Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2264 |
| ensemblid | ENSG00000160867.15 |
| hgncid | 3691 |
| symbol | FGFR4 |
| name | fibroblast growth factor receptor 4 |
| refseq_nuc | NM_213647.3 |
| refseq_prot | NP_998812.1 |
| ensembl_nuc | ENST00000292408.9 |
| ensembl_prot | ENSP00000292408.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 177086915 |
| end | 177098144 |
| strand | + |
| ver | v1.2 |
| region | chr5:177086915-177098144 |
| region5000 | chr5:177081915-177103144 |
| regionname0 | FGFR4_chr5_177086915_177098144 |
| regionname5000 | FGFR4_chr5_177081915_177103144 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 802 | 109 | 11 | 23 | 55 | 6 | 14 | 35 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0002 | 0/0 | 802 | 106 | 1 | 21 | 64 | 3 | 17 | 47 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0003 | 0/0 | 802 | 89 | 48 | 20 | 3 | 5 | 13 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0004 | 1/1 | 802 | 46 | 29 | 10 | 0 | 2 | 3 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0005 | 0/0 | 802 | 7 | 0 | 0 | 7 | 0 | 0 | 6 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0006 | 0/0 | 796 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(791): Show |
chr5 | 177081915 | 177103144 |
| a0007 | 0/0 | 802 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0008 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(802): Show |
chr5 | 177081915 | 177103144 |
| a0009 | 0/0 | 802 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0010 | 0/0 | 802 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0011 | 0/0 | 802 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0012 | 0/0 | 802 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0013 | 0/0 | 802 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0014 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(792): Show |
chr5 | 177081915 | 177103144 |
| a0015 | 0/0 | 802 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0016 | 0/0 | 802 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0017 | 0/0 | 802 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0018 | 0/0 | 802 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0019 | 0/0 | 802 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| a0020 | 0/0 | 802 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | MRLLL others(797): Show |
chr5 | 177081915 | 177103144 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2406 | 107 | 11 | 22 | 55 | 5 | 14 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0001c0020 | 0/0 | 2406 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0001c0025 | 0/0 | 2406 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0002c0002 | 0/0 | 2406 | 104 | 1 | 21 | 63 | 3 | 16 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0002c0014 | 0/0 | 2406 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0002c0016 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0003c0004 | 0/0 | 2406 | 35 | 11 | 11 | 0 | 4 | 9 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0003c0005 | 0/0 | 2406 | 27 | 17 | 5 | 3 | 0 | 2 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0003c0006 | 0/0 | 2406 | 14 | 9 | 2 | 0 | 1 | 2 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0003c0007 | 0/0 | 2406 | 9 | 7 | 2 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0003c0010 | 0/0 | 2406 | 4 | 4 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0004c0003 | 1/1 | 2406 | 37 | 24 | 7 | 0 | 2 | 2 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0004c0009 | 0/0 | 2406 | 7 | 5 | 1 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0004c0011 | 0/0 | 2406 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0005c0008 | 0/0 | 2406 | 7 | 0 | 0 | 7 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0006c0023 | 0/0 | 2388 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2383): Show |
chr5 | 177081915 | 177103144 | ||
| a0007c0013 | 0/0 | 2406 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0008c0018 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2416): Show |
chr5 | 177081915 | 177103144 | ||
| a0009c0024 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0010c0029 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0011c0030 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0012c0019 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0013c0022 | 0/0 | 2406 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0014c0015 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2386): Show |
chr5 | 177081915 | 177103144 | ||
| a0015c0017 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0016c0028 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0017c0021 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0018c0012 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0019c0027 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 | ||
| a0020c0026 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | ATGCG others(2401): Show |
chr5 | 177081915 | 177103144 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3093 | 105 | 11 | 22 | 54 | 5 | 13 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0001c0001t0008 | 0/0 | 3093 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0001c0001t0010 | 0/0 | 3093 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0001c0020t0001 | 0/0 | 3093 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0001c0025t0001 | 0/0 | 3093 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0002c0002t0001 | 0/0 | 3093 | 98 | 1 | 20 | 62 | 3 | 12 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0002c0002t0004 | 0/0 | 3078 | 4 | 0 | 1 | 0 | 0 | 3 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3073): Show |
chr5 | 177081915 | 177103144 |
| a0002c0002t0009 | 0/0 | 3093 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0002c0002t0011 | 0/0 | 3093 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0002c0014t0001 | 0/0 | 3093 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0002c0016t0001 | 0/0 | 3093 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0003c0004t0001 | 0/0 | 3093 | 11 | 10 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0003c0004t0003 | 0/0 | 3093 | 24 | 1 | 10 | 0 | 4 | 9 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0003c0005t0002 | 0/0 | 3093 | 27 | 17 | 5 | 3 | 0 | 2 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0003c0006t0001 | 0/0 | 3093 | 14 | 9 | 2 | 0 | 1 | 2 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0003c0007t0001 | 0/0 | 3093 | 9 | 7 | 2 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0003c0010t0001 | 0/0 | 3093 | 4 | 4 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0004c0003t0001 | 1/1 | 3093 | 35 | 22 | 7 | 0 | 2 | 2 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0004c0003t0005 | 0/0 | 3093 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0004c0009t0001 | 0/0 | 3093 | 5 | 4 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0004c0009t0005 | 0/0 | 3093 | 2 | 1 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0004c0011t0001 | 0/0 | 3093 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0005c0008t0001 | 0/0 | 3093 | 7 | 0 | 0 | 7 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0006c0023t0001 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3070): Show |
chr5 | 177081915 | 177103144 |
| a0007c0013t0001 | 0/0 | 3093 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0008c0018t0001 | 0/0 | 3108 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3103): Show |
chr5 | 177081915 | 177103144 |
| a0009c0024t0001 | 0/0 | 3093 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0010c0029t0001 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0011c0030t0002 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0012c0019t0001 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0013c0022t0001 | 0/0 | 3093 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0014c0015t0007 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3073): Show |
chr5 | 177081915 | 177103144 |
| a0015c0017t0001 | 0/0 | 3093 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0016c0028t0001 | 0/0 | 3093 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0017c0021t0001 | 0/0 | 3093 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0018c0012t0001 | 0/0 | 3093 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0019c0027t0003 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3088): Show |
chr5 | 177081915 | 177103144 |
| a0020c0026t0006 | 0/0 | 3123 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | CATTC others(3118): Show |
chr5 | 177081915 | 177103144 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 65 | 3 | 11 | 41 | 3 | 7 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0020t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0001c0025t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0004 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0006 | 0/0 | 8 | 0 | 6 | 1 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0013 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0022 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0004g0007 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0009g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0002t0011g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0014t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0002c0016t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0003g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0003g0005 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0003g0012 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0003g0017 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0003g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0004t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0005t0002g0003 | 0/0 | 10 | 4 | 5 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0005t0002g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0005t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0005t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0005t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0005t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0005t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0005t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0005t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0005t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0005t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0005t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0006t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0006t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0006t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0006t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0006t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0006t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0006t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0006t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0006t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0007t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0007t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0007t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0007t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0007t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0007t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0003c0010t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0003t0001g0002 | 1/1 | 15 | 2 | 7 | 0 | 2 | 2 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0003t0001g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0003t0001g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0003t0001g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0003t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0003t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0009t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0009t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0009t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0009t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0009t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0009t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0004c0011t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0005c0008t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0005c0008t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0005c0008t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0005c0008t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0006c0023t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0007c0013t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0008c0018t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0009c0024t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0010c0029t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0011c0030t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0012c0019t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0013c0022t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0014c0015t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0015c0017t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0016c0028t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0017c0021t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0018c0012t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0019c0027t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| a0020c0026t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0020 | t0001 | g0117 | EUR | GBR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00140 | hp1 | a0003 | c0004 | t0003 | g0042 | EUR | GBR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00140 | hp2 | a0003 | c0004 | t0003 | g0012 | EUR | GBR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0061 | EUR | FIN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00280 | hp2 | a0003 | c0004 | t0003 | g0012 | EUR | FIN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00323 | hp2 | a0004 | c0003 | t0001 | g0002 | EUR | FIN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00558 | hp1 | a0002 | c0002 | t0011 | g0102 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00639 | hp1 | a0003 | c0004 | t0003 | g0020 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00639 | hp2 | a0003 | c0004 | t0003 | g0012 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00642 | hp1 | a0003 | c0005 | t0002 | g0003 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00733 | hp1 | a0003 | c0004 | t0001 | g0046 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00738 | hp2 | a0006 | c0023 | t0001 | g0113 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00741 | hp1 | a0003 | c0005 | t0002 | g0003 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG00741 | hp2 | a0004 | c0003 | t0001 | g0002 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01070 | hp2 | a0004 | c0011 | t0001 | g0002 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01071 | hp2 | a0004 | c0011 | t0001 | g0002 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01081 | hp1 | a0007 | c0013 | t0001 | g0123 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01081 | hp2 | a0004 | c0003 | t0001 | g0002 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01106 | hp1 | a0003 | c0004 | t0003 | g0017 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01109 | hp1 | a0003 | c0007 | t0001 | g0143 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01167 | hp1 | a0003 | c0007 | t0001 | g0141 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01167 | hp2 | a0003 | c0004 | t0003 | g0042 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01168 | hp2 | a0003 | c0006 | t0001 | g0031 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01243 | hp1 | a0004 | c0009 | t0005 | g0147 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01243 | hp2 | a0003 | c0006 | t0001 | g0054 | AMR | PUR | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01255 | hp1 | a0003 | c0004 | t0003 | g0012 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01256 | hp2 | a0004 | c0003 | t0001 | g0002 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01258 | hp2 | a0004 | c0003 | t0001 | g0002 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01261 | hp2 | a0001 | c0025 | t0001 | g0001 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01346 | hp2 | a0003 | c0004 | t0003 | g0079 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01358 | hp2 | a0004 | c0003 | t0001 | g0002 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01361 | hp2 | a0003 | c0004 | t0003 | g0004 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01433 | hp1 | a0004 | c0003 | t0001 | g0002 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01433 | hp2 | a0003 | c0004 | t0003 | g0004 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01496 | hp2 | a0004 | c0003 | t0001 | g0002 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01515 | hp1 | a0003 | c0006 | t0001 | g0031 | EUR | IBS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0007 | EUR | IBS | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01884 | hp1 | a0003 | c0004 | t0001 | g0078 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01884 | hp2 | a0003 | c0005 | t0002 | g0124 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01891 | hp1 | a0004 | c0003 | t0001 | g0010 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01891 | hp2 | a0003 | c0007 | t0001 | g0140 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01928 | hp1 | a0003 | c0005 | t0002 | g0003 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01952 | hp2 | a0003 | c0005 | t0002 | g0003 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02004 | hp1 | a0003 | c0004 | t0003 | g0017 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02015 | hp1 | a0008 | c0018 | t0001 | g0133 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02015 | hp2 | a0003 | c0005 | t0002 | g0003 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02055 | hp1 | a0003 | c0005 | t0002 | g0065 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02055 | hp2 | a0003 | c0005 | t0002 | g0003 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02071 | hp1 | a0009 | c0024 | t0001 | g0001 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02071 | hp2 | a0003 | c0005 | t0002 | g0126 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02145 | hp1 | a0003 | c0004 | t0001 | g0087 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02145 | hp2 | a0003 | c0005 | t0002 | g0009 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | CDX | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CDX | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | CDX | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02257 | hp1 | a0004 | c0003 | t0001 | g0021 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02257 | hp2 | a0004 | c0003 | t0001 | g0002 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02258 | hp1 | a0010 | c0029 | t0001 | g0155 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02258 | hp2 | a0004 | c0003 | t0001 | g0021 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02280 | hp1 | a0003 | c0005 | t0002 | g0066 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02280 | hp2 | a0004 | c0009 | t0001 | g0144 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02300 | hp1 | a0002 | c0002 | t0004 | g0094 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02300 | hp2 | a0003 | c0004 | t0003 | g0017 | AMR | PEL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02451 | hp1 | a0004 | c0003 | t0001 | g0153 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02523 | hp1 | a0005 | c0008 | t0001 | g0004 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02602 | hp2 | a0003 | c0005 | t0002 | g0033 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02615 | hp2 | a0003 | c0006 | t0001 | g0015 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02622 | hp1 | a0003 | c0004 | t0001 | g0046 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02622 | hp2 | a0003 | c0007 | t0001 | g0048 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02630 | hp1 | a0003 | c0004 | t0001 | g0127 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02630 | hp2 | a0003 | c0005 | t0002 | g0003 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02647 | hp1 | a0004 | c0003 | t0001 | g0152 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02647 | hp2 | a0003 | c0005 | t0002 | g0003 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02683 | hp1 | a0002 | c0002 | t0004 | g0007 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02698 | hp1 | a0003 | c0004 | t0003 | g0086 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02723 | hp1 | a0004 | c0003 | t0001 | g0010 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02723 | hp2 | a0003 | c0006 | t0001 | g0055 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0100 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02735 | hp2 | a0003 | c0006 | t0001 | g0051 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02738 | hp1 | a0004 | c0003 | t0001 | g0002 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02738 | hp2 | a0004 | c0009 | t0001 | g0150 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02809 | hp1 | a0004 | c0003 | t0001 | g0154 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02809 | hp2 | a0003 | c0010 | t0001 | g0016 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02818 | hp1 | a0003 | c0004 | t0001 | g0137 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02818 | hp2 | a0004 | c0003 | t0001 | g0011 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02886 | hp1 | a0011 | c0030 | t0002 | g0003 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02886 | hp2 | a0003 | c0005 | t0002 | g0003 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02895 | hp1 | a0004 | c0003 | t0001 | g0010 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02895 | hp2 | a0003 | c0010 | t0001 | g0016 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02896 | hp2 | a0003 | c0006 | t0001 | g0049 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02897 | hp2 | a0003 | c0010 | t0001 | g0016 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02922 | hp1 | a0003 | c0005 | t0002 | g0009 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02922 | hp2 | a0004 | c0003 | t0001 | g0021 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02965 | hp1 | a0004 | c0009 | t0005 | g0148 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02965 | hp2 | a0003 | c0004 | t0001 | g0132 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02970 | hp1 | a0003 | c0004 | t0001 | g0138 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02970 | hp2 | a0003 | c0005 | t0002 | g0009 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02976 | hp1 | a0012 | c0019 | t0001 | g0029 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02976 | hp2 | a0004 | c0009 | t0001 | g0029 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03017 | hp2 | a0003 | c0005 | t0002 | g0033 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03041 | hp1 | a0003 | c0007 | t0001 | g0048 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03041 | hp2 | a0004 | c0003 | t0001 | g0011 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03098 | hp1 | a0004 | c0009 | t0001 | g0029 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03098 | hp2 | a0004 | c0003 | t0001 | g0011 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03130 | hp1 | a0004 | c0003 | t0001 | g0156 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03130 | hp2 | a0003 | c0007 | t0001 | g0028 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03139 | hp2 | a0004 | c0003 | t0005 | g0145 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03195 | hp1 | a0004 | c0003 | t0001 | g0002 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03195 | hp2 | a0004 | c0003 | t0001 | g0010 | AFR | ESN | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03209 | hp2 | a0003 | c0007 | t0001 | g0028 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03225 | hp1 | a0003 | c0007 | t0001 | g0028 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03225 | hp2 | a0004 | c0009 | t0001 | g0149 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03239 | hp1 | a0004 | c0003 | t0001 | g0002 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03453 | hp1 | a0004 | c0003 | t0001 | g0011 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03453 | hp2 | a0003 | c0006 | t0001 | g0030 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03486 | hp1 | a0003 | c0005 | t0002 | g0057 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03486 | hp2 | a0004 | c0003 | t0005 | g0146 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03490 | hp1 | a0002 | c0002 | t0004 | g0007 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03490 | hp2 | a0001 | c0001 | t0010 | g0001 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0024 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0024 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03492 | hp2 | a0002 | c0002 | t0004 | g0007 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03540 | hp1 | a0003 | c0005 | t0002 | g0134 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03540 | hp2 | a0003 | c0006 | t0001 | g0056 | AFR | GWD | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0077 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03579 | hp2 | a0003 | c0005 | t0002 | g0009 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03654 | hp1 | a0003 | c0004 | t0003 | g0005 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03654 | hp2 | a0002 | c0002 | t0009 | g0064 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03704 | hp1 | a0003 | c0006 | t0001 | g0050 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0101 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0098 | SAS | PJL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0084 | SAS | BEB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03927 | hp1 | a0002 | c0014 | t0001 | g0018 | SAS | BEB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03927 | hp2 | a0003 | c0004 | t0003 | g0024 | SAS | BEB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | BEB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03942 | hp2 | a0003 | c0004 | t0003 | g0005 | SAS | BEB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0110 | SAS | STU | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0093 | SAS | BEB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG04199 | hp1 | a0003 | c0004 | t0003 | g0076 | SAS | STU | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG04199 | hp2 | a0003 | c0004 | t0003 | g0088 | SAS | STU | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG04204 | hp2 | a0003 | c0004 | t0003 | g0004 | SAS | STU | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG04228 | hp1 | a0013 | c0022 | t0001 | g0001 | SAS | STU | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG04228 | hp2 | a0003 | c0004 | t0003 | g0005 | SAS | STU | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18522 | hp1 | a0003 | c0005 | t0002 | g0135 | AFR | YRI | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18522 | hp2 | a0004 | c0003 | t0001 | g0011 | AFR | YRI | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | CHB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | CHB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18906 | hp1 | a0003 | c0007 | t0001 | g0142 | AFR | YRI | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18906 | hp2 | a0003 | c0006 | t0001 | g0015 | AFR | YRI | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18941 | hp2 | a0005 | c0008 | t0001 | g0129 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18945 | hp2 | a0002 | c0016 | t0001 | g0004 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18948 | hp2 | a0005 | c0008 | t0001 | g0041 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18950 | hp1 | a0005 | c0008 | t0001 | g0004 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18970 | hp2 | a0014 | c0015 | t0007 | g0037 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18985 | hp2 | a0015 | c0017 | t0001 | g0073 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18986 | hp1 | a0016 | c0028 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18999 | hp1 | a0005 | c0008 | t0001 | g0025 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19009 | hp1 | a0005 | c0008 | t0001 | g0004 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19030 | hp1 | a0004 | c0003 | t0001 | g0010 | AFR | LWK | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19030 | hp2 | a0004 | c0003 | t0001 | g0021 | AFR | LWK | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19043 | hp1 | a0003 | c0005 | t0002 | g0068 | AFR | LWK | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19043 | hp2 | a0003 | c0005 | t0002 | g0009 | AFR | LWK | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19067 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19070 | hp2 | a0005 | c0008 | t0001 | g0004 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19084 | hp1 | a0017 | c0021 | t0001 | g0063 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19084 | hp2 | a0018 | c0012 | t0001 | g0111 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19089 | hp1 | a0003 | c0005 | t0002 | g0052 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | YRI | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA20129 | hp1 | a0003 | c0005 | t0002 | g0009 | AFR | ASW | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ASW | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA20752 | hp2 | a0003 | c0004 | t0003 | g0017 | EUR | TSI | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0022 | EUR | TSI | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA20805 | hp2 | a0004 | c0003 | t0001 | g0002 | EUR | TSI | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA20905 | hp1 | a0003 | c0004 | t0003 | g0081 | SAS | GIH | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | GIH | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01123 | hp1 | a0003 | c0005 | t0002 | g0003 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02109 | hp2 | a0003 | c0006 | t0001 | g0015 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02486 | hp1 | a0004 | c0003 | t0001 | g0010 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02559 | hp1 | a0003 | c0004 | t0003 | g0085 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG02559 | hp2 | a0004 | c0003 | t0001 | g0011 | AFR | ACB | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03471 | hp1 | a0003 | c0010 | t0001 | g0016 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG06807 | hp1 | a0003 | c0006 | t0001 | g0030 | AFR | USA | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| HG06807 | hp2 | a0003 | c0004 | t0001 | g0136 | AFR | USA | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA20300 | hp1 | a0003 | c0004 | t0001 | g0109 | AFR | USA | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA20300 | hp2 | a0019 | c0027 | t0003 | g0069 | AFR | USA | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA21309 | hp1 | a0003 | c0006 | t0001 | g0015 | AFR | LWK | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| NA21309 | hp2 | a0020 | c0026 | t0006 | g0125 | AFR | LWK | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| homoSapiens | chm13v2 | a0004 | c0003 | t0001 | g0002 | REF | REF | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| homoSapiens | grch38p0 | a0004 | c0003 | t0001 | g0002 | REF | REF | FGFR4_chr5_177081915_177103144 | FGFR4 | chr5 | 177081915 | 177103144 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177089630 | G | A | 7 | a0002 a0005 a0007 others(4): Show |
118 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
missense_variant | MODERATE | c.28G>A | p.Val10Ile | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/18 | 244/3093 | 28/2409 | 10/802 | chr5 | 177089630 | |||
| chr5:177090422 | G | A | 1 | a0012 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.124G>A | p.Glu42Lys | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 3/18 | 340/3093 | 124/2409 | 42/802 | chr5 | 177090422 | |||
| chr5:177090473 | C | T | 1 | a0016 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.175C>T | p.Arg59Trp | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 3/18 | 391/3093 | 175/2409 | 59/802 | chr5 | 177090473 | |||
| chr5:177090768 | G | C | 1 | a0018 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.379G>C | p.Asp127His | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 4/18 | 595/3093 | 379/2409 | 127/802 | chr5 | 177090768 | |||
| chr5:177090796 | C | T | 17 | a0001 a0002 a0003 others(14): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
missense_variant | MODERATE | c.407C>T | p.Pro136Leu | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 4/18 | 623/3093 | 407/2409 | 136/802 | chr5 | 177090796 | |||
| chr5:177091036 | A | G | 1 | a0005 | 7 | HG02523.hp1 NA18941.hp2 NA18948.hp2 others(4): Show |
missense_variant | MODERATE | c.535A>G | p.Thr179Ala | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 5/18 | 751/3093 | 535/2409 | 179/802 | chr5 | 177091036 | |||
| chr5:177093242 | G | A | 6 | a0001 a0006 a0009 others(3): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(111): Show |
missense_variant | MODERATE | c.1162G>A | p.Gly388Arg | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 9/18 | 1378/3093 | 1162/2409 | 388/802 | chr5 | 177093242 | |||
| chr5:177093282 | G | C | 1 | a0017 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.1202G>C | p.Arg401Pro | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 9/18 | 1418/3093 | 1202/2409 | 401/802 | chr5 | 177093282 | |||
| chr5:177093431 | G | A | 1 | a0013 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1277G>A | p.Gly426Asp | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 10/18 | 1493/3093 | 1277/2409 | 426/802 | chr5 | 177093431 | |||
| chr5:177093442 | T | C | 1 | a0010 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1288T>C | p.Ser430Pro | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 10/18 | 1504/3093 | 1288/2409 | 430/802 | chr5 | 177093442 | |||
| chr5:177093464 | G | A | 1 | a0020 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1310G>A | p.Arg437His | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 10/18 | 1526/3093 | 1310/2409 | 437/802 | chr5 | 177093464 | |||
| chr5:177093493 | G | A | 1 | a0011 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1339G>A | p.Ala447Thr | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 10/18 | 1555/3093 | 1339/2409 | 447/802 | chr5 | 177093493 | |||
| chr5:177093756 | GGCCGTCA others(11): Show |
G | 1 | a0006 | 1 | HG00738.hp2 | disruptive_inframe_deletion&splice_region_variant | MODERATE | c.1502_1519delCCGTCA others(12): Show |
p.Ala501_Lys506del | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/18 | 1718/3093 | 1502/2409 | 501/802 | INFO_REALIGN_3_PRIME | chr5 | 177093756 | ||
| chr5:177095691 | G | C | 1 | a0007 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1789G>C | p.Ala597Pro | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 13/18 | 2005/3093 | 1789/2409 | 597/802 | chr5 | 177095691 | |||
| chr5:177095692 | C | G | 1 | a0007 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1790C>G | p.Ala597Gly | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 13/18 | 2006/3093 | 1790/2409 | 597/802 | chr5 | 177095692 | |||
| chr5:177096141 | G | C | 1 | a0007 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1906G>C | p.Gly636Arg | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 14/18 | 2122/3093 | 1906/2409 | 636/802 | chr5 | 177096141 | |||
| chr5:177096312 | C | G | 1 | a0019 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1970C>G | p.Ala657Gly | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/18 | 2186/3093 | 1970/2409 | 657/802 | chr5 | 177096312 | |||
| chr5:177096333 | G | T | 1 | a0015 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.1991G>T | p.Arg664Leu | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/18 | 2207/3093 | 1991/2409 | 664/802 | chr5 | 177096333 | |||
| chr5:177096355 | C | G | 1 | a0019 | 1 | NA20300.hp2 | missense_variant&splice_region_variant | MODERATE | c.2013C>G | p.Asp671Glu | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/18 | 2229/3093 | 2013/2409 | 671/802 | chr5 | 177096355 | |||
| chr5:177096356 | G | T | 1 | a0019 | 1 | NA20300.hp2 | missense_variant&splice_region_variant | MODERATE | c.2014G>T | p.Val672Leu | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/18 | 2230/3093 | 2014/2409 | 672/802 | chr5 | 177096356 | |||
| chr5:177096357 | T | C | 1 | a0019 | 1 | NA20300.hp2 | missense_variant&splice_region_variant | MODERATE | c.2015T>C | p.Val672Ala | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/18 | 2231/3093 | 2015/2409 | 672/802 | chr5 | 177096357 | |||
| chr5:177096726 | A | T | 1 | a0019 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.2138A>T | p.His713Leu | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/18 | 2354/3093 | 2138/2409 | 713/802 | chr5 | 177096726 | |||
| chr5:177096728 | T | G | 1 | a0019 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.2140T>G | p.Cys714Gly | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/18 | 2356/3093 | 2140/2409 | 714/802 | chr5 | 177096728 | |||
| chr5:177096729 | G | C | 1 | a0019 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.2141G>C | p.Cys714Ser | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/18 | 2357/3093 | 2141/2409 | 714/802 | chr5 | 177096729 | |||
| chr5:177096731 | C | T | 1 | a0019 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.2143C>T | p.Pro715Ser | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/18 | 2359/3093 | 2143/2409 | 715/802 | chr5 | 177096731 | |||
| chr5:177097606 | C | A | 1 | a0009 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.2339C>A | p.Ser780Tyr | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 2555/3093 | 2339/2409 | 780/802 | chr5 | 177097606 | |||
| chr5:177097639 | CCAGCTCC others(8): Show |
C | 1 | a0014 | 1 | NA18970.hp2 | conservative_inframe_deletion | MODERATE | c.2374_2388delAGCTCC others(9): Show |
p.Ser792_Phe796del | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 2590/3093 | 2374/2409 | 792/802 | INFO_REALIGN_3_PRIME | chr5 | 177097639 | ||
| chr5:177097655 | C | A | 1 | a0014 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.2388C>A | p.Phe796Leu | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 2604/3093 | 2388/2409 | 796/802 | chr5 | 177097655 | |||
| chr5:177097657 | G | A | 1 | a0014 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.2390G>A | p.Gly797Glu | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 2606/3093 | 2390/2409 | 797/802 | chr5 | 177097657 | |||
| chr5:177097660 | C | G | 1 | a0014 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.2393C>G | p.Ser798Cys | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 2609/3093 | 2393/2409 | 798/802 | chr5 | 177097660 | |||
| chr5:177097662 | G | A | 1 | a0014 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.2395G>A | p.Gly799Arg | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 2611/3093 | 2395/2409 | 799/802 | chr5 | 177097662 | |||
| chr5:177097670 | G | T | 1 | a0014 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.2403G>T | p.Gln801His | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 2619/3093 | 2403/2409 | 801/802 | chr5 | 177097670 | |||
| chr5:177097671 | A | C | 1 | a0014 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.2404A>C | p.Thr802Pro | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 2620/3093 | 2404/2409 | 802/802 | chr5 | 177097671 | |||
| chr5:177097672 | C | A | 1 | a0014 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.2405C>A | p.Thr802Lys | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 2621/3093 | 2405/2409 | 802/802 | chr5 | 177097672 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177090460 | T | G | 25 | a0001c0001 a0001c0020 a0001c0025 others(22): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
synonymous_variant | LOW | c.162T>G | p.Arg54Arg | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 3/18 | 378/3093 | 162/2409 | 54/802 | chr5 | 177090460 | |||
| chr5:177090800 | G | A | 1 | a0001c0020 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.411G>A | p.Ser137Ser | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 4/18 | 627/3093 | 411/2409 | 137/802 | chr5 | 177090800 | |||
| chr5:177090990 | T | C | 1 | a0003c0010 | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.489T>C | p.Pro163Pro | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 5/18 | 705/3093 | 489/2409 | 163/802 | chr5 | 177090990 | |||
| chr5:177091765 | C | T | 1 | a0003c0007 | 9 | HG01109.hp1 HG01167.hp1 HG01891.hp2 others(6): Show |
synonymous_variant | LOW | c.684C>T | p.Asn228Asn | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 6/18 | 900/3093 | 684/2409 | 228/802 | chr5 | 177091765 | |||
| chr5:177091783 | C | T | 25 | a0001c0001 a0001c0020 a0001c0025 others(22): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
synonymous_variant | LOW | c.702C>T | p.Arg234Arg | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 6/18 | 918/3093 | 702/2409 | 234/802 | chr5 | 177091783 | |||
| chr5:177092729 | C | T | 1 | a0004c0011 | 2 | HG01070.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.1002C>T | p.Leu334Leu | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 8/18 | 1218/3093 | 1002/2409 | 334/802 | chr5 | 177092729 | |||
| chr5:177093495 | C | T | 1 | a0001c0025 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1341C>T | p.Ala447Ala | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 10/18 | 1557/3093 | 1341/2409 | 447/802 | chr5 | 177093495 | |||
| chr5:177095561 | C | T | 2 | a0003c0006 a0020c0026 |
15 | HG01168.hp2 HG01243.hp2 HG01515.hp1 others(12): Show |
synonymous_variant | LOW | c.1659C>T | p.Ala553Ala | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 13/18 | 1875/3093 | 1659/2409 | 553/802 | chr5 | 177095561 | |||
| chr5:177096313 | G | C | 1 | a0019c0027 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.1971G>C | p.Ala657Ala | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/18 | 2187/3093 | 1971/2409 | 657/802 | chr5 | 177096313 | |||
| chr5:177097364 | G | A | 1 | a0002c0014 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.2226G>A | p.Ala742Ala | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 17/18 | 2442/3093 | 2226/2409 | 742/802 | chr5 | 177097364 | |||
| chr5:177097619 | C | T | 1 | a0002c0016 | 1 | NA18945.hp2 | synonymous_variant | LOW | c.2352C>T | p.His784His | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 2568/3093 | 2352/2409 | 784/802 | chr5 | 177097619 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177087007 | CGGAGGAG others(8): Show |
C | 1 | a0002c0002t0004 | 4 | HG02300.hp1 HG02683.hp1 HG03490.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-107_-93delGAGGAGC others(8): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/18 | 2565 | INFO_REALIGN_3_PRIME | chr5 | 177087007 | |||||
| chr5:177087029 | G | GCCAGGTG others(23): Show |
1 | a0020c0026t0006 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-85_-84insAGGTGAGC others(22): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/18 | 2556 | INFO_REALIGN_3_PRIME | chr5 | 177087029 | |||||
| chr5:177097677 | G | A | 1 | a0014c0015t0007 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 1 | chr5 | 177097677 | ||||||
| chr5:177097678 | C | T | 1 | a0014c0015t0007 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 2 | chr5 | 177097678 | ||||||
| chr5:177097679 | A | G | 1 | a0014c0015t0007 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3A>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 3 | chr5 | 177097679 | ||||||
| chr5:177097686 | A | T | 1 | a0014c0015t0007 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10A>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 10 | chr5 | 177097686 | ||||||
| chr5:177097702 | A | T | 2 | a0004c0003t0005 a0004c0009t0005 |
4 | HG01243.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*26A>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 26 | chr5 | 177097702 | ||||||
| chr5:177097713 | G | C | 1 | a0014c0015t0007 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*37G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 37 | chr5 | 177097713 | ||||||
| chr5:177097715 | C | T | 1 | a0014c0015t0007 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*39C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 39 | chr5 | 177097715 | ||||||
| chr5:177097796 | C | T | 1 | a0002c0002t0011 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*120C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 120 | chr5 | 177097796 | ||||||
| chr5:177097906 | C | T | 1 | a0001c0001t0010 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*230C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 230 | chr5 | 177097906 | ||||||
| chr5:177097996 | T | C | 1 | a0001c0001t0008 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*320T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 320 | chr5 | 177097996 | ||||||
| chr5:177098022 | G | C | 1 | a0001c0001t0008 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*346G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 346 | chr5 | 177098022 | ||||||
| chr5:177098028 | G | C | 2 | a0003c0004t0003 a0019c0027t0003 |
25 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*352G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 352 | chr5 | 177098028 | ||||||
| chr5:177098038 | G | A | 1 | a0001c0001t0010 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*362G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 362 | chr5 | 177098038 | ||||||
| chr5:177098070 | G | A | 2 | a0003c0005t0002 a0011c0030t0002 |
28 | HG00642.hp1 HG00741.hp1 HG01123.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*394G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 394 | chr5 | 177098070 | ||||||
| chr5:177098092 | A | T | 1 | a0002c0002t0009 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*416A>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 18/18 | 416 | chr5 | 177098092 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177087218 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-54+141C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177087218 | |||||||
| chr5:177087454 | C | T | 1 | a0002c0002t0001g0157 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-54+377C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177087454 | |||||||
| chr5:177087594 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(167): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-54+517T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177087594 | |||||||
| chr5:177087651 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-54+574C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177087651 | |||||||
| chr5:177087749 | G | C | 1 | a0003c0006t0001g0030 | 2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-54+672G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177087749 | |||||||
| chr5:177087780 | ACAG | A | 9 | a0004c0003t0005g0145 a0004c0003t0005g0146 a0004c0009t0001g0029 others(6): Show |
10 | HG01243.hp1 HG02280.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.-54+707_-54+709del others(3): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 177087780 | ||||||
| chr5:177088112 | G | A | 1 | a0004c0009t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-54+1035G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177088112 | |||||||
| chr5:177088157 | A | G | 9 | a0004c0003t0005g0145 a0004c0003t0005g0146 a0004c0009t0001g0029 others(6): Show |
10 | HG01243.hp1 HG02280.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.-54+1080A>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177088157 | |||||||
| chr5:177088169 | C | T | 6 | a0003c0007t0001g0028 a0003c0007t0001g0048 a0003c0007t0001g0140 others(3): Show |
9 | HG01109.hp1 HG01167.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-54+1092C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177088169 | |||||||
| chr5:177088190 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-54+1113C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177088190 | |||||||
| chr5:177088590 | A | AC | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(167): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-53-958dupC | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 177088590 | ||||||
| chr5:177088772 | G | A | 5 | a0003c0007t0001g0028 a0003c0007t0001g0048 a0003c0007t0001g0140 others(2): Show |
8 | HG01167.hp1 HG01891.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53-778G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177088772 | |||||||
| chr5:177088814 | G | GTGTGCCC | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(167): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-53-736_-53-735ins others(7): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177088814 | |||||||
| chr5:177088815 | C | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(167): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-53-735C>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177088815 | |||||||
| chr5:177088865 | AG | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(158): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-53-684delG | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177088865 | |||||||
| chr5:177089049 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG01069.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.-53-501C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177089049 | |||||||
| chr5:177089227 | A | G | 3 | a0003c0004t0001g0136 a0003c0004t0001g0137 a0003c0004t0001g0138 |
3 | HG02818.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-53-323A>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177089227 | |||||||
| chr5:177089536 | C | G | 2 | a0004c0009t0001g0144 a0004c0009t0001g0150 |
2 | HG02280.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-53-14C>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177089536 | |||||||
| chr5:177089539 | C | T | 3 | a0003c0005t0002g0009 a0003c0005t0002g0134 a0003c0005t0002g0135 |
8 | HG02145.hp2 HG02922.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53-11C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177089539 | |||||||
| chr5:177089541 | C | T | 6 | a0003c0007t0001g0028 a0003c0007t0001g0048 a0003c0007t0001g0140 others(3): Show |
9 | HG01109.hp1 HG01167.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53-9C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 1/17 | chr5 | 177089541 | |||||||
| chr5:177089795 | C | T | 1 | a0003c0004t0001g0046 | 2 | HG00733.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.91+102C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | chr5 | 177089795 | |||||||
| chr5:177089827 | C | G | 5 | a0003c0007t0001g0028 a0003c0007t0001g0048 a0003c0007t0001g0140 others(2): Show |
8 | HG01167.hp1 HG01891.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+134C>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | chr5 | 177089827 | |||||||
| chr5:177089952 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(167): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.91+259A>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | chr5 | 177089952 | |||||||
| chr5:177089953 | C | T | 1 | a0008c0018t0001g0133 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.91+260C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | chr5 | 177089953 | |||||||
| chr5:177090057 | G | C | 5 | a0003c0006t0001g0015 a0003c0006t0001g0031 a0003c0006t0001g0049 others(2): Show |
9 | HG01168.hp2 HG01515.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-333G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | chr5 | 177090057 | |||||||
| chr5:177090073 | G | A | 1 | a0003c0004t0001g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.92-317G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | chr5 | 177090073 | |||||||
| chr5:177090098 | T | TTG | 4 | a0003c0004t0001g0046 a0004c0009t0001g0029 a0004c0009t0001g0149 others(1): Show |
6 | HG00733.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-278_92-277dupGT | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 177090098 | ||||||
| chr5:177090135 | C | CGTGT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(142): Show |
307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.92-238_92-235dupGT others(2): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 177090135 | ||||||
| chr5:177090135 | C | CGTGTGT | 7 | a0001c0001t0001g0131 a0002c0002t0001g0128 a0002c0002t0001g0130 others(4): Show |
7 | HG00099.hp2 HG02071.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-240_92-235dupGT others(4): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 177090135 | ||||||
| chr5:177090135 | C | CGTGTGTG others(1): Show |
5 | a0003c0004t0001g0046 a0003c0004t0001g0132 a0003c0004t0001g0136 others(2): Show |
6 | HG00733.hp1 HG02622.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-242_92-235dupGT others(6): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 177090135 | ||||||
| chr5:177090135 | C | CGTGTGTG others(3): Show |
1 | a0003c0004t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.92-244_92-235dupGT others(8): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 177090135 | ||||||
| chr5:177090169 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(158): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.92-221G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | chr5 | 177090169 | |||||||
| chr5:177090198 | G | A | 1 | a0003c0007t0001g0140 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.92-192G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | chr5 | 177090198 | |||||||
| chr5:177090211 | G | C | 3 | a0003c0004t0001g0136 a0003c0004t0001g0137 a0003c0004t0001g0138 |
3 | HG02818.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.92-179G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | chr5 | 177090211 | |||||||
| chr5:177090291 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(167): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.92-99A>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | chr5 | 177090291 | |||||||
| chr5:177090325 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(167): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.92-65T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | chr5 | 177090325 | |||||||
| chr5:177090330 | C | T | 1 | a0003c0005t0002g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.92-60C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 2/17 | chr5 | 177090330 | |||||||
| chr5:177090884 | G | A | 1 | a0003c0004t0001g0046 | 2 | HG00733.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.437-54G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 4/17 | chr5 | 177090884 | |||||||
| chr5:177090892 | G | A | 1 | a0003c0004t0001g0046 | 2 | HG00733.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.437-46G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 4/17 | chr5 | 177090892 | |||||||
| chr5:177091314 | A | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(158): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.603+210A>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 5/17 | chr5 | 177091314 | |||||||
| chr5:177091425 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(167): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.604-260T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 5/17 | chr5 | 177091425 | |||||||
| chr5:177091664 | G | A | 1 | a0004c0003t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.604-21G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 5/17 | chr5 | 177091664 | |||||||
| chr5:177091676 | T | C | 1 | a0003c0007t0001g0048 | 2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.604-9T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 5/17 | chr5 | 177091676 | |||||||
| chr5:177091943 | A | G | 3 | a0004c0009t0001g0029 a0004c0009t0001g0149 a0012c0019t0001g0029 |
4 | HG02976.hp1 HG02976.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.727+135A>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 6/17 | chr5 | 177091943 | |||||||
| chr5:177092176 | G | GGAAGGTT others(6): Show |
1 | a0003c0007t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.728-143_728-131dup others(13): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 177092176 | ||||||
| chr5:177092286 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(172): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.728-35G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 6/17 | chr5 | 177092286 | |||||||
| chr5:177092507 | T | TAAAGGTA others(8): Show |
1 | a0008c0018t0001g0133 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.916_918+12dupAAGGT others(10): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 177092507 | ||||||
| chr5:177092515 | A | G | 6 | a0003c0007t0001g0028 a0003c0007t0001g0048 a0003c0007t0001g0140 others(3): Show |
9 | HG01109.hp1 HG01167.hp1 HG01891.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.918+4A>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 7/17 | chr5 | 177092515 | |||||||
| chr5:177092565 | TG | T | 10 | a0003c0006t0001g0015 a0003c0006t0001g0030 a0003c0006t0001g0031 others(7): Show |
15 | HG01168.hp2 HG01243.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.918+60delG | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 177092565 | ||||||
| chr5:177092808 | ATGCTGCG others(36): Show |
A | 1 | a0004c0009t0005g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1057+27_1057+69del others(43): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 177092808 | ||||||
| chr5:177092872 | TTGGCCTG others(7): Show |
T | 1 | a0001c0001t0001g0032 | 2 | HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1057+96_1057+109de others(15): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 177092872 | ||||||
| chr5:177092984 | G | A | 1 | a0003c0005t0002g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1058-154G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 8/17 | chr5 | 177092984 | |||||||
| chr5:177093582 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1397+31G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 10/17 | chr5 | 177093582 | |||||||
| chr5:177093847 | G | A | 2 | a0002c0002t0001g0059 a0003c0005t0002g0057 |
2 | HG03486.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1519+72G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177093847 | |||||||
| chr5:177093864 | C | T | 1 | a0003c0006t0001g0056 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1519+89C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177093864 | |||||||
| chr5:177093974 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1519+199G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177093974 | |||||||
| chr5:177094007 | G | A | 1 | a0002c0002t0001g0061 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1519+232G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177094007 | |||||||
| chr5:177094011 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1519+236C>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177094011 | |||||||
| chr5:177094136 | TG | T | 7 | a0003c0007t0001g0028 a0003c0007t0001g0048 a0003c0007t0001g0140 others(4): Show |
10 | HG01109.hp1 HG01167.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1519+364delG | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 177094136 | ||||||
| chr5:177094333 | GGCTCATA others(14): Show |
G | 1 | a0002c0002t0009g0064 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1519+559_1519+579d others(23): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177094333 | |||||||
| chr5:177094403 | G | A | 1 | a0003c0005t0002g0134 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1519+628G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177094403 | |||||||
| chr5:177094409 | T | A | 2 | a0003c0005t0002g0065 a0003c0005t0002g0066 |
2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1519+634T>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177094409 | |||||||
| chr5:177094414 | TGTGTCAG others(72): Show |
T | 1 | a0007c0013t0001g0123 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1519+640_1519+718d others(81): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177094414 | |||||||
| chr5:177094455 | C | T | 73 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0006 others(70): Show |
118 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1519+680C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177094455 | |||||||
| chr5:177094641 | G | A | 1 | a0002c0002t0001g0067 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1520-689G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177094641 | |||||||
| chr5:177094791 | A | T | 1 | a0002c0002t0001g0122 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1520-539A>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177094791 | |||||||
| chr5:177095035 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(28): Show |
111 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1520-295C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177095035 | |||||||
| chr5:177095061 | G | A | 13 | a0003c0005t0002g0003 a0003c0005t0002g0009 a0003c0005t0002g0033 others(10): Show |
28 | HG00642.hp1 HG00741.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.1520-269G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177095061 | |||||||
| chr5:177095076 | T | C | 1 | a0006c0023t0001g0113 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1520-254T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177095076 | |||||||
| chr5:177095077 | C | T | 1 | a0006c0023t0001g0113 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1520-253C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177095077 | |||||||
| chr5:177095153 | A | G | 1 | a0003c0004t0003g0042 | 2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1520-177A>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177095153 | |||||||
| chr5:177095156 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1520-174C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177095156 | |||||||
| chr5:177095254 | T | G | 1 | a0007c0013t0001g0123 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1520-76T>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177095254 | |||||||
| chr5:177095313 | G | A | 1 | a0004c0003t0001g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1520-17G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 11/17 | chr5 | 177095313 | |||||||
| chr5:177095727 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(138): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
splice_region_variant&intron_variant | LOW | c.1821+4C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 13/17 | chr5 | 177095727 | |||||||
| chr5:177095855 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1821+132G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 13/17 | chr5 | 177095855 | |||||||
| chr5:177096185 | G | A | 4 | a0004c0003t0005g0145 a0004c0003t0005g0146 a0004c0009t0005g0147 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1944+6G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 14/17 | chr5 | 177096185 | |||||||
| chr5:177096205 | T | TGGGGGTG others(139): Show |
1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1944+33_1944+34ins others(146): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 177096205 | ||||||
| chr5:177096225 | G | C | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1944+46G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 14/17 | chr5 | 177096225 | |||||||
| chr5:177096228 | C | CG | 7 | a0002c0002t0001g0070 a0002c0002t0001g0071 a0002c0002t0001g0072 others(4): Show |
7 | HG01167.hp1 HG01243.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1944+53dupG | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 177096228 | ||||||
| chr5:177096228 | C | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1944+49C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 14/17 | chr5 | 177096228 | |||||||
| chr5:177096284 | C | G | 1 | a0007c0013t0001g0123 | 1 | HG01081.hp1 | splice_region_variant&intron_variant | LOW | c.1945-3C>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 14/17 | chr5 | 177096284 | |||||||
| chr5:177096364 | C | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | splice_region_variant&intron_variant | LOW | c.2015+7C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096364 | |||||||
| chr5:177096400 | C | G | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2015+43C>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096400 | |||||||
| chr5:177096402 | A | G | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2015+45A>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096402 | |||||||
| chr5:177096423 | G | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2015+66G>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096423 | |||||||
| chr5:177096425 | C | G | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2015+68C>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096425 | |||||||
| chr5:177096442 | T | G | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2015+85T>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096442 | |||||||
| chr5:177096444 | G | A | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2015+87G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096444 | |||||||
| chr5:177096445 | A | G | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2015+88A>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096445 | |||||||
| chr5:177096469 | G | A | 1 | a0015c0017t0001g0073 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2015+112G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096469 | |||||||
| chr5:177096470 | A | C | 1 | a0015c0017t0001g0073 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2015+113A>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096470 | |||||||
| chr5:177096472 | C | A | 1 | a0015c0017t0001g0073 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2015+115C>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096472 | |||||||
| chr5:177096479 | G | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2015+122G>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096479 | |||||||
| chr5:177096541 | C | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2016-63C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096541 | |||||||
| chr5:177096550 | G | C | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2016-54G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096550 | |||||||
| chr5:177096551 | C | G | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2016-53C>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096551 | |||||||
| chr5:177096561 | C | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(167): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.2016-43C>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096561 | |||||||
| chr5:177096563 | G | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2016-41G>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096563 | |||||||
| chr5:177096575 | G | C | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2016-29G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096575 | |||||||
| chr5:177096591 | G | C | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2016-13G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096591 | |||||||
| chr5:177096592 | C | G | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2016-12C>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096592 | |||||||
| chr5:177096596 | A | C | 1 | a0004c0003t0005g0145 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.2016-8A>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096596 | |||||||
| chr5:177096596 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(153): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
splice_region_variant&intron_variant | LOW | c.2016-8A>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 15/17 | chr5 | 177096596 | |||||||
| chr5:177096746 | G | C | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | splice_region_variant&intron_variant | LOW | c.2153+5G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096746 | |||||||
| chr5:177096748 | C | G | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | splice_region_variant&intron_variant | LOW | c.2153+7C>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096748 | |||||||
| chr5:177096757 | G | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2153+16G>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096757 | |||||||
| chr5:177096786 | C | A | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2153+45C>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096786 | |||||||
| chr5:177096790 | T | C | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2153+49T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096790 | |||||||
| chr5:177096791 | C | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2153+50C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096791 | |||||||
| chr5:177096797 | T | G | 11 | a0003c0006t0001g0015 a0003c0006t0001g0030 a0003c0006t0001g0031 others(8): Show |
16 | HG01168.hp2 HG01243.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.2153+56T>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096797 | |||||||
| chr5:177096804 | G | T | 1 | a0003c0006t0001g0051 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2153+63G>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096804 | |||||||
| chr5:177096807 | C | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2153+66C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096807 | |||||||
| chr5:177096808 | T | C | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2153+67T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096808 | |||||||
| chr5:177096820 | C | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2153+79C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096820 | |||||||
| chr5:177096822 | G | C | 1 | a0003c0007t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2153+81G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096822 | |||||||
| chr5:177096824 | C | G | 1 | a0003c0007t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2153+83C>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096824 | |||||||
| chr5:177096854 | G | T | 1 | a0002c0002t0001g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2153+113G>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096854 | |||||||
| chr5:177096860 | C | CTCCTCTT others(5): Show |
1 | a0003c0010t0001g0016 | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2153+124_2153+125i others(14): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096860 | ||||||
| chr5:177096860 | C | T | 13 | a0003c0005t0002g0003 a0003c0005t0002g0009 a0003c0005t0002g0033 others(10): Show |
28 | HG00642.hp1 HG00741.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.2153+119C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096860 | |||||||
| chr5:177096862 | C | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2153+121C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096862 | |||||||
| chr5:177096869 | T | C | 16 | a0002c0014t0001g0018 a0003c0005t0002g0003 a0003c0005t0002g0009 others(13): Show |
34 | HG00642.hp1 HG00741.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.2153+128T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096869 | |||||||
| chr5:177096874 | C | T | 2 | a0003c0006t0001g0031 a0003c0006t0001g0050 |
3 | HG01168.hp2 HG01515.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2153+133C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096874 | |||||||
| chr5:177096875 | T | C | 1 | a0002c0002t0001g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2153+134T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096875 | |||||||
| chr5:177096877 | C | CCTCTCCT others(5): Show |
1 | a0007c0013t0001g0123 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2153+139_2153+140i others(14): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096877 | ||||||
| chr5:177096878 | C | CTCCTCCT others(5): Show |
1 | a0003c0004t0001g0046 | 2 | HG00733.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2153+149_2153+160d others(14): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096878 | ||||||
| chr5:177096878 | C | CTCCTCCT others(17): Show |
1 | a0003c0005t0002g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2153+145_2153+146i others(26): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096878 | ||||||
| chr5:177096878 | C | CTCCTCCT others(44): Show |
1 | a0003c0005t0002g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2153+145_2153+146i others(53): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096878 | ||||||
| chr5:177096878 | C | CTCCTCCT others(59): Show |
1 | a0003c0005t0002g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2153+145_2153+146i others(68): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096878 | ||||||
| chr5:177096878 | C | CTCCTCCT others(86): Show |
3 | a0003c0005t0002g0003 a0003c0005t0002g0124 a0011c0030t0002g0003 |
5 | HG01884.hp2 HG02055.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2153+145_2153+146i others(95): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096878 | ||||||
| chr5:177096878 | C | CTCCTCCT others(115): Show |
1 | a0003c0005t0002g0052 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2153+145_2153+146i others(124): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096878 | ||||||
| chr5:177096878 | C | CTCCTCCT others(113): Show |
6 | a0003c0005t0002g0003 a0003c0005t0002g0009 a0003c0005t0002g0033 others(3): Show |
17 | HG00642.hp1 HG00741.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.2153+145_2153+146i others(122): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096878 | ||||||
| chr5:177096881 | C | CTCCTCTC others(245): Show |
1 | a0004c0009t0005g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2153+145_2153+146i others(254): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096881 | ||||||
| chr5:177096890 | T | C | 2 | a0004c0009t0005g0148 a0007c0013t0001g0123 |
2 | HG01081.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2153+149T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096890 | |||||||
| chr5:177096900 | T | G | 1 | a0002c0002t0009g0064 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2153+159T>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096900 | |||||||
| chr5:177096905 | T | TCCTCCTC others(237): Show |
1 | a0004c0003t0005g0145 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2153+164_2153+165i others(246): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096905 | |||||||
| chr5:177096905 | T | TTCC | 7 | a0002c0002t0001g0112 a0003c0006t0001g0015 a0003c0006t0001g0031 others(4): Show |
11 | HG00673.hp1 HG01168.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.2153+173_2153+175d others(5): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(53): Show |
2 | a0003c0004t0001g0137 a0003c0004t0001g0138 |
2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2153+175_2153+176i others(62): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(23): Show |
3 | a0001c0001t0001g0080 a0003c0007t0001g0028 a0003c0007t0001g0141 |
5 | HG01167.hp1 HG03130.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2153+175_2153+176i others(32): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(110): Show |
3 | a0003c0007t0001g0048 a0003c0007t0001g0140 a0003c0007t0001g0143 |
4 | HG01109.hp1 HG01891.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2153+175_2153+176i others(119): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(68): Show |
2 | a0003c0004t0001g0127 a0003c0004t0001g0132 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2153+175_2153+176i others(77): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(110): Show |
5 | a0003c0006t0001g0030 a0003c0006t0001g0050 a0003c0006t0001g0054 others(2): Show |
6 | HG01243.hp2 HG02723.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2153+175_2153+176i others(119): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(245): Show |
1 | a0001c0001t0001g0001 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2153+175_2153+176i others(254): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(230): Show |
1 | a0001c0001t0001g0001 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2153+175_2153+176i others(239): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(131): Show |
2 | a0004c0009t0001g0029 a0012c0019t0001g0029 |
3 | HG02976.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2153+175_2153+176i others(140): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(292): Show |
1 | a0006c0023t0001g0113 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2153+175_2153+176i others(301): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(53): Show |
3 | a0001c0001t0001g0008 a0001c0001t0001g0116 a0003c0004t0003g0079 |
8 | HG01346.hp2 HG02135.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.2153+175_2153+176i others(62): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(68): Show |
2 | a0003c0004t0001g0077 a0003c0004t0001g0078 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2153+175_2153+176i others(77): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(350): Show |
1 | a0002c0002t0001g0074 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2153+175_2153+176i others(359): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(116): Show |
1 | a0002c0002t0001g0034 | 2 | HG01106.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2153+175_2153+176i others(125): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(293): Show |
1 | a0002c0002t0001g0035 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2153+175_2153+176i others(302): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(287): Show |
1 | a0003c0004t0003g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2153+175_2153+176i others(296): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(245): Show |
1 | a0001c0001t0001g0001 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2153+175_2153+176i others(254): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(299): Show |
1 | a0001c0001t0001g0001 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2153+175_2153+176i others(308): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(176): Show |
1 | a0001c0001t0001g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2153+175_2153+176i others(185): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(230): Show |
1 | a0001c0001t0001g0044 | 2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2153+175_2153+176i others(239): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(230): Show |
15 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0032 others(12): Show |
50 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.2153+175_2153+176i others(239): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(299): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0131 others(2): Show |
28 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.2153+175_2153+176i others(308): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(231): Show |
1 | a0001c0001t0008g0001 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2153+175_2153+176i others(240): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(239): Show |
2 | a0004c0003t0005g0146 a0004c0009t0005g0147 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2153+175_2153+176i others(248): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(161): Show |
1 | a0001c0001t0001g0001 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2153+175_2153+176i others(170): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(215): Show |
2 | a0001c0001t0001g0001 a0013c0022t0001g0001 |
2 | HG04228.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2153+175_2153+176i others(224): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(299): Show |
1 | a0001c0001t0001g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2153+175_2153+176i others(308): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(284): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0114 others(2): Show |
7 | HG00099.hp1 HG00642.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.2153+175_2153+176i others(293): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096905 | T | TTCCTCCT others(8): Show |
1 | a0010c0029t0001g0155 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2153+199_2153+213d others(17): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096905 | ||||||
| chr5:177096910 | C | CCTCCTCC others(107): Show |
1 | a0001c0001t0001g0151 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2153+175_2153+176i others(116): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096910 | ||||||
| chr5:177096910 | C | CCTCCTCC others(161): Show |
1 | a0001c0001t0001g0115 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2153+175_2153+176i others(170): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096910 | ||||||
| chr5:177096917 | T | C | 87 | a0001c0001t0001g0027 a0001c0001t0001g0119 a0001c0001t0001g0120 others(84): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.2153+176T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096917 | |||||||
| chr5:177096918 | T | C | 1 | a0002c0002t0009g0064 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2153+177T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096918 | |||||||
| chr5:177096919 | C | T | 1 | a0002c0002t0009g0064 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2153+178C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096919 | |||||||
| chr5:177096920 | C | T | 82 | a0001c0001t0001g0027 a0001c0001t0001g0119 a0001c0001t0001g0120 others(79): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.2153+179C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096920 | |||||||
| chr5:177096926 | C | T | 1 | a0003c0007t0001g0142 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2153+185C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096926 | |||||||
| chr5:177096928 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0151 |
2 | HG03239.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2153+187C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096928 | |||||||
| chr5:177096928 | CCTCTTCC others(47): Show |
C | 2 | a0004c0003t0001g0010 a0004c0003t0001g0153 |
7 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2153+214_2153+267d others(56): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096928 | ||||||
| chr5:177096932 | T | C | 4 | a0002c0002t0001g0013 a0002c0002t0001g0074 a0003c0004t0001g0109 others(1): Show |
4 | HG00544.hp2 HG02148.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.2153+191T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096932 | |||||||
| chr5:177096932 | T | TTCCTCCT others(224): Show |
1 | a0004c0003t0001g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2153+213_2153+214i others(233): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096932 | ||||||
| chr5:177096932 | T | TTCCTCCT others(389): Show |
1 | a0004c0003t0001g0011 | 6 | HG02559.hp2 HG02818.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2153+213_2153+214i others(398): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096932 | ||||||
| chr5:177096935 | C | CTCCTCCT others(407): Show |
1 | a0001c0001t0001g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2153+213_2153+214i others(416): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096935 | ||||||
| chr5:177096944 | C | T | 4 | a0002c0002t0001g0005 a0002c0002t0001g0128 a0003c0005t0002g0065 others(1): Show |
5 | HG02055.hp1 HG02280.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.2153+203C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096944 | |||||||
| chr5:177096947 | T | C | 3 | a0003c0004t0003g0079 a0003c0005t0002g0065 a0003c0005t0002g0066 |
3 | HG01346.hp2 HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2153+206T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096947 | |||||||
| chr5:177096947 | T | TTCCTCCT others(62): Show |
1 | a0003c0004t0003g0012 | 2 | HG00639.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.2153+213_2153+214i others(71): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096947 | ||||||
| chr5:177096947 | T | TTCCTCCT others(65): Show |
1 | a0003c0004t0003g0088 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2153+213_2153+214i others(74): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096947 | ||||||
| chr5:177096947 | T | TTCCTCCT others(113): Show |
1 | a0003c0004t0003g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2153+213_2153+214i others(122): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096947 | ||||||
| chr5:177096947 | T | TTCCTCCT others(79): Show |
1 | a0002c0002t0001g0082 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2153+213_2153+214i others(88): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096947 | ||||||
| chr5:177096949 | C | CCTCCTCC others(107): Show |
1 | a0004c0009t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2153+213_2153+214i others(116): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096949 | ||||||
| chr5:177096949 | C | CCTCCTCC others(23): Show |
1 | a0004c0009t0001g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2153+213_2153+214i others(32): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096949 | ||||||
| chr5:177096953 | C | CTCCTCCT others(2): Show |
3 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0112 |
3 | HG00673.hp1 NA19057.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2153+213_2153+214i others(11): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096953 | ||||||
| chr5:177096953 | C | CTCCTCCT others(32): Show |
1 | a0002c0002t0001g0023 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2153+213_2153+214i others(41): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096953 | ||||||
| chr5:177096954 | T | TCCTCCTC others(83): Show |
1 | a0007c0013t0001g0123 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2153+213_2153+214i others(92): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096954 | |||||||
| chr5:177096955 | T | C | 110 | a0001c0001t0001g0027 a0001c0001t0001g0120 a0002c0002t0001g0004 others(107): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.2153+214T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096955 | |||||||
| chr5:177096956 | C | CTCCTCT | 75 | a0001c0001t0001g0027 a0001c0001t0001g0120 a0002c0002t0001g0004 others(72): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2153+220_2153+221i others(8): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096956 | ||||||
| chr5:177096956 | C | CTCCTCTT others(29): Show |
1 | a0002c0002t0001g0022 | 2 | NA19240.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2153+220_2153+221i others(38): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096956 | ||||||
| chr5:177096956 | C | CTCCTCTT others(80): Show |
1 | a0003c0006t0001g0031 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2153+220_2153+221i others(89): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096956 | ||||||
| chr5:177096956 | C | CTCCTCTT others(212): Show |
1 | a0003c0004t0001g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2153+220_2153+221i others(221): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096956 | ||||||
| chr5:177096956 | C | CTCCTCTT others(137): Show |
1 | a0002c0002t0001g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2153+220_2153+221i others(146): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096956 | ||||||
| chr5:177096956 | C | CTCCTCTT others(80): Show |
1 | a0003c0006t0001g0031 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2153+220_2153+221i others(89): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096956 | ||||||
| chr5:177096958 | C | CCTCTTCC others(68): Show |
1 | a0003c0004t0003g0081 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2153+220_2153+221i others(77): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096958 | ||||||
| chr5:177096959 | C | CTCTTCCT others(59): Show |
1 | a0008c0018t0001g0133 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2153+220_2153+221i others(68): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096959 | ||||||
| chr5:177096959 | C | CTCTTCCT others(101): Show |
1 | a0002c0002t0001g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2153+220_2153+221i others(110): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096959 | ||||||
| chr5:177096959 | C | CTCTTCCT others(104): Show |
1 | a0002c0002t0001g0036 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2153+220_2153+221i others(113): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096959 | ||||||
| chr5:177096959 | C | T | 2 | a0003c0005t0002g0065 a0003c0005t0002g0066 |
2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2153+218C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096959 | |||||||
| chr5:177096961 | C | CTTCCTCC others(89): Show |
1 | a0003c0004t0003g0017 | 3 | HG01106.hp1 HG02300.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2153+220_2153+221i others(98): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096961 | |||||||
| chr5:177096961 | C | CTTCCTCC others(86): Show |
1 | a0003c0004t0003g0017 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2153+220_2153+221i others(95): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096961 | |||||||
| chr5:177096962 | C | T | 3 | a0002c0002t0001g0083 a0003c0004t0003g0085 a0003c0010t0001g0016 |
6 | HG02559.hp1 HG02809.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2153+221C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096962 | |||||||
| chr5:177096964 | G | C | 101 | a0001c0001t0001g0027 a0001c0001t0001g0120 a0002c0002t0001g0004 others(98): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.2153+223G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096964 | |||||||
| chr5:177096964 | G | T | 1 | a0004c0009t0005g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2153+223G>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096964 | |||||||
| chr5:177096971 | T | C | 13 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0034 others(10): Show |
22 | HG00673.hp1 HG01106.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.2153+230T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096971 | |||||||
| chr5:177096977 | C | CTCCTCCT others(23): Show |
1 | a0003c0007t0001g0142 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2153+240_2153+241i others(32): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096977 | ||||||
| chr5:177096977 | C | T | 3 | a0003c0004t0003g0085 a0003c0007t0001g0028 a0003c0010t0001g0016 |
6 | HG02559.hp1 HG02809.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2153+236C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096977 | |||||||
| chr5:177096979 | C | CCTCTTCC others(83): Show |
1 | a0001c0001t0001g0080 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2153+240_2153+241i others(92): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096979 | ||||||
| chr5:177096979 | C | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2153+238C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096979 | |||||||
| chr5:177096981 | T | C | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2153+240T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096981 | |||||||
| chr5:177096982 | T | C | 113 | a0001c0001t0001g0027 a0001c0001t0001g0080 a0001c0001t0001g0115 others(110): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.2153+241T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096982 | |||||||
| chr5:177096982 | T | TCTCTTCC others(158): Show |
1 | a0004c0009t0001g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2153+259_2153+260i others(167): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096982 | ||||||
| chr5:177096982 | T | TCTCTTCC others(293): Show |
1 | a0003c0007t0001g0140 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2153+274_2153+275i others(302): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096982 | ||||||
| chr5:177096982 | T | TCTCTTCC others(215): Show |
1 | a0001c0001t0001g0121 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2153+274_2153+275i others(224): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096982 | ||||||
| chr5:177096982 | T | TCTCTTCC others(86): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0116 |
6 | HG02135.hp2 HG03209.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.2153+267_2153+268i others(95): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096982 | ||||||
| chr5:177096982 | T | TCTCTTCC others(155): Show |
1 | a0001c0001t0001g0008 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2153+267_2153+268i others(164): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096982 | ||||||
| chr5:177096986 | T | C | 19 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0036 others(16): Show |
30 | HG00544.hp2 HG00673.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.2153+245T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096986 | |||||||
| chr5:177096986 | T | TTCCTCCT others(149): Show |
1 | a0002c0002t0001g0038 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2153+274_2153+275i others(158): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096986 | ||||||
| chr5:177096986 | T | TTCCTCCT others(161): Show |
1 | a0003c0004t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2153+274_2153+275i others(170): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096986 | ||||||
| chr5:177096986 | T | TTCCTCCT others(85): Show |
1 | a0003c0006t0001g0054 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2153+256_2153+257i others(94): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096986 | ||||||
| chr5:177096986 | T | TTCCTCCT others(116): Show |
1 | a0003c0005t0002g0134 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2153+255_2153+256i others(125): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096986 | ||||||
| chr5:177096986 | T | TTCCTCCT others(155): Show |
1 | a0003c0005t0002g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2153+255_2153+256i others(164): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096986 | ||||||
| chr5:177096986 | T | TTCCTCCT others(2): Show |
3 | a0003c0006t0001g0015 a0003c0006t0001g0049 a0020c0026t0006g0125 |
6 | HG02109.hp2 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2153+252_2153+253i others(11): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096986 | ||||||
| chr5:177096986 | T | TTCCTCTC others(76): Show |
1 | a0018c0012t0001g0111 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2153+250_2153+251i others(85): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096986 | ||||||
| chr5:177096987 | T | C | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2153+246T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096987 | |||||||
| chr5:177096988 | C | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2153+247C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096988 | |||||||
| chr5:177096990 | T | TTCCTCCT others(7): Show |
1 | a0003c0006t0001g0051 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2153+249_2153+250i others(16): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096990 | |||||||
| chr5:177096992 | C | T | 2 | a0003c0004t0003g0085 a0003c0010t0001g0016 |
5 | HG02559.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2153+251C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096992 | |||||||
| chr5:177096997 | C | CCTCTTCC others(16): Show |
1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2153+267_2153+268i others(25): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177096997 | ||||||
| chr5:177096997 | C | T | 9 | a0003c0005t0002g0003 a0003c0005t0002g0009 a0003c0005t0002g0033 others(6): Show |
24 | HG00642.hp1 HG00741.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.2153+256C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177096997 | |||||||
| chr5:177097001 | T | C | 21 | a0002c0002t0001g0012 a0002c0002t0001g0022 a0002c0002t0001g0074 others(18): Show |
33 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.2153+260T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097001 | |||||||
| chr5:177097001 | T | TTCC | 3 | a0002c0002t0001g0096 a0002c0002t0001g0097 a0002c0002t0001g0098 |
3 | HG03710.hp2 NA18944.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2153+272_2153+274d others(5): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCC | 2 | a0002c0002t0001g0024 a0003c0004t0003g0024 |
3 | HG03491.hp1 HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2153+269_2153+274d others(8): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCCT others(26): Show |
2 | a0002c0002t0001g0039 a0002c0002t0001g0157 |
3 | HG02027.hp1 HG02293.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2153+274_2153+275i others(35): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCCT others(38): Show |
1 | a0002c0002t0001g0090 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2153+274_2153+275i others(47): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCCT others(65): Show |
1 | a0002c0002t0001g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2153+274_2153+275i others(74): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCCT others(62): Show |
1 | a0002c0002t0001g0091 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2153+274_2153+275i others(71): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCCT others(56): Show |
1 | a0002c0002t0001g0092 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2153+274_2153+275i others(65): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCCT others(83): Show |
2 | a0002c0002t0001g0037 a0014c0015t0007g0037 |
2 | HG00438.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.2153+274_2153+275i others(92): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCCT others(59): Show |
1 | a0002c0002t0004g0094 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2153+274_2153+275i others(68): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCCT others(74): Show |
1 | a0003c0004t0001g0077 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2153+274_2153+275i others(83): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCCT others(143): Show |
1 | a0003c0007t0001g0048 | 2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2153+274_2153+275i others(152): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCCT others(146): Show |
1 | a0003c0007t0001g0143 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2153+274_2153+275i others(155): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCCT others(86): Show |
1 | a0003c0006t0001g0055 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2153+274_2153+275i others(95): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCCT others(164): Show |
1 | a0003c0004t0001g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2153+274_2153+275i others(173): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCCTCCT others(65): Show |
1 | a0003c0004t0001g0078 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2153+274_2153+275i others(74): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097001 | T | TTCTCCTC others(7): Show |
1 | a0001c0001t0001g0118 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2153+262_2153+263i others(16): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097001 | ||||||
| chr5:177097003 | C | CCTCCTTC others(149): Show |
2 | a0003c0005t0002g0065 a0003c0005t0002g0066 |
2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2153+267_2153+268i others(158): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097003 | ||||||
| chr5:177097004 | C | CTCCTCCT others(101): Show |
1 | a0002c0002t0001g0093 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2153+274_2153+275i others(110): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097004 | ||||||
| chr5:177097012 | C | T | 10 | a0001c0001t0001g0120 a0003c0005t0002g0003 a0003c0005t0002g0009 others(7): Show |
25 | HG00642.hp1 HG00741.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.2153+271C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097012 | |||||||
| chr5:177097013 | C | T | 1 | a0002c0002t0001g0083 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2153+272C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097013 | |||||||
| chr5:177097013 | CTCT | C | 8 | a0001c0001t0001g0014 a0002c0002t0001g0018 a0002c0002t0001g0019 others(5): Show |
17 | HG00438.hp2 HG00733.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2153+275_2154-274d others(5): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097013 | ||||||
| chr5:177097016 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0032 others(95): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.2153+275T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097016 | |||||||
| chr5:177097016 | T | TTCC | 3 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0112 |
3 | HG00673.hp1 NA19057.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2154-264_2154-262d others(5): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097016 | ||||||
| chr5:177097016 | T | TTCCTCC | 2 | a0002c0002t0001g0004 a0003c0006t0001g0031 |
3 | HG01168.hp2 HG01515.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.2154-267_2154-262d others(8): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097016 | ||||||
| chr5:177097016 | T | TTCCTCCT others(2): Show |
2 | a0002c0002t0001g0004 a0003c0004t0003g0042 |
3 | HG00140.hp1 HG01167.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2154-270_2154-262d others(11): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097016 | ||||||
| chr5:177097016 | T | TTCCTCCT others(74): Show |
1 | a0004c0003t0001g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2154-254_2154-253i others(83): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097016 | ||||||
| chr5:177097016 | T | TTTCTCCT others(41): Show |
1 | a0004c0009t0001g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2154-275_2154-274i others(50): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097016 | ||||||
| chr5:177097019 | C | CTCCTCCT others(95): Show |
1 | a0002c0002t0001g0006 | 8 | HG01192.hp1 HG01261.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154-262_2154-261i others(104): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097019 | ||||||
| chr5:177097019 | C | CTCCTCCT others(92): Show |
2 | a0002c0002t0001g0007 a0002c0002t0004g0007 |
6 | HG01516.hp2 HG02155.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.2154-262_2154-261i others(101): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097019 | ||||||
| chr5:177097019 | C | CTCCTCCT others(83): Show |
2 | a0003c0006t0001g0030 a0003c0006t0001g0056 |
3 | HG03453.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2154-262_2154-261i others(92): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097019 | ||||||
| chr5:177097019 | C | T | 1 | a0002c0002t0001g0074 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2154-273C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097019 | |||||||
| chr5:177097022 | C | CTCCTCCT others(92): Show |
1 | a0002c0002t0001g0099 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2154-262_2154-261i others(101): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097022 | ||||||
| chr5:177097022 | C | CTCCTCCT others(83): Show |
1 | a0002c0002t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2154-262_2154-261i others(92): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097022 | ||||||
| chr5:177097022 | C | CTCCTCCT others(92): Show |
2 | a0002c0002t0001g0025 a0005c0008t0001g0025 |
3 | HG00609.hp1 NA18999.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2154-262_2154-261i others(101): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097022 | ||||||
| chr5:177097022 | C | CTCCTCCT others(83): Show |
1 | a0002c0002t0001g0101 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2154-262_2154-261i others(92): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097022 | ||||||
| chr5:177097022 | C | CTCCTCCT others(80): Show |
1 | a0002c0002t0011g0102 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2154-262_2154-261i others(89): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097022 | ||||||
| chr5:177097022 | C | CTCCTTCT others(110): Show |
1 | a0003c0005t0002g0135 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2154-266_2154-265i others(119): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097022 | ||||||
| chr5:177097022 | C | CTCCTTCT others(95): Show |
6 | a0003c0005t0002g0003 a0003c0005t0002g0033 a0003c0005t0002g0052 others(3): Show |
16 | HG00642.hp1 HG00741.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.2154-266_2154-265i others(104): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097022 | ||||||
| chr5:177097022 | C | T | 3 | a0003c0005t0002g0065 a0003c0005t0002g0066 a0003c0005t0002g0134 |
3 | HG02055.hp1 HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2154-270C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097022 | |||||||
| chr5:177097025 | C | CTCCTCCT others(95): Show |
1 | a0002c0002t0009g0064 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2154-262_2154-261i others(104): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097025 | ||||||
| chr5:177097025 | C | CTTCTCTT others(92): Show |
1 | a0003c0005t0002g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2154-266_2154-265i others(101): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097025 | ||||||
| chr5:177097027 | C | T | 1 | a0003c0005t0002g0009 | 6 | HG02145.hp2 HG02922.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2154-265C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097027 | |||||||
| chr5:177097028 | C | T | 1 | a0002c0002t0001g0083 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2154-264C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097028 | |||||||
| chr5:177097031 | T | C | 88 | a0001c0001t0001g0027 a0002c0002t0001g0004 a0002c0002t0001g0005 others(85): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.2154-261T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097031 | |||||||
| chr5:177097031 | T | TTCCTCCT others(104): Show |
1 | a0003c0006t0001g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2154-254_2154-253i others(113): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097031 | ||||||
| chr5:177097033 | C | CTCCTCCT others(3): Show |
1 | a0018c0012t0001g0111 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2154-259_2154-258i others(12): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097033 | |||||||
| chr5:177097033 | C | T | 1 | a0003c0004t0001g0046 | 2 | HG00733.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2154-259C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097033 | |||||||
| chr5:177097034 | C | T | 4 | a0003c0004t0001g0087 a0003c0004t0003g0017 a0003c0004t0003g0085 others(1): Show |
7 | HG01106.hp1 HG02004.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2154-258C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097034 | |||||||
| chr5:177097037 | C | CTCCTCTT others(146): Show |
1 | a0003c0004t0001g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2154-254_2154-253i others(155): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097037 | ||||||
| chr5:177097037 | C | CTCCTCTT others(143): Show |
1 | a0003c0004t0001g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2154-254_2154-253i others(152): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097037 | ||||||
| chr5:177097039 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0027 others(142): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2154-253T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097039 | |||||||
| chr5:177097040 | C | CTCCTCCT others(98): Show |
1 | a0002c0002t0001g0013 | 2 | HG02148.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2154-245_2154-244i others(107): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097040 | ||||||
| chr5:177097040 | C | CTCCTCCT others(95): Show |
1 | a0002c0002t0001g0013 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2154-245_2154-244i others(104): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097040 | ||||||
| chr5:177097040 | C | CTCCTCCT others(95): Show |
1 | a0002c0002t0001g0013 | 2 | NA18944.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.2154-245_2154-244i others(104): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097040 | ||||||
| chr5:177097040 | C | CTCCTCT | 4 | a0003c0004t0003g0004 a0003c0004t0003g0005 a0003c0004t0003g0079 others(1): Show |
7 | HG01346.hp2 HG01361.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.2154-247_2154-246i others(8): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097040 | ||||||
| chr5:177097040 | C | CTCCTCTT others(83): Show |
1 | a0012c0019t0001g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2154-247_2154-246i others(92): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097040 | ||||||
| chr5:177097040 | C | CTCCTCTT others(98): Show |
1 | a0004c0009t0001g0029 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2154-247_2154-246i others(107): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097040 | ||||||
| chr5:177097040 | C | CTCTTCCT others(95): Show |
1 | a0003c0005t0002g0009 | 6 | HG02145.hp2 HG02922.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2154-250_2154-249i others(104): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097040 | ||||||
| chr5:177097040 | C | T | 2 | a0002c0002t0001g0012 a0003c0004t0003g0012 |
3 | HG00140.hp2 HG00280.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.2154-252C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097040 | |||||||
| chr5:177097042 | C | CCTCCTCT others(164): Show |
1 | a0015c0017t0001g0073 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2154-245_2154-244i others(173): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097042 | ||||||
| chr5:177097043 | C | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0032 others(27): Show |
105 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.2154-249C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097043 | |||||||
| chr5:177097046 | C | T | 4 | a0002c0002t0001g0026 a0002c0002t0001g0034 a0002c0002t0001g0110 others(1): Show |
7 | HG01106.hp2 HG01358.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.2154-246C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097046 | |||||||
| chr5:177097047 | T | C | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2154-245T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097047 | |||||||
| chr5:177097048 | G | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0027 others(137): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.2154-244G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097048 | |||||||
| chr5:177097048 | G | GCTCCTCT others(23): Show |
1 | a0003c0004t0003g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2154-227_2154-226i others(32): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097048 | ||||||
| chr5:177097048 | G | T | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2154-244G>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097048 | |||||||
| chr5:177097049 | C | T | 2 | a0002c0002t0001g0061 a0002c0002t0001g0130 |
2 | HG00280.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2154-243C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097049 | |||||||
| chr5:177097051 | CCTCTTCC others(8): Show |
C | 1 | a0004c0003t0001g0021 | 4 | HG02257.hp1 HG02258.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154-211_2154-197d others(17): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097051 | ||||||
| chr5:177097052 | C | T | 2 | a0001c0001t0001g0027 a0002c0002t0001g0005 |
3 | HG01934.hp1 NA18959.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2154-240C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097052 | |||||||
| chr5:177097055 | T | C | 37 | a0001c0001t0001g0027 a0002c0002t0001g0004 a0002c0002t0001g0005 others(34): Show |
52 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2154-237T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097055 | |||||||
| chr5:177097055 | T | TTCCTCCT others(59): Show |
1 | a0003c0004t0001g0046 | 2 | HG00733.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2154-227_2154-226i others(68): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097055 | ||||||
| chr5:177097055 | T | TTCCTCCT others(100): Show |
1 | a0002c0002t0001g0107 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2154-227_2154-226i others(109): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097055 | ||||||
| chr5:177097058 | C | T | 1 | a0002c0002t0001g0104 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2154-234C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097058 | |||||||
| chr5:177097061 | C | T | 2 | a0002c0002t0001g0034 a0002c0002t0001g0110 |
3 | HG01106.hp2 HG01358.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2154-231C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097061 | |||||||
| chr5:177097063 | C | CCTCCTCT others(131): Show |
1 | a0003c0007t0001g0140 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2154-227_2154-226i others(140): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097063 | ||||||
| chr5:177097063 | C | CCTCCTCT others(203): Show |
1 | a0003c0007t0001g0048 | 2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2154-227_2154-226i others(212): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097063 | ||||||
| chr5:177097063 | C | CCTCCTCT others(200): Show |
1 | a0003c0007t0001g0143 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2154-227_2154-226i others(209): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097063 | ||||||
| chr5:177097064 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2154-228C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097064 | |||||||
| chr5:177097066 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(150): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.2154-226T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097066 | |||||||
| chr5:177097066 | T | TCTCTTCC others(437): Show |
1 | a0003c0007t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2154-212_2154-211i others(446): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097066 | ||||||
| chr5:177097067 | C | T | 1 | a0002c0002t0001g0108 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2154-225C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097067 | |||||||
| chr5:177097069 | C | CTTCCTCC others(77): Show |
1 | a0004c0003t0001g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2154-212_2154-211i others(86): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097069 | ||||||
| chr5:177097069 | C | T | 1 | a0002c0002t0001g0034 | 2 | HG01106.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2154-223C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097069 | |||||||
| chr5:177097070 | T | C | 34 | a0001c0001t0001g0027 a0001c0001t0001g0121 a0002c0002t0001g0005 others(31): Show |
52 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.2154-222T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097070 | |||||||
| chr5:177097073 | C | CTCCTCCT others(158): Show |
1 | a0003c0004t0003g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2154-212_2154-211i others(167): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097073 | ||||||
| chr5:177097073 | C | T | 2 | a0002c0002t0001g0040 a0007c0013t0001g0123 |
3 | HG01081.hp1 NA18971.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.2154-219C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097073 | |||||||
| chr5:177097073 | CTCCTCCT others(5): Show |
C | 1 | a0002c0002t0001g0038 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2154-211_2154-200d others(14): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097073 | ||||||
| chr5:177097078 | C | CCTCCTCC others(104): Show |
1 | a0002c0002t0001g0005 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2154-212_2154-211i others(113): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(86): Show |
1 | a0002c0002t0001g0004 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2154-212_2154-211i others(95): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(122): Show |
1 | a0002c0002t0001g0018 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2154-212_2154-211i others(131): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(116): Show |
1 | a0002c0002t0001g0004 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2154-212_2154-211i others(125): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(95): Show |
2 | a0003c0004t0003g0004 a0003c0004t0003g0024 |
2 | HG03927.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2154-212_2154-211i others(104): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(98): Show |
1 | a0003c0004t0003g0042 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2154-212_2154-211i others(107): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(128): Show |
2 | a0002c0002t0001g0024 a0005c0008t0001g0129 |
3 | HG03491.hp1 HG03492.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.2154-212_2154-211i others(137): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(92): Show |
1 | a0003c0004t0003g0004 | 2 | HG01361.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.2154-212_2154-211i others(101): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(95): Show |
1 | a0003c0004t0003g0042 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2154-212_2154-211i others(104): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(125): Show |
7 | a0002c0002t0001g0018 a0002c0002t0001g0060 a0002c0002t0001g0067 others(4): Show |
11 | HG00438.hp2 HG01943.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.2154-212_2154-211i others(134): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(104): Show |
2 | a0001c0001t0001g0027 a0002c0002t0001g0122 |
2 | HG02293.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.2154-212_2154-211i others(113): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(68): Show |
4 | a0002c0002t0001g0020 a0002c0002t0001g0022 a0002c0002t0001g0023 others(1): Show |
6 | HG00673.hp1 NA18612.hp1 NA19057.hp2 others(3): Show |
intron_variant | MODIFIER | c.2154-212_2154-211i others(77): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(101): Show |
3 | a0001c0001t0001g0027 a0002c0002t0001g0005 a0002c0002t0001g0130 |
4 | HG01934.hp1 HG02165.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154-212_2154-211i others(110): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(80): Show |
1 | a0003c0004t0003g0020 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2154-212_2154-211i others(89): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(116): Show |
1 | a0002c0002t0001g0004 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2154-212_2154-211i others(125): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(83): Show |
1 | a0003c0004t0003g0012 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2154-212_2154-211i others(92): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(80): Show |
1 | a0003c0004t0003g0012 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2154-212_2154-211i others(89): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(95): Show |
1 | a0002c0002t0001g0005 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2154-212_2154-211i others(104): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(77): Show |
1 | a0003c0004t0003g0005 | 3 | HG03654.hp1 HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2154-212_2154-211i others(86): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(62): Show |
1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2154-212_2154-211i others(71): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(110): Show |
2 | a0002c0002t0001g0005 a0002c0002t0001g0012 |
2 | HG00738.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2154-212_2154-211i others(119): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(152): Show |
1 | a0002c0002t0001g0075 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2154-212_2154-211i others(161): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(107): Show |
1 | a0002c0002t0001g0061 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2154-212_2154-211i others(116): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCC others(101): Show |
1 | a0002c0002t0001g0026 | 2 | NA18969.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2154-212_2154-211i others(110): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCT others(98): Show |
2 | a0002c0002t0001g0020 a0002c0002t0001g0072 |
2 | NA18747.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.2154-212_2154-211i others(107): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCT others(245): Show |
1 | a0003c0010t0001g0016 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2154-212_2154-211i others(254): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCT others(236): Show |
1 | a0003c0010t0001g0016 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2154-212_2154-211i others(245): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCCTCT others(236): Show |
1 | a0003c0010t0001g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2154-212_2154-211i others(245): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCTTCC others(131): Show |
1 | a0002c0002t0001g0005 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2154-212_2154-211i others(140): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCTTCC others(95): Show |
1 | a0002c0002t0001g0026 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2154-212_2154-211i others(104): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CCTCTTCC others(14): Show |
1 | a0003c0004t0003g0012 | 2 | HG00639.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.2154-212_2154-211i others(23): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097078 | C | CTTCCTCC others(92): Show |
1 | a0002c0002t0001g0020 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2154-214_2154-213i others(101): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097078 | |||||||
| chr5:177097078 | C | G | 1 | a0002c0002t0001g0034 | 2 | HG01106.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2154-214C>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097078 | |||||||
| chr5:177097078 | C | T | 1 | a0002c0002t0001g0013 | 5 | HG00544.hp1 HG02148.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154-214C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097078 | |||||||
| chr5:177097078 | CCTT | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0044 others(2): Show |
9 | HG00673.hp2 HG01928.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.2154-211_2154-209d others(5): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097078 | ||||||
| chr5:177097079 | CTTCTCTT others(23): Show |
C | 1 | a0019c0027t0003g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2154-211_2154-182d others(32): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097079 | ||||||
| chr5:177097081 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(155): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2154-211T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097081 | |||||||
| chr5:177097081 | T | G | 1 | a0004c0003t0001g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2154-211T>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097081 | |||||||
| chr5:177097085 | T | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0032 others(40): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.2154-207T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097085 | |||||||
| chr5:177097085 | T | TTCCTCCT others(443): Show |
1 | a0003c0007t0001g0028 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2154-191_2154-190i others(452): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097085 | ||||||
| chr5:177097085 | T | TTCCTCCT others(446): Show |
1 | a0003c0007t0001g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2154-191_2154-190i others(455): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097085 | ||||||
| chr5:177097085 | T | TTCCTCCT others(159): Show |
1 | a0001c0001t0001g0008 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2154-193_2154-192i others(168): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097085 | ||||||
| chr5:177097085 | T | TTCCTCCT others(140): Show |
1 | a0001c0001t0001g0115 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2154-193_2154-192i others(149): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097085 | ||||||
| chr5:177097087 | C | G | 1 | a0002c0002t0001g0013 | 5 | HG00544.hp1 HG02148.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154-205C>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097087 | |||||||
| chr5:177097088 | C | CTCCTCCT others(428): Show |
1 | a0003c0007t0001g0142 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2154-191_2154-190i others(437): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097088 | ||||||
| chr5:177097088 | C | CTCCTCCT others(14): Show |
1 | a0010c0029t0001g0155 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2154-190_2154-170d others(23): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097088 | ||||||
| chr5:177097088 | C | T | 1 | a0004c0003t0001g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2154-204C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097088 | |||||||
| chr5:177097091 | C | CTCCTCCT others(178): Show |
1 | a0003c0006t0001g0051 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2154-191_2154-190i others(187): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097091 | ||||||
| chr5:177097091 | C | T | 1 | a0003c0005t0002g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2154-201C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097091 | |||||||
| chr5:177097093 | C | CCTCCTCT others(53): Show |
1 | a0004c0003t0005g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2154-193_2154-192i others(62): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097093 | ||||||
| chr5:177097093 | C | T | 60 | a0001c0001t0001g0120 a0001c0001t0001g0151 a0002c0002t0001g0006 others(57): Show |
93 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.2154-199C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097093 | |||||||
| chr5:177097094 | C | CTCCTCCT others(179): Show |
1 | a0002c0002t0001g0103 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2154-191_2154-190i others(188): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097094 | ||||||
| chr5:177097094 | C | CTCTTCCT others(101): Show |
1 | a0002c0002t0001g0106 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2154-196_2154-195i others(110): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097094 | ||||||
| chr5:177097094 | C | T | 1 | a0002c0002t0001g0013 | 5 | HG00544.hp1 HG02148.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154-198C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097094 | |||||||
| chr5:177097096 | C | CCTCTTCC others(47): Show |
1 | a0004c0009t0001g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2154-193_2154-192i others(56): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097096 | ||||||
| chr5:177097097 | C | CTCTTCCT others(80): Show |
1 | a0004c0003t0005g0145 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2154-193_2154-192i others(89): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097097 | ||||||
| chr5:177097097 | C | CTCTTCCT others(65): Show |
1 | a0004c0009t0005g0147 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2154-193_2154-192i others(74): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097097 | ||||||
| chr5:177097097 | C | T | 1 | a0003c0004t0003g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2154-195C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097097 | |||||||
| chr5:177097099 | C | CCTCCTCC others(440): Show |
1 | a0003c0007t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2154-191_2154-190i others(449): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097099 | ||||||
| chr5:177097100 | C | CTCCTCCT others(77): Show |
1 | a0003c0004t0001g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2154-191_2154-190i others(86): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097100 | ||||||
| chr5:177097100 | C | CTCCTCCT others(248): Show |
1 | a0003c0004t0001g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2154-191_2154-190i others(257): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097100 | ||||||
| chr5:177097100 | C | CTCCTCCT others(98): Show |
1 | a0002c0002t0001g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2154-191_2154-190i others(107): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097100 | ||||||
| chr5:177097100 | C | CTCCTCCT others(83): Show |
4 | a0002c0002t0001g0022 a0002c0002t0001g0039 a0002c0002t0001g0083 others(1): Show |
5 | HG02027.hp1 HG02293.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154-191_2154-190i others(92): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097100 | ||||||
| chr5:177097100 | C | CTCCTCCT others(260): Show |
1 | a0003c0006t0001g0015 | 2 | HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2154-191_2154-190i others(269): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097100 | ||||||
| chr5:177097100 | C | CTCCTCCT others(194): Show |
1 | a0003c0006t0001g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2154-191_2154-190i others(203): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097100 | ||||||
| chr5:177097100 | C | CTCCTCCT others(188): Show |
1 | a0003c0006t0001g0015 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2154-191_2154-190i others(197): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097100 | ||||||
| chr5:177097100 | C | CTCCTCCT others(185): Show |
1 | a0020c0026t0006g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2154-191_2154-190i others(194): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097100 | ||||||
| chr5:177097100 | C | CTCCTCCT others(68): Show |
1 | a0004c0009t0001g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2154-191_2154-190i others(77): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097100 | ||||||
| chr5:177097100 | C | CTCCTCCT others(65): Show |
1 | a0001c0001t0001g0008 | 4 | NA18947.hp1 NA18990.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154-191_2154-190i others(74): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097100 | ||||||
| chr5:177097100 | C | CTCCTCCT others(104): Show |
1 | a0001c0001t0001g0080 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2154-191_2154-190i others(113): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097100 | ||||||
| chr5:177097100 | C | CTCCTCCT others(131): Show |
1 | a0001c0001t0001g0008 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2154-191_2154-190i others(140): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097100 | ||||||
| chr5:177097100 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0027 others(58): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.2154-192C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097100 | |||||||
| chr5:177097102 | G | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(103): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.2154-190G>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097102 | |||||||
| chr5:177097102 | G | GCTCCTCT others(8): Show |
2 | a0001c0001t0001g0121 a0002c0002t0001g0074 |
2 | HG00544.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2154-171_2154-157d others(17): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097102 | ||||||
| chr5:177097102 | GCTCCTCT others(8): Show |
G | 5 | a0004c0003t0001g0010 a0004c0003t0001g0011 a0004c0003t0001g0152 others(2): Show |
15 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.2154-171_2154-157d others(17): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097102 | ||||||
| chr5:177097103 | C | CTCCTCCT others(86): Show |
1 | a0001c0001t0001g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2154-184_2154-183i others(95): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097103 | ||||||
| chr5:177097103 | C | T | 2 | a0001c0001t0001g0045 a0017c0021t0001g0063 |
3 | HG00673.hp2 NA18943.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2154-189C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097103 | |||||||
| chr5:177097106 | C | T | 1 | a0001c0001t0001g0044 | 2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2154-186C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097106 | |||||||
| chr5:177097109 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(83): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.2154-183T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097109 | |||||||
| chr5:177097109 | T | TTCCTCCT others(2): Show |
3 | a0002c0002t0001g0084 a0003c0005t0002g0057 a0008c0018t0001g0133 |
3 | HG02015.hp1 HG03486.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2154-177_2154-169d others(11): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097109 | ||||||
| chr5:177097109 | T | TTCCTCCT others(107): Show |
4 | a0002c0002t0001g0071 a0002c0002t0001g0095 a0002c0002t0001g0104 others(1): Show |
4 | NA18959.hp1 NA18960.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154-169_2154-168i others(116): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097109 | ||||||
| chr5:177097109 | T | TTCCTCCT others(104): Show |
1 | a0002c0002t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2154-169_2154-168i others(113): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097109 | ||||||
| chr5:177097109 | T | TTCCTCCT others(17): Show |
53 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0025 others(50): Show |
85 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.2154-180_2154-157d others(26): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097109 | ||||||
| chr5:177097109 | T | TTCCTCCT others(122): Show |
8 | a0002c0002t0001g0019 a0002c0002t0001g0040 a0002c0002t0001g0041 others(5): Show |
12 | HG01255.hp2 HG02129.hp2 HG03710.hp2 others(9): Show |
intron_variant | MODIFIER | c.2154-157_2154-156i others(131): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097109 | ||||||
| chr5:177097109 | T | TTCCTCCT others(71): Show |
2 | a0002c0002t0001g0059 a0002c0002t0001g0105 |
2 | HG00423.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2154-157_2154-156i others(80): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097109 | ||||||
| chr5:177097109 | T | TTCCTCCT others(17): Show |
1 | a0004c0009t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2154-173_2154-172i others(26): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097109 | ||||||
| chr5:177097109 | T | TTCCTCCT others(20): Show |
1 | a0004c0003t0005g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2154-173_2154-172i others(29): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097109 | ||||||
| chr5:177097109 | T | TTCCTCCT others(215): Show |
1 | a0001c0001t0001g0151 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2154-173_2154-172i others(224): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097109 | ||||||
| chr5:177097112 | C | CTCCTCCT others(5): Show |
1 | a0003c0005t0002g0033 | 2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2154-168_2154-157d others(14): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097112 | ||||||
| chr5:177097114 | C | CCTCCTCC others(19): Show |
1 | a0007c0013t0001g0123 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2154-157_2154-156i others(28): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097114 | ||||||
| chr5:177097114 | C | CCTCCTCT others(257): Show |
1 | a0003c0006t0001g0049 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2154-172_2154-171i others(266): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097114 | ||||||
| chr5:177097119 | T | TCCTCTTC others(62): Show |
1 | a0004c0009t0005g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2154-161_2154-160i others(71): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097119 | ||||||
| chr5:177097127 | C | CTCCTCCT others(371): Show |
1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2154-157_2154-156i others(380): Show |
FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 177097127 | ||||||
| chr5:177097229 | C | G | 1 | a0003c0007t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2154-63C>G | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097229 | |||||||
| chr5:177097231 | G | T | 1 | a0003c0007t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2154-61G>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097231 | |||||||
| chr5:177097232 | T | C | 1 | a0003c0007t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2154-60T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 16/17 | chr5 | 177097232 | |||||||
| chr5:177097464 | C | T | 2 | a0001c0020t0001g0117 a0006c0023t0001g0113 |
2 | HG00099.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.2260-63C>T | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 17/17 | chr5 | 177097464 | |||||||
| chr5:177097465 | G | A | 1 | a0003c0010t0001g0016 | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2260-62G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 17/17 | chr5 | 177097465 | |||||||
| chr5:177097472 | T | C | 1 | a0002c0002t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2260-55T>C | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 17/17 | chr5 | 177097472 | |||||||
| chr5:177097475 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2260-52G>A | FGFR4 | ENSG00000160867.15 | transcript | ENST00000292408.9 | protein_coding | 17/17 | chr5 | 177097475 |