Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2260 |
| ensemblid | ENSG00000077782.23 |
| hgncid | 3688 |
| symbol | FGFR1 |
| name | fibroblast growth factor receptor 1 |
| refseq_nuc | NM_023110.3 |
| refseq_prot | NP_075598.2 |
| ensembl_nuc | ENST00000447712.7 |
| ensembl_prot | ENSP00000400162.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 38411143 |
| end | 38468635 |
| strand | - |
| ver | v1.2 |
| region | chr8:38411143-38468635 |
| region5000 | chr8:38406143-38473635 |
| regionname0 | FGFR1_chr8_38411143_38468635 |
| regionname5000 | FGFR1_chr8_38406143_38473635 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 822 | 323 | 63 | 63 | 147 | 14 | 34 | 106 | FGFR1_chr8_38406143_38473635 | FGFR1 | MWSWK others(817): Show |
chr8 | 38406143 | 38473635 |
| a0002 | 0/0 | 822 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | MWSWK others(817): Show |
chr8 | 38406143 | 38473635 |
| a0003 | 0/0 | 822 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | FGFR1_chr8_38406143_38473635 | FGFR1 | MWSWK others(817): Show |
chr8 | 38406143 | 38473635 |
| a0004 | 0/0 | 822 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | MWSWK others(817): Show |
chr8 | 38406143 | 38473635 |
| a0005 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | MWSWK others(817): Show |
chr8 | 38406143 | 38473635 |
| a0006 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | MWSWK others(817): Show |
chr8 | 38406143 | 38473635 |
| a0007 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | MWSWK others(817): Show |
chr8 | 38406143 | 38473635 |
| a0008 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | MWSWK others(817): Show |
chr8 | 38406143 | 38473635 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2466 | 316 | 61 | 60 | 146 | 14 | 33 | FGFR1_chr8_38406143_38473635 | FGFR1 | ATGTG others(2461): Show |
chr8 | 38406143 | 38473635 | ||
| a0001c0003 | 0/0 | 2466 | 3 | 0 | 3 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | ATGTG others(2461): Show |
chr8 | 38406143 | 38473635 | ||
| a0001c0008 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | ATGTG others(2461): Show |
chr8 | 38406143 | 38473635 | ||
| a0001c0009 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | ATGTG others(2461): Show |
chr8 | 38406143 | 38473635 | ||
| a0001c0011 | 0/0 | 2466 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | ATGTG others(2461): Show |
chr8 | 38406143 | 38473635 | ||
| a0001c0012 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | ATGTG others(2461): Show |
chr8 | 38406143 | 38473635 | ||
| a0002c0002 | 0/0 | 2466 | 4 | 3 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | ATGTG others(2461): Show |
chr8 | 38406143 | 38473635 | ||
| a0003c0004 | 0/0 | 2466 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | ATGTG others(2461): Show |
chr8 | 38406143 | 38473635 | ||
| a0004c0005 | 0/0 | 2466 | 2 | 0 | 0 | 0 | 0 | 2 | FGFR1_chr8_38406143_38473635 | FGFR1 | ATGTG others(2461): Show |
chr8 | 38406143 | 38473635 | ||
| a0005c0010 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | ATGTG others(2461): Show |
chr8 | 38406143 | 38473635 | ||
| a0006c0007 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | ATGTG others(2461): Show |
chr8 | 38406143 | 38473635 | ||
| a0007c0006 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | ATGTG others(2461): Show |
chr8 | 38406143 | 38473635 | ||
| a0008c0013 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | ATGTG others(2461): Show |
chr8 | 38406143 | 38473635 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5697 | 105 | 22 | 19 | 47 | 2 | 14 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0002 | 0/1 | 5697 | 83 | 9 | 14 | 40 | 5 | 14 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0003 | 0/0 | 5697 | 69 | 4 | 13 | 44 | 6 | 2 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0004 | 0/0 | 5697 | 19 | 3 | 7 | 8 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0005 | 0/0 | 5697 | 14 | 14 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0006 | 0/0 | 5697 | 3 | 0 | 3 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0007 | 0/0 | 5697 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0008 | 0/0 | 5697 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0009 | 0/0 | 5697 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0010 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0011 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0012 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0014 | 0/0 | 5697 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0015 | 0/0 | 5697 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0016 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0017 | 0/0 | 5697 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0018 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0019 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0021 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0022 | 0/0 | 5697 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0023 | 0/0 | 5697 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0024 | 0/0 | 5697 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0025 | 0/0 | 5697 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0026 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0027 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0001t0028 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0003t0001 | 0/0 | 5697 | 3 | 0 | 3 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0008t0002 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0009t0013 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0011t0001 | 0/0 | 5697 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0001c0012t0020 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0002c0002t0001 | 0/0 | 5697 | 4 | 3 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0003c0004t0003 | 0/0 | 5697 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0004c0005t0002 | 0/0 | 5697 | 2 | 0 | 0 | 0 | 0 | 2 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0005c0010t0002 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0006c0007t0003 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0007c0006t0003 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| a0008c0013t0003 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | GCATA others(5692): Show |
chr8 | 38406143 | 38473635 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0010 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0292 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0007g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0009g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0009g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0010g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0011g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0012g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0014g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0015g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0016g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0017g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0018g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0019g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0021g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0022g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0023g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0024g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0025g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0026g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0027g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0001t0028g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0008t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0009t0013g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0011t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0001c0012t0020g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0003c0004t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0003c0004t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0003c0004t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0004c0005t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0004c0005t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0005c0010t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0006c0007t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0007c0006t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| a0008c0013t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0161 | EUR | GBR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0299 | EUR | GBR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0171 | EUR | GBR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0307 | EUR | GBR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0271 | EUR | FIN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0164 | EUR | FIN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0172 | EUR | FIN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00408 | hp1 | a0001 | c0001 | t0007 | g0165 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00609 | hp1 | a0001 | c0001 | t0007 | g0192 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0197 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00735 | hp1 | a0001 | c0001 | t0023 | g0257 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0250 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01074 | hp1 | a0001 | c0001 | t0022 | g0207 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0105 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0245 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0251 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0204 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0196 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0277 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0264 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0263 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0265 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0195 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0290 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0175 | EUR | IBS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0233 | EUR | IBS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0173 | EUR | IBS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0270 | EUR | IBS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0168 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01943 | hp2 | a0001 | c0001 | t0014 | g0007 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0051 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0036 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0169 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0324 | AFR | ACB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02071 | hp2 | a0005 | c0010 | t0002 | g0304 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | CDX | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | CDX | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | CDX | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | CDX | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | ACB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02572 | hp1 | a0001 | c0001 | t0019 | g0103 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0326 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0328 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0005 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02735 | hp2 | a0001 | c0001 | t0015 | g0087 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02818 | hp2 | a0001 | c0012 | t0020 | g0206 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0332 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0325 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0319 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0327 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0057 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0323 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0321 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0004 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0320 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0331 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0200 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0055 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03654 | hp2 | a0001 | c0011 | t0001 | g0059 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | STU | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0269 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03834 | hp1 | a0001 | c0001 | t0017 | g0098 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03834 | hp2 | a0004 | c0005 | t0002 | g0311 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0309 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03942 | hp2 | a0004 | c0005 | t0002 | g0278 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | STU | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | STU | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | STU | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0298 | AFR | YRI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0333 | AFR | YRI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | CHB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | CHB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18747 | hp2 | a0001 | c0001 | t0018 | g0137 | EAS | CHB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18906 | hp2 | a0001 | c0001 | t0016 | g0064 | AFR | YRI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18941 | hp2 | a0003 | c0004 | t0003 | g0162 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18942 | hp2 | a0001 | c0001 | t0021 | g0289 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18943 | hp2 | a0003 | c0004 | t0003 | g0121 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18956 | hp1 | a0001 | c0001 | t0009 | g0066 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18965 | hp1 | a0006 | c0007 | t0003 | g0177 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18975 | hp1 | a0001 | c0001 | t0009 | g0145 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18995 | hp2 | a0003 | c0004 | t0003 | g0156 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19002 | hp1 | a0001 | c0008 | t0002 | g0276 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19010 | hp2 | a0007 | c0006 | t0003 | g0030 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19030 | hp1 | a0001 | c0001 | t0027 | g0330 | AFR | LWK | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19074 | hp1 | a0008 | c0013 | t0003 | g0180 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19090 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0315 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0322 | AFR | YRI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ASW | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | ASW | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA20752 | hp1 | a0001 | c0001 | t0024 | g0317 | EUR | TSI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0262 | SAS | GIH | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0268 | SAS | GIH | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG01123 | hp2 | a0001 | c0001 | t0025 | g0316 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG03471 | hp2 | a0001 | c0001 | t0028 | g0318 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0329 | AFR | USA | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | USA | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA21309 | hp1 | a0001 | c0009 | t0013 | g0006 | AFR | LWK | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| NA21309 | hp2 | a0001 | c0001 | t0026 | g0334 | AFR | LWK | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0292 | REF | REF | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0010 | REF | REF | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38413783 | G | A | 1 | a0002 | 4 | HG01167.hp2 HG03139.hp1 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.2314C>T | p.Pro772Ser | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 3057/5697 | 2314/2469 | 772/822 | chr8 | 38413783 | |||
| chr8:38414019 | T | C | 1 | a0005 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.2191A>G | p.Met731Val | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 17/18 | 2934/5697 | 2191/2469 | 731/822 | chr8 | 38414019 | |||
| chr8:38429720 | G | A | 1 | a0003 | 3 | NA18941.hp2 NA18943.hp2 NA18995.hp2 |
missense_variant | MODERATE | c.320C>T | p.Ser107Leu | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/18 | 1063/5697 | 320/2469 | 107/822 | chr8 | 38429720 | |||
| chr8:38429736 | C | T | 1 | a0006 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.304G>A | p.Val102Ile | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/18 | 1047/5697 | 304/2469 | 102/822 | chr8 | 38429736 | |||
| chr8:38429864 | T | A | 1 | a0008 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.176A>T | p.Asp59Val | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/18 | 919/5697 | 176/2469 | 59/822 | chr8 | 38429864 | |||
| chr8:38429879 | C | T | 1 | a0007 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.161G>A | p.Arg54His | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/18 | 904/5697 | 161/2469 | 54/822 | chr8 | 38429879 | |||
| chr8:38457381 | C | G | 1 | a0004 | 2 | HG03834.hp2 HG03942.hp2 |
missense_variant | MODERATE | c.66G>C | p.Arg22Ser | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/18 | 809/5697 | 66/2469 | 22/822 | chr8 | 38457381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38413948 | C | T | 1 | a0001c0003 | 3 | HG00642.hp1 HG01175.hp2 HG01261.hp2 |
synonymous_variant | LOW | c.2262G>A | p.Leu754Leu | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 17/18 | 3005/5697 | 2262/2469 | 754/822 | chr8 | 38413948 | |||
| chr8:38419719 | C | T | 1 | a0001c0009 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1098G>A | p.Pro366Pro | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/18 | 1841/5697 | 1098/2469 | 366/822 | chr8 | 38419719 | |||
| chr8:38427942 | G | A | 1 | a0001c0011 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.600C>T | p.Asp200Asp | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/18 | 1343/5697 | 600/2469 | 200/822 | chr8 | 38427942 | |||
| chr8:38429704 | G | A | 1 | a0001c0012 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.336C>T | p.Thr112Thr | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/18 | 1079/5697 | 336/2469 | 112/822 | chr8 | 38429704 | |||
| chr8:38429719 | C | T | 1 | a0001c0008 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.321G>A | p.Ser107Ser | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/18 | 1064/5697 | 321/2469 | 107/822 | chr8 | 38429719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38411287 | T | G | 1 | a0001c0001t0027 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2341A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 2341 | chr8 | 38411287 | ||||||
| chr8:38411410 | A | T | 1 | a0001c0001t0008 | 2 | HG02976.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2218T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 2218 | chr8 | 38411410 | ||||||
| chr8:38411440 | A | G | 1 | a0001c0001t0016 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2188T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 2188 | chr8 | 38411440 | ||||||
| chr8:38411529 | A | C | 1 | a0001c0001t0006 | 3 | HG01928.hp1 HG01952.hp2 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2099T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 2099 | chr8 | 38411529 | ||||||
| chr8:38411646 | T | G | 1 | a0001c0001t0017 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1982A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1982 | chr8 | 38411646 | ||||||
| chr8:38411729 | G | C | 1 | a0001c0001t0019 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1899C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1899 | chr8 | 38411729 | ||||||
| chr8:38411800 | C | T | 1 | a0001c0001t0018 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1828G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1828 | chr8 | 38411800 | ||||||
| chr8:38411996 | T | C | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(15): Show |
107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1632A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1632 | chr8 | 38411996 | ||||||
| chr8:38412134 | C | T | 1 | a0001c0001t0015 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1494G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1494 | chr8 | 38412134 | ||||||
| chr8:38412204 | C | T | 1 | a0001c0009t0013 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1424G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1424 | chr8 | 38412204 | ||||||
| chr8:38412267 | C | G | 1 | a0001c0001t0012 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1361G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1361 | chr8 | 38412267 | ||||||
| chr8:38412301 | C | T | 1 | a0001c0001t0007 | 2 | HG00408.hp1 HG00609.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1327G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1327 | chr8 | 38412301 | ||||||
| chr8:38412576 | G | A | 1 | a0001c0001t0009 | 2 | NA18956.hp1 NA18975.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1052C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1052 | chr8 | 38412576 | ||||||
| chr8:38412602 | A | G | 1 | a0001c0001t0022 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1026T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1026 | chr8 | 38412602 | ||||||
| chr8:38413008 | G | A | 1 | a0001c0001t0023 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*620C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 620 | chr8 | 38413008 | ||||||
| chr8:38413059 | G | A | 1 | a0001c0001t0028 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*569C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 569 | chr8 | 38413059 | ||||||
| chr8:38413408 | A | G | 1 | a0001c0001t0021 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*220T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 220 | chr8 | 38413408 | ||||||
| chr8:38468016 | C | T | 1 | a0001c0001t0014 | 1 | HG01943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-124G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 10570 | chr8 | 38468016 | ||||||
| chr8:38468140 | C | T | 1 | a0001c0009t0013 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-248G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 10694 | chr8 | 38468140 | ||||||
| chr8:38468230 | A | C | 1 | a0001c0001t0012 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-338T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 10784 | chr8 | 38468230 | ||||||
| chr8:38468249 | T | C | 1 | a0001c0012t0020 | 1 | HG02818.hp2 | 5_prime_UTR_variant | MODIFIER | c.-357A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 10803 | chr8 | 38468249 | ||||||
| chr8:38468250 | G | A | 2 | a0001c0001t0024 a0001c0001t0025 |
2 | HG01123.hp2 NA20752.hp1 |
5_prime_UTR_variant | MODIFIER | c.-358C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 10804 | chr8 | 38468250 | ||||||
| chr8:38468277 | C | T | 5 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0026 others(2): Show |
18 | HG02055.hp1 HG02630.hp1 HG02647.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-385G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 10831 | chr8 | 38468277 | ||||||
| chr8:38468528 | G | A | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0021 others(7): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-636C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | chr8 | 38468528 | |||||||
| chr8:38468591 | G | A | 4 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(1): Show |
17 | HG02055.hp1 HG02630.hp1 HG02647.hp1 others(14): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-699C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | chr8 | 38468591 | |||||||
| chr8:38468596 | C | G | 1 | a0001c0001t0010 | 1 | NA19090.hp1 | 5_prime_UTR_variant | MODIFIER | c.-704G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 11150 | chr8 | 38468596 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38413882 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2292+36G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 17/17 | chr8 | 38413882 | |||||||
| chr8:38414331 | G | A | 2 | a0001c0001t0003g0187 a0001c0001t0004g0315 |
2 | NA18966.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2049-42C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 15/17 | chr8 | 38414331 | |||||||
| chr8:38414344 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2049-55G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 15/17 | chr8 | 38414344 | |||||||
| chr8:38415024 | C | G | 86 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0017 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1855-123G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415024 | |||||||
| chr8:38415064 | C | A | 84 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0025 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1855-163G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415064 | |||||||
| chr8:38415066 | C | G | 1 | a0001c0001t0002g0242 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1855-165G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415066 | |||||||
| chr8:38415136 | G | A | 1 | a0001c0001t0004g0306 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1855-235C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415136 | |||||||
| chr8:38415269 | A | C | 1 | a0001c0001t0004g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1855-368T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415269 | |||||||
| chr8:38415296 | T | C | 52 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0047 others(49): Show |
52 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1855-395A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415296 | |||||||
| chr8:38415400 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1854+470G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415400 | |||||||
| chr8:38415434 | T | C | 90 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0017 others(87): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1854+436A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415434 | |||||||
| chr8:38415441 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1854+429C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415441 | |||||||
| chr8:38415468 | A | AT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0026 others(38): Show |
42 | HG00438.hp2 HG00558.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1854+401dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415468 | |||||||
| chr8:38415468 | A | T | 1 | a0001c0001t0001g0023 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1854+402T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415468 | |||||||
| chr8:38415468 | AT | A | 12 | a0001c0001t0001g0042 a0001c0001t0001g0148 a0001c0001t0002g0252 others(9): Show |
12 | HG00099.hp2 HG01081.hp2 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.1854+401delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415468 | |||||||
| chr8:38415568 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1854+302C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415568 | |||||||
| chr8:38415747 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1854+123G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415747 | |||||||
| chr8:38416212 | A | C | 1 | a0001c0001t0012g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1664-152T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416212 | |||||||
| chr8:38416429 | C | G | 3 | a0001c0001t0002g0312 a0001c0001t0008g0055 a0001c0001t0008g0057 |
3 | HG02895.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1664-369G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416429 | |||||||
| chr8:38416448 | A | AT | 182 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(179): Show |
183 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1664-389dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416448 | |||||||
| chr8:38416448 | A | ATT | 15 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0063 others(12): Show |
15 | HG00735.hp2 HG00741.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1664-390_1664-389d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416448 | |||||||
| chr8:38416448 | ATT | A | 11 | a0001c0001t0003g0017 a0001c0001t0003g0113 a0001c0001t0003g0125 others(8): Show |
11 | HG02572.hp1 HG02723.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1664-390_1664-389d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416448 | |||||||
| chr8:38416448 | ATTT | A | 74 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0025 others(71): Show |
75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1664-391_1664-389d others(5): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416448 | |||||||
| chr8:38416448 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0012g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1664-401_1664-389d others(15): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416448 | |||||||
| chr8:38416541 | C | T | 2 | a0001c0001t0003g0082 a0001c0001t0003g0203 |
2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1664-481G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416541 | |||||||
| chr8:38416551 | G | A | 1 | a0001c0001t0004g0241 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1664-491C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416551 | |||||||
| chr8:38416604 | C | T | 1 | a0001c0001t0012g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1664-544G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416604 | |||||||
| chr8:38416613 | G | A | 1 | a0001c0001t0012g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1664-553C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416613 | |||||||
| chr8:38416657 | G | C | 1 | a0001c0001t0001g0014 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1664-597C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416657 | |||||||
| chr8:38416672 | C | G | 1 | a0001c0009t0013g0006 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1664-612G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416672 | |||||||
| chr8:38416675 | C | G | 101 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0017 others(98): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1664-615G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416675 | |||||||
| chr8:38416718 | G | T | 3 | a0001c0001t0001g0076 a0001c0001t0002g0221 a0008c0013t0003g0180 |
3 | NA19011.hp1 NA19074.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1663+588C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416718 | |||||||
| chr8:38416840 | C | T | 8 | a0001c0001t0001g0054 a0001c0001t0001g0069 a0001c0001t0001g0089 others(5): Show |
8 | HG00423.hp2 HG02074.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1663+466G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416840 | |||||||
| chr8:38416901 | C | T | 2 | a0001c0001t0003g0173 a0001c0001t0003g0175 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1663+405G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416901 | |||||||
| chr8:38416965 | A | G | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1663+341T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416965 | |||||||
| chr8:38417241 | G | T | 1 | a0001c0001t0028g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1663+65C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38417241 | |||||||
| chr8:38417268 | C | G | 2 | a0001c0001t0001g0040 a0001c0001t0002g0282 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1663+38G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38417268 | |||||||
| chr8:38417637 | G | A | 1 | a0001c0001t0003g0065 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1553-221C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 11/17 | chr8 | 38417637 | |||||||
| chr8:38418520 | A | G | 2 | a0001c0001t0002g0252 a0001c0001t0002g0253 |
2 | NA19012.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1285-147T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38418520 | |||||||
| chr8:38418735 | G | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0144 |
2 | NA18952.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1285-362C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38418735 | |||||||
| chr8:38418929 | G | A | 1 | a0006c0007t0003g0177 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1285-556C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38418929 | |||||||
| chr8:38419027 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1284+506A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38419027 | |||||||
| chr8:38419084 | C | T | 1 | a0001c0001t0026g0334 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1284+449G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38419084 | |||||||
| chr8:38419230 | C | T | 3 | a0001c0001t0003g0002 a0001c0001t0003g0171 a0001c0001t0004g0277 |
4 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284+303G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38419230 | |||||||
| chr8:38419276 | CA | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0041 others(4): Show |
8 | HG01257.hp1 HG01361.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1284+256delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38419276 | |||||||
| chr8:38419779 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1082-44C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38419779 | |||||||
| chr8:38419786 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1082-51G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38419786 | |||||||
| chr8:38419971 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1082-236G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38419971 | |||||||
| chr8:38420156 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1082-421G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38420156 | |||||||
| chr8:38420292 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1082-557C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38420292 | |||||||
| chr8:38420750 | C | T | 1 | a0001c0001t0012g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1082-1015G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38420750 | |||||||
| chr8:38420920 | G | A | 2 | a0001c0001t0002g0303 a0005c0010t0002g0304 |
2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1081+877C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38420920 | |||||||
| chr8:38420929 | G | A | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1081+868C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38420929 | |||||||
| chr8:38421006 | C | G | 1 | a0001c0001t0002g0280 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1081+791G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421006 | |||||||
| chr8:38421176 | C | G | 1 | a0001c0001t0012g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1081+621G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421176 | |||||||
| chr8:38421211 | C | T | 22 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0119 others(19): Show |
22 | HG00597.hp1 HG00609.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.1081+586G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421211 | |||||||
| chr8:38421219 | G | A | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1081+578C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421219 | |||||||
| chr8:38421461 | G | C | 1 | a0001c0001t0003g0081 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1081+336C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421461 | |||||||
| chr8:38421461 | G | T | 1 | a0001c0001t0002g0300 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1081+336C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421461 | |||||||
| chr8:38421547 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1081+250C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421547 | |||||||
| chr8:38421730 | G | A | 3 | a0001c0001t0003g0017 a0001c0001t0019g0103 a0001c0009t0013g0006 |
3 | HG02572.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1081+67C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421730 | |||||||
| chr8:38421746 | C | T | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1081+51G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421746 | |||||||
| chr8:38421777 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1081+20C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421777 | |||||||
| chr8:38422000 | G | A | 2 | a0001c0001t0002g0290 a0001c0001t0002g0299 |
2 | HG00099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.937-59C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422000 | |||||||
| chr8:38422123 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.937-182C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422123 | |||||||
| chr8:38422223 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.937-282G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422223 | |||||||
| chr8:38422231 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0093 |
2 | HG02040.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.937-290C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422231 | |||||||
| chr8:38422255 | G | A | 3 | a0001c0001t0003g0017 a0001c0001t0019g0103 a0001c0009t0013g0006 |
3 | HG02572.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.937-314C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422255 | |||||||
| chr8:38422312 | C | T | 2 | a0001c0001t0003g0082 a0001c0001t0003g0203 |
2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.937-371G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422312 | |||||||
| chr8:38422351 | C | T | 8 | a0001c0001t0001g0102 a0001c0001t0002g0243 a0001c0001t0002g0248 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.937-410G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422351 | |||||||
| chr8:38422380 | C | T | 1 | a0001c0001t0012g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.937-439G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422380 | |||||||
| chr8:38422459 | T | C | 3 | a0001c0001t0003g0017 a0001c0001t0019g0103 a0001c0009t0013g0006 |
3 | HG02572.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.937-518A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422459 | |||||||
| chr8:38422646 | C | T | 1 | a0001c0001t0009g0066 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.937-705G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422646 | |||||||
| chr8:38422995 | A | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0149 |
2 | HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.937-1054T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422995 | |||||||
| chr8:38423233 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.936+1276G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423233 | |||||||
| chr8:38423312 | G | GT | 26 | a0001c0001t0001g0060 a0001c0001t0001g0069 a0001c0001t0001g0074 others(23): Show |
27 | HG00140.hp1 HG00438.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.936+1196dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423312 | |||||||
| chr8:38423312 | G | GTT | 88 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0003g0020 others(85): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.936+1195_936+1196d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423312 | |||||||
| chr8:38423356 | C | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0069 a0001c0001t0002g0213 others(1): Show |
4 | NA18939.hp2 NA18968.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+1153G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423356 | |||||||
| chr8:38423530 | C | T | 4 | a0001c0001t0003g0108 a0001c0001t0003g0187 a0001c0001t0004g0236 others(1): Show |
4 | NA18957.hp2 NA18961.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+979G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423530 | |||||||
| chr8:38423552 | C | A | 3 | a0001c0001t0003g0113 a0001c0001t0003g0114 a0001c0001t0003g0150 |
3 | NA18953.hp1 NA19056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.936+957G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423552 | |||||||
| chr8:38423573 | G | A | 3 | a0001c0001t0002g0312 a0001c0001t0008g0055 a0001c0001t0008g0057 |
3 | HG02895.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.936+936C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423573 | |||||||
| chr8:38423603 | C | T | 2 | a0001c0001t0004g0246 a0001c0001t0012g0005 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.936+906G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423603 | |||||||
| chr8:38423662 | T | TA | 41 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0045 others(38): Show |
41 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.936+846dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423662 | |||||||
| chr8:38423662 | TA | T | 26 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0090 others(23): Show |
26 | HG00408.hp1 HG00609.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.936+846delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423662 | |||||||
| chr8:38423739 | C | A | 1 | a0001c0001t0004g0246 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.936+770G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423739 | |||||||
| chr8:38423854 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.936+655C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423854 | |||||||
| chr8:38424057 | A | C | 2 | a0001c0001t0004g0263 a0001c0001t0004g0265 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.936+452T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38424057 | |||||||
| chr8:38424131 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.936+378C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38424131 | |||||||
| chr8:38424140 | G | A | 84 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0003g0002 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.936+369C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38424140 | |||||||
| chr8:38424366 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.936+143G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38424366 | |||||||
| chr8:38424396 | G | A | 5 | a0001c0001t0003g0120 a0001c0001t0003g0136 a0001c0001t0003g0154 others(2): Show |
5 | HG00621.hp2 HG02155.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.936+113C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38424396 | |||||||
| chr8:38424776 | C | T | 50 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0047 others(47): Show |
50 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.746-77G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38424776 | |||||||
| chr8:38424875 | G | A | 3 | a0001c0001t0003g0193 a0001c0001t0004g0231 a0001c0001t0004g0234 |
3 | HG00621.hp1 HG02165.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.746-176C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38424875 | |||||||
| chr8:38424971 | T | G | 5 | a0001c0001t0003g0017 a0001c0001t0003g0082 a0001c0001t0003g0203 others(2): Show |
5 | HG01243.hp1 HG02572.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-272A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38424971 | |||||||
| chr8:38425054 | G | A | 2 | a0001c0001t0008g0055 a0001c0001t0008g0057 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.746-355C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425054 | |||||||
| chr8:38425136 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.746-437G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425136 | |||||||
| chr8:38425145 | CT | C | 81 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0003g0002 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.746-447delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425145 | |||||||
| chr8:38425428 | G | T | 2 | a0001c0001t0019g0103 a0001c0009t0013g0006 |
2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.745+694C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425428 | |||||||
| chr8:38425541 | C | A | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.745+581G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425541 | |||||||
| chr8:38425586 | A | T | 1 | a0001c0001t0001g0142 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.745+536T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425586 | |||||||
| chr8:38425656 | C | T | 2 | a0001c0001t0002g0281 a0001c0001t0005g0322 |
2 | HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.745+466G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425656 | |||||||
| chr8:38425690 | C | A | 83 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0003g0002 others(80): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.745+432G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425690 | |||||||
| chr8:38425828 | C | T | 2 | a0001c0001t0003g0065 a0001c0001t0009g0145 |
2 | NA18975.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.745+294G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425828 | |||||||
| chr8:38425851 | C | A | 1 | a0001c0001t0028g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.745+271G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425851 | |||||||
| chr8:38425916 | C | T | 3 | a0001c0001t0003g0118 a0001c0001t0003g0130 a0001c0001t0003g0131 |
3 | NA18970.hp1 NA19007.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.745+206G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425916 | |||||||
| chr8:38426493 | C | T | 81 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0003g0002 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.622-248G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38426493 | |||||||
| chr8:38426545 | A | G | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.622-300T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38426545 | |||||||
| chr8:38426598 | C | T | 2 | a0001c0001t0019g0103 a0001c0009t0013g0006 |
2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.622-353G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38426598 | |||||||
| chr8:38426871 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.622-626C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38426871 | |||||||
| chr8:38426934 | G | A | 2 | a0001c0001t0002g0308 a0001c0001t0002g0309 |
2 | HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.622-689C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38426934 | |||||||
| chr8:38427028 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0049 |
2 | HG01928.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.622-783T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427028 | |||||||
| chr8:38427063 | C | T | 81 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0003g0002 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.622-818G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427063 | |||||||
| chr8:38427088 | CAG | C | 79 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0003g0002 others(76): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.621+831_621+832del others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427088 | |||||||
| chr8:38427105 | T | TA | 92 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0080 others(89): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.621+815dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427105 | |||||||
| chr8:38427122 | T | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0079 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.621+799A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427122 | |||||||
| chr8:38427476 | C | T | 19 | a0001c0001t0003g0025 a0001c0001t0003g0035 a0001c0001t0003g0113 others(16): Show |
19 | HG00673.hp1 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.621+445G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427476 | |||||||
| chr8:38427477 | G | A | 2 | a0001c0001t0004g0246 a0001c0001t0012g0005 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.621+444C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427477 | |||||||
| chr8:38427777 | A | G | 1 | a0001c0001t0012g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.621+144T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427777 | |||||||
| chr8:38427894 | C | G | 1 | a0001c0001t0027g0330 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.621+27G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427894 | |||||||
| chr8:38428101 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG00408.hp2 | splice_region_variant&intron_variant | LOW | c.449-8C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 4/17 | chr8 | 38428101 | |||||||
| chr8:38428175 | C | G | 2 | a0001c0001t0003g0017 a0001c0001t0005g0326 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.449-82G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 4/17 | chr8 | 38428175 | |||||||
| chr8:38428216 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.449-123C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 4/17 | chr8 | 38428216 | |||||||
| chr8:38428439 | T | C | 1 | a0001c0003t0001g0196 | 1 | HG01175.hp2 | splice_region_variant&intron_variant | LOW | c.359-4A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38428439 | |||||||
| chr8:38428707 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(42): Show |
46 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.359-272C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38428707 | |||||||
| chr8:38428805 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0002g0281 a0001c0001t0005g0322 others(1): Show |
4 | HG03130.hp2 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-370T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38428805 | |||||||
| chr8:38428955 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.359-520T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38428955 | |||||||
| chr8:38429017 | T | C | 1 | a0001c0001t0002g0307 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.359-582A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38429017 | |||||||
| chr8:38429119 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.358+563T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38429119 | |||||||
| chr8:38429293 | C | G | 85 | a0001c0001t0001g0077 a0001c0001t0003g0002 a0001c0001t0003g0017 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.358+389G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38429293 | |||||||
| chr8:38429384 | G | A | 2 | a0002c0002t0001g0204 a0002c0002t0001g0205 |
2 | HG01167.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.358+298C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38429384 | |||||||
| chr8:38429469 | C | A | 1 | a0001c0001t0002g0284 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.358+213G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38429469 | |||||||
| chr8:38429496 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0005g0332 a0001c0001t0005g0333 |
3 | HG02622.hp1 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.358+186T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38429496 | |||||||
| chr8:38429962 | G | A | 1 | a0001c0001t0003g0193 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.92-14C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38429962 | |||||||
| chr8:38430037 | C | T | 82 | a0001c0001t0001g0077 a0001c0001t0003g0002 a0001c0001t0003g0017 others(79): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.92-89G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430037 | |||||||
| chr8:38430234 | G | GGATCA | 330 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(327): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.92-287_92-286insTG others(3): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430234 | |||||||
| chr8:38430295 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.92-347C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430295 | |||||||
| chr8:38430415 | C | T | 1 | a0001c0001t0003g0187 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.92-467G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430415 | |||||||
| chr8:38430449 | C | T | 2 | a0001c0001t0003g0161 a0001c0001t0003g0186 |
2 | HG00099.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.92-501G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430449 | |||||||
| chr8:38430688 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0022g0207 |
2 | HG01074.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.92-740C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430688 | |||||||
| chr8:38430764 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0005g0321 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92-816C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430764 | |||||||
| chr8:38431048 | C | G | 80 | a0001c0001t0001g0077 a0001c0001t0003g0002 a0001c0001t0003g0025 others(77): Show |
81 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.92-1100G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431048 | |||||||
| chr8:38431054 | T | G | 1 | a0001c0001t0024g0317 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.92-1106A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431054 | |||||||
| chr8:38431285 | G | A | 1 | a0001c0001t0003g0020 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.92-1337C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431285 | |||||||
| chr8:38431312 | G | A | 1 | a0001c0001t0004g0246 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92-1364C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431312 | |||||||
| chr8:38431326 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.92-1378C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431326 | |||||||
| chr8:38431384 | T | C | 2 | a0001c0001t0019g0103 a0001c0009t0013g0006 |
2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.92-1436A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431384 | |||||||
| chr8:38431415 | G | A | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-1467C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431415 | |||||||
| chr8:38431419 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.92-1471G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431419 | |||||||
| chr8:38431712 | G | A | 14 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0182 others(11): Show |
14 | HG00597.hp1 HG00609.hp2 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.92-1764C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431712 | |||||||
| chr8:38431790 | G | A | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-1842C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431790 | |||||||
| chr8:38431854 | C | T | 2 | a0001c0001t0004g0246 a0001c0001t0012g0005 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.92-1906G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431854 | |||||||
| chr8:38431928 | T | C | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-1980A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431928 | |||||||
| chr8:38432232 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.92-2284G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432232 | |||||||
| chr8:38432357 | C | A | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-2409G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432357 | |||||||
| chr8:38432410 | A | AT | 27 | a0001c0001t0001g0056 a0001c0001t0001g0079 a0001c0001t0001g0122 others(24): Show |
27 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.92-2463dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432410 | |||||||
| chr8:38432410 | AT | A | 19 | a0001c0001t0001g0073 a0001c0001t0001g0092 a0001c0001t0001g0100 others(16): Show |
19 | HG00099.hp2 HG00140.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.92-2463delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432410 | |||||||
| chr8:38432769 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.92-2821A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432769 | |||||||
| chr8:38432891 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-2943G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432891 | |||||||
| chr8:38432904 | C | CCA | 18 | a0001c0001t0003g0002 a0001c0001t0003g0017 a0001c0001t0003g0081 others(15): Show |
19 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.92-2957_92-2956ins others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432904 | |||||||
| chr8:38432906 | G | A | 65 | a0001c0001t0001g0077 a0001c0001t0003g0025 a0001c0001t0003g0035 others(62): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.92-2958C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432906 | |||||||
| chr8:38432908 | G | C | 18 | a0001c0001t0003g0002 a0001c0001t0003g0017 a0001c0001t0003g0081 others(15): Show |
19 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.92-2960C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432908 | |||||||
| chr8:38432908 | G | GC | 168 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(165): Show |
168 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.92-2961dupG | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432908 | |||||||
| chr8:38432916 | C | G | 1 | a0001c0001t0003g0163 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.92-2968G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432916 | |||||||
| chr8:38432919 | T | A | 4 | a0001c0001t0004g0246 a0001c0001t0012g0005 a0001c0001t0019g0103 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-2971A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432919 | |||||||
| chr8:38432919 | T | C | 98 | a0001c0001t0001g0077 a0001c0001t0003g0002 a0001c0001t0003g0017 others(95): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.92-2971A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432919 | |||||||
| chr8:38432921 | C | T | 1 | a0001c0001t0003g0179 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.92-2973G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432921 | |||||||
| chr8:38433163 | C | T | 2 | a0001c0001t0004g0246 a0001c0001t0012g0005 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.92-3215G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433163 | |||||||
| chr8:38433294 | C | T | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-3346G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433294 | |||||||
| chr8:38433413 | C | G | 3 | a0001c0001t0003g0025 a0001c0001t0003g0169 a0001c0001t0006g0168 |
3 | HG01928.hp1 HG01952.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.92-3465G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433413 | |||||||
| chr8:38433562 | G | A | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-3614C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433562 | |||||||
| chr8:38433582 | G | T | 2 | a0001c0001t0002g0270 a0001c0001t0002g0271 |
2 | HG00280.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.92-3634C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433582 | |||||||
| chr8:38433583 | C | T | 2 | a0001c0001t0002g0270 a0001c0001t0002g0271 |
2 | HG00280.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.92-3635G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433583 | |||||||
| chr8:38433601 | G | A | 1 | a0001c0001t0004g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.92-3653C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433601 | |||||||
| chr8:38433670 | T | C | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-3722A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433670 | |||||||
| chr8:38433694 | G | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0005g0319 others(7): Show |
10 | HG02055.hp1 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-3746C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433694 | |||||||
| chr8:38433910 | T | C | 4 | a0001c0001t0001g0178 a0001c0001t0002g0209 a0001c0001t0002g0259 others(1): Show |
4 | NA18947.hp1 NA18953.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-3962A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433910 | |||||||
| chr8:38433965 | C | G | 1 | a0001c0001t0001g0091 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.92-4017G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433965 | |||||||
| chr8:38434030 | G | C | 2 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.92-4082C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434030 | |||||||
| chr8:38434168 | T | C | 2 | a0001c0001t0002g0255 a0001c0001t0002g0269 |
2 | HG03831.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.92-4220A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434168 | |||||||
| chr8:38434318 | T | C | 88 | a0001c0001t0001g0077 a0001c0001t0003g0002 a0001c0001t0003g0020 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.92-4370A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434318 | |||||||
| chr8:38434320 | TTGC | T | 6 | a0001c0001t0003g0035 a0001c0001t0003g0105 a0001c0001t0003g0114 others(3): Show |
6 | HG01081.hp2 HG01167.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-4375_92-4373del others(3): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434320 | |||||||
| chr8:38434327 | TG | T | 5 | a0001c0001t0003g0002 a0001c0001t0003g0159 a0001c0001t0003g0160 others(2): Show |
6 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-4380delC | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434327 | |||||||
| chr8:38434327 | TGC | T | 77 | a0001c0001t0001g0077 a0001c0001t0003g0020 a0001c0001t0003g0024 others(74): Show |
77 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.92-4381_92-4380del others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434327 | |||||||
| chr8:38434329 | C | T | 5 | a0001c0001t0003g0002 a0001c0001t0003g0159 a0001c0001t0003g0160 others(2): Show |
6 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-4381G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434329 | |||||||
| chr8:38434329 | CT | C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0061 a0001c0001t0001g0119 others(3): Show |
6 | HG02683.hp2 HG02818.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-4382delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434329 | |||||||
| chr8:38434346 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.92-4398A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434346 | |||||||
| chr8:38434487 | T | C | 1 | a0001c0001t0003g0115 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.92-4539A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434487 | |||||||
| chr8:38434629 | A | C | 92 | a0001c0001t0001g0077 a0001c0001t0003g0002 a0001c0001t0003g0017 others(89): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.92-4681T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434629 | |||||||
| chr8:38434697 | G | C | 1 | a0001c0001t0001g0008 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92-4749C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434697 | |||||||
| chr8:38434748 | C | A | 51 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0047 others(48): Show |
51 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.92-4800G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434748 | |||||||
| chr8:38434807 | A | G | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-4859T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434807 | |||||||
| chr8:38434821 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0144 |
2 | NA18952.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.92-4873G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434821 | |||||||
| chr8:38434948 | A | T | 90 | a0001c0001t0001g0077 a0001c0001t0003g0002 a0001c0001t0003g0020 others(87): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.92-5000T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434948 | |||||||
| chr8:38435090 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.92-5142C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435090 | |||||||
| chr8:38435166 | G | A | 2 | a0001c0001t0003g0082 a0001c0001t0003g0203 |
2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.92-5218C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435166 | |||||||
| chr8:38435295 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92-5347G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435295 | |||||||
| chr8:38435304 | C | T | 1 | a0001c0003t0001g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.92-5356G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435304 | |||||||
| chr8:38435320 | A | G | 3 | a0001c0001t0003g0118 a0001c0001t0003g0130 a0001c0001t0003g0131 |
3 | NA18970.hp1 NA19007.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.92-5372T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435320 | |||||||
| chr8:38435376 | G | A | 23 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0060 others(20): Show |
23 | HG02015.hp2 HG02040.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.92-5428C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435376 | |||||||
| chr8:38435384 | T | G | 2 | a0001c0001t0003g0082 a0001c0001t0003g0203 |
2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.92-5436A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435384 | |||||||
| chr8:38435700 | T | G | 2 | a0004c0005t0002g0278 a0004c0005t0002g0311 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.92-5752A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435700 | |||||||
| chr8:38435735 | G | A | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-5787C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435735 | |||||||
| chr8:38435903 | A | G | 1 | a0001c0001t0028g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.92-5955T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435903 | |||||||
| chr8:38435945 | G | A | 89 | a0001c0001t0001g0048 a0001c0001t0001g0077 a0001c0001t0001g0090 others(86): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.92-5997C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435945 | |||||||
| chr8:38435959 | T | C | 97 | a0001c0001t0001g0048 a0001c0001t0001g0077 a0001c0001t0001g0090 others(94): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.92-6011A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435959 | |||||||
| chr8:38435998 | G | A | 1 | a0001c0001t0004g0246 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92-6050C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435998 | |||||||
| chr8:38436269 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.92-6321C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38436269 | |||||||
| chr8:38436280 | G | A | 4 | a0001c0001t0003g0120 a0001c0001t0003g0136 a0001c0001t0003g0154 others(1): Show |
4 | HG00621.hp2 HG02155.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-6332C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38436280 | |||||||
| chr8:38436409 | C | A | 9 | a0001c0001t0001g0029 a0001c0001t0001g0060 a0001c0001t0001g0083 others(6): Show |
9 | HG02040.hp1 NA18947.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-6461G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38436409 | |||||||
| chr8:38436416 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.92-6468G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38436416 | |||||||
| chr8:38437616 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.92-7668T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38437616 | |||||||
| chr8:38437735 | G | T | 1 | a0001c0001t0002g0296 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.92-7787C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38437735 | |||||||
| chr8:38437824 | A | G | 1 | a0001c0001t0001g0027 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.92-7876T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38437824 | |||||||
| chr8:38438024 | G | A | 51 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0047 others(48): Show |
51 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.92-8076C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438024 | |||||||
| chr8:38438172 | C | T | 2 | a0001c0001t0002g0252 a0001c0001t0002g0253 |
2 | NA19012.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.92-8224G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438172 | |||||||
| chr8:38438201 | T | TCA | 28 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0067 others(25): Show |
28 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.92-8255_92-8254dup others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438201 | |||||||
| chr8:38438225 | T | C | 94 | a0001c0001t0001g0077 a0001c0001t0002g0242 a0001c0001t0003g0002 others(91): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.92-8277A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438225 | |||||||
| chr8:38438286 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.92-8338T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438286 | |||||||
| chr8:38438384 | A | G | 2 | a0001c0001t0003g0017 a0001c0001t0003g0082 |
2 | HG03540.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.92-8436T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438384 | |||||||
| chr8:38438410 | A | G | 101 | a0001c0001t0001g0016 a0001c0001t0001g0077 a0001c0001t0002g0242 others(98): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.92-8462T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438410 | |||||||
| chr8:38438542 | C | CA | 16 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0045 others(13): Show |
16 | HG01074.hp1 HG01192.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.92-8595dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438542 | |||||||
| chr8:38438560 | G | A | 1 | a0001c0001t0004g0306 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.92-8612C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438560 | |||||||
| chr8:38438690 | A | G | 1 | a0001c0001t0002g0284 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92-8742T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438690 | |||||||
| chr8:38438813 | C | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | NA18969.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.92-8865G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438813 | |||||||
| chr8:38438816 | C | T | 1 | a0001c0001t0004g0251 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.92-8868G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438816 | |||||||
| chr8:38438901 | T | C | 1 | a0001c0001t0002g0290 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.92-8953A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438901 | |||||||
| chr8:38438907 | A | G | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-8959T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438907 | |||||||
| chr8:38438984 | G | A | 1 | a0001c0001t0027g0330 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.92-9036C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438984 | |||||||
| chr8:38439253 | C | T | 1 | a0001c0001t0003g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.92-9305G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439253 | |||||||
| chr8:38439299 | G | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0134 a0001c0001t0002g0230 |
3 | HG01361.hp1 NA18973.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.92-9351C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439299 | |||||||
| chr8:38439469 | A | C | 1 | a0001c0001t0002g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.92-9521T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439469 | |||||||
| chr8:38439571 | C | A | 1 | a0001c0001t0002g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.92-9623G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439571 | |||||||
| chr8:38439596 | G | A | 1 | a0003c0004t0003g0121 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.92-9648C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439596 | |||||||
| chr8:38439863 | T | TCTCGCAC others(3): Show |
1 | a0001c0001t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.92-9916_92-9915ins others(10): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439863 | |||||||
| chr8:38439866 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.92-9918A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439866 | |||||||
| chr8:38439905 | G | A | 4 | a0001c0001t0003g0118 a0001c0001t0003g0130 a0001c0001t0003g0131 others(1): Show |
4 | NA18970.hp1 NA18986.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-9957C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439905 | |||||||
| chr8:38440242 | G | A | 1 | a0001c0001t0003g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.92-10294C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38440242 | |||||||
| chr8:38440566 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.92-10618C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38440566 | |||||||
| chr8:38441029 | C | G | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.92-11081G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38441029 | |||||||
| chr8:38441048 | C | A | 1 | a0001c0001t0019g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92-11100G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38441048 | |||||||
| chr8:38441129 | C | T | 78 | a0001c0001t0001g0077 a0001c0001t0002g0242 a0001c0001t0003g0002 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.92-11181G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38441129 | |||||||
| chr8:38441304 | T | C | 1 | a0001c0001t0004g0251 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.92-11356A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38441304 | |||||||
| chr8:38441901 | G | A | 167 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(164): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.92-11953C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38441901 | |||||||
| chr8:38442106 | T | C | 78 | a0001c0001t0001g0077 a0001c0001t0002g0242 a0001c0001t0003g0002 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.92-12158A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442106 | |||||||
| chr8:38442192 | G | A | 1 | a0001c0001t0003g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.92-12244C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442192 | |||||||
| chr8:38442197 | G | C | 168 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0019 others(165): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.92-12249C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442197 | |||||||
| chr8:38442362 | G | GGTGTGGG others(7): Show |
1 | a0001c0001t0001g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.92-12415_92-12414i others(16): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | |||||||
| chr8:38442362 | G | GGTGTGT | 4 | a0001c0001t0002g0303 a0001c0001t0003g0158 a0001c0001t0003g0186 others(1): Show |
4 | HG00642.hp2 HG02071.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-12420_92-12415d others(8): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | |||||||
| chr8:38442362 | G | GGTGTGTG others(1): Show |
13 | a0001c0001t0001g0060 a0001c0001t0001g0095 a0001c0001t0001g0101 others(10): Show |
13 | HG00642.hp1 HG02809.hp1 NA18953.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-12422_92-12415d others(10): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | |||||||
| chr8:38442362 | G | GGTGTGTG others(3): Show |
64 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0056 others(61): Show |
64 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.92-12424_92-12415d others(12): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | |||||||
| chr8:38442362 | G | GGTGTGTG others(5): Show |
43 | a0001c0001t0001g0067 a0001c0001t0001g0076 a0001c0001t0001g0078 others(40): Show |
44 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.92-12426_92-12415d others(14): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | |||||||
| chr8:38442362 | G | GGTGTGTG others(7): Show |
16 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0097 others(13): Show |
16 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.92-12428_92-12415d others(16): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | |||||||
| chr8:38442362 | G | GGTGTGTG others(9): Show |
7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0080 others(4): Show |
7 | HG01934.hp2 HG01993.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-12430_92-12415d others(18): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | |||||||
| chr8:38442362 | G | GGTGTGTG others(13): Show |
3 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG01257.hp2 HG01258.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.92-12434_92-12415d others(22): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | |||||||
| chr8:38442362 | G | GGTGTGTG others(15): Show |
1 | a0001c0009t0013g0006 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-12436_92-12415d others(24): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | |||||||
| chr8:38442362 | GGT | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(144): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.92-12416_92-12415d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | |||||||
| chr8:38442383 | G | GTGTGTGT others(6): Show |
1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.92-12448_92-12436d others(15): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442383 | |||||||
| chr8:38442727 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.92-12779C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442727 | |||||||
| chr8:38442792 | C | T | 1 | a0001c0001t0005g0329 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.92-12844G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442792 | |||||||
| chr8:38442920 | A | G | 1 | a0001c0001t0019g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92-12972T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442920 | |||||||
| chr8:38442929 | C | T | 1 | a0001c0001t0003g0025 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.92-12981G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442929 | |||||||
| chr8:38443133 | G | A | 1 | a0001c0001t0003g0167 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.92-13185C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443133 | |||||||
| chr8:38443173 | C | A | 2 | a0001c0001t0003g0152 a0001c0001t0003g0153 |
2 | NA18944.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.92-13225G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443173 | |||||||
| chr8:38443212 | T | A | 170 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(167): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.92-13264A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443212 | |||||||
| chr8:38443496 | C | CA | 7 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0054 others(4): Show |
7 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-13549dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443496 | |||||||
| chr8:38443496 | CA | C | 167 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(164): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.92-13549delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443496 | |||||||
| chr8:38443564 | T | C | 73 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0047 others(70): Show |
73 | HG00423.hp1 HG00558.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.92-13616A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443564 | |||||||
| chr8:38443594 | G | C | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-13646C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443594 | |||||||
| chr8:38443617 | G | A | 1 | a0001c0001t0002g0279 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.92-13669C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443617 | |||||||
| chr8:38443851 | C | T | 1 | a0001c0001t0003g0179 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.91+13505G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443851 | |||||||
| chr8:38443921 | C | T | 1 | a0001c0001t0002g0300 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+13435G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443921 | |||||||
| chr8:38443970 | G | A | 1 | a0001c0001t0014g0007 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.91+13386C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443970 | |||||||
| chr8:38444051 | C | CA | 46 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0019 others(43): Show |
46 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.91+13304dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444051 | |||||||
| chr8:38444051 | CA | C | 101 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0021 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.91+13304delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444051 | |||||||
| chr8:38444051 | CAA | C | 6 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0002g0209 others(3): Show |
6 | HG01069.hp2 HG03492.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+13303_91+13304d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444051 | |||||||
| chr8:38444051 | CAAAAAAA | C | 56 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0047 others(53): Show |
56 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.91+13298_91+13304d others(9): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444051 | |||||||
| chr8:38444051 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0159 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.91+13293_91+13304d others(14): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444051 | |||||||
| chr8:38444231 | C | G | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13125G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444231 | |||||||
| chr8:38444242 | G | A | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13114C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444242 | |||||||
| chr8:38444243 | A | C | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13113T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444243 | |||||||
| chr8:38444244 | G | C | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13112C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444244 | |||||||
| chr8:38444252 | A | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13104T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444252 | |||||||
| chr8:38444261 | C | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13095G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444261 | |||||||
| chr8:38444263 | G | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13093C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444263 | |||||||
| chr8:38444265 | T | A | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13091A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444265 | |||||||
| chr8:38444269 | T | G | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13087A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444269 | |||||||
| chr8:38444271 | C | A | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13085G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444271 | |||||||
| chr8:38444281 | C | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13075G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444281 | |||||||
| chr8:38444283 | A | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13073T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444283 | |||||||
| chr8:38444285 | C | G | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13071G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444285 | |||||||
| chr8:38444286 | C | G | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13070G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444286 | |||||||
| chr8:38444293 | C | A | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13063G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444293 | |||||||
| chr8:38444297 | C | A | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13059G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444297 | |||||||
| chr8:38444299 | T | A | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13057A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444299 | |||||||
| chr8:38444314 | C | A | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13042G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444314 | |||||||
| chr8:38444331 | C | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13025G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444331 | |||||||
| chr8:38444341 | G | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13015C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444341 | |||||||
| chr8:38444343 | G | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13013C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444343 | |||||||
| chr8:38444350 | G | C | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13006C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444350 | |||||||
| chr8:38444352 | A | G | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13004T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444352 | |||||||
| chr8:38444355 | C | G | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13001G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444355 | |||||||
| chr8:38444356 | T | C | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13000A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444356 | |||||||
| chr8:38444358 | A | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12998T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444358 | |||||||
| chr8:38444369 | A | C | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12987T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444369 | |||||||
| chr8:38444370 | T | A | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12986A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444370 | |||||||
| chr8:38444372 | A | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12984T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444372 | |||||||
| chr8:38444379 | T | C | 1 | a0001c0001t0005g0331 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.91+12977A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444379 | |||||||
| chr8:38444385 | G | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12971C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444385 | |||||||
| chr8:38444387 | G | GT | 24 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0063 others(21): Show |
24 | HG00438.hp1 HG00738.hp1 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.91+12968dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444387 | |||||||
| chr8:38444387 | G | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12969C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444387 | |||||||
| chr8:38444387 | GT | G | 7 | a0001c0001t0001g0102 a0001c0001t0001g0181 a0001c0001t0002g0291 others(4): Show |
7 | HG01070.hp2 HG01071.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+12968delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444387 | |||||||
| chr8:38444391 | T | TG | 55 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0047 others(52): Show |
55 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.91+12964_91+12965i others(3): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444391 | |||||||
| chr8:38444403 | C | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12953G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444403 | |||||||
| chr8:38444415 | G | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12941C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444415 | |||||||
| chr8:38444439 | A | G | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12917T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444439 | |||||||
| chr8:38444442 | A | G | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12914T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444442 | |||||||
| chr8:38444449 | C | A | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12907G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444449 | |||||||
| chr8:38444453 | A | G | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12903T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444453 | |||||||
| chr8:38444454 | T | A | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12902A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444454 | |||||||
| chr8:38444485 | C | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12871G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444485 | |||||||
| chr8:38444489 | A | C | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12867T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444489 | |||||||
| chr8:38444491 | T | A | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12865A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444491 | |||||||
| chr8:38444493 | A | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12863T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444493 | |||||||
| chr8:38444496 | C | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12860G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444496 | |||||||
| chr8:38444510 | C | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12846G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444510 | |||||||
| chr8:38444512 | C | A | 2 | a0001c0001t0012g0005 a0001c0012t0020g0206 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.91+12844G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444512 | |||||||
| chr8:38444526 | G | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12830C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444526 | |||||||
| chr8:38444529 | T | C | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12827A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444529 | |||||||
| chr8:38444546 | G | A | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12810C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444546 | |||||||
| chr8:38444548 | G | C | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12808C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444548 | |||||||
| chr8:38444556 | A | AT | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0002g0226 others(3): Show |
6 | HG02615.hp1 HG03225.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+12799dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444556 | |||||||
| chr8:38444556 | A | ATTTTTTT | 123 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0047 others(120): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.91+12793_91+12799d others(9): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444556 | |||||||
| chr8:38444556 | A | ATTTTTTT others(1): Show |
20 | a0001c0001t0001g0062 a0001c0001t0001g0078 a0001c0001t0001g0083 others(17): Show |
20 | HG01175.hp2 HG01261.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.91+12792_91+12799d others(10): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444556 | |||||||
| chr8:38444585 | T | A | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+12771A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444585 | |||||||
| chr8:38444588 | T | A | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12768A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444588 | |||||||
| chr8:38444589 | A | T | 1 | a0001c0001t0003g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12767T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444589 | |||||||
| chr8:38444591 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0019g0103 a0001c0009t0013g0006 |
3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.91+12765G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444591 | |||||||
| chr8:38444603 | G | A | 1 | a0001c0001t0003g0025 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.91+12753C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444603 | |||||||
| chr8:38444710 | C | A | 1 | a0001c0001t0001g0029 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.91+12646G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444710 | |||||||
| chr8:38445125 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.91+12231C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445125 | |||||||
| chr8:38445126 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.91+12230G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445126 | |||||||
| chr8:38445199 | C | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0141 |
2 | HG00673.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.91+12157G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445199 | |||||||
| chr8:38445234 | C | A | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+12122G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445234 | |||||||
| chr8:38445447 | C | T | 61 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0046 others(58): Show |
61 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.91+11909G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445447 | |||||||
| chr8:38445510 | G | T | 1 | a0001c0001t0001g0029 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.91+11846C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445510 | |||||||
| chr8:38445608 | G | A | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+11748C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445608 | |||||||
| chr8:38445702 | T | C | 8 | a0001c0001t0005g0319 a0001c0001t0005g0320 a0001c0001t0005g0323 others(5): Show |
8 | HG02055.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.91+11654A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445702 | |||||||
| chr8:38445707 | T | A | 4 | a0001c0001t0003g0017 a0001c0001t0003g0082 a0001c0001t0012g0005 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+11649A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445707 | |||||||
| chr8:38445710 | T | A | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.91+11646A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445710 | |||||||
| chr8:38445981 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0019g0103 a0001c0009t0013g0006 |
3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.91+11375G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445981 | |||||||
| chr8:38446205 | C | CT | 20 | a0001c0001t0001g0049 a0001c0001t0001g0056 a0001c0001t0001g0061 others(17): Show |
20 | HG00438.hp1 HG01123.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.91+11150dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446205 | |||||||
| chr8:38446205 | CT | C | 10 | a0001c0001t0001g0009 a0001c0001t0002g0223 a0001c0001t0002g0273 others(7): Show |
10 | HG01070.hp1 HG01070.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+11150delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446205 | |||||||
| chr8:38446228 | TA | T | 4 | a0001c0001t0001g0016 a0001c0001t0015g0087 a0001c0001t0019g0103 others(1): Show |
4 | HG02572.hp1 HG02630.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+11127delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446228 | |||||||
| chr8:38446229 | A | T | 56 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0047 others(53): Show |
56 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.91+11127T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446229 | |||||||
| chr8:38446336 | G | A | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+11020C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446336 | |||||||
| chr8:38446371 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0002g0300 a0001c0001t0019g0103 others(1): Show |
4 | HG02572.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+10985G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446371 | |||||||
| chr8:38446372 | G | A | 1 | a0001c0001t0017g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.91+10984C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446372 | |||||||
| chr8:38446461 | T | A | 55 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0047 others(52): Show |
55 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.91+10895A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446461 | |||||||
| chr8:38446471 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0019g0103 a0001c0009t0013g0006 |
3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.91+10885T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446471 | |||||||
| chr8:38446606 | G | T | 1 | a0001c0001t0003g0172 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.91+10750C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446606 | |||||||
| chr8:38446716 | A | G | 1 | a0001c0001t0004g0245 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.91+10640T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446716 | |||||||
| chr8:38446816 | A | G | 1 | a0001c0001t0004g0298 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.91+10540T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446816 | |||||||
| chr8:38446907 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.91+10449C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446907 | |||||||
| chr8:38446926 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0019g0103 a0001c0009t0013g0006 |
3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.91+10430C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446926 | |||||||
| chr8:38447094 | A | C | 1 | a0001c0001t0002g0233 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.91+10262T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447094 | |||||||
| chr8:38447096 | CA | C | 3 | a0001c0001t0001g0053 a0001c0001t0021g0289 a0001c0008t0002g0276 |
3 | HG01361.hp1 NA18942.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.91+10259delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447096 | |||||||
| chr8:38447097 | AAAC | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0110 a0001c0001t0002g0295 |
3 | HG01070.hp2 HG01099.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.91+10256_91+10258d others(5): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447097 | |||||||
| chr8:38447097 | AAACACAC others(4): Show |
A | 1 | a0001c0001t0003g0123 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.91+10248_91+10258d others(13): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447097 | |||||||
| chr8:38447098 | A | AAC | 7 | a0001c0001t0001g0052 a0001c0001t0001g0132 a0001c0001t0001g0144 others(4): Show |
7 | HG01975.hp2 HG02135.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+10256_91+10257d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | A | AACAC | 7 | a0001c0001t0001g0037 a0001c0001t0001g0068 a0001c0001t0001g0104 others(4): Show |
7 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+10254_91+10257d others(6): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | A | AACACACA others(3): Show |
2 | a0001c0001t0001g0044 a0001c0001t0002g0239 |
2 | HG02293.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.91+10248_91+10257d others(12): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | AAC | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(43): Show |
46 | HG00323.hp2 HG00423.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.91+10256_91+10257d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | AACAC | A | 58 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(55): Show |
58 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.91+10254_91+10257d others(6): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | AACACAC | A | 42 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0018 others(39): Show |
42 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.91+10252_91+10257d others(8): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | AACACACA others(1): Show |
A | 36 | a0001c0001t0001g0019 a0001c0001t0001g0047 a0001c0001t0001g0116 others(33): Show |
37 | HG00408.hp2 HG00642.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.91+10250_91+10257d others(10): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | AACACACA others(3): Show |
A | 11 | a0001c0001t0001g0046 a0001c0001t0001g0062 a0001c0001t0001g0077 others(8): Show |
11 | HG00140.hp1 HG00621.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.91+10248_91+10257d others(12): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | AACACACA others(5): Show |
A | 51 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0048 others(48): Show |
51 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.91+10246_91+10257d others(14): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | AACACACA others(7): Show |
A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0060 a0001c0001t0001g0063 others(8): Show |
11 | HG00597.hp2 HG01261.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+10244_91+10257d others(16): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | AACACACA others(9): Show |
A | 2 | a0001c0001t0001g0084 a0001c0001t0002g0229 |
2 | NA19087.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.91+10242_91+10257d others(18): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | AACACACA others(11): Show |
A | 2 | a0001c0001t0002g0299 a0001c0001t0003g0017 |
2 | HG00099.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.91+10240_91+10257d others(20): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | AACACACA others(13): Show |
A | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.91+10238_91+10257d others(22): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | AACACACA others(17): Show |
A | 1 | a0001c0001t0015g0087 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.91+10234_91+10257d others(26): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447098 | AACACACA others(21): Show |
A | 1 | a0001c0001t0002g0262 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.91+10230_91+10257d others(30): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | |||||||
| chr8:38447116 | C | T | 9 | a0001c0001t0001g0122 a0001c0001t0001g0183 a0001c0001t0001g0184 others(6): Show |
9 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.91+10240G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447116 | |||||||
| chr8:38447118 | C | T | 1 | a0001c0003t0001g0195 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.91+10238G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447118 | |||||||
| chr8:38447141 | ACACACAC others(4): Show |
A | 2 | a0001c0001t0001g0029 a0008c0013t0003g0180 |
2 | NA19063.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.91+10204_91+10214d others(13): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447141 | |||||||
| chr8:38447151 | A | C | 6 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0288 others(3): Show |
6 | HG03710.hp1 NA18942.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+10205T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447151 | |||||||
| chr8:38447153 | C | A | 2 | a0001c0001t0001g0053 a0001c0001t0005g0321 |
2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.91+10203G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447153 | |||||||
| chr8:38447376 | C | A | 3 | a0001c0003t0001g0195 a0001c0003t0001g0196 a0001c0003t0001g0197 |
3 | HG00642.hp1 HG01175.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.91+9980G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447376 | |||||||
| chr8:38447640 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.91+9716T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447640 | |||||||
| chr8:38447677 | T | C | 62 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0046 others(59): Show |
62 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.91+9679A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447677 | |||||||
| chr8:38447769 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.91+9587G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447769 | |||||||
| chr8:38447776 | C | T | 62 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0046 others(59): Show |
62 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.91+9580G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447776 | |||||||
| chr8:38447966 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.91+9390G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447966 | |||||||
| chr8:38447968 | C | A | 3 | a0001c0001t0003g0002 a0001c0001t0003g0171 a0001c0001t0004g0277 |
4 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+9388G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447968 | |||||||
| chr8:38448006 | A | G | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+9350T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448006 | |||||||
| chr8:38448278 | AT | A | 58 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(55): Show |
58 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.91+9077delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448278 | |||||||
| chr8:38448331 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.91+9025C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448331 | |||||||
| chr8:38448348 | C | T | 1 | a0001c0001t0003g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91+9008G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448348 | |||||||
| chr8:38448432 | A | G | 1 | a0001c0001t0003g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91+8924T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448432 | |||||||
| chr8:38448478 | C | G | 1 | a0001c0001t0003g0129 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.91+8878G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448478 | |||||||
| chr8:38448659 | G | A | 1 | a0001c0001t0002g0300 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+8697C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448659 | |||||||
| chr8:38448785 | T | C | 1 | a0001c0001t0006g0036 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.91+8571A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448785 | |||||||
| chr8:38448838 | C | A | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+8518G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448838 | |||||||
| chr8:38448904 | G | A | 1 | a0001c0001t0003g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91+8452C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448904 | |||||||
| chr8:38448909 | C | T | 1 | a0001c0001t0002g0279 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.91+8447G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448909 | |||||||
| chr8:38448918 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.91+8438C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448918 | |||||||
| chr8:38449089 | G | A | 1 | a0001c0001t0003g0190 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.91+8267C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449089 | |||||||
| chr8:38449136 | G | GA | 4 | a0001c0001t0001g0013 a0001c0001t0001g0100 a0001c0001t0002g0260 others(1): Show |
4 | HG02809.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+8219dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449136 | |||||||
| chr8:38449156 | T | A | 1 | a0001c0001t0002g0300 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+8200A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449156 | |||||||
| chr8:38449320 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.91+8036A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449320 | |||||||
| chr8:38449335 | T | C | 1 | a0001c0001t0001g0029 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.91+8021A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449335 | |||||||
| chr8:38449344 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0019g0103 a0001c0009t0013g0006 |
3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.91+8012G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449344 | |||||||
| chr8:38449409 | C | G | 63 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0046 others(60): Show |
63 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.91+7947G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449409 | |||||||
| chr8:38449553 | C | T | 1 | a0001c0001t0004g0250 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.91+7803G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449553 | |||||||
| chr8:38449625 | G | A | 2 | a0001c0001t0004g0246 a0001c0001t0027g0330 |
2 | HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.91+7731C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449625 | |||||||
| chr8:38449656 | C | A | 1 | a0001c0001t0002g0249 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.91+7700G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449656 | |||||||
| chr8:38449665 | A | ACCATTCT | 64 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0047 others(61): Show |
64 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.91+7690_91+7691ins others(7): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449665 | |||||||
| chr8:38449665 | A | T | 1 | a0001c0001t0001g0029 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.91+7691T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449665 | |||||||
| chr8:38449685 | C | T | 9 | a0001c0001t0003g0020 a0001c0001t0003g0024 a0001c0001t0003g0033 others(6): Show |
9 | NA18982.hp1 NA19001.hp1 NA19007.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+7671G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449685 | |||||||
| chr8:38449725 | G | C | 1 | a0001c0001t0003g0201 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.91+7631C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449725 | |||||||
| chr8:38449728 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.91+7628C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449728 | |||||||
| chr8:38450097 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0002g0260 a0001c0001t0002g0261 |
3 | HG02965.hp1 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.91+7259G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450097 | |||||||
| chr8:38450213 | G | A | 2 | a0001c0001t0012g0005 a0001c0012t0020g0206 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.91+7143C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450213 | |||||||
| chr8:38450218 | C | A | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+7138G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450218 | |||||||
| chr8:38450352 | G | T | 1 | a0001c0001t0003g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91+7004C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450352 | |||||||
| chr8:38450353 | A | T | 1 | a0001c0001t0003g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91+7003T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450353 | |||||||
| chr8:38450427 | T | G | 2 | a0001c0001t0004g0246 a0001c0001t0027g0330 |
2 | HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.91+6929A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450427 | |||||||
| chr8:38450449 | T | G | 1 | a0001c0001t0001g0023 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.91+6907A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450449 | |||||||
| chr8:38450467 | G | A | 2 | a0001c0001t0003g0176 a0006c0007t0003g0177 |
2 | NA18965.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.91+6889C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450467 | |||||||
| chr8:38450517 | T | C | 1 | a0001c0001t0002g0300 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+6839A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450517 | |||||||
| chr8:38450649 | T | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0043 others(8): Show |
11 | HG01243.hp2 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.91+6707A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450649 | |||||||
| chr8:38450869 | T | C | 12 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0182 others(9): Show |
12 | HG00597.hp1 HG00609.hp2 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.91+6487A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450869 | |||||||
| chr8:38451064 | C | A | 1 | a0001c0001t0012g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+6292G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451064 | |||||||
| chr8:38451339 | T | C | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+6017A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451339 | |||||||
| chr8:38451510 | G | A | 1 | a0001c0001t0003g0111 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.91+5846C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451510 | |||||||
| chr8:38451717 | A | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0100 a0001c0001t0002g0260 others(1): Show |
4 | HG02809.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+5639T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451717 | |||||||
| chr8:38451916 | G | T | 2 | a0001c0001t0003g0017 a0001c0001t0003g0082 |
2 | HG03540.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.91+5440C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451916 | |||||||
| chr8:38451919 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.91+5437A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451919 | |||||||
| chr8:38451943 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.91+5413G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451943 | |||||||
| chr8:38452148 | G | A | 4 | a0001c0001t0003g0120 a0001c0001t0003g0136 a0001c0001t0003g0154 others(1): Show |
4 | HG00621.hp2 HG02155.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+5208C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452148 | |||||||
| chr8:38452192 | GACACACA others(13): Show |
G | 1 | a0001c0009t0013g0006 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.91+5144_91+5163del others(20): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452192 | |||||||
| chr8:38452200 | G | GAC | 4 | a0001c0001t0001g0053 a0001c0001t0001g0086 a0001c0001t0021g0289 others(1): Show |
4 | HG01361.hp1 HG02055.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+5154_91+5155dup others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | |||||||
| chr8:38452200 | GAC | G | 28 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0019 others(25): Show |
28 | HG00597.hp2 HG01070.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.91+5154_91+5155del others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | |||||||
| chr8:38452200 | GACAC | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(72): Show |
76 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.91+5152_91+5155del others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | |||||||
| chr8:38452200 | GACACAC | G | 46 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0046 others(43): Show |
46 | HG00423.hp2 HG00438.hp2 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.91+5150_91+5155del others(6): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | |||||||
| chr8:38452200 | GACACACA others(1): Show |
G | 51 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0045 others(48): Show |
51 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.91+5148_91+5155del others(8): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | |||||||
| chr8:38452200 | GACACACA others(3): Show |
G | 89 | a0001c0001t0001g0067 a0001c0001t0001g0076 a0001c0001t0001g0077 others(86): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.91+5146_91+5155del others(10): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | |||||||
| chr8:38452200 | GACACACA others(5): Show |
G | 6 | a0001c0001t0003g0120 a0001c0001t0003g0136 a0001c0001t0003g0154 others(3): Show |
6 | HG00621.hp2 HG02155.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+5144_91+5155del others(12): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | |||||||
| chr8:38452200 | GACACACA others(7): Show |
G | 6 | a0001c0001t0001g0028 a0001c0001t0002g0210 a0001c0001t0002g0262 others(3): Show |
6 | NA18944.hp1 NA18962.hp1 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+5142_91+5155del others(14): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | |||||||
| chr8:38452200 | GACACACA others(9): Show |
G | 5 | a0001c0001t0003g0113 a0001c0001t0003g0114 a0001c0001t0003g0150 others(2): Show |
5 | HG00673.hp1 NA18612.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+5140_91+5155del others(16): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | |||||||
| chr8:38452200 | GACACACA others(13): Show |
G | 3 | a0001c0001t0003g0017 a0001c0001t0004g0250 a0001c0001t0004g0251 |
3 | HG01070.hp1 HG01167.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.91+5136_91+5155del others(20): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | |||||||
| chr8:38452210 | C | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0005g0333 |
3 | HG02622.hp1 NA18522.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.91+5146G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452210 | |||||||
| chr8:38452212 | C | G | 2 | a0001c0001t0002g0237 a0001c0001t0004g0236 |
2 | NA18957.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.91+5144G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452212 | |||||||
| chr8:38452214 | C | G | 1 | a0001c0001t0005g0332 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.91+5142G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452214 | |||||||
| chr8:38452216 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.91+5140G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452216 | |||||||
| chr8:38452218 | C | G | 1 | a0001c0001t0012g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+5138G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452218 | |||||||
| chr8:38452220 | C | G | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.91+5136G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452220 | |||||||
| chr8:38452727 | A | T | 1 | a0001c0001t0003g0015 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.91+4629T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452727 | |||||||
| chr8:38452739 | G | A | 1 | a0003c0004t0003g0121 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.91+4617C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452739 | |||||||
| chr8:38452849 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.91+4507G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452849 | |||||||
| chr8:38452980 | A | T | 2 | a0001c0001t0001g0185 a0001c0001t0004g0231 |
2 | HG00621.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.91+4376T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452980 | |||||||
| chr8:38452980 | AAATT | A | 9 | a0001c0001t0003g0020 a0001c0001t0003g0024 a0001c0001t0003g0033 others(6): Show |
9 | NA18982.hp1 NA19001.hp1 NA19007.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+4372_91+4375del others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452980 | |||||||
| chr8:38452984 | T | A | 3 | a0001c0001t0002g0222 a0001c0001t0002g0226 a0001c0001t0002g0227 |
3 | NA18964.hp1 NA18991.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.91+4372A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452984 | |||||||
| chr8:38453112 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.91+4244A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453112 | |||||||
| chr8:38453215 | A | G | 1 | a0001c0001t0002g0300 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+4141T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453215 | |||||||
| chr8:38453285 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.91+4071G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453285 | |||||||
| chr8:38453392 | T | G | 84 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0002g0208 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.91+3964A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453392 | |||||||
| chr8:38453483 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(119): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.91+3873G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453483 | |||||||
| chr8:38453720 | C | G | 1 | a0001c0001t0012g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+3636G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453720 | |||||||
| chr8:38453875 | G | A | 1 | a0001c0001t0005g0321 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.91+3481C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453875 | |||||||
| chr8:38453903 | C | A | 8 | a0001c0001t0001g0016 a0001c0001t0002g0300 a0001c0001t0003g0017 others(5): Show |
8 | HG02572.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+3453G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453903 | |||||||
| chr8:38453907 | C | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(318): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.91+3449G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453907 | |||||||
| chr8:38454052 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+3304G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454052 | |||||||
| chr8:38454076 | T | A | 1 | a0004c0005t0002g0278 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.91+3280A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454076 | |||||||
| chr8:38454119 | A | T | 1 | a0001c0001t0001g0029 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.91+3237T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454119 | |||||||
| chr8:38454124 | C | T | 1 | a0001c0001t0004g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.91+3232G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454124 | |||||||
| chr8:38454155 | C | T | 4 | a0001c0001t0003g0118 a0001c0001t0003g0130 a0001c0001t0003g0131 others(1): Show |
4 | NA18970.hp1 NA18986.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+3201G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454155 | |||||||
| chr8:38454289 | A | C | 3 | a0001c0001t0001g0008 a0001c0001t0005g0332 a0001c0001t0005g0333 |
3 | HG02622.hp1 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.91+3067T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454289 | |||||||
| chr8:38454788 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.91+2568T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454788 | |||||||
| chr8:38454820 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.91+2536T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454820 | |||||||
| chr8:38454973 | C | CT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(120): Show |
124 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.91+2382dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454973 | |||||||
| chr8:38454973 | C | CTT | 9 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0001c0001t0001g0117 others(6): Show |
9 | HG01952.hp2 HG02080.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.91+2381_91+2382dup others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454973 | |||||||
| chr8:38454973 | CT | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0097 a0001c0001t0003g0017 others(4): Show |
7 | HG01496.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+2382delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454973 | |||||||
| chr8:38455017 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.91+2339G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38455017 | |||||||
| chr8:38455049 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0002g0229 a0001c0001t0002g0279 |
3 | NA18965.hp2 NA19063.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.91+2307G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38455049 | |||||||
| chr8:38455330 | G | A | 1 | a0001c0001t0002g0301 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+2026C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38455330 | |||||||
| chr8:38455382 | G | A | 3 | a0001c0001t0002g0222 a0001c0001t0002g0226 a0001c0001t0002g0227 |
3 | NA18964.hp1 NA18991.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.91+1974C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38455382 | |||||||
| chr8:38455550 | C | T | 1 | a0001c0001t0003g0015 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.91+1806G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38455550 | |||||||
| chr8:38455824 | C | T | 1 | a0001c0001t0003g0127 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.91+1532G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38455824 | |||||||
| chr8:38456122 | C | T | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.91+1234G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456122 | |||||||
| chr8:38456286 | A | G | 1 | a0001c0001t0003g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+1070T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456286 | |||||||
| chr8:38456394 | G | T | 2 | a0001c0001t0012g0005 a0001c0012t0020g0206 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.91+962C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456394 | |||||||
| chr8:38456415 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.91+941G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456415 | |||||||
| chr8:38456432 | C | T | 3 | a0001c0001t0002g0303 a0001c0001t0003g0193 a0005c0010t0002g0304 |
3 | HG02071.hp2 HG02083.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.91+924G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456432 | |||||||
| chr8:38456625 | T | C | 1 | a0001c0001t0017g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.91+731A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456625 | |||||||
| chr8:38456709 | T | A | 2 | a0001c0001t0012g0005 a0001c0012t0020g0206 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.91+647A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456709 | |||||||
| chr8:38456716 | G | A | 1 | a0001c0001t0003g0193 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.91+640C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456716 | |||||||
| chr8:38456768 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0019g0103 a0001c0009t0013g0006 |
3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.91+588C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456768 | |||||||
| chr8:38456906 | A | G | 1 | a0001c0001t0006g0036 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.91+450T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456906 | |||||||
| chr8:38457146 | C | T | 1 | a0001c0001t0003g0203 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.91+210G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38457146 | |||||||
| chr8:38457299 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0005g0332 a0001c0001t0005g0333 |
3 | HG02622.hp1 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.91+57G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38457299 | |||||||
| chr8:38457306 | T | A | 1 | a0001c0001t0012g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+50A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38457306 | |||||||
| chr8:38457553 | C | A | 1 | a0001c0001t0001g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-88-19G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38457553 | |||||||
| chr8:38457756 | C | T | 1 | a0001c0001t0003g0193 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-88-222G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38457756 | |||||||
| chr8:38457882 | C | G | 1 | a0001c0001t0004g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-88-348G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38457882 | |||||||
| chr8:38457883 | T | C | 17 | a0001c0001t0001g0102 a0001c0001t0001g0110 a0001c0001t0001g0178 others(14): Show |
17 | HG00099.hp2 HG00140.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-88-349A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38457883 | |||||||
| chr8:38457903 | A | C | 2 | a0001c0001t0004g0246 a0001c0001t0027g0330 |
2 | HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-88-369T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38457903 | |||||||
| chr8:38458062 | C | T | 1 | a0001c0001t0003g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-88-528G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458062 | |||||||
| chr8:38458265 | G | A | 1 | a0001c0001t0019g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-88-731C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458265 | |||||||
| chr8:38458349 | T | C | 26 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0056 others(23): Show |
26 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.-88-815A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458349 | |||||||
| chr8:38458362 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0002g0300 a0001c0001t0019g0103 others(1): Show |
4 | HG02572.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-88-828C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458362 | |||||||
| chr8:38458420 | A | G | 1 | a0001c0001t0002g0254 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-88-886T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458420 | |||||||
| chr8:38458489 | C | A | 2 | a0001c0001t0003g0179 a0008c0013t0003g0180 |
2 | NA18952.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-88-955G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458489 | |||||||
| chr8:38458682 | A | G | 4 | a0001c0001t0001g0181 a0001c0001t0004g0263 a0001c0001t0004g0264 others(1): Show |
4 | HG01243.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-88-1148T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458682 | |||||||
| chr8:38458942 | G | C | 2 | a0004c0005t0002g0278 a0004c0005t0002g0311 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-88-1408C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458942 | |||||||
| chr8:38458992 | AAGCACTG others(17): Show |
A | 1 | a0001c0001t0002g0223 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-88-1482_-88-1459d others(26): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458992 | |||||||
| chr8:38459146 | T | C | 2 | a0001c0001t0005g0331 a0001c0001t0027g0330 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-88-1612A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459146 | |||||||
| chr8:38459316 | G | A | 4 | a0001c0001t0002g0209 a0001c0001t0002g0259 a0001c0001t0002g0301 others(1): Show |
4 | NA18947.hp1 NA18963.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.-88-1782C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459316 | |||||||
| chr8:38459331 | C | T | 84 | a0001c0001t0001g0067 a0001c0001t0001g0106 a0001c0001t0001g0107 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.-88-1797G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459331 | |||||||
| chr8:38459427 | A | C | 1 | a0001c0001t0004g0315 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-88-1893T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459427 | |||||||
| chr8:38459437 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-88-1903A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459437 | |||||||
| chr8:38459712 | A | C | 3 | a0002c0002t0001g0058 a0002c0002t0001g0204 a0002c0002t0001g0205 |
3 | HG01167.hp2 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-88-2178T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459712 | |||||||
| chr8:38459880 | T | C | 195 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0029 others(192): Show |
196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-88-2346A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459880 | |||||||
| chr8:38459891 | T | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(36): Show |
40 | HG00597.hp2 HG01257.hp1 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.-88-2357A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459891 | |||||||
| chr8:38459958 | A | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(230): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-88-2424T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459958 | |||||||
| chr8:38460136 | T | C | 2 | a0001c0001t0003g0108 a0001c0001t0003g0187 |
2 | NA18961.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-88-2602A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460136 | |||||||
| chr8:38460145 | T | C | 1 | a0001c0001t0003g0015 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-88-2611A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460145 | |||||||
| chr8:38460165 | G | A | 1 | a0001c0001t0003g0081 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-88-2631C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460165 | |||||||
| chr8:38460457 | T | C | 1 | a0001c0012t0020g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-88-2923A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460457 | |||||||
| chr8:38460553 | C | T | 1 | a0001c0001t0002g0262 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-88-3019G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460553 | |||||||
| chr8:38460649 | T | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(35): Show |
39 | HG00597.hp2 HG01167.hp2 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.-88-3115A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460649 | |||||||
| chr8:38460819 | G | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(141): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-88-3285C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460819 | |||||||
| chr8:38460903 | T | C | 1 | a0001c0001t0019g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-88-3369A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460903 | |||||||
| chr8:38461197 | A | G | 3 | a0001c0001t0001g0202 a0001c0001t0003g0201 a0002c0002t0001g0200 |
3 | HG02717.hp2 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-88-3663T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461197 | |||||||
| chr8:38461263 | A | C | 2 | a0001c0001t0002g0252 a0001c0001t0002g0253 |
2 | NA19012.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-88-3729T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461263 | |||||||
| chr8:38461321 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-88-3787G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461321 | |||||||
| chr8:38461363 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
6 | HG02615.hp1 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-88-3829C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461363 | |||||||
| chr8:38461420 | C | T | 1 | a0001c0001t0026g0334 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-88-3886G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461420 | |||||||
| chr8:38461456 | T | G | 1 | a0001c0003t0001g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-88-3922A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461456 | |||||||
| chr8:38461696 | C | T | 2 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-88-4162G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461696 | |||||||
| chr8:38461733 | A | AT | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-88-4200dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461733 | |||||||
| chr8:38461740 | G | C | 2 | a0001c0001t0002g0303 a0005c0010t0002g0304 |
2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-88-4206C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461740 | |||||||
| chr8:38461831 | G | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(37): Show |
41 | HG00597.hp2 HG01257.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.-88-4297C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461831 | |||||||
| chr8:38462187 | A | G | 1 | a0001c0001t0002g0313 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-88-4653T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462187 | |||||||
| chr8:38462211 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(37): Show |
41 | HG00597.hp2 HG01257.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.-88-4677T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462211 | |||||||
| chr8:38462238 | G | T | 1 | a0001c0001t0003g0065 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-88-4704C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462238 | |||||||
| chr8:38462504 | A | C | 1 | a0001c0001t0002g0233 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-88-4970T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462504 | |||||||
| chr8:38462513 | A | AT | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(4): Show |
7 | HG02615.hp1 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-88-4980dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462513 | |||||||
| chr8:38462513 | A | T | 2 | a0001c0001t0001g0049 a0001c0001t0004g0250 |
2 | HG01070.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.-88-4979T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462513 | |||||||
| chr8:38462765 | G | A | 1 | a0001c0001t0002g0305 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-89+5216C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462765 | |||||||
| chr8:38462855 | T | G | 1 | a0001c0001t0004g0245 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-89+5126A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462855 | |||||||
| chr8:38462902 | C | CT | 35 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0212 others(32): Show |
35 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-89+5078dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462902 | |||||||
| chr8:38462902 | CT | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(163): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-89+5078delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462902 | |||||||
| chr8:38462980 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-89+5001A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462980 | |||||||
| chr8:38463056 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-89+4925C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38463056 | |||||||
| chr8:38463371 | T | C | 4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0100 others(1): Show |
4 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89+4610A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38463371 | |||||||
| chr8:38463395 | A | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
9 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-89+4586T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38463395 | |||||||
| chr8:38463458 | T | C | 1 | a0001c0001t0002g0307 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-89+4523A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38463458 | |||||||
| chr8:38463558 | T | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0009t0013g0006 |
3 | HG02622.hp1 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-89+4423A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38463558 | |||||||
| chr8:38463861 | G | T | 1 | a0001c0001t0002g0252 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-89+4120C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38463861 | |||||||
| chr8:38464035 | T | C | 315 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(312): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-89+3946A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464035 | |||||||
| chr8:38464081 | G | A | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-89+3900C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464081 | |||||||
| chr8:38464089 | C | T | 108 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0002g0208 others(105): Show |
108 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-89+3892G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464089 | |||||||
| chr8:38464179 | G | T | 1 | a0001c0001t0026g0334 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-89+3802C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464179 | |||||||
| chr8:38464312 | C | CA | 16 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0049 others(13): Show |
16 | HG00597.hp2 HG00741.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-89+3668dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464312 | |||||||
| chr8:38464312 | CA | C | 88 | a0001c0001t0001g0023 a0001c0001t0001g0106 a0001c0001t0001g0107 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.-89+3668delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464312 | |||||||
| chr8:38464312 | CAA | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0083 others(28): Show |
31 | HG01175.hp1 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.-89+3667_-89+3668d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464312 | |||||||
| chr8:38464312 | CAAA | C | 147 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0060 others(144): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-89+3666_-89+3668d others(5): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464312 | |||||||
| chr8:38464572 | C | T | 6 | a0001c0001t0001g0202 a0001c0001t0003g0201 a0001c0001t0003g0203 others(3): Show |
6 | HG01167.hp2 HG01243.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89+3409G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464572 | |||||||
| chr8:38464713 | C | T | 2 | a0001c0001t0003g0113 a0001c0001t0003g0114 |
2 | NA18953.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-89+3268G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464713 | |||||||
| chr8:38464828 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(205): Show |
209 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.-89+3153T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464828 | |||||||
| chr8:38464917 | C | A | 1 | a0001c0001t0001g0104 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-89+3064G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464917 | |||||||
| chr8:38465102 | G | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(33): Show |
37 | HG00597.hp2 HG01257.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.-89+2879C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465102 | |||||||
| chr8:38465118 | T | G | 3 | a0001c0003t0001g0195 a0001c0003t0001g0196 a0001c0003t0001g0197 |
3 | HG00642.hp1 HG01175.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-89+2863A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465118 | |||||||
| chr8:38465148 | C | G | 19 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0212 others(16): Show |
19 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.-89+2833G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465148 | |||||||
| chr8:38465196 | C | A | 1 | a0001c0001t0026g0334 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-89+2785G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465196 | |||||||
| chr8:38465685 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-89+2296G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465685 | |||||||
| chr8:38465692 | G | T | 1 | a0001c0001t0003g0112 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-89+2289C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465692 | |||||||
| chr8:38465874 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-89+2107A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465874 | |||||||
| chr8:38466006 | G | GT | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0011g0004 others(1): Show |
4 | HG02622.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89+1974dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466006 | |||||||
| chr8:38466175 | A | G | 5 | a0001c0001t0002g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | HG01070.hp1 HG01123.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89+1806T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466175 | |||||||
| chr8:38466240 | C | T | 1 | a0001c0001t0003g0111 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-89+1741G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466240 | |||||||
| chr8:38466247 | C | G | 114 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0002g0208 others(111): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-89+1734G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466247 | |||||||
| chr8:38466255 | G | C | 1 | a0001c0001t0012g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-89+1726C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466255 | |||||||
| chr8:38466758 | T | A | 3 | a0001c0001t0002g0313 a0001c0001t0002g0314 a0001c0001t0004g0315 |
3 | HG00423.hp2 NA18969.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-89+1223A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466758 | |||||||
| chr8:38466763 | C | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(40): Show |
44 | HG00597.hp2 HG01167.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.-89+1218G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466763 | |||||||
| chr8:38466823 | G | A | 52 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0060 others(49): Show |
52 | HG00323.hp1 HG00558.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.-89+1158C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466823 | |||||||
| chr8:38466888 | ACACCC | A | 17 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(14): Show |
17 | HG00323.hp1 HG01069.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89+1088_-89+1092d others(7): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466888 | |||||||
| chr8:38466891 | CCCCA | C | 14 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0067 others(11): Show |
14 | HG01257.hp2 HG01258.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-89+1086_-89+1089d others(6): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466891 | |||||||
| chr8:38466895 | A | C | 3 | a0001c0001t0001g0056 a0001c0001t0008g0055 a0001c0001t0008g0057 |
3 | HG02976.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-89+1086T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466895 | |||||||
| chr8:38466895 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-89+1086T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466895 | |||||||
| chr8:38466895 | AC | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(218): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.-89+1085delG | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466895 | |||||||
| chr8:38466900 | C | G | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | NA18947.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.-89+1081G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466900 | |||||||
| chr8:38466906 | A | C | 48 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(45): Show |
48 | HG00323.hp1 HG00558.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.-89+1075T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466906 | |||||||
| chr8:38466908 | C | A | 111 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0210 others(108): Show |
111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-89+1073G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466908 | |||||||
| chr8:38467001 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-89+980C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467001 | |||||||
| chr8:38467098 | G | A | 148 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0060 others(145): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.-89+883C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467098 | |||||||
| chr8:38467120 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-89+861G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467120 | |||||||
| chr8:38467298 | C | T | 1 | a0001c0001t0028g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-89+683G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467298 | |||||||
| chr8:38467613 | G | A | 97 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0110 others(94): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.-89+368C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467613 | |||||||
| chr8:38467650 | G | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-89+331C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467650 | |||||||
| chr8:38467753 | G | A | 7 | a0001c0001t0001g0202 a0001c0001t0003g0201 a0001c0001t0003g0203 others(4): Show |
7 | HG01167.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-89+228C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467753 | |||||||
| chr8:38467767 | C | T | 1 | a0001c0001t0022g0207 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-89+214G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467767 | |||||||
| chr8:38467893 | G | A | 110 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0210 others(107): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-89+88C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467893 |