr8:11810718 | C | T | 6 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(3): Show |
6 | HG02896.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+868C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810718 | |||||||
| chr8:11810768 | G | A | 6 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(3): Show |
6 | HG02896.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+918G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810768 | |||||||
| chr8:11810854 | G | C | 2 | a0001c0001t0001g0395 a0001c0001t0001g0396 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.381+1004G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810854 | |||||||
| chr8:11810878 | G | C | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.381+1028G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810878 | |||||||
| chr8:11810923 | G | T | 1 | a0001c0003t0001g0099 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.381+1073G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11810923 | |||||||
| chr8:11810933 | T | TA | 12 | a0001c0002t0001g0202 a0001c0002t0003g0183 a0001c0002t0003g0199 others(9): Show |
13 | HG01255.hp1 HG01361.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.381+1108dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810933 | ||||||
| chr8:11810933 | T | TAA | 97 | a0001c0001t0001g0297 a0001c0002t0001g0032 a0001c0002t0001g0056 others(94): Show |
111 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.381+1107_381+1108d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810933 | ||||||
| chr8:11810933 | T | TAAA | 9 | a0001c0002t0002g0274 a0001c0002t0003g0052 a0001c0002t0003g0195 others(6): Show |
9 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.381+1106_381+1108d others(5): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810933 | ||||||
| chr8:11810933 | TA | T | 162 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(159): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.381+1108delA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810933 | ||||||
| chr8:11810933 | TAA | T | 73 | a0001c0001t0001g0038 a0001c0001t0001g0207 a0001c0001t0001g0281 others(70): Show |
79 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.381+1107_381+1108d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11810933 | ||||||
| chr8:11811040 | T | C | 1 | a0001c0004t0001g0141 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.381+1190T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811040 | |||||||
| chr8:11811050 | T | G | 47 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0078 others(44): Show |
59 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.381+1200T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811050 | |||||||
| chr8:11811087 | G | A | 1 | a0002c0007t0002g0348 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.381+1237G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811087 | |||||||
| chr8:11811115 | A | T | 1 | a0001c0003t0013g0404 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.381+1265A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811115 | |||||||
| chr8:11811181 | T | G | 1 | a0001c0003t0002g0161 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.381+1331T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811181 | |||||||
| chr8:11811242 | C | G | 11 | a0001c0004t0001g0133 a0001c0004t0001g0154 a0001c0004t0002g0021 others(8): Show |
13 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+1392C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811242 | |||||||
| chr8:11811258 | C | T | 115 | a0001c0001t0001g0211 a0001c0002t0001g0032 a0001c0002t0001g0056 others(112): Show |
129 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.381+1408C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811258 | |||||||
| chr8:11811275 | G | A | 3 | a0001c0001t0010g0043 a0001c0004t0010g0179 a0006c0023t0017g0042 |
3 | HG02622.hp2 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.381+1425G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811275 | |||||||
| chr8:11811370 | C | G | 2 | a0001c0008t0001g0134 a0001c0008t0001g0157 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.381+1520C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811370 | |||||||
| chr8:11811456 | G | C | 1 | a0001c0004t0002g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.381+1606G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811456 | |||||||
| chr8:11811552 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.381+1702T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811552 | |||||||
| chr8:11811617 | T | A | 1 | a0001c0005t0002g0149 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.381+1767T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811617 | |||||||
| chr8:11811757 | C | A | 1 | a0001c0001t0001g0393 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.381+1907C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811757 | |||||||
| chr8:11811855 | G | A | 1 | a0001c0006t0002g0185 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.381+2005G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811855 | |||||||
| chr8:11811931 | G | C | 113 | a0001c0001t0001g0211 a0001c0002t0001g0032 a0001c0002t0001g0056 others(110): Show |
127 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.381+2081G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811931 | |||||||
| chr8:11811944 | A | G | 5 | a0001c0001t0001g0211 a0001c0002t0003g0251 a0001c0002t0003g0398 others(2): Show |
5 | HG02027.hp1 HG02132.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+2094A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811944 | |||||||
| chr8:11811976 | C | G | 1 | a0001c0001t0002g0367 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.381+2126C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11811976 | |||||||
| chr8:11812006 | C | G | 1 | a0001c0001t0002g0119 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.381+2156C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812006 | |||||||
| chr8:11812015 | A | T | 1 | a0001c0002t0003g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.381+2165A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812015 | |||||||
| chr8:11812064 | G | A | 1 | a0001c0001t0001g0349 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.381+2214G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812064 | |||||||
| chr8:11812088 | G | A | 1 | a0001c0002t0003g0220 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.381+2238G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812088 | |||||||
| chr8:11812140 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.381+2290C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812140 | |||||||
| chr8:11812153 | G | C | 1 | a0001c0001t0001g0299 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.381+2303G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812153 | |||||||
| chr8:11812167 | G | A | 1 | a0001c0001t0002g0350 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.381+2317G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812167 | |||||||
| chr8:11812222 | C | T | 2 | a0001c0008t0001g0134 a0001c0008t0001g0157 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.381+2372C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812222 | |||||||
| chr8:11812237 | T | G | 6 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(3): Show |
6 | HG00733.hp2 HG02738.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+2387T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812237 | |||||||
| chr8:11812400 | G | A | 1 | a0001c0003t0001g0080 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.381+2550G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812400 | |||||||
| chr8:11812415 | C | T | 2 | a0001c0006t0006g0193 a0001c0028t0002g0373 |
2 | HG00741.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.381+2565C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812415 | |||||||
| chr8:11812509 | C | T | 1 | a0001c0002t0005g0248 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.381+2659C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812509 | |||||||
| chr8:11812585 | T | A | 1 | a0001c0018t0001g0372 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.381+2735T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812585 | |||||||
| chr8:11812596 | A | T | 54 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0122 others(51): Show |
66 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.381+2746A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812596 | |||||||
| chr8:11812635 | G | A | 1 | a0001c0002t0001g0221 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.381+2785G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812635 | |||||||
| chr8:11812677 | T | C | 2 | a0001c0003t0002g0403 a0001c0003t0013g0404 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.381+2827T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812677 | |||||||
| chr8:11812678 | A | G | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.381+2828A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812678 | |||||||
| chr8:11812679 | G | T | 1 | a0001c0001t0001g0299 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.381+2829G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812679 | |||||||
| chr8:11812709 | C | G | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.381+2859C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812709 | |||||||
| chr8:11812749 | T | A | 1 | a0001c0003t0001g0081 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.381+2899T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812749 | |||||||
| chr8:11812763 | T | C | 55 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0078 others(52): Show |
67 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.381+2913T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812763 | |||||||
| chr8:11812772 | G | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0300 a0001c0001t0001g0301 others(4): Show |
8 | HG01074.hp2 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+2922G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812772 | |||||||
| chr8:11812781 | T | C | 1 | a0001c0015t0002g0181 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.381+2931T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812781 | |||||||
| chr8:11812815 | A | G | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.381+2965A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812815 | |||||||
| chr8:11812874 | G | T | 1 | a0001c0002t0003g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.381+3024G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812874 | |||||||
| chr8:11812886 | G | A | 3 | a0001c0001t0010g0043 a0001c0004t0010g0179 a0006c0023t0017g0042 |
3 | HG02622.hp2 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.381+3036G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812886 | |||||||
| chr8:11812889 | A | G | 1 | a0001c0001t0001g0347 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.381+3039A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812889 | |||||||
| chr8:11812911 | A | G | 3 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0202 |
3 | NA18971.hp2 NA18998.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.381+3061A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812911 | |||||||
| chr8:11812931 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.381+3081C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812931 | |||||||
| chr8:11812933 | C | A | 1 | a0001c0001t0002g0107 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.381+3083C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11812933 | |||||||
| chr8:11813020 | T | C | 1 | a0001c0015t0002g0181 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.381+3170T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813020 | |||||||
| chr8:11813038 | TCCAAGGC | T | 51 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0122 others(48): Show |
63 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.381+3189_381+3195d others(9): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813038 | |||||||
| chr8:11813080 | C | T | 1 | a0001c0002t0003g0246 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.381+3230C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813080 | |||||||
| chr8:11813089 | A | G | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.381+3239A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813089 | |||||||
| chr8:11813149 | G | A | 2 | a0001c0004t0001g0133 a0001c0004t0001g0140 |
2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.381+3299G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813149 | |||||||
| chr8:11813157 | A | T | 1 | a0001c0003t0002g0161 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.381+3307A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813157 | |||||||
| chr8:11813197 | C | G | 2 | a0001c0002t0003g0216 a0001c0002t0003g0217 |
2 | NA18959.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.381+3347C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813197 | |||||||
| chr8:11813275 | T | C | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.381+3425T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813275 | |||||||
| chr8:11813352 | G | C | 1 | a0001c0001t0001g0351 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.381+3502G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813352 | |||||||
| chr8:11813376 | A | G | 6 | a0001c0004t0001g0154 a0001c0008t0001g0134 a0001c0008t0001g0155 others(3): Show |
6 | HG01891.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+3526A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813376 | |||||||
| chr8:11813423 | C | T | 57 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0078 others(54): Show |
69 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.381+3573C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813423 | |||||||
| chr8:11813440 | A | G | 1 | a0001c0001t0002g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.381+3590A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813440 | |||||||
| chr8:11813514 | C | G | 1 | a0001c0002t0003g0245 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.381+3664C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813514 | |||||||
| chr8:11813532 | G | A | 122 | a0001c0001t0001g0305 a0001c0001t0003g0010 a0001c0001t0003g0271 others(119): Show |
138 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.381+3682G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813532 | |||||||
| chr8:11813554 | A | G | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.381+3704A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813554 | |||||||
| chr8:11813578 | G | T | 1 | a0001c0003t0003g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.381+3728G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813578 | |||||||
| chr8:11813599 | C | T | 6 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0058 others(3): Show |
6 | HG00733.hp2 HG02738.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+3749C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813599 | |||||||
| chr8:11813632 | G | A | 1 | a0001c0015t0002g0181 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.381+3782G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813632 | |||||||
| chr8:11813637 | A | G | 10 | a0001c0004t0001g0154 a0001c0004t0002g0021 a0001c0004t0002g0022 others(7): Show |
12 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+3787A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813637 | |||||||
| chr8:11813670 | C | T | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+3820C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813670 | |||||||
| chr8:11813711 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.381+3861G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813711 | |||||||
| chr8:11813803 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+3953G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813803 | |||||||
| chr8:11813853 | T | C | 202 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0078 others(199): Show |
235 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(232): Show |
intron_variant | MODIFIER | c.381+4003T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813853 | |||||||
| chr8:11813886 | G | A | 1 | a0001c0004t0001g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+4036G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813886 | |||||||
| chr8:11813892 | A | G | 1 | a0001c0001t0001g0346 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.381+4042A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813892 | |||||||
| chr8:11813906 | CA | C | 36 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0122 others(33): Show |
48 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.381+4057delA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813906 | |||||||
| chr8:11813957 | C | G | 7 | a0001c0005t0002g0023 a0001c0005t0002g0070 a0001c0005t0002g0136 others(4): Show |
8 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+4107C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11813957 | |||||||
| chr8:11814095 | C | G | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.381+4245C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814095 | |||||||
| chr8:11814097 | C | G | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.381+4247C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814097 | |||||||
| chr8:11814150 | A | G | 34 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0078 others(31): Show |
44 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.381+4300A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814150 | |||||||
| chr8:11814280 | G | A | 5 | a0001c0005t0002g0070 a0001c0005t0002g0136 a0001c0005t0002g0137 others(2): Show |
5 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+4430G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814280 | |||||||
| chr8:11814291 | A | C | 2 | a0001c0001t0002g0101 a0001c0003t0002g0161 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.381+4441A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814291 | |||||||
| chr8:11814300 | G | GT | 66 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(63): Show |
71 | HG00544.hp2 HG00639.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.381+4467dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11814300 | ||||||
| chr8:11814300 | G | GTT | 71 | a0001c0001t0001g0078 a0001c0001t0001g0182 a0001c0001t0001g0207 others(68): Show |
80 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.381+4466_381+4467d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11814300 | ||||||
| chr8:11814300 | GT | G | 7 | a0001c0001t0001g0306 a0001c0001t0001g0347 a0001c0001t0001g0349 others(4): Show |
9 | HG01169.hp1 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+4467delT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11814300 | ||||||
| chr8:11814353 | C | G | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.381+4503C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814353 | |||||||
| chr8:11814380 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.381+4530G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814380 | |||||||
| chr8:11814422 | C | G | 1 | a0001c0001t0010g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.381+4572C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814422 | |||||||
| chr8:11814423 | T | C | 1 | a0001c0001t0002g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.381+4573T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814423 | |||||||
| chr8:11814433 | G | A | 2 | a0001c0006t0006g0193 a0001c0028t0002g0373 |
2 | HG00741.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.381+4583G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814433 | |||||||
| chr8:11814462 | T | A | 3 | a0001c0001t0010g0043 a0001c0004t0010g0179 a0006c0023t0017g0042 |
3 | HG02622.hp2 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.381+4612T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814462 | |||||||
| chr8:11814475 | A | AC | 11 | a0001c0004t0001g0154 a0001c0004t0002g0021 a0001c0004t0002g0022 others(8): Show |
13 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+4627dupC | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11814475 | ||||||
| chr8:11814488 | C | T | 1 | a0008c0020t0002g0059 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.381+4638C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814488 | |||||||
| chr8:11814496 | C | G | 1 | a0001c0004t0002g0130 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.381+4646C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814496 | |||||||
| chr8:11814502 | T | C | 1 | a0001c0005t0002g0023 | 2 | HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.381+4652T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814502 | |||||||
| chr8:11814519 | C | T | 28 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(25): Show |
33 | HG00741.hp2 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.381+4669C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814519 | |||||||
| chr8:11814714 | C | G | 2 | a0001c0003t0002g0403 a0001c0003t0013g0404 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.381+4864C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814714 | |||||||
| chr8:11814748 | A | T | 1 | a0001c0002t0003g0052 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.381+4898A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814748 | |||||||
| chr8:11814774 | A | G | 1 | a0001c0002t0003g0242 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.381+4924A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814774 | |||||||
| chr8:11814805 | GAT | G | 25 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(22): Show |
36 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.381+4957_381+4958d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11814805 | ||||||
| chr8:11814844 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.381+4994T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814844 | |||||||
| chr8:11814925 | T | G | 5 | a0001c0004t0010g0179 a0001c0006t0001g0383 a0001c0013t0002g0180 others(2): Show |
5 | HG02145.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+5075T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814925 | |||||||
| chr8:11814943 | T | C | 1 | a0001c0015t0002g0181 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.381+5093T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814943 | |||||||
| chr8:11814972 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 |
3 | HG02970.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.381+5122A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11814972 | |||||||
| chr8:11815005 | C | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0374 |
2 | HG01099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.381+5155C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815005 | |||||||
| chr8:11815020 | C | T | 1 | a0010c0026t0004g0262 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.381+5170C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815020 | |||||||
| chr8:11815041 | C | A | 1 | a0001c0005t0012g0049 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.381+5191C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815041 | |||||||
| chr8:11815042 | C | T | 2 | a0001c0003t0002g0403 a0001c0003t0013g0404 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.381+5192C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815042 | |||||||
| chr8:11815061 | C | G | 1 | a0001c0001t0002g0119 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.381+5211C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815061 | |||||||
| chr8:11815065 | G | A | 1 | a0001c0002t0003g0266 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.381+5215G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815065 | |||||||
| chr8:11815089 | A | C | 5 | a0001c0003t0001g0095 a0001c0003t0001g0096 a0001c0003t0001g0097 others(2): Show |
5 | NA18962.hp2 NA18968.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+5239A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815089 | |||||||
| chr8:11815114 | T | C | 3 | a0001c0001t0002g0051 a0001c0001t0002g0060 a0001c0003t0003g0062 |
3 | HG00733.hp2 HG02738.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.381+5264T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815114 | |||||||
| chr8:11815130 | G | A | 2 | a0001c0004t0002g0024 a0001c0004t0002g0168 |
3 | HG02559.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.381+5280G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815130 | |||||||
| chr8:11815133 | G | A | 4 | a0001c0001t0002g0013 a0001c0001t0002g0159 a0001c0001t0002g0367 others(1): Show |
6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+5283G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815133 | |||||||
| chr8:11815150 | A | G | 1 | a0001c0001t0003g0271 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.381+5300A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815150 | |||||||
| chr8:11815181 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.381+5331C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815181 | |||||||
| chr8:11815203 | C | G | 1 | a0001c0001t0001g0341 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.381+5353C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815203 | |||||||
| chr8:11815211 | A | G | 27 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(24): Show |
38 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.381+5361A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815211 | |||||||
| chr8:11815263 | C | A | 1 | a0001c0001t0001g0387 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.381+5413C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815263 | |||||||
| chr8:11815364 | T | C | 1 | a0001c0010t0002g0069 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.381+5514T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815364 | |||||||
| chr8:11815390 | T | C | 27 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(24): Show |
38 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.381+5540T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815390 | |||||||
| chr8:11815451 | T | G | 24 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(21): Show |
35 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.381+5601T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815451 | |||||||
| chr8:11815508 | T | G | 1 | a0001c0002t0003g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.381+5658T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815508 | |||||||
| chr8:11815524 | A | G | 58 | a0001c0001t0002g0051 a0001c0001t0002g0060 a0001c0001t0002g0064 others(55): Show |
72 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.381+5674A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815524 | |||||||
| chr8:11815546 | T | A | 35 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(32): Show |
46 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.381+5696T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815546 | |||||||
| chr8:11815659 | T | A | 3 | a0001c0004t0007g0025 a0001c0004t0007g0176 a0001c0016t0002g0169 |
4 | HG01070.hp2 HG01071.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+5809T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815659 | |||||||
| chr8:11815769 | C | T | 2 | a0001c0001t0002g0101 a0001c0003t0002g0161 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.381+5919C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815769 | |||||||
| chr8:11815879 | C | T | 5 | a0001c0001t0008g0044 a0001c0001t0008g0047 a0001c0001t0008g0048 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-5871C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815879 | |||||||
| chr8:11815907 | A | G | 26 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(23): Show |
36 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.382-5843A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815907 | |||||||
| chr8:11815923 | T | C | 1 | a0008c0020t0002g0059 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.382-5827T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815923 | |||||||
| chr8:11815970 | G | A | 26 | a0001c0001t0002g0051 a0001c0001t0002g0060 a0001c0001t0002g0158 others(23): Show |
29 | HG00323.hp2 HG00733.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.382-5780G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815970 | |||||||
| chr8:11815976 | T | C | 192 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(189): Show |
215 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.382-5774T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815976 | |||||||
| chr8:11815992 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.382-5758C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815992 | |||||||
| chr8:11815994 | G | T | 4 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-5756G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11815994 | |||||||
| chr8:11816081 | C | T | 7 | a0001c0005t0002g0023 a0001c0005t0002g0070 a0001c0005t0002g0136 others(4): Show |
8 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-5669C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816081 | |||||||
| chr8:11816092 | C | G | 26 | a0001c0001t0002g0051 a0001c0001t0002g0060 a0001c0001t0002g0158 others(23): Show |
29 | HG00323.hp2 HG00733.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.382-5658C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816092 | |||||||
| chr8:11816143 | G | T | 3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0391 |
3 | HG02056.hp2 NA19060.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.382-5607G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816143 | |||||||
| chr8:11816191 | T | C | 5 | a0001c0004t0002g0068 a0001c0006t0001g0383 a0001c0013t0002g0180 others(2): Show |
5 | HG02145.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-5559T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816191 | |||||||
| chr8:11816245 | G | C | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00544.hp2 NA18941.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-5505G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816245 | |||||||
| chr8:11816310 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.382-5440C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816310 | |||||||
| chr8:11816449 | T | G | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
4 | HG02970.hp2 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-5301T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816449 | |||||||
| chr8:11816476 | G | C | 23 | a0001c0001t0001g0078 a0001c0001t0002g0015 a0001c0001t0002g0018 others(20): Show |
25 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.382-5274G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816476 | |||||||
| chr8:11816480 | C | T | 23 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(20): Show |
26 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-5270C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816480 | |||||||
| chr8:11816566 | T | C | 23 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(20): Show |
26 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-5184T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816566 | |||||||
| chr8:11816568 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 |
3 | HG02970.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.382-5182T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816568 | |||||||
| chr8:11816610 | G | A | 3 | a0001c0001t0002g0051 a0001c0001t0002g0060 a0001c0003t0003g0062 |
3 | HG00733.hp2 HG02738.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.382-5140G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816610 | |||||||
| chr8:11816628 | C | G | 41 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(38): Show |
52 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.382-5122C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816628 | |||||||
| chr8:11816683 | G | A | 1 | a0001c0002t0003g0216 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.382-5067G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816683 | |||||||
| chr8:11816689 | G | C | 34 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(31): Show |
45 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.382-5061G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816689 | |||||||
| chr8:11816749 | T | G | 133 | a0001c0001t0001g0211 a0001c0001t0001g0280 a0001c0001t0001g0281 others(130): Show |
147 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.382-5001T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816749 | |||||||
| chr8:11816755 | T | G | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
4 | HG02970.hp2 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-4995T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816755 | |||||||
| chr8:11816780 | G | C | 4 | a0001c0001t0002g0013 a0001c0001t0002g0159 a0001c0001t0002g0367 others(1): Show |
6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-4970G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816780 | |||||||
| chr8:11816782 | G | C | 4 | a0001c0006t0001g0383 a0001c0013t0002g0180 a0001c0015t0002g0181 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-4968G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816782 | |||||||
| chr8:11816783 | G | A | 3 | a0001c0001t0002g0051 a0001c0001t0002g0060 a0001c0003t0003g0062 |
3 | HG00733.hp2 HG02738.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.382-4967G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816783 | |||||||
| chr8:11816792 | A | G | 23 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(20): Show |
26 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-4958A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816792 | |||||||
| chr8:11816830 | T | A | 1 | a0001c0001t0001g0305 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.382-4920T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816830 | |||||||
| chr8:11816852 | C | T | 4 | a0001c0006t0001g0383 a0001c0013t0002g0180 a0001c0015t0002g0181 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-4898C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816852 | |||||||
| chr8:11816871 | C | A | 1 | a0001c0003t0001g0375 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.382-4879C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816871 | |||||||
| chr8:11816904 | G | T | 1 | a0001c0002t0005g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.382-4846G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816904 | |||||||
| chr8:11816963 | G | T | 4 | a0001c0006t0001g0383 a0001c0013t0002g0180 a0001c0015t0002g0181 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-4787G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816963 | |||||||
| chr8:11816969 | A | G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0159 a0001c0001t0002g0367 others(1): Show |
6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-4781A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11816969 | |||||||
| chr8:11817039 | G | A | 4 | a0001c0001t0002g0013 a0001c0001t0002g0159 a0001c0001t0002g0367 others(1): Show |
6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-4711G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817039 | |||||||
| chr8:11817276 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.382-4474T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817276 | |||||||
| chr8:11817284 | A | C | 59 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(56): Show |
73 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.382-4466A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817284 | |||||||
| chr8:11817388 | TG | T | 4 | a0002c0007t0001g0035 a0002c0007t0001g0313 a0002c0007t0001g0352 others(1): Show |
5 | HG00323.hp1 HG00642.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-4361delG | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817388 | |||||||
| chr8:11817446 | G | T | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00544.hp2 NA18941.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-4304G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817446 | |||||||
| chr8:11817502 | T | C | 10 | a0001c0002t0003g0184 a0001c0002t0003g0189 a0001c0002t0003g0203 others(7): Show |
10 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-4248T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817502 | |||||||
| chr8:11817685 | T | A | 1 | a0001c0001t0001g0385 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.382-4065T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817685 | |||||||
| chr8:11817694 | G | C | 1 | a0001c0001t0002g0129 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382-4056G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817694 | |||||||
| chr8:11817739 | T | A | 264 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(261): Show |
302 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(299): Show |
intron_variant | MODIFIER | c.382-4011T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817739 | |||||||
| chr8:11817790 | T | A | 1 | a0001c0002t0003g0030 | 2 | NA18979.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.382-3960T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817790 | |||||||
| chr8:11817795 | T | A | 3 | a0001c0001t0002g0051 a0001c0001t0002g0060 a0001c0003t0003g0062 |
3 | HG00733.hp2 HG02738.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.382-3955T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817795 | |||||||
| chr8:11817809 | C | T | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.382-3941C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817809 | |||||||
| chr8:11817822 | A | AT | 193 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 others(190): Show |
215 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.382-3917dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11817822 | ||||||
| chr8:11817822 | A | ATT | 50 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0122 others(47): Show |
64 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.382-3918_382-3917d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11817822 | ||||||
| chr8:11817854 | A | G | 265 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(262): Show |
304 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(301): Show |
intron_variant | MODIFIER | c.382-3896A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817854 | |||||||
| chr8:11817907 | T | A | 3 | a0001c0013t0002g0180 a0001c0015t0002g0181 a0006c0023t0017g0042 |
3 | HG02145.hp2 HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.382-3843T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817907 | |||||||
| chr8:11817936 | C | G | 10 | a0001c0003t0002g0403 a0001c0003t0013g0404 a0001c0005t0001g0138 others(7): Show |
11 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.382-3814C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11817936 | |||||||
| chr8:11818008 | A | G | 4 | a0001c0004t0002g0068 a0001c0013t0002g0180 a0001c0015t0002g0181 others(1): Show |
4 | HG02145.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-3742A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818008 | |||||||
| chr8:11818018 | A | C | 1 | a0001c0002t0001g0032 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.382-3732A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818018 | |||||||
| chr8:11818022 | A | T | 186 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 others(183): Show |
207 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.382-3728A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818022 | |||||||
| chr8:11818089 | T | A | 54 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0078 others(51): Show |
68 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.382-3661T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818089 | |||||||
| chr8:11818161 | A | T | 1 | a0001c0002t0001g0032 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.382-3589A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818161 | |||||||
| chr8:11818164 | T | A | 1 | a0001c0002t0001g0032 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.382-3586T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818164 | |||||||
| chr8:11818166 | T | C | 1 | a0001c0002t0001g0032 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.382-3584T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818166 | |||||||
| chr8:11818377 | C | G | 17 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0078 others(14): Show |
18 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.382-3373C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818377 | |||||||
| chr8:11818391 | G | A | 20 | a0001c0003t0002g0403 a0001c0003t0013g0404 a0001c0004t0001g0154 others(17): Show |
23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.382-3359G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818391 | |||||||
| chr8:11818409 | A | G | 1 | a0001c0004t0001g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.382-3341A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818409 | |||||||
| chr8:11818534 | T | C | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.382-3216T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818534 | |||||||
| chr8:11818554 | G | GT | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 |
3 | HG02970.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.382-3195dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11818554 | ||||||
| chr8:11818561 | T | C | 1 | a0001c0002t0001g0196 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.382-3189T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818561 | |||||||
| chr8:11818572 | T | C | 4 | a0001c0004t0002g0068 a0001c0013t0002g0180 a0001c0015t0002g0181 others(1): Show |
4 | HG02145.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-3178T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818572 | |||||||
| chr8:11818585 | T | C | 25 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(22): Show |
36 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.382-3165T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818585 | |||||||
| chr8:11818609 | T | A | 5 | a0001c0001t0011g0045 a0001c0001t0011g0046 a0001c0004t0001g0148 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-3141T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818609 | |||||||
| chr8:11818667 | G | C | 1 | a0001c0001t0002g0107 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.382-3083G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818667 | |||||||
| chr8:11818692 | T | C | 2 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | NA18957.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.382-3058T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818692 | |||||||
| chr8:11818752 | C | T | 1 | a0001c0006t0001g0356 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.382-2998C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818752 | |||||||
| chr8:11818759 | G | A | 4 | a0001c0004t0002g0068 a0001c0013t0002g0180 a0001c0015t0002g0181 others(1): Show |
4 | HG02145.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-2991G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818759 | |||||||
| chr8:11818762 | G | A | 7 | a0001c0005t0002g0023 a0001c0005t0002g0070 a0001c0005t0002g0136 others(4): Show |
8 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-2988G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818762 | |||||||
| chr8:11818800 | T | C | 2 | a0001c0001t0001g0212 a0001c0006t0001g0399 |
2 | HG00544.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.382-2950T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818800 | |||||||
| chr8:11818802 | T | C | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-2948T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818802 | |||||||
| chr8:11818813 | C | G | 4 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0202 others(1): Show |
4 | NA18971.hp2 NA18998.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-2937C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818813 | |||||||
| chr8:11818821 | C | T | 1 | a0001c0005t0002g0149 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.382-2929C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818821 | |||||||
| chr8:11818880 | A | G | 4 | a0001c0004t0002g0068 a0001c0013t0002g0180 a0001c0015t0002g0181 others(1): Show |
4 | HG02145.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-2870A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818880 | |||||||
| chr8:11818886 | T | G | 3 | a0001c0002t0003g0028 a0001c0002t0003g0197 a0001c0002t0003g0198 |
4 | NA18948.hp1 NA18966.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-2864T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818886 | |||||||
| chr8:11818920 | A | G | 3 | a0003c0012t0001g0340 a0003c0012t0018g0339 a0012c0030t0001g0139 |
3 | HG00597.hp2 NA19075.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.382-2830A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818920 | |||||||
| chr8:11818946 | C | G | 14 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0122 others(11): Show |
15 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.382-2804C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818946 | |||||||
| chr8:11818955 | C | G | 2 | a0001c0001t0001g0395 a0001c0001t0001g0396 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.382-2795C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818955 | |||||||
| chr8:11818984 | C | T | 1 | a0001c0002t0003g0238 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.382-2766C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11818984 | |||||||
| chr8:11819004 | C | G | 1 | a0001c0004t0002g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.382-2746C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819004 | |||||||
| chr8:11819010 | T | G | 56 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(53): Show |
70 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.382-2740T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819010 | |||||||
| chr8:11819025 | G | T | 2 | a0001c0004t0002g0024 a0001c0004t0002g0168 |
3 | HG02559.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.382-2725G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819025 | |||||||
| chr8:11819057 | A | G | 1 | a0001c0004t0002g0172 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.382-2693A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819057 | |||||||
| chr8:11819083 | A | G | 237 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(234): Show |
271 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.382-2667A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819083 | |||||||
| chr8:11819173 | G | A | 52 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0122 others(49): Show |
66 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.382-2577G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819173 | |||||||
| chr8:11819193 | A | T | 237 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(234): Show |
271 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.382-2557A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819193 | |||||||
| chr8:11819272 | C | A | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.382-2478C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819272 | |||||||
| chr8:11819350 | A | G | 237 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(234): Show |
271 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.382-2400A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819350 | |||||||
| chr8:11819396 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.382-2354C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819396 | |||||||
| chr8:11819455 | T | G | 53 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0122 others(50): Show |
67 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.382-2295T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819455 | |||||||
| chr8:11819458 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.382-2292C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819458 | |||||||
| chr8:11819460 | TTCTG | T | 10 | a0001c0003t0002g0403 a0001c0003t0013g0404 a0001c0005t0001g0138 others(7): Show |
11 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.382-2286_382-2283d others(6): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11819460 | ||||||
| chr8:11819485 | C | A | 51 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0122 others(48): Show |
65 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.382-2265C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819485 | |||||||
| chr8:11819487 | A | G | 53 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0122 others(50): Show |
67 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.382-2263A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819487 | |||||||
| chr8:11819516 | C | G | 2 | a0001c0002t0001g0221 a0001c0002t0001g0237 |
2 | HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.382-2234C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819516 | |||||||
| chr8:11819549 | A | T | 1 | a0001c0001t0001g0338 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.382-2201A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819549 | |||||||
| chr8:11819601 | C | T | 24 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(21): Show |
35 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.382-2149C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819601 | |||||||
| chr8:11819612 | A | G | 1 | a0001c0002t0003g0236 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.382-2138A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819612 | |||||||
| chr8:11819615 | C | A | 4 | a0001c0004t0002g0068 a0001c0013t0002g0180 a0001c0015t0002g0181 others(1): Show |
4 | HG02145.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-2135C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819615 | |||||||
| chr8:11819741 | T | A | 170 | a0001c0001t0001g0207 a0001c0001t0001g0211 a0001c0001t0001g0305 others(167): Show |
187 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.382-2009T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819741 | |||||||
| chr8:11819781 | C | G | 262 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(259): Show |
299 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.382-1969C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819781 | |||||||
| chr8:11819791 | G | A | 1 | a0001c0002t0001g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.382-1959G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819791 | |||||||
| chr8:11819796 | G | C | 209 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 others(206): Show |
232 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.382-1954G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819796 | |||||||
| chr8:11819853 | C | T | 1 | a0001c0002t0001g0196 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.382-1897C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819853 | |||||||
| chr8:11819914 | A | G | 1 | a0001c0001t0001g0378 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.382-1836A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819914 | |||||||
| chr8:11819915 | G | A | 1 | a0001c0001t0009g0017 | 2 | HG02129.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.382-1835G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819915 | |||||||
| chr8:11819949 | C | T | 252 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0122 others(249): Show |
287 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.382-1801C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819949 | |||||||
| chr8:11819959 | T | C | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-1791T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819959 | |||||||
| chr8:11819963 | T | G | 237 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(234): Show |
271 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.382-1787T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819963 | |||||||
| chr8:11819976 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.382-1774T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11819976 | |||||||
| chr8:11820009 | G | C | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.382-1741G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820009 | |||||||
| chr8:11820013 | C | T | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-1737C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820013 | |||||||
| chr8:11820015 | T | C | 27 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(24): Show |
38 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.382-1735T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820015 | |||||||
| chr8:11820054 | T | C | 1 | a0001c0002t0003g0252 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.382-1696T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820054 | |||||||
| chr8:11820104 | G | T | 1 | a0001c0005t0001g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.382-1646G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820104 | |||||||
| chr8:11820131 | G | A | 1 | a0001c0001t0001g0393 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.382-1619G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820131 | |||||||
| chr8:11820135 | A | C | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(110): Show |
124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.382-1615A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820135 | |||||||
| chr8:11820142 | A | G | 8 | a0001c0005t0001g0138 a0001c0005t0002g0023 a0001c0005t0002g0070 others(5): Show |
9 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.382-1608A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820142 | |||||||
| chr8:11820215 | G | C | 2 | a0001c0002t0001g0221 a0001c0002t0001g0237 |
2 | HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.382-1535G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820215 | |||||||
| chr8:11820241 | A | G | 6 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0194 others(3): Show |
6 | NA18939.hp2 NA18950.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-1509A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820241 | |||||||
| chr8:11820265 | C | G | 7 | a0001c0005t0002g0023 a0001c0005t0002g0070 a0001c0005t0002g0136 others(4): Show |
8 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-1485C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820265 | |||||||
| chr8:11820294 | C | A | 3 | a0001c0003t0002g0403 a0001c0003t0013g0404 a0001c0005t0001g0138 |
3 | HG03041.hp1 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.382-1456C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820294 | |||||||
| chr8:11820296 | T | A | 56 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0122 others(53): Show |
68 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.382-1454T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820296 | |||||||
| chr8:11820396 | A | C | 30 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(27): Show |
34 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.382-1354A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820396 | |||||||
| chr8:11820419 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 |
3 | HG02970.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.382-1331C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820419 | |||||||
| chr8:11820456 | A | C | 1 | a0001c0003t0003g0286 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.382-1294A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820456 | |||||||
| chr8:11820470 | G | T | 1 | a0001c0002t0003g0192 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.382-1280G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820470 | |||||||
| chr8:11820471 | G | T | 2 | a0001c0013t0002g0180 a0006c0023t0017g0042 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.382-1279G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820471 | |||||||
| chr8:11820481 | TTGCTGAG others(1): Show |
T | 194 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 others(191): Show |
215 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.382-1265_382-1258d others(10): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 11820481 | ||||||
| chr8:11820493 | G | A | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-1257G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820493 | |||||||
| chr8:11820558 | C | G | 2 | a0001c0001t0001g0337 a0001c0001t0001g0378 |
2 | HG01192.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.382-1192C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820558 | |||||||
| chr8:11820658 | G | A | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.382-1092G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820658 | |||||||
| chr8:11820665 | G | A | 2 | a0001c0001t0001g0346 a0001c0001t0001g0379 |
2 | NA19057.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.382-1085G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820665 | |||||||
| chr8:11820712 | C | A | 1 | a0001c0001t0001g0315 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.382-1038C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820712 | |||||||
| chr8:11820766 | A | G | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-984A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820766 | |||||||
| chr8:11820776 | G | A | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.382-974G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820776 | |||||||
| chr8:11820806 | C | A | 1 | a0001c0001t0011g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.382-944C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820806 | |||||||
| chr8:11820878 | C | G | 1 | a0001c0002t0001g0201 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.382-872C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820878 | |||||||
| chr8:11820895 | G | A | 261 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0077 others(258): Show |
297 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(294): Show |
intron_variant | MODIFIER | c.382-855G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820895 | |||||||
| chr8:11820938 | C | A | 1 | a0001c0004t0001g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.382-812C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820938 | |||||||
| chr8:11820992 | A | G | 254 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0077 others(251): Show |
290 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.382-758A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820992 | |||||||
| chr8:11820996 | C | G | 1 | a0001c0001t0011g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.382-754C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11820996 | |||||||
| chr8:11821055 | C | G | 7 | a0001c0005t0002g0023 a0001c0005t0002g0070 a0001c0005t0002g0136 others(4): Show |
8 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-695C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821055 | |||||||
| chr8:11821064 | T | C | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.382-686T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821064 | |||||||
| chr8:11821082 | T | A | 1 | a0001c0001t0002g0060 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.382-668T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821082 | |||||||
| chr8:11821159 | A | C | 254 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0077 others(251): Show |
290 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.382-591A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821159 | |||||||
| chr8:11821190 | A | G | 1 | a0001c0001t0002g0159 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.382-560A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821190 | |||||||
| chr8:11821208 | G | C | 3 | a0001c0001t0001g0342 a0001c0001t0001g0395 a0001c0001t0001g0396 |
3 | HG01515.hp2 HG01517.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.382-542G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821208 | |||||||
| chr8:11821235 | G | C | 1 | a0001c0003t0003g0354 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.382-515G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821235 | |||||||
| chr8:11821315 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.382-435G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821315 | |||||||
| chr8:11821420 | A | C | 9 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(6): Show |
11 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.382-330A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821420 | |||||||
| chr8:11821523 | G | A | 1 | a0001c0002t0003g0258 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.382-227G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821523 | |||||||
| chr8:11821608 | C | G | 1 | a0001c0004t0006g0146 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.382-142C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821608 | |||||||
| chr8:11821648 | C | T | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-102C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821648 | |||||||
| chr8:11821668 | C | T | 9 | a0001c0001t0002g0119 a0001c0004t0002g0001 a0001c0004t0002g0026 others(6): Show |
15 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.382-82C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821668 | |||||||
| chr8:11821728 | G | C | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00544.hp2 NA18941.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-22G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821728 | |||||||
| chr8:11821735 | C | T | 1 | a0001c0001t0001g0359 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.382-15C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 3/7 | chr8 | 11821735 | |||||||
| chr8:11821936 | A | G | 2 | a0001c0003t0002g0403 a0001c0003t0013g0404 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.510+58A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11821936 | |||||||
| chr8:11821955 | G | A | 4 | a0001c0001t0002g0013 a0001c0001t0002g0159 a0001c0001t0002g0367 others(1): Show |
6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+77G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11821955 | |||||||
| chr8:11821963 | G | A | 1 | a0001c0002t0003g0366 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.510+85G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11821963 | |||||||
| chr8:11822022 | C | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0159 a0001c0001t0002g0367 others(1): Show |
6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+144C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822022 | |||||||
| chr8:11822049 | C | A | 2 | a0001c0001t0001g0294 a0001c0001t0001g0297 |
2 | HG02015.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.510+171C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822049 | |||||||
| chr8:11822056 | A | C | 1 | a0001c0006t0005g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.510+178A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822056 | |||||||
| chr8:11822173 | G | C | 1 | a0001c0013t0002g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.510+295G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822173 | |||||||
| chr8:11822201 | G | T | 9 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(6): Show |
11 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.510+323G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822201 | |||||||
| chr8:11822265 | T | A | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.510+387T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822265 | |||||||
| chr8:11822272 | CA | C | 9 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(6): Show |
11 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.510+395delA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822272 | |||||||
| chr8:11822274 | G | A | 35 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(32): Show |
46 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.510+396G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822274 | |||||||
| chr8:11822284 | G | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0159 a0001c0001t0002g0367 others(1): Show |
6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+406G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822284 | |||||||
| chr8:11822326 | C | T | 1 | a0001c0005t0001g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.510+448C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822326 | |||||||
| chr8:11822331 | C | CT | 37 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(34): Show |
48 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.510+456dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11822331 | ||||||
| chr8:11822494 | A | G | 2 | a0001c0004t0002g0130 a0001c0004t0002g0131 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.510+616A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822494 | |||||||
| chr8:11822519 | A | G | 2 | a0001c0003t0002g0403 a0001c0003t0013g0404 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.510+641A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822519 | |||||||
| chr8:11822608 | G | A | 2 | a0001c0013t0002g0180 a0006c0023t0017g0042 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.510+730G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822608 | |||||||
| chr8:11822625 | G | GC | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.510+748dupC | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11822625 | ||||||
| chr8:11822639 | C | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0159 a0001c0001t0002g0367 others(1): Show |
6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+761C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822639 | |||||||
| chr8:11822769 | T | C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+891T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822769 | |||||||
| chr8:11822793 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.510+915G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822793 | |||||||
| chr8:11822828 | G | C | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.510+950G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822828 | |||||||
| chr8:11822897 | T | G | 1 | a0001c0001t0001g0342 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.510+1019T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822897 | |||||||
| chr8:11822959 | A | T | 55 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(52): Show |
69 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.510+1081A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822959 | |||||||
| chr8:11822966 | A | T | 2 | a0001c0003t0002g0403 a0001c0003t0013g0404 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.510+1088A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11822966 | |||||||
| chr8:11823001 | C | T | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.510+1123C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823001 | |||||||
| chr8:11823026 | C | T | 193 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0077 others(190): Show |
214 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.510+1148C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823026 | |||||||
| chr8:11823032 | G | A | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.510+1154G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823032 | |||||||
| chr8:11823101 | A | C | 2 | a0001c0004t0006g0164 a0001c0004t0006g0165 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.510+1223A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823101 | |||||||
| chr8:11823160 | T | A | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1282T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823160 | |||||||
| chr8:11823161 | G | T | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.510+1283G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823161 | |||||||
| chr8:11823193 | CAGTCCTC others(28): Show |
C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1317_510+1351d others(37): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11823193 | ||||||
| chr8:11823210 | C | T | 1 | a0001c0013t0002g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.510+1332C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823210 | |||||||
| chr8:11823236 | T | A | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1358T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823236 | |||||||
| chr8:11823250 | T | C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1372T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823250 | |||||||
| chr8:11823251 | T | C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1373T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823251 | |||||||
| chr8:11823254 | A | C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1376A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823254 | |||||||
| chr8:11823255 | A | C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1377A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823255 | |||||||
| chr8:11823256 | G | GGTCCCCC others(85): Show |
1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1379_510+1380i others(94): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11823256 | ||||||
| chr8:11823260 | T | G | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.510+1382T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823260 | |||||||
| chr8:11823377 | C | G | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.510+1499C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823377 | |||||||
| chr8:11823541 | G | C | 1 | a0001c0003t0001g0087 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.510+1663G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823541 | |||||||
| chr8:11823543 | T | C | 9 | a0001c0002t0003g0225 a0001c0002t0003g0251 a0001c0002t0003g0276 others(6): Show |
9 | HG00423.hp2 HG02132.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+1665T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823543 | |||||||
| chr8:11823623 | G | C | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.510+1745G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823623 | |||||||
| chr8:11823626 | A | T | 1 | a0001c0004t0006g0146 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.510+1748A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823626 | |||||||
| chr8:11823655 | C | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0159 a0001c0001t0002g0367 others(1): Show |
6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+1777C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823655 | |||||||
| chr8:11823672 | A | G | 2 | a0001c0003t0003g0020 a0001c0003t0003g0102 |
3 | NA18968.hp1 NA18971.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.510+1794A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823672 | |||||||
| chr8:11823694 | T | C | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.510+1816T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823694 | |||||||
| chr8:11823737 | A | G | 110 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(107): Show |
120 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.510+1859A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823737 | |||||||
| chr8:11823758 | T | A | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.510+1880T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823758 | |||||||
| chr8:11823805 | A | G | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.510+1927A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823805 | |||||||
| chr8:11823831 | C | T | 9 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(6): Show |
11 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.510+1953C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823831 | |||||||
| chr8:11823837 | G | T | 1 | a0001c0002t0003g0366 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.510+1959G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823837 | |||||||
| chr8:11823844 | A | C | 1 | a0001c0001t0001g0342 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.510+1966A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823844 | |||||||
| chr8:11823879 | G | A | 29 | a0001c0001t0001g0078 a0001c0001t0002g0064 a0001c0001t0002g0065 others(26): Show |
40 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.510+2001G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823879 | |||||||
| chr8:11823883 | A | G | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.510+2005A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823883 | |||||||
| chr8:11823943 | A | T | 24 | a0001c0001t0010g0043 a0001c0004t0002g0021 a0001c0004t0002g0022 others(21): Show |
27 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.510+2065A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823943 | |||||||
| chr8:11823946 | G | C | 1 | a0001c0001t0001g0317 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.510+2068G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823946 | |||||||
| chr8:11823956 | G | A | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.511-2068G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11823956 | |||||||
| chr8:11824007 | G | C | 1 | a0001c0003t0001g0272 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.511-2017G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824007 | |||||||
| chr8:11824027 | G | C | 1 | a0001c0005t0001g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.511-1997G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824027 | |||||||
| chr8:11824028 | C | A | 1 | a0001c0005t0001g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.511-1996C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824028 | |||||||
| chr8:11824078 | G | C | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-1946G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824078 | |||||||
| chr8:11824089 | T | C | 1 | a0001c0002t0003g0209 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.511-1935T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824089 | |||||||
| chr8:11824106 | C | G | 2 | a0001c0013t0002g0180 a0006c0023t0017g0042 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.511-1918C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824106 | |||||||
| chr8:11824227 | T | TA | 9 | a0001c0005t0001g0138 a0001c0005t0002g0023 a0001c0005t0002g0070 others(6): Show |
10 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.511-1795dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11824227 | ||||||
| chr8:11824304 | A | C | 1 | a0001c0002t0003g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.511-1720A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824304 | |||||||
| chr8:11824316 | C | T | 257 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0077 others(254): Show |
294 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.511-1708C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824316 | |||||||
| chr8:11824329 | T | C | 179 | a0001c0001t0001g0282 a0001c0001t0001g0291 a0001c0001t0001g0316 others(176): Show |
199 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.511-1695T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824329 | |||||||
| chr8:11824385 | C | G | 2 | a0001c0001t0002g0065 a0001c0001t0002g0066 |
2 | HG02738.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.511-1639C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824385 | |||||||
| chr8:11824402 | A | G | 9 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(6): Show |
11 | HG01891.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.511-1622A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824402 | |||||||
| chr8:11824482 | A | T | 1 | a0001c0006t0005g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.511-1542A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824482 | |||||||
| chr8:11824484 | C | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0077 others(14): Show |
18 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.511-1540C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824484 | |||||||
| chr8:11824541 | C | T | 1 | a0001c0021t0001g0073 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.511-1483C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824541 | |||||||
| chr8:11824606 | T | TC | 140 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(137): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.511-1417dupC | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11824606 | ||||||
| chr8:11824638 | G | C | 2 | a0001c0001t0001g0395 a0001c0001t0001g0396 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.511-1386G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824638 | |||||||
| chr8:11824659 | C | T | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-1365C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824659 | |||||||
| chr8:11824664 | T | C | 1 | a0001c0005t0012g0049 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.511-1360T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824664 | |||||||
| chr8:11824738 | CTGT | C | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-1275_511-1273d others(5): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11824738 | ||||||
| chr8:11824758 | C | T | 173 | a0001c0001t0001g0316 a0001c0001t0001g0334 a0001c0001t0001g0390 others(170): Show |
191 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.511-1266C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824758 | |||||||
| chr8:11824767 | A | G | 1 | a0001c0005t0001g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.511-1257A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824767 | |||||||
| chr8:11824794 | G | T | 1 | a0001c0002t0001g0196 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.511-1230G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824794 | |||||||
| chr8:11824796 | C | T | 2 | a0001c0001t0002g0101 a0001c0003t0002g0161 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.511-1228C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824796 | |||||||
| chr8:11824797 | G | A | 2 | a0001c0002t0003g0247 a0001c0002t0003g0290 |
2 | HG03017.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.511-1227G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824797 | |||||||
| chr8:11824821 | C | G | 8 | a0001c0001t0002g0013 a0001c0001t0002g0159 a0001c0001t0002g0367 others(5): Show |
10 | HG02258.hp1 HG02486.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.511-1203C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824821 | |||||||
| chr8:11824837 | G | A | 1 | a0001c0002t0003g0204 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.511-1187G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824837 | |||||||
| chr8:11824909 | G | C | 9 | a0001c0001t0002g0119 a0001c0004t0002g0001 a0001c0004t0002g0026 others(6): Show |
15 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.511-1115G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824909 | |||||||
| chr8:11824936 | C | T | 1 | a0001c0001t0001g0333 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.511-1088C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824936 | |||||||
| chr8:11824937 | G | T | 7 | a0001c0004t0006g0142 a0001c0004t0006g0144 a0001c0004t0006g0145 others(4): Show |
7 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.511-1087G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824937 | |||||||
| chr8:11824939 | C | G | 170 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(167): Show |
186 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.511-1085C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824939 | |||||||
| chr8:11824967 | T | C | 224 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(221): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.511-1057T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824967 | |||||||
| chr8:11824968 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.511-1056C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11824968 | |||||||
| chr8:11825047 | T | C | 15 | a0001c0005t0001g0138 a0001c0005t0002g0023 a0001c0005t0002g0070 others(12): Show |
16 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.511-977T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825047 | |||||||
| chr8:11825057 | C | A | 223 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(220): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.511-967C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825057 | |||||||
| chr8:11825097 | A | G | 1 | a0001c0002t0003g0290 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.511-927A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825097 | |||||||
| chr8:11825142 | G | C | 1 | a0001c0006t0002g0260 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.511-882G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825142 | |||||||
| chr8:11825146 | A | G | 1 | a0001c0004t0002g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.511-878A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825146 | |||||||
| chr8:11825161 | A | G | 6 | a0001c0001t0010g0043 a0001c0004t0002g0021 a0001c0004t0002g0022 others(3): Show |
8 | HG02622.hp2 HG02717.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.511-863A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825161 | |||||||
| chr8:11825189 | C | T | 4 | a0001c0001t0001g0332 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
4 | HG00597.hp1 HG03831.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-835C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825189 | |||||||
| chr8:11825213 | T | C | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-811T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825213 | |||||||
| chr8:11825262 | G | C | 191 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(188): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.511-762G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825262 | |||||||
| chr8:11825263 | C | T | 6 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0094 others(3): Show |
6 | HG02129.hp2 NA18939.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-761C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825263 | |||||||
| chr8:11825280 | G | T | 1 | a0001c0001t0001g0331 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.511-744G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825280 | |||||||
| chr8:11825349 | G | C | 25 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(22): Show |
36 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.511-675G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825349 | |||||||
| chr8:11825369 | C | G | 1 | a0001c0004t0010g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.511-655C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825369 | |||||||
| chr8:11825369 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.511-655C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825369 | |||||||
| chr8:11825392 | T | A | 25 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(22): Show |
36 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.511-632T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825392 | |||||||
| chr8:11825405 | G | C | 3 | a0001c0002t0003g0226 a0001c0002t0003g0227 a0001c0002t0005g0248 |
3 | HG02080.hp1 NA18949.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.511-619G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825405 | |||||||
| chr8:11825431 | T | C | 1 | a0001c0002t0001g0032 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.511-593T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825431 | |||||||
| chr8:11825501 | G | C | 399 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(396): Show |
449 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(446): Show |
intron_variant | MODIFIER | c.511-523G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825501 | |||||||
| chr8:11825539 | CA | C | 319 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(316): Show |
354 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.511-464delA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11825539 | ||||||
| chr8:11825539 | CAA | C | 43 | a0001c0001t0001g0379 a0001c0001t0001g0385 a0001c0001t0001g0393 others(40): Show |
53 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.511-465_511-464del others(2): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11825539 | ||||||
| chr8:11825560 | A | C | 1 | a0001c0004t0002g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.511-464A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825560 | |||||||
| chr8:11825584 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.511-440G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825584 | |||||||
| chr8:11825601 | C | A | 1 | a0001c0002t0003g0269 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.511-423C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825601 | |||||||
| chr8:11825635 | T | C | 4 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(1): Show |
6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-389T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825635 | |||||||
| chr8:11825655 | C | G | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-369C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825655 | |||||||
| chr8:11825685 | T | A | 1 | a0001c0001t0002g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.511-339T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825685 | |||||||
| chr8:11825686 | C | A | 1 | a0001c0001t0002g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.511-338C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825686 | |||||||
| chr8:11825686 | C | CA | 352 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(349): Show |
387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.511-328dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 11825686 | ||||||
| chr8:11825697 | T | A | 26 | a0001c0001t0001g0078 a0001c0001t0002g0013 a0001c0001t0002g0015 others(23): Show |
29 | HG00099.hp1 HG00639.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.511-327T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825697 | |||||||
| chr8:11825821 | C | T | 5 | a0001c0005t0001g0138 a0001c0008t0001g0134 a0001c0008t0001g0155 others(2): Show |
5 | HG01891.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-203C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825821 | |||||||
| chr8:11825836 | A | G | 401 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(398): Show |
451 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(448): Show |
intron_variant | MODIFIER | c.511-188A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825836 | |||||||
| chr8:11825882 | G | C | 1 | a0001c0002t0003g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.511-142G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825882 | |||||||
| chr8:11825893 | T | A | 1 | a0001c0001t0002g0119 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.511-131T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825893 | |||||||
| chr8:11825940 | G | C | 6 | a0001c0003t0001g0187 a0001c0003t0001g0263 a0001c0003t0001g0272 others(3): Show |
6 | NA18951.hp1 NA18979.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-84G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825940 | |||||||
| chr8:11825987 | T | G | 4 | a0001c0002t0003g0228 a0001c0003t0003g0020 a0001c0003t0003g0102 others(1): Show |
5 | HG02071.hp2 NA18968.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-37T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 4/7 | chr8 | 11825987 | |||||||
| chr8:11826233 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+18T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826233 | |||||||
| chr8:11826291 | G | A | 2 | a0001c0001t0001g0316 a0001c0002t0003g0031 |
3 | HG03654.hp1 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.702+76G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826291 | |||||||
| chr8:11826309 | T | C | 177 | a0001c0001t0001g0207 a0001c0001t0001g0316 a0001c0001t0002g0057 others(174): Show |
197 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.702+94T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826309 | |||||||
| chr8:11826355 | C | A | 367 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(364): Show |
413 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(410): Show |
intron_variant | MODIFIER | c.702+140C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826355 | |||||||
| chr8:11826355 | C | T | 29 | a0001c0001t0001g0078 a0001c0001t0002g0013 a0001c0001t0002g0015 others(26): Show |
33 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.702+140C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826355 | |||||||
| chr8:11826365 | G | T | 5 | a0001c0005t0001g0138 a0001c0008t0001g0134 a0001c0008t0001g0155 others(2): Show |
5 | HG01891.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+150G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826365 | |||||||
| chr8:11826538 | G | A | 1 | a0001c0002t0003g0252 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.702+323G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826538 | |||||||
| chr8:11826562 | C | A | 174 | a0001c0001t0001g0207 a0001c0001t0001g0316 a0001c0001t0002g0057 others(171): Show |
192 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.702+347C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826562 | |||||||
| chr8:11826563 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+348C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826563 | |||||||
| chr8:11826604 | A | G | 1 | a0001c0004t0002g0170 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.702+389A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826604 | |||||||
| chr8:11826612 | G | C | 2 | a0001c0002t0003g0197 a0001c0003t0004g0386 |
2 | NA18940.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.702+397G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826612 | |||||||
| chr8:11826632 | C | A | 398 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(395): Show |
448 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(445): Show |
intron_variant | MODIFIER | c.702+417C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826632 | |||||||
| chr8:11826756 | G | C | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.702+541G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826756 | |||||||
| chr8:11826757 | G | C | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.702+542G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826757 | |||||||
| chr8:11826779 | C | T | 7 | a0001c0005t0001g0138 a0001c0005t0012g0040 a0001c0005t0012g0049 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.702+564C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826779 | |||||||
| chr8:11826884 | C | G | 1 | a0001c0002t0003g0259 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.702+669C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826884 | |||||||
| chr8:11826888 | G | C | 1 | a0001c0003t0001g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.702+673G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826888 | |||||||
| chr8:11826894 | G | A | 170 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(167): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.702+679G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826894 | |||||||
| chr8:11826950 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.702+735C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826950 | |||||||
| chr8:11826954 | A | G | 174 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(171): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.702+739A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11826954 | |||||||
| chr8:11827031 | A | G | 2 | a0001c0001t0002g0101 a0001c0003t0002g0161 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.702+816A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827031 | |||||||
| chr8:11827115 | T | A | 3 | a0001c0001t0001g0074 a0001c0001t0011g0045 a0001c0001t0011g0046 |
3 | HG02109.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.702+900T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827115 | |||||||
| chr8:11827168 | C | T | 2 | a0001c0005t0012g0040 a0001c0005t0012g0049 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.702+953C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827168 | |||||||
| chr8:11827212 | A | G | 19 | a0001c0001t0002g0119 a0001c0004t0002g0001 a0001c0004t0002g0024 others(16): Show |
29 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.702+997A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827212 | |||||||
| chr8:11827278 | T | G | 27 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(24): Show |
38 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.702+1063T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827278 | |||||||
| chr8:11827292 | T | G | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.702+1077T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827292 | |||||||
| chr8:11827397 | A | G | 2 | a0001c0004t0002g0178 a0001c0011t0002g0014 |
3 | HG01891.hp2 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.702+1182A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827397 | |||||||
| chr8:11827413 | G | C | 3 | a0001c0001t0002g0051 a0001c0001t0002g0060 a0001c0001t0002g0388 |
3 | HG00733.hp2 HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.702+1198G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827413 | |||||||
| chr8:11827428 | G | C | 2 | a0001c0001t0001g0318 a0001c0001t0001g0376 |
2 | HG01074.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.702+1213G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827428 | |||||||
| chr8:11827440 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.702+1225C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827440 | |||||||
| chr8:11827441 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.702+1226G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827441 | |||||||
| chr8:11827447 | G | T | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1232G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827447 | |||||||
| chr8:11827449 | T | C | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1234T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827449 | |||||||
| chr8:11827458 | G | A | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1243G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827458 | |||||||
| chr8:11827459 | A | G | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1244A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827459 | |||||||
| chr8:11827461 | T | G | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1246T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827461 | |||||||
| chr8:11827462 | G | C | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1247G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827462 | |||||||
| chr8:11827465 | T | G | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1250T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827465 | |||||||
| chr8:11827477 | C | A | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.702+1262C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827477 | |||||||
| chr8:11827501 | G | C | 179 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0295 others(176): Show |
199 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.702+1286G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827501 | |||||||
| chr8:11827575 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.702+1360G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827575 | |||||||
| chr8:11827589 | T | C | 1 | a0001c0003t0003g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.702+1374T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827589 | |||||||
| chr8:11827606 | A | G | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.702+1391A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827606 | |||||||
| chr8:11827658 | G | A | 1 | a0001c0004t0001g0154 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.702+1443G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827658 | |||||||
| chr8:11827667 | A | T | 395 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(392): Show |
445 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(442): Show |
intron_variant | MODIFIER | c.702+1452A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827667 | |||||||
| chr8:11827669 | T | C | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+1454T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827669 | |||||||
| chr8:11827676 | G | A | 1 | a0001c0001t0001g0319 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.702+1461G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827676 | |||||||
| chr8:11827688 | A | G | 7 | a0001c0005t0001g0138 a0001c0005t0012g0040 a0001c0005t0012g0049 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.702+1473A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827688 | |||||||
| chr8:11827811 | T | C | 398 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(395): Show |
448 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(445): Show |
intron_variant | MODIFIER | c.702+1596T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827811 | |||||||
| chr8:11827833 | A | G | 262 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(259): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.702+1618A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827833 | |||||||
| chr8:11827837 | C | T | 4 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(1): Show |
6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+1622C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827837 | |||||||
| chr8:11827871 | C | G | 4 | a0001c0003t0002g0403 a0001c0003t0013g0404 a0001c0015t0002g0181 others(1): Show |
4 | HG02886.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+1656C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827871 | |||||||
| chr8:11827875 | TAAAAC | T | 5 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 others(2): Show |
5 | HG02572.hp1 HG02970.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+1685_702+1689d others(7): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11827875 | ||||||
| chr8:11827875 | TAAAACAA others(3): Show |
T | 1 | a0002c0009t0001g0174 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.702+1680_702+1689d others(12): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11827875 | ||||||
| chr8:11827895 | C | CA | 5 | a0001c0001t0001g0038 a0001c0004t0006g0146 a0002c0007t0001g0035 others(2): Show |
6 | HG00323.hp1 HG01081.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.702+1684dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11827895 | ||||||
| chr8:11827899 | A | C | 1 | a0001c0001t0001g0338 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.702+1684A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827899 | |||||||
| chr8:11827900 | C | A | 197 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(194): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.702+1685C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827900 | |||||||
| chr8:11827900 | C | CA | 15 | a0001c0005t0001g0138 a0001c0005t0002g0023 a0001c0005t0002g0070 others(12): Show |
16 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.702+1693dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11827900 | ||||||
| chr8:11827928 | A | T | 2 | a0001c0001t0001g0319 a0001c0001t0001g0330 |
2 | NA18941.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.702+1713A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827928 | |||||||
| chr8:11827944 | A | G | 26 | a0001c0001t0002g0013 a0001c0001t0002g0015 a0001c0001t0002g0018 others(23): Show |
30 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.702+1729A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827944 | |||||||
| chr8:11827996 | G | A | 8 | a0001c0001t0006g0380 a0001c0004t0006g0142 a0001c0004t0006g0144 others(5): Show |
8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.702+1781G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11827996 | |||||||
| chr8:11828027 | C | T | 179 | a0001c0001t0001g0207 a0001c0001t0001g0212 a0001c0001t0001g0295 others(176): Show |
199 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.702+1812C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828027 | |||||||
| chr8:11828035 | C | T | 1 | a0001c0004t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+1820C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828035 | |||||||
| chr8:11828040 | A | G | 7 | a0001c0005t0001g0138 a0001c0005t0012g0040 a0001c0005t0012g0049 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.702+1825A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828040 | |||||||
| chr8:11828066 | G | A | 1 | a0001c0006t0002g0233 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.702+1851G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828066 | |||||||
| chr8:11828074 | C | T | 8 | a0001c0001t0006g0380 a0001c0004t0006g0142 a0001c0004t0006g0144 others(5): Show |
8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.702+1859C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828074 | |||||||
| chr8:11828082 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.702+1867G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828082 | |||||||
| chr8:11828101 | C | G | 2 | a0001c0001t0002g0101 a0001c0003t0002g0161 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.702+1886C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828101 | |||||||
| chr8:11828152 | G | A | 1 | a0001c0002t0003g0245 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.702+1937G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828152 | |||||||
| chr8:11828155 | G | A | 25 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(22): Show |
36 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.702+1940G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828155 | |||||||
| chr8:11828163 | C | T | 1 | a0001c0008t0001g0134 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.702+1948C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828163 | |||||||
| chr8:11828171 | C | A | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.702+1956C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828171 | |||||||
| chr8:11828235 | C | T | 178 | a0001c0001t0001g0207 a0001c0001t0001g0212 a0001c0001t0001g0295 others(175): Show |
198 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.703-2009C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828235 | |||||||
| chr8:11828243 | G | A | 398 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(395): Show |
448 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(445): Show |
intron_variant | MODIFIER | c.703-2001G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828243 | |||||||
| chr8:11828256 | C | G | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.703-1988C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828256 | |||||||
| chr8:11828264 | C | T | 8 | a0001c0001t0006g0380 a0001c0004t0006g0142 a0001c0004t0006g0144 others(5): Show |
8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.703-1980C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828264 | |||||||
| chr8:11828292 | AAAAC | A | 26 | a0001c0001t0002g0013 a0001c0001t0002g0015 a0001c0001t0002g0018 others(23): Show |
30 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.703-1941_703-1938d others(6): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11828292 | ||||||
| chr8:11828300 | C | G | 179 | a0001c0001t0001g0207 a0001c0001t0001g0212 a0001c0001t0001g0295 others(176): Show |
199 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.703-1944C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828300 | |||||||
| chr8:11828310 | C | A | 3 | a0001c0001t0004g0336 a0001c0002t0003g0266 a0001c0002t0003g0267 |
3 | HG01952.hp2 HG01975.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.703-1934C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828310 | |||||||
| chr8:11828416 | T | A | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703-1828T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828416 | |||||||
| chr8:11828463 | A | T | 1 | a0001c0001t0002g0067 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.703-1781A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828463 | |||||||
| chr8:11828466 | G | C | 25 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(22): Show |
36 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.703-1778G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828466 | |||||||
| chr8:11828472 | C | G | 229 | a0001c0001t0001g0207 a0001c0001t0001g0212 a0001c0001t0001g0295 others(226): Show |
265 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.703-1772C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828472 | |||||||
| chr8:11828550 | A | G | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.703-1694A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828550 | |||||||
| chr8:11828580 | T | C | 45 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(42): Show |
59 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.703-1664T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828580 | |||||||
| chr8:11828677 | G | C | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703-1567G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828677 | |||||||
| chr8:11828695 | T | C | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.703-1549T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828695 | |||||||
| chr8:11828797 | G | C | 1 | a0001c0001t0001g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.703-1447G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828797 | |||||||
| chr8:11828904 | C | T | 1 | a0001c0014t0016g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.703-1340C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828904 | |||||||
| chr8:11828910 | A | G | 253 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 others(250): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.703-1334A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828910 | |||||||
| chr8:11828911 | A | G | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703-1333A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828911 | |||||||
| chr8:11828944 | A | G | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703-1300A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828944 | |||||||
| chr8:11828957 | C | G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0159 a0001c0001t0002g0367 others(1): Show |
6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-1287C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828957 | |||||||
| chr8:11828958 | T | A | 1 | a0001c0001t0001g0338 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.703-1286T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828958 | |||||||
| chr8:11828978 | T | G | 398 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(395): Show |
448 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(445): Show |
intron_variant | MODIFIER | c.703-1266T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11828978 | |||||||
| chr8:11829000 | C | G | 2 | a0001c0005t0012g0040 a0001c0005t0012g0049 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.703-1244C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829000 | |||||||
| chr8:11829061 | G | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-1183G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829061 | |||||||
| chr8:11829071 | G | C | 1 | a0001c0028t0002g0373 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.703-1173G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829071 | |||||||
| chr8:11829146 | CTTG | C | 136 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(133): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.703-1092_703-1090d others(5): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11829146 | ||||||
| chr8:11829175 | A | T | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.703-1069A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829175 | |||||||
| chr8:11829193 | A | G | 1 | a0001c0002t0003g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.703-1051A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829193 | |||||||
| chr8:11829199 | A | C | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.703-1045A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829199 | |||||||
| chr8:11829248 | A | G | 3 | a0001c0001t0002g0051 a0001c0001t0002g0060 a0001c0001t0002g0388 |
3 | HG00733.hp2 HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.703-996A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829248 | |||||||
| chr8:11829261 | A | G | 19 | a0001c0001t0002g0015 a0001c0001t0010g0043 a0001c0004t0002g0068 others(16): Show |
21 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.703-983A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829261 | |||||||
| chr8:11829326 | G | C | 129 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.703-918G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829326 | |||||||
| chr8:11829396 | T | G | 2 | a0001c0015t0002g0181 a0001c0017t0002g0041 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.703-848T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829396 | |||||||
| chr8:11829403 | C | G | 26 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(23): Show |
37 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.703-841C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829403 | |||||||
| chr8:11829482 | T | A | 400 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(397): Show |
450 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(447): Show |
intron_variant | MODIFIER | c.703-762T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829482 | |||||||
| chr8:11829525 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.703-719G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829525 | |||||||
| chr8:11829545 | T | G | 16 | a0001c0001t0002g0015 a0001c0005t0001g0138 a0001c0005t0002g0023 others(13): Show |
18 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.703-699T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829545 | |||||||
| chr8:11829546 | T | A | 16 | a0001c0001t0002g0015 a0001c0005t0001g0138 a0001c0005t0002g0023 others(13): Show |
18 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.703-698T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829546 | |||||||
| chr8:11829549 | C | G | 2 | a0001c0001t0008g0044 a0001c0001t0008g0048 |
2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.703-695C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829549 | |||||||
| chr8:11829551 | G | A | 2 | a0001c0005t0012g0040 a0001c0005t0012g0049 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.703-693G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829551 | |||||||
| chr8:11829553 | T | C | 1 | a0001c0002t0001g0363 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.703-691T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829553 | |||||||
| chr8:11829577 | G | A | 7 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(4): Show |
7 | NA18941.hp1 NA18956.hp2 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-667G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829577 | |||||||
| chr8:11829614 | C | T | 7 | a0001c0004t0006g0142 a0001c0004t0006g0144 a0001c0004t0006g0145 others(4): Show |
7 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-630C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829614 | |||||||
| chr8:11829622 | C | CT | 4 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(1): Show |
6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-621dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11829622 | ||||||
| chr8:11829650 | G | A | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(104): Show |
118 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.703-594G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829650 | |||||||
| chr8:11829796 | T | A | 1 | a0001c0002t0003g0251 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.703-448T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829796 | |||||||
| chr8:11829799 | G | C | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.703-445G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829799 | |||||||
| chr8:11829831 | A | T | 2 | a0001c0002t0003g0204 a0001c0002t0003g0247 |
2 | HG01358.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.703-413A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829831 | |||||||
| chr8:11829834 | G | GT | 50 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0077 others(47): Show |
64 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.703-401dupT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11829834 | ||||||
| chr8:11829844 | G | T | 14 | a0001c0001t0002g0013 a0001c0001t0002g0159 a0001c0001t0002g0367 others(11): Show |
16 | HG02258.hp1 HG02486.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.703-400G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829844 | |||||||
| chr8:11829845 | T | G | 2 | a0001c0015t0002g0181 a0001c0017t0002g0041 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.703-399T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829845 | |||||||
| chr8:11829884 | T | TTTTTTTT others(40): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.703-359_703-358ins others(47): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11829884 | ||||||
| chr8:11829884 | T | TTTTTTTT others(42): Show |
1 | a0001c0001t0001g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.703-359_703-358ins others(49): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11829884 | ||||||
| chr8:11829884 | T | TTTTTTTT others(59): Show |
1 | a0001c0001t0002g0129 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.703-359_703-358ins others(66): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 11829884 | ||||||
| chr8:11829887 | A | G | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-357A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829887 | |||||||
| chr8:11829935 | C | T | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.703-309C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11829935 | |||||||
| chr8:11830002 | C | T | 1 | a0001c0001t0008g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.703-242C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830002 | |||||||
| chr8:11830009 | G | A | 174 | a0001c0001t0001g0295 a0001c0001t0002g0057 a0001c0001t0002g0058 others(171): Show |
192 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.703-235G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830009 | |||||||
| chr8:11830050 | C | A | 1 | a0001c0002t0003g0259 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.703-194C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830050 | |||||||
| chr8:11830149 | A | C | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.703-95A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830149 | |||||||
| chr8:11830155 | G | T | 2 | a0001c0002t0003g0238 a0001c0002t0003g0252 |
2 | HG02129.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.703-89G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830155 | |||||||
| chr8:11830174 | C | T | 7 | a0001c0005t0001g0138 a0001c0005t0012g0040 a0001c0005t0012g0049 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-70C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830174 | |||||||
| chr8:11830190 | A | T | 1 | a0001c0003t0001g0375 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.703-54A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830190 | |||||||
| chr8:11830235 | T | C | 1 | a0001c0013t0002g0177 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.703-9T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 5/7 | chr8 | 11830235 | |||||||
| chr8:11830429 | G | C | 399 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(396): Show |
449 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(446): Show |
intron_variant | MODIFIER | c.879+9G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830429 | |||||||
| chr8:11830434 | C | A | 4 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(1): Show |
6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+14C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830434 | |||||||
| chr8:11830450 | C | T | 169 | a0001c0001t0001g0295 a0001c0001t0002g0057 a0001c0001t0002g0058 others(166): Show |
187 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.879+30C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830450 | |||||||
| chr8:11830464 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.879+44G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830464 | |||||||
| chr8:11830489 | T | G | 8 | a0001c0001t0001g0034 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
9 | HG01074.hp2 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.879+69T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830489 | |||||||
| chr8:11830546 | C | G | 15 | a0001c0001t0001g0295 a0001c0002t0003g0052 a0001c0002t0003g0053 others(12): Show |
15 | HG01928.hp2 HG01943.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.879+126C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830546 | |||||||
| chr8:11830564 | A | T | 1 | a0001c0008t0001g0134 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.879+144A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830564 | |||||||
| chr8:11830567 | C | T | 1 | a0001c0013t0002g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.879+147C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830567 | |||||||
| chr8:11830628 | A | T | 6 | a0001c0001t0002g0015 a0001c0005t0002g0070 a0001c0005t0002g0136 others(3): Show |
7 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+208A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830628 | |||||||
| chr8:11830639 | T | C | 315 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(312): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.879+219T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830639 | |||||||
| chr8:11830654 | C | A | 1 | a0002c0009t0002g0166 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.879+234C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830654 | |||||||
| chr8:11830795 | G | A | 30 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(27): Show |
43 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.879+375G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830795 | |||||||
| chr8:11830826 | C | T | 4 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(1): Show |
6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+406C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830826 | |||||||
| chr8:11830833 | G | T | 30 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(27): Show |
43 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.879+413G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830833 | |||||||
| chr8:11830884 | T | C | 4 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(1): Show |
6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+464T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830884 | |||||||
| chr8:11830953 | G | A | 1 | a0002c0009t0002g0005 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.879+533G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830953 | |||||||
| chr8:11830976 | A | C | 192 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(189): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.880-542A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11830976 | |||||||
| chr8:11831004 | C | G | 1 | a0001c0001t0001g0402 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.880-514C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831004 | |||||||
| chr8:11831098 | G | A | 4 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(1): Show |
6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-420G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831098 | |||||||
| chr8:11831110 | A | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0122 a0001c0001t0001g0123 others(3): Show |
7 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-408A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831110 | |||||||
| chr8:11831167 | C | G | 4 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(1): Show |
6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-351C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831167 | |||||||
| chr8:11831251 | T | G | 5 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(2): Show |
7 | HG02717.hp1 HG02723.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-267T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831251 | |||||||
| chr8:11831303 | C | G | 1 | a0001c0001t0002g0129 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.880-215C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831303 | |||||||
| chr8:11831322 | G | A | 8 | a0001c0002t0003g0225 a0001c0002t0003g0251 a0001c0002t0003g0276 others(5): Show |
8 | HG00423.hp2 HG02132.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-196G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831322 | |||||||
| chr8:11831378 | A | G | 2 | a0001c0003t0001g0082 a0001c0003t0001g0083 |
2 | NA18942.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.880-140A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831378 | |||||||
| chr8:11831451 | C | T | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.880-67C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | chr8 | 11831451 | |||||||
| chr8:11831499 | CTCT | C | 49 | a0001c0002t0001g0032 a0001c0002t0001g0056 a0001c0002t0001g0061 others(46): Show |
55 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.880-14_880-12delCT others(1): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 11831499 | ||||||
| chr8:11831712 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1032+42T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11831712 | |||||||
| chr8:11831719 | T | G | 319 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(316): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.1032+49T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11831719 | |||||||
| chr8:11831882 | G | C | 1 | a0001c0003t0001g0284 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1032+212G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11831882 | |||||||
| chr8:11832100 | A | G | 1 | a0001c0013t0002g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1032+430A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832100 | |||||||
| chr8:11832237 | C | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0122 a0001c0001t0001g0123 others(11): Show |
15 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1032+567C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832237 | |||||||
| chr8:11832249 | A | G | 38 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(35): Show |
51 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1032+579A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832249 | |||||||
| chr8:11832250 | CTAGGTT | C | 38 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(35): Show |
51 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1032+581_1032+586d others(8): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832250 | |||||||
| chr8:11832254 | G | A | 114 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(111): Show |
125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1032+584G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832254 | |||||||
| chr8:11832282 | C | T | 1 | a0001c0004t0002g0170 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1032+612C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832282 | |||||||
| chr8:11832363 | C | T | 13 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(10): Show |
13 | HG00544.hp2 HG00597.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.1032+693C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832363 | |||||||
| chr8:11832367 | C | T | 3 | a0001c0001t0001g0344 a0001c0001t0001g0345 a0001c0006t0001g0215 |
3 | NA18953.hp1 NA18957.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1032+697C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832367 | |||||||
| chr8:11832442 | C | G | 1 | a0001c0003t0001g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1032+772C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832442 | |||||||
| chr8:11832516 | C | T | 26 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(23): Show |
37 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1032+846C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832516 | |||||||
| chr8:11832535 | G | C | 2 | a0001c0002t0003g0184 a0001c0002t0015g0222 |
2 | HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1032+865G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832535 | |||||||
| chr8:11832551 | C | CAAAA | 8 | a0001c0003t0001g0050 a0001c0003t0001g0079 a0001c0003t0001g0092 others(5): Show |
8 | HG01891.hp1 HG02074.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1032+903_1032+906d others(6): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA | 11 | a0001c0001t0001g0037 a0001c0001t0002g0057 a0001c0001t0002g0058 others(8): Show |
12 | HG01358.hp2 HG01515.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1032+900_1032+906d others(9): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(1): Show |
35 | a0001c0001t0002g0051 a0001c0001t0002g0060 a0001c0001t0002g0101 others(32): Show |
37 | HG00558.hp1 HG00621.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1032+899_1032+906d others(10): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(2): Show |
31 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0109 others(28): Show |
34 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1032+898_1032+906d others(11): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(3): Show |
10 | a0001c0001t0002g0018 a0001c0001t0002g0112 a0001c0001t0002g0114 others(7): Show |
11 | HG00323.hp2 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1032+897_1032+906d others(12): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0377 a0001c0002t0001g0063 |
2 | HG00140.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1032+896_1032+906d others(13): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0002g0158 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1032+895_1032+906d others(14): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(6): Show |
4 | a0001c0001t0002g0015 a0001c0001t0002g0163 a0001c0005t0002g0136 others(1): Show |
5 | HG01168.hp2 HG01169.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+894_1032+906d others(15): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(7): Show |
6 | a0001c0001t0001g0292 a0001c0001t0001g0316 a0001c0001t0001g0364 others(3): Show |
7 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1032+893_1032+906d others(16): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(8): Show |
30 | a0001c0001t0001g0012 a0001c0001t0001g0301 a0001c0001t0001g0311 others(27): Show |
32 | HG00544.hp2 HG00621.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1032+892_1032+906d others(17): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(9): Show |
34 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0036 others(31): Show |
39 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.1032+891_1032+906d others(18): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(10): Show |
15 | a0001c0001t0001g0211 a0001c0001t0001g0282 a0001c0001t0001g0299 others(12): Show |
15 | HG01243.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1032+890_1032+906d others(19): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(11): Show |
6 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0357 others(3): Show |
6 | HG01515.hp2 HG01517.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1032+889_1032+906d others(20): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(12): Show |
5 | a0001c0001t0001g0212 a0001c0001t0001g0297 a0001c0001t0001g0359 others(2): Show |
7 | HG00438.hp1 HG00544.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.1032+888_1032+906d others(21): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(13): Show |
4 | a0001c0001t0001g0291 a0001c0001t0001g0337 a0001c0004t0001g0148 others(1): Show |
4 | HG00597.hp2 HG02258.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1032+887_1032+906d others(22): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0321 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1032+886_1032+906d others(23): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(15): Show |
5 | a0001c0001t0001g0207 a0001c0001t0001g0300 a0001c0001t0001g0306 others(2): Show |
5 | HG01978.hp1 HG02630.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+885_1032+906d others(24): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0003g0271 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1032+883_1032+906d others(26): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0338 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1032+882_1032+906d others(27): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | CAA | C | 7 | a0001c0001t0002g0129 a0001c0002t0003g0210 a0001c0002t0003g0228 others(4): Show |
7 | HG02572.hp1 NA18940.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1032+905_1032+906d others(4): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | CAAA | C | 120 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0077 others(117): Show |
137 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1032+904_1032+906d others(5): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | CAAAA | C | 7 | a0001c0001t0008g0047 a0001c0002t0003g0198 a0001c0002t0003g0242 others(4): Show |
7 | HG01943.hp1 NA18906.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.1032+903_1032+906d others(6): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832551 | CAAAAAAA others(3): Show |
C | 1 | a0003c0012t0001g0329 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1032+897_1032+906d others(12): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11832551 | ||||||
| chr8:11832576 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0362 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1032+906_1032+907i others(19): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832576 | |||||||
| chr8:11832576 | A | AT | 4 | a0001c0001t0002g0065 a0001c0001t0006g0380 a0001c0004t0002g0068 others(1): Show |
4 | HG01255.hp1 HG02738.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+906_1032+907i others(3): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832576 | |||||||
| chr8:11832576 | A | T | 30 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0067 others(27): Show |
41 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1032+906A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832576 | |||||||
| chr8:11832577 | G | T | 38 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(35): Show |
51 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1032+907G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832577 | |||||||
| chr8:11832579 | C | G | 2 | a0001c0013t0002g0180 a0006c0023t0017g0042 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1032+909C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832579 | |||||||
| chr8:11832583 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1032+913G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832583 | |||||||
| chr8:11832587 | C | T | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1032+917C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832587 | |||||||
| chr8:11832597 | T | C | 321 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(318): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1032+927T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832597 | |||||||
| chr8:11832617 | T | C | 3 | a0001c0014t0016g0143 a0001c0015t0002g0181 a0001c0017t0002g0041 |
3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1032+947T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832617 | |||||||
| chr8:11832621 | C | T | 3 | a0001c0014t0016g0143 a0001c0015t0002g0181 a0001c0017t0002g0041 |
3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1032+951C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832621 | |||||||
| chr8:11832661 | C | T | 61 | a0001c0001t0002g0101 a0001c0002t0001g0032 a0001c0002t0001g0056 others(58): Show |
67 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1032+991C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832661 | |||||||
| chr8:11832668 | C | A | 1 | a0001c0003t0001g0106 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1032+998C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832668 | |||||||
| chr8:11832668 | C | G | 1 | a0001c0001t0003g0271 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1032+998C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832668 | |||||||
| chr8:11832671 | A | T | 2 | a0001c0001t0008g0044 a0001c0001t0008g0048 |
2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1032+1001A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832671 | |||||||
| chr8:11832724 | C | T | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1032+1054C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832724 | |||||||
| chr8:11832725 | G | A | 4 | a0001c0001t0002g0013 a0001c0001t0002g0159 a0001c0001t0002g0367 others(1): Show |
6 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1032+1055G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832725 | |||||||
| chr8:11832786 | C | A | 1 | a0001c0001t0001g0341 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1032+1116C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832786 | |||||||
| chr8:11832862 | T | C | 2 | a0001c0002t0001g0221 a0001c0002t0001g0237 |
2 | HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1032+1192T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832862 | |||||||
| chr8:11832883 | C | G | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1032+1213C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832883 | |||||||
| chr8:11832894 | G | A | 38 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(35): Show |
51 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1032+1224G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832894 | |||||||
| chr8:11832907 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1032+1237C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832907 | |||||||
| chr8:11832913 | G | A | 150 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(147): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1032+1243G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832913 | |||||||
| chr8:11832919 | C | G | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1032+1249C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832919 | |||||||
| chr8:11832955 | C | A | 1 | a0001c0002t0003g0259 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1032+1285C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11832955 | |||||||
| chr8:11833007 | A | T | 1 | a0001c0002t0001g0268 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1032+1337A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833007 | |||||||
| chr8:11833010 | C | G | 5 | a0001c0001t0008g0044 a0001c0001t0008g0047 a0001c0001t0008g0048 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+1340C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833010 | |||||||
| chr8:11833010 | C | T | 1 | a0001c0004t0006g0142 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1032+1340C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833010 | |||||||
| chr8:11833013 | C | A | 1 | a0001c0002t0004g0072 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1032+1343C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833013 | |||||||
| chr8:11833025 | C | T | 8 | a0001c0001t0006g0380 a0001c0004t0006g0142 a0001c0004t0006g0144 others(5): Show |
8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1032+1355C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833025 | |||||||
| chr8:11833048 | A | T | 1 | a0001c0001t0001g0393 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1032+1378A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833048 | |||||||
| chr8:11833164 | C | T | 1 | a0001c0002t0001g0363 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1032+1494C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833164 | |||||||
| chr8:11833165 | C | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0118 |
2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1032+1495C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833165 | |||||||
| chr8:11833291 | C | A | 1 | a0001c0002t0003g0226 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1032+1621C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833291 | |||||||
| chr8:11833361 | C | G | 7 | a0001c0001t0002g0015 a0001c0005t0002g0070 a0001c0005t0002g0136 others(4): Show |
8 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1032+1691C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833361 | |||||||
| chr8:11833367 | G | C | 1 | a0001c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1032+1697G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833367 | |||||||
| chr8:11833406 | A | G | 37 | a0001c0001t0001g0078 a0001c0001t0002g0018 a0001c0001t0002g0051 others(34): Show |
41 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1032+1736A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833406 | |||||||
| chr8:11833432 | C | G | 2 | a0001c0004t0002g0130 a0001c0004t0002g0131 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1032+1762C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833432 | |||||||
| chr8:11833504 | A | T | 9 | a0001c0001t0006g0380 a0001c0004t0006g0142 a0001c0004t0006g0144 others(6): Show |
9 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1032+1834A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833504 | |||||||
| chr8:11833517 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1032+1847T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833517 | |||||||
| chr8:11833615 | G | A | 1 | a0001c0004t0001g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1032+1945G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833615 | |||||||
| chr8:11833633 | G | T | 116 | a0001c0001t0001g0019 a0001c0001t0001g0078 a0001c0001t0001g0122 others(113): Show |
131 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.1032+1963G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833633 | |||||||
| chr8:11833636 | G | A | 2 | a0001c0001t0002g0117 a0001c0001t0002g0350 |
2 | HG01358.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1032+1966G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833636 | |||||||
| chr8:11833694 | C | G | 4 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(1): Show |
6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1032+2024C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833694 | |||||||
| chr8:11833696 | T | A | 403 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(400): Show |
453 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(450): Show |
intron_variant | MODIFIER | c.1032+2026T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833696 | |||||||
| chr8:11833801 | T | G | 289 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(286): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1032+2131T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833801 | |||||||
| chr8:11833821 | T | C | 395 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(392): Show |
445 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(442): Show |
intron_variant | MODIFIER | c.1032+2151T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833821 | |||||||
| chr8:11833866 | G | A | 1 | a0001c0014t0016g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1032+2196G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833866 | |||||||
| chr8:11833884 | C | T | 63 | a0001c0001t0002g0101 a0001c0002t0001g0032 a0001c0002t0001g0056 others(60): Show |
69 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1032+2214C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11833884 | |||||||
| chr8:11834116 | C | T | 6 | a0001c0001t0002g0015 a0001c0005t0002g0136 a0001c0005t0002g0137 others(3): Show |
7 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1032+2446C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834116 | |||||||
| chr8:11834129 | C | G | 1 | a0001c0001t0001g0306 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1032+2459C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834129 | |||||||
| chr8:11834165 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1032+2495T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834165 | |||||||
| chr8:11834322 | C | G | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1032+2652C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834322 | |||||||
| chr8:11834430 | T | G | 194 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0077 others(191): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1032+2760T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834430 | |||||||
| chr8:11834489 | C | T | 3 | a0001c0014t0016g0143 a0001c0015t0002g0181 a0001c0017t0002g0041 |
3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1032+2819C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834489 | |||||||
| chr8:11834589 | C | CA | 63 | a0001c0001t0002g0101 a0001c0002t0001g0032 a0001c0002t0001g0056 others(60): Show |
69 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1032+2922dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11834589 | ||||||
| chr8:11834594 | G | C | 398 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(395): Show |
448 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(445): Show |
intron_variant | MODIFIER | c.1032+2924G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834594 | |||||||
| chr8:11834598 | C | G | 1 | a0001c0001t0001g0394 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1032+2928C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834598 | |||||||
| chr8:11834619 | T | C | 126 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(123): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1032+2949T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834619 | |||||||
| chr8:11834831 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1032+3161T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834831 | |||||||
| chr8:11834898 | C | T | 25 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(22): Show |
36 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1032+3228C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834898 | |||||||
| chr8:11834952 | T | A | 5 | a0001c0001t0002g0101 a0001c0002t0002g0274 a0001c0003t0002g0161 others(2): Show |
5 | HG02809.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+3282T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834952 | |||||||
| chr8:11834972 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1032+3302C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11834972 | |||||||
| chr8:11835060 | G | T | 180 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0034 others(177): Show |
197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1033-3328G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835060 | |||||||
| chr8:11835070 | G | C | 5 | a0001c0005t0001g0138 a0001c0008t0001g0134 a0001c0008t0001g0155 others(2): Show |
5 | HG01891.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1033-3318G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835070 | |||||||
| chr8:11835112 | A | T | 1 | a0001c0002t0001g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1033-3276A>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835112 | |||||||
| chr8:11835129 | C | T | 33 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0051 others(30): Show |
36 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1033-3259C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835129 | |||||||
| chr8:11835157 | C | T | 1 | a0001c0014t0016g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1033-3231C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835157 | |||||||
| chr8:11835206 | T | C | 7 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0094 others(4): Show |
7 | NA18939.hp2 NA18943.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1033-3182T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835206 | |||||||
| chr8:11835314 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1033-3074C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835314 | |||||||
| chr8:11835315 | G | A | 5 | a0001c0001t0002g0101 a0001c0002t0002g0274 a0001c0003t0002g0161 others(2): Show |
5 | HG02809.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1033-3073G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835315 | |||||||
| chr8:11835322 | C | G | 4 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(1): Show |
6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033-3066C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835322 | |||||||
| chr8:11835332 | C | T | 107 | a0001c0001t0003g0010 a0001c0001t0003g0271 a0001c0001t0004g0257 others(104): Show |
121 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1033-3056C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835332 | |||||||
| chr8:11835345 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1033-3043C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835345 | |||||||
| chr8:11835362 | A | G | 1 | a0001c0002t0003g0265 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1033-3026A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835362 | |||||||
| chr8:11835371 | C | T | 1 | a0001c0006t0001g0383 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1033-3017C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835371 | |||||||
| chr8:11835393 | C | G | 1 | a0001c0001t0011g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1033-2995C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835393 | |||||||
| chr8:11835413 | C | T | 1 | a0001c0002t0003g0366 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1033-2975C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835413 | |||||||
| chr8:11835468 | T | G | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1033-2920T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835468 | |||||||
| chr8:11835472 | G | A | 1 | a0001c0002t0003g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1033-2916G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835472 | |||||||
| chr8:11835539 | A | G | 59 | a0001c0002t0001g0032 a0001c0002t0001g0056 a0001c0002t0001g0061 others(56): Show |
65 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1033-2849A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835539 | |||||||
| chr8:11835624 | C | G | 1 | a0001c0003t0003g0286 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1033-2764C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835624 | |||||||
| chr8:11835670 | C | A | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1033-2718C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835670 | |||||||
| chr8:11835715 | A | G | 7 | a0001c0005t0001g0138 a0001c0005t0012g0040 a0001c0005t0012g0049 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1033-2673A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835715 | |||||||
| chr8:11835869 | G | T | 346 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(343): Show |
393 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(390): Show |
intron_variant | MODIFIER | c.1033-2519G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835869 | |||||||
| chr8:11835870 | A | C | 8 | a0001c0001t0002g0015 a0001c0005t0002g0023 a0001c0005t0002g0070 others(5): Show |
10 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1033-2518A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835870 | |||||||
| chr8:11835877 | T | C | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1033-2511T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835877 | |||||||
| chr8:11835897 | G | A | 25 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(22): Show |
36 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1033-2491G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835897 | |||||||
| chr8:11835930 | G | T | 397 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(394): Show |
447 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(444): Show |
intron_variant | MODIFIER | c.1033-2458G>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835930 | |||||||
| chr8:11835932 | G | A | 1 | a0001c0002t0003g0203 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1033-2456G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835932 | |||||||
| chr8:11835946 | T | A | 1 | a0001c0013t0002g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1033-2442T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835946 | |||||||
| chr8:11835948 | A | C | 1 | a0001c0003t0001g0288 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1033-2440A>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11835948 | |||||||
| chr8:11835971 | T | TAAAA | 8 | a0001c0001t0001g0281 a0001c0001t0001g0304 a0001c0001t0001g0310 others(5): Show |
8 | HG01257.hp1 HG01358.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1033-2396_1033-239 others(8): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | T | TAAAAA | 128 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0034 others(125): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1033-2397_1033-239 others(9): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | T | TAAAAAA | 126 | a0001c0001t0001g0011 a0001c0001t0001g0074 a0001c0001t0001g0122 others(123): Show |
138 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1033-2398_1033-239 others(10): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | T | TAAAAAAA | 31 | a0001c0001t0001g0211 a0001c0001t0001g0315 a0001c0001t0001g0325 others(28): Show |
35 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1033-2399_1033-239 others(11): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | T | TAAAAAAA others(1): Show |
8 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(5): Show |
8 | HG01358.hp1 HG02071.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.1033-2400_1033-239 others(12): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | T | TAAAAAAA others(3): Show |
5 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0094 others(2): Show |
5 | NA18939.hp2 NA18943.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1033-2402_1033-239 others(14): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | T | TAAAAAAA others(4): Show |
3 | a0001c0001t0002g0060 a0001c0001t0002g0160 a0008c0020t0002g0059 |
3 | HG00639.hp2 HG02738.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1033-2403_1033-239 others(15): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | T | TAAAAAAA others(5): Show |
11 | a0001c0001t0002g0109 a0001c0001t0002g0111 a0001c0001t0002g0116 others(8): Show |
11 | HG00323.hp2 HG00738.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1033-2404_1033-239 others(16): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | T | TAAAAAAA others(6): Show |
6 | a0001c0001t0002g0018 a0001c0001t0002g0107 a0001c0001t0002g0108 others(3): Show |
7 | HG00099.hp1 HG01106.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033-2405_1033-239 others(17): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | T | TAAAAAAA others(7): Show |
1 | a0001c0001t0002g0051 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1033-2406_1033-239 others(18): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | T | TAAAAAAA others(9): Show |
3 | a0001c0001t0002g0159 a0001c0001t0002g0367 a0001c0004t0002g0135 |
3 | HG02258.hp1 HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1033-2408_1033-239 others(20): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | T | TAAAAAAA others(10): Show |
1 | a0001c0001t0002g0112 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1033-2409_1033-239 others(21): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | T | TAAAAAAA others(11): Show |
1 | a0001c0001t0002g0013 | 3 | HG02922.hp1 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1033-2410_1033-239 others(22): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | TA | T | 8 | a0001c0001t0001g0305 a0001c0001t0010g0043 a0001c0004t0002g0021 others(5): Show |
10 | HG02040.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1033-2393delA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11835971 | TAAAAAAA others(2): Show |
T | 34 | a0001c0001t0002g0015 a0001c0001t0002g0064 a0001c0001t0002g0065 others(31): Show |
47 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1033-2401_1033-239 others(13): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11835971 | ||||||
| chr8:11836039 | C | G | 398 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(395): Show |
448 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(445): Show |
intron_variant | MODIFIER | c.1033-2349C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836039 | |||||||
| chr8:11836068 | G | A | 29 | a0001c0001t0002g0018 a0001c0001t0002g0051 a0001c0001t0002g0057 others(26): Show |
30 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1033-2320G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836068 | |||||||
| chr8:11836112 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1033-2276C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836112 | |||||||
| chr8:11836121 | C | G | 1 | a0001c0021t0001g0073 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1033-2267C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836121 | |||||||
| chr8:11836139 | C | A | 1 | a0001c0001t0002g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1033-2249C>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836139 | |||||||
| chr8:11836148 | A | G | 2 | a0001c0001t0001g0126 a0001c0004t0001g0154 |
2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1033-2240A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836148 | |||||||
| chr8:11836149 | T | A | 1 | a0001c0002t0003g0252 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1033-2239T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836149 | |||||||
| chr8:11836150 | C | G | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1033-2238C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836150 | |||||||
| chr8:11836152 | T | TA | 216 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(213): Show |
245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1033-2221dupA | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11836152 | ||||||
| chr8:11836152 | T | TAA | 11 | a0001c0001t0001g0311 a0001c0001t0002g0064 a0001c0001t0002g0065 others(8): Show |
11 | HG02738.hp1 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1033-2222_1033-222 others(6): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11836152 | ||||||
| chr8:11836152 | T | TAAA | 40 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0051 others(37): Show |
45 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1033-2223_1033-222 others(7): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11836152 | ||||||
| chr8:11836171 | A | G | 1 | a0001c0002t0001g0363 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1033-2217A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836171 | |||||||
| chr8:11836196 | C | T | 2 | a0001c0003t0003g0020 a0001c0003t0003g0102 |
3 | NA18968.hp1 NA18971.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1033-2192C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836196 | |||||||
| chr8:11836234 | ATTTTATG others(4): Show |
A | 2 | a0001c0001t0010g0043 a0001c0004t0010g0179 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1033-2151_1033-214 others(15): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11836234 | ||||||
| chr8:11836261 | C | T | 3 | a0001c0001t0001g0126 a0001c0004t0001g0154 a0001c0005t0001g0125 |
3 | HG02559.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1033-2127C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836261 | |||||||
| chr8:11836333 | T | G | 3 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1033-2055T>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836333 | |||||||
| chr8:11836410 | T | C | 191 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(188): Show |
207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1033-1978T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836410 | |||||||
| chr8:11836437 | C | T | 1 | a0001c0002t0015g0222 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1033-1951C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836437 | |||||||
| chr8:11836469 | G | C | 1 | a0001c0028t0002g0373 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1033-1919G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836469 | |||||||
| chr8:11836485 | C | T | 5 | a0001c0001t0002g0101 a0001c0002t0002g0274 a0001c0003t0002g0161 others(2): Show |
5 | HG02809.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1033-1903C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836485 | |||||||
| chr8:11836587 | C | T | 1 | a0001c0006t0005g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1033-1801C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836587 | |||||||
| chr8:11836790 | C | G | 3 | a0001c0001t0001g0326 a0001c0001t0001g0328 a0001c0001t0001g0334 |
3 | HG00738.hp2 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1033-1598C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836790 | |||||||
| chr8:11836855 | G | A | 7 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0094 others(4): Show |
7 | NA18939.hp2 NA18943.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1033-1533G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836855 | |||||||
| chr8:11836903 | C | G | 1 | a0001c0003t0002g0161 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1033-1485C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836903 | |||||||
| chr8:11836961 | C | T | 1 | a0001c0002t0003g0254 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1033-1427C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11836961 | |||||||
| chr8:11837095 | G | C | 112 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 others(109): Show |
128 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1033-1293G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837095 | |||||||
| chr8:11837132 | C | T | 8 | a0001c0001t0006g0380 a0001c0004t0006g0142 a0001c0004t0006g0144 others(5): Show |
8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1033-1256C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837132 | |||||||
| chr8:11837141 | C | T | 13 | a0001c0001t0002g0018 a0001c0001t0002g0108 a0001c0001t0002g0109 others(10): Show |
14 | HG00099.hp1 HG00738.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1033-1247C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837141 | |||||||
| chr8:11837209 | C | T | 3 | a0001c0014t0016g0143 a0001c0015t0002g0181 a0001c0017t0002g0041 |
3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1033-1179C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837209 | |||||||
| chr8:11837231 | T | A | 10 | a0001c0001t0002g0158 a0001c0001t0002g0162 a0001c0001t0002g0163 others(7): Show |
10 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1033-1157T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837231 | |||||||
| chr8:11837234 | TTTTG | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0122 a0001c0001t0001g0123 others(7): Show |
11 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1033-1146_1033-114 others(8): Show |
FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11837234 | ||||||
| chr8:11837242 | GT | G | 3 | a0001c0014t0016g0143 a0001c0015t0002g0181 a0001c0017t0002g0041 |
3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1033-1140delT | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 11837242 | ||||||
| chr8:11837256 | G | C | 32 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0051 others(29): Show |
35 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1033-1132G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837256 | |||||||
| chr8:11837358 | T | A | 1 | a0001c0001t0001g0338 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1033-1030T>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837358 | |||||||
| chr8:11837382 | C | T | 2 | a0001c0003t0002g0403 a0001c0003t0013g0404 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1033-1006C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837382 | |||||||
| chr8:11837411 | T | C | 1 | a0001c0002t0003g0366 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1033-977T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837411 | |||||||
| chr8:11837455 | C | T | 1 | a0001c0002t0003g0258 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1033-933C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837455 | |||||||
| chr8:11837463 | C | G | 7 | a0001c0005t0001g0138 a0001c0005t0012g0040 a0001c0005t0012g0049 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1033-925C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837463 | |||||||
| chr8:11837477 | G | A | 22 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0107 others(19): Show |
25 | HG00099.hp1 HG00639.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1033-911G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837477 | |||||||
| chr8:11837490 | C | T | 1 | a0007c0019t0001g0335 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1033-898C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837490 | |||||||
| chr8:11837526 | C | G | 2 | a0001c0001t0001g0395 a0001c0001t0001g0396 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1033-862C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837526 | |||||||
| chr8:11837551 | G | A | 32 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0051 others(29): Show |
35 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1033-837G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837551 | |||||||
| chr8:11837622 | C | T | 1 | a0002c0009t0002g0166 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1033-766C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837622 | |||||||
| chr8:11837652 | T | C | 3 | a0001c0014t0016g0143 a0001c0015t0002g0181 a0001c0017t0002g0041 |
3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1033-736T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837652 | |||||||
| chr8:11837874 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1033-514G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837874 | |||||||
| chr8:11837903 | C | G | 4 | a0001c0004t0002g0021 a0001c0004t0002g0022 a0001c0004t0002g0130 others(1): Show |
6 | HG02717.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033-485C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837903 | |||||||
| chr8:11837925 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1033-463C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837925 | |||||||
| chr8:11837994 | G | A | 1 | a0002c0009t0002g0166 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1033-394G>A | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11837994 | |||||||
| chr8:11838046 | G | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0182 |
3 | HG02970.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1033-342G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838046 | |||||||
| chr8:11838110 | C | T | 1 | a0001c0001t0010g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1033-278C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838110 | |||||||
| chr8:11838124 | C | T | 1 | a0001c0001t0010g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1033-264C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838124 | |||||||
| chr8:11838134 | G | C | 1 | a0001c0001t0006g0380 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1033-254G>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838134 | |||||||
| chr8:11838140 | C | T | 1 | a0001c0004t0002g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1033-248C>T | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838140 | |||||||
| chr8:11838154 | T | C | 2 | a0001c0004t0002g0130 a0001c0004t0002g0131 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1033-234T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838154 | |||||||
| chr8:11838191 | C | G | 3 | a0001c0014t0016g0143 a0001c0015t0002g0181 a0001c0017t0002g0041 |
3 | HG02886.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1033-197C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838191 | |||||||
| chr8:11838222 | C | G | 8 | a0001c0001t0006g0380 a0001c0004t0006g0142 a0001c0004t0006g0144 others(5): Show |
8 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1033-166C>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838222 | |||||||
| chr8:11838225 | A | G | 1 | a0001c0002t0001g0363 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1033-163A>G | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838225 | |||||||
| chr8:11838226 | T | C | 7 | a0001c0002t0003g0184 a0001c0002t0003g0203 a0001c0002t0003g0218 others(4): Show |
7 | HG00735.hp2 HG01070.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033-162T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838226 | |||||||
| chr8:11838363 | T | C | 308 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(305): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1033-25T>C | FDFT1 | ENSG00000079459.14 | transcript | ENST00000220584.9 | protein_coding | 7/7 | chr8 | 11838363 |