Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2218 |
| ensemblid | ENSG00000106692.15 |
| hgncid | 3622 |
| symbol | FKTN |
| name | fukutin |
| refseq_nuc | NM_001079802.2 |
| refseq_prot | NP_001073270.1 |
| ensembl_nuc | ENST00000357998.10 |
| ensembl_prot | ENSP00000350687.6 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 105558131 |
| end | 105641118 |
| strand | + |
| ver | v1.2 |
| region | chr9:105558131-105641118 |
| region5000 | chr9:105553131-105646118 |
| regionname0 | FKTN_chr9_105558131_105641118 |
| regionname5000 | FKTN_chr9_105553131_105646118 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 461 | 302 | 57 | 41 | 167 | 8 | 28 | 135 | FKTN_chr9_105553131_105646118 | FKTN | MSRIN others(456): Show |
chr9 | 105553131 | 105646118 |
| a0002 | 0/1 | 461 | 48 | 14 | 13 | 14 | 4 | 2 | 10 | FKTN_chr9_105553131_105646118 | FKTN | MSRIN others(456): Show |
chr9 | 105553131 | 105646118 |
| a0003 | 0/0 | 461 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | MSRIN others(456): Show |
chr9 | 105553131 | 105646118 |
| a0004 | 0/0 | 461 | 9 | 1 | 6 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | MSRIN others(456): Show |
chr9 | 105553131 | 105646118 |
| a0005 | 0/0 | 461 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | MSRIN others(456): Show |
chr9 | 105553131 | 105646118 |
| a0006 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | MSRIN others(456): Show |
chr9 | 105553131 | 105646118 |
| a0007 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | MSRIN others(456): Show |
chr9 | 105553131 | 105646118 |
| a0008 | 0/0 | 461 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | MSRIN others(456): Show |
chr9 | 105553131 | 105646118 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1383 | 291 | 49 | 41 | 164 | 8 | 28 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0001c0005 | 0/0 | 1383 | 5 | 5 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0001c0006 | 0/0 | 1383 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0001c0008 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0001c0013 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0001c0015 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0002c0002 | 0/1 | 1383 | 47 | 14 | 12 | 14 | 4 | 2 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0002c0011 | 0/0 | 1383 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0003c0003 | 0/0 | 1383 | 13 | 13 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0004c0004 | 0/0 | 1383 | 8 | 0 | 6 | 0 | 2 | 0 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0004c0010 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0005c0007 | 0/0 | 1383 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0006c0009 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0007c0014 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 | ||
| a0008c0012 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | ATGAG others(1378): Show |
chr9 | 105553131 | 105646118 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 7455 | 84 | 7 | 14 | 51 | 2 | 9 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0002 | 0/0 | 7455 | 81 | 10 | 12 | 53 | 3 | 3 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0003 | 0/0 | 7455 | 54 | 1 | 12 | 33 | 2 | 6 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0005 | 0/0 | 7455 | 6 | 0 | 0 | 0 | 1 | 5 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0006 | 0/0 | 7454 | 16 | 14 | 1 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7449): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0007 | 0/0 | 7455 | 7 | 0 | 0 | 7 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0009 | 0/0 | 7455 | 4 | 0 | 0 | 4 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0010 | 0/0 | 7455 | 4 | 4 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0011 | 0/0 | 7454 | 4 | 4 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7449): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0012 | 0/0 | 7455 | 4 | 3 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0016 | 0/0 | 7455 | 2 | 0 | 0 | 0 | 0 | 2 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0017 | 0/0 | 7455 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0018 | 0/0 | 7454 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7449): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0027 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0029 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0030 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0031 | 0/0 | 7491 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7486): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0032 | 0/0 | 7455 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0033 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0034 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0035 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0036 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0037 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0038 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0039 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0040 | 0/0 | 7455 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0042 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0044 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0045 | 0/0 | 7455 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0046 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0047 | 0/0 | 7454 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7449): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0048 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0049 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0001t0050 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0005t0013 | 0/0 | 7455 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0005t0019 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0005t0026 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0006t0014 | 0/0 | 7454 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7449): Show |
chr9 | 105553131 | 105646118 |
| a0001c0006t0015 | 0/0 | 7454 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7449): Show |
chr9 | 105553131 | 105646118 |
| a0001c0008t0003 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0013t0002 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0001c0015t0002 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0002c0002t0001 | 0/0 | 7455 | 9 | 0 | 1 | 8 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0002c0002t0004 | 0/1 | 7455 | 27 | 9 | 10 | 2 | 3 | 2 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0002c0002t0008 | 0/0 | 7455 | 5 | 0 | 1 | 4 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0002c0002t0020 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0002c0002t0021 | 0/0 | 7455 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0002c0002t0022 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0002c0002t0023 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0002c0002t0024 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0002c0002t0025 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0002c0011t0004 | 0/0 | 7455 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0003c0003t0001 | 0/0 | 7455 | 11 | 11 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0003c0003t0004 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0003c0003t0028 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0004c0004t0005 | 0/0 | 7455 | 8 | 0 | 6 | 0 | 2 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0004c0010t0041 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0005c0007t0005 | 0/0 | 7455 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0006c0009t0015 | 0/0 | 7454 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7449): Show |
chr9 | 105553131 | 105646118 |
| a0007c0014t0043 | 0/0 | 7455 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| a0008c0012t0004 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | TAAAG others(7450): Show |
chr9 | 105553131 | 105646118 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0007 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0005g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0006g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0006g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0006g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0007g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0007g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0009g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0009g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0009g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0011g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0011g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0012g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0012g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0012g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0012g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0016g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0016g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0017g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0018g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0018g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0027g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0029g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0030g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0031g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0032g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0033g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0034g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0035g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0036g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0037g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0038g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0039g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0040g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0042g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0044g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0045g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0046g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0047g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0048g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0049g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0001t0050g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0005t0013g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0005t0013g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0005t0019g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0005t0026g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0006t0014g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0006t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0006t0015g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0008t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0013t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0001c0015t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0008g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0008g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0020g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0021g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0022g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0023g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0024g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0002t0025g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0002c0011t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0003c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0003c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0003c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0003c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0003c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0003c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0003c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0003c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0003c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0003c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0003c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0003c0003t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0003c0003t0028g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0004c0004t0005g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0004c0004t0005g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0004c0004t0005g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0004c0004t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0004c0004t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0004c0010t0041g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0005c0007t0005g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0005c0007t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0006c0009t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0007c0014t0043g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| a0008c0012t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00099 | hp2 | a0002 | c0002 | t0004 | g0032 | EUR | GBR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00140 | hp1 | a0004 | c0004 | t0005 | g0044 | EUR | GBR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0109 | EUR | GBR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0243 | EUR | FIN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | FIN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0088 | EUR | FIN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0029 | EUR | FIN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00597 | hp1 | a0002 | c0002 | t0008 | g0201 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00609 | hp1 | a0001 | c0008 | t0003 | g0094 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00609 | hp2 | a0001 | c0001 | t0037 | g0163 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00639 | hp2 | a0002 | c0002 | t0004 | g0183 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | CHS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00735 | hp1 | a0004 | c0004 | t0005 | g0250 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00735 | hp2 | a0002 | c0002 | t0004 | g0190 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG00741 | hp2 | a0002 | c0002 | t0004 | g0186 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01069 | hp1 | a0002 | c0002 | t0004 | g0191 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01074 | hp2 | a0002 | c0002 | t0004 | g0196 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01099 | hp2 | a0004 | c0004 | t0005 | g0042 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01167 | hp2 | a0004 | c0004 | t0005 | g0043 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01168 | hp1 | a0004 | c0004 | t0005 | g0044 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01192 | hp1 | a0002 | c0011 | t0004 | g0066 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01192 | hp2 | a0004 | c0004 | t0005 | g0042 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01243 | hp1 | a0002 | c0002 | t0004 | g0068 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0038 | AMR | PUR | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01255 | hp2 | a0001 | c0001 | t0012 | g0062 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01257 | hp2 | a0002 | c0002 | t0004 | g0184 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01358 | hp2 | a0002 | c0002 | t0004 | g0185 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01361 | hp1 | a0002 | c0002 | t0004 | g0211 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01516 | hp1 | a0002 | c0002 | t0004 | g0033 | EUR | IBS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01516 | hp2 | a0002 | c0002 | t0021 | g0210 | EUR | IBS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01517 | hp1 | a0002 | c0002 | t0004 | g0033 | EUR | IBS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0078 | EUR | IBS | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01884 | hp1 | a0001 | c0001 | t0010 | g0057 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01884 | hp2 | a0002 | c0002 | t0004 | g0206 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0230 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG01993 | hp2 | a0002 | c0002 | t0004 | g0067 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02004 | hp1 | a0002 | c0002 | t0008 | g0200 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02027 | hp1 | a0002 | c0002 | t0004 | g0182 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02055 | hp1 | a0002 | c0002 | t0004 | g0179 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02056 | hp2 | a0001 | c0001 | t0034 | g0113 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02071 | hp1 | a0001 | c0001 | t0048 | g0087 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02071 | hp2 | a0001 | c0001 | t0042 | g0258 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02080 | hp2 | a0001 | c0001 | t0017 | g0021 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02083 | hp1 | a0001 | c0001 | t0017 | g0021 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02148 | hp1 | a0001 | c0001 | t0032 | g0111 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | CDX | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | CDX | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | CDX | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CDX | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0065 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02258 | hp1 | a0001 | c0005 | t0013 | g0035 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02258 | hp2 | a0001 | c0001 | t0018 | g0038 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0055 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02280 | hp2 | a0002 | c0002 | t0022 | g0202 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02300 | hp1 | a0004 | c0004 | t0005 | g0043 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02451 | hp1 | a0003 | c0003 | t0001 | g0225 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02451 | hp2 | a0001 | c0005 | t0026 | g0181 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02572 | hp2 | a0001 | c0001 | t0011 | g0204 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02615 | hp2 | a0005 | c0007 | t0005 | g0039 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02622 | hp1 | a0002 | c0002 | t0020 | g0213 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0041 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0228 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0245 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0247 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02647 | hp2 | a0002 | c0002 | t0023 | g0203 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0226 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02723 | hp1 | a0001 | c0001 | t0027 | g0268 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02723 | hp2 | a0001 | c0006 | t0015 | g0054 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02738 | hp2 | a0002 | c0002 | t0004 | g0207 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0223 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0058 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0235 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02896 | hp1 | a0002 | c0002 | t0004 | g0197 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02896 | hp2 | a0001 | c0001 | t0029 | g0103 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02897 | hp1 | a0002 | c0002 | t0004 | g0198 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02965 | hp1 | a0005 | c0007 | t0005 | g0239 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0222 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02970 | hp2 | a0002 | c0002 | t0024 | g0199 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03041 | hp1 | a0001 | c0005 | t0013 | g0180 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0063 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03098 | hp2 | a0001 | c0001 | t0046 | g0060 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0233 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03130 | hp2 | a0004 | c0010 | t0041 | g0061 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0205 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03225 | hp2 | a0002 | c0002 | t0004 | g0034 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0059 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03486 | hp1 | a0001 | c0006 | t0014 | g0051 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03486 | hp2 | a0001 | c0005 | t0019 | g0189 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0040 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0040 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03492 | hp2 | a0002 | c0002 | t0004 | g0032 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03516 | hp1 | a0001 | c0006 | t0014 | g0052 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03516 | hp2 | a0002 | c0002 | t0004 | g0187 | AFR | ESN | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03540 | hp1 | a0007 | c0014 | t0043 | g0070 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0227 | AFR | GWD | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03579 | hp1 | a0003 | c0003 | t0004 | g0238 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03579 | hp2 | a0002 | c0002 | t0004 | g0195 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0232 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03669 | hp1 | a0001 | c0001 | t0045 | g0231 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03669 | hp2 | a0001 | c0001 | t0016 | g0155 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | STU | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0242 | SAS | STU | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0248 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0019 | SAS | PJL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | BEB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03831 | hp2 | a0001 | c0001 | t0040 | g0244 | SAS | BEB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | BEB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | BEB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | BEB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0081 | SAS | BEB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG04228 | hp1 | a0001 | c0001 | t0016 | g0115 | SAS | STU | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0240 | AFR | YRI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18522 | hp2 | a0005 | c0007 | t0005 | g0039 | AFR | YRI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | CHB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | CHB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | YRI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18945 | hp1 | a0001 | c0001 | t0039 | g0158 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18948 | hp1 | a0002 | c0002 | t0008 | g0008 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18951 | hp2 | a0002 | c0002 | t0008 | g0008 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18952 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18957 | hp1 | a0001 | c0001 | t0009 | g0305 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18959 | hp2 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18961 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18966 | hp2 | a0001 | c0001 | t0031 | g0003 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18972 | hp2 | a0001 | c0001 | t0036 | g0002 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18974 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18977 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18981 | hp1 | a0001 | c0001 | t0050 | g0005 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18983 | hp2 | a0001 | c0001 | t0033 | g0169 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18988 | hp1 | a0001 | c0015 | t0002 | g0026 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18988 | hp2 | a0002 | c0002 | t0008 | g0008 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18990 | hp1 | a0001 | c0001 | t0044 | g0011 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18999 | hp1 | a0001 | c0001 | t0030 | g0150 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19001 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19002 | hp2 | a0001 | c0001 | t0049 | g0098 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19007 | hp1 | a0001 | c0001 | t0009 | g0278 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19009 | hp1 | a0001 | c0001 | t0035 | g0123 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19030 | hp1 | a0001 | c0001 | t0047 | g0234 | AFR | LWK | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0237 | AFR | LWK | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19043 | hp1 | a0002 | c0002 | t0025 | g0194 | AFR | LWK | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0041 | AFR | LWK | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19057 | hp1 | a0001 | c0001 | t0007 | g0173 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19060 | hp2 | a0002 | c0002 | t0004 | g0192 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19067 | hp1 | a0008 | c0012 | t0004 | g0212 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0102 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19083 | hp2 | a0001 | c0013 | t0002 | g0307 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19090 | hp1 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19090 | hp2 | a0001 | c0001 | t0038 | g0159 | EAS | JPT | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0308 | AFR | YRI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | ASW | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA20129 | hp2 | a0003 | c0003 | t0001 | g0224 | AFR | ASW | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0029 | EUR | TSI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA20752 | hp2 | a0004 | c0004 | t0005 | g0249 | EUR | TSI | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0082 | SAS | GIH | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0241 | SAS | GIH | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02109 | hp1 | a0001 | c0001 | t0018 | g0221 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02109 | hp2 | a0001 | c0005 | t0013 | g0035 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0208 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG02559 | hp2 | a0002 | c0002 | t0004 | g0034 | AFR | ACB | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0064 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG03471 | hp2 | a0006 | c0009 | t0015 | g0053 | AFR | MSL | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG06807 | hp1 | a0001 | c0001 | t0010 | g0056 | AFR | USA | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| HG06807 | hp2 | a0003 | c0003 | t0028 | g0229 | AFR | USA | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA20300 | hp1 | a0001 | c0001 | t0011 | g0209 | AFR | USA | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | USA | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA21309 | hp1 | a0002 | c0002 | t0004 | g0188 | AFR | LWK | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0236 | AFR | LWK | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0004 | g0193 | REF | REF | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0272 | REF | REF | FKTN_chr9_105553131_105646118 | FKTN | chr9 | 105553131 | 105646118 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:105573742 | CA | C | 1 | a0001 | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
splice_region_variant | LOW | c.-90delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 105573742 | ||||||
| chr9:105601145 | C | T | 1 | a0004 | 8 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
missense_variant&splice_region_variant | MODERATE | c.166C>T | p.Arg56Cys | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/11 | 381/7455 | 166/1386 | 56/461 | chr9 | 105601145 | |||
| chr9:105601146 | G | A | 1 | a0004 | 1 | HG03130.hp2 | missense_variant&splice_region_variant | MODERATE | c.167G>A | p.Arg56His | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/11 | 382/7455 | 167/1386 | 56/461 | chr9 | 105601146 | |||
| chr9:105604218 | G | A | 1 | a0003 | 13 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
missense_variant | MODERATE | c.373G>A | p.Gly125Ser | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/11 | 588/7455 | 373/1386 | 125/461 | chr9 | 105604218 | |||
| chr9:105604453 | G | A | 2 | a0002 a0008 |
48 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
missense_variant | MODERATE | c.608G>A | p.Arg203Gln | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/11 | 823/7455 | 608/1386 | 203/461 | chr9 | 105604453 | |||
| chr9:105607839 | C | T | 1 | a0005 | 3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.668C>T | p.Thr223Ile | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/11 | 883/7455 | 668/1386 | 223/461 | chr9 | 105607839 | |||
| chr9:105607926 | A | T | 1 | a0006 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.755A>T | p.Tyr252Phe | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/11 | 970/7455 | 755/1386 | 252/461 | chr9 | 105607926 | |||
| chr9:105615351 | C | T | 1 | a0008 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.854C>T | p.Ala285Val | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/11 | 1069/7455 | 854/1386 | 285/461 | chr9 | 105615351 | |||
| chr9:105635214 | A | G | 1 | a0007 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1336A>G | p.Asn446Asp | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1551/7455 | 1336/1386 | 446/461 | chr9 | 105635214 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:105575062 | G | A | 1 | a0001c0008 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.30G>A | p.Leu10Leu | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/11 | 245/7455 | 30/1386 | 10/461 | chr9 | 105575062 | |||
| chr9:105575074 | G | A | 2 | a0001c0006 a0006c0009 |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
synonymous_variant | LOW | c.42G>A | p.Thr14Thr | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/11 | 257/7455 | 42/1386 | 14/461 | chr9 | 105575074 | |||
| chr9:105575075 | C | T | 1 | a0001c0015 | 1 | NA18988.hp1 | synonymous_variant | LOW | c.43C>T | p.Leu15Leu | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/11 | 258/7455 | 43/1386 | 15/461 | chr9 | 105575075 | |||
| chr9:105618074 | C | A | 3 | a0001c0005 a0002c0002 a0008c0012 |
52 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(49): Show |
synonymous_variant | LOW | c.1026C>A | p.Leu342Leu | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/11 | 1241/7455 | 1026/1386 | 342/461 | chr9 | 105618074 | |||
| chr9:105635108 | T | C | 1 | a0001c0013 | 1 | NA19083.hp2 | synonymous_variant | LOW | c.1230T>C | p.His410His | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1445/7455 | 1230/1386 | 410/461 | chr9 | 105635108 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:105558154 | CT | C | 3 | a0001c0006t0014 a0001c0006t0015 a0006c0009t0015 |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-191delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/11 | 16878 | chr9 | 105558154 | ||||||
| chr9:105573677 | G | C | 14 | a0001c0005t0013 a0001c0005t0019 a0001c0005t0026 others(11): Show |
45 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-158G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/11 | 1356 | chr9 | 105573677 | ||||||
| chr9:105573727 | A | T | 1 | a0001c0001t0012 | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-108A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/11 | 1306 | chr9 | 105573727 | ||||||
| chr9:105573739 | T | C | 1 | a0001c0001t0027 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-96T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/11 | 1294 | chr9 | 105573739 | ||||||
| chr9:105574988 | G | T | 2 | a0001c0005t0013 a0001c0005t0026 |
4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-45G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/11 | 45 | chr9 | 105574988 | ||||||
| chr9:105635318 | G | T | 1 | a0002c0002t0025 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*54G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 54 | chr9 | 105635318 | ||||||
| chr9:105635343 | C | T | 1 | a0001c0001t0050 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*79C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 79 | chr9 | 105635343 | ||||||
| chr9:105635563 | C | A | 1 | a0003c0003t0028 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*299C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 299 | chr9 | 105635563 | ||||||
| chr9:105635785 | A | G | 1 | a0002c0002t0024 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*521A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 521 | chr9 | 105635785 | ||||||
| chr9:105636041 | C | A | 1 | a0001c0001t0016 | 2 | HG03669.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*777C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 777 | chr9 | 105636041 | ||||||
| chr9:105636050 | T | G | 16 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0016 others(13): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*786T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 786 | chr9 | 105636050 | ||||||
| chr9:105636070 | G | C | 1 | a0001c0001t0011 | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*806G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 806 | chr9 | 105636070 | ||||||
| chr9:105636082 | C | T | 1 | a0001c0005t0026 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*818C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 818 | chr9 | 105636082 | ||||||
| chr9:105636241 | C | T | 1 | a0001c0001t0018 | 2 | HG02109.hp1 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*977C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 977 | chr9 | 105636241 | ||||||
| chr9:105636282 | T | A | 1 | a0002c0002t0008 | 5 | HG00597.hp1 HG02004.hp1 NA18948.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1018T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1018 | chr9 | 105636282 | ||||||
| chr9:105636397 | A | G | 8 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0038 others(5): Show |
62 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1133A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1133 | chr9 | 105636397 | ||||||
| chr9:105636493 | A | G | 2 | a0002c0002t0022 a0002c0002t0023 |
2 | HG02280.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1229A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1229 | chr9 | 105636493 | ||||||
| chr9:105636513 | C | T | 1 | a0001c0001t0037 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1249C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1249 | chr9 | 105636513 | ||||||
| chr9:105636553 | G | A | 1 | a0001c0001t0029 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1289G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1289 | chr9 | 105636553 | ||||||
| chr9:105636587 | C | T | 3 | a0001c0006t0014 a0001c0006t0015 a0006c0009t0015 |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1323C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1323 | chr9 | 105636587 | ||||||
| chr9:105636902 | A | G | 1 | a0001c0001t0047 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1638A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1638 | chr9 | 105636902 | ||||||
| chr9:105637107 | A | T | 2 | a0001c0001t0007 a0001c0001t0036 |
8 | NA18952.hp2 NA18961.hp2 NA18972.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1843A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1843 | chr9 | 105637107 | ||||||
| chr9:105637123 | G | C | 1 | a0001c0001t0012 | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1859G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1859 | chr9 | 105637123 | ||||||
| chr9:105637162 | A | G | 2 | a0001c0006t0015 a0006c0009t0015 |
2 | HG02723.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1898A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 1898 | chr9 | 105637162 | ||||||
| chr9:105637321 | G | A | 1 | a0001c0001t0038 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2057G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2057 | chr9 | 105637321 | ||||||
| chr9:105637544 | T | C | 9 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0038 others(6): Show |
63 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2280T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2280 | chr9 | 105637544 | ||||||
| chr9:105637562 | C | G | 2 | a0001c0001t0010 a0001c0001t0012 |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2298C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2298 | chr9 | 105637562 | ||||||
| chr9:105637691 | G | T | 1 | a0002c0002t0024 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2427G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2427 | chr9 | 105637691 | ||||||
| chr9:105637856 | T | C | 1 | a0004c0010t0041 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2592T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2592 | chr9 | 105637856 | ||||||
| chr9:105637904 | G | A | 1 | a0001c0001t0048 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2640G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2640 | chr9 | 105637904 | ||||||
| chr9:105638052 | C | T | 1 | a0002c0002t0021 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2788C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2788 | chr9 | 105638052 | ||||||
| chr9:105638149 | G | A | 1 | a0002c0002t0022 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2885G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2885 | chr9 | 105638149 | ||||||
| chr9:105638174 | C | A | 2 | a0001c0001t0017 a0001c0001t0048 |
3 | HG02071.hp1 HG02080.hp2 HG02083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2910C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2910 | chr9 | 105638174 | ||||||
| chr9:105638194 | G | T | 1 | a0001c0001t0035 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2930G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2930 | chr9 | 105638194 | ||||||
| chr9:105638259 | T | G | 3 | a0001c0006t0014 a0001c0006t0015 a0006c0009t0015 |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2995T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 2995 | chr9 | 105638259 | ||||||
| chr9:105638360 | G | C | 1 | a0001c0001t0036 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3096G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3096 | chr9 | 105638360 | ||||||
| chr9:105638390 | C | G | 1 | a0001c0001t0046 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3126C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3126 | chr9 | 105638390 | ||||||
| chr9:105638616 | C | A | 1 | a0001c0001t0030 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3352C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3352 | chr9 | 105638616 | ||||||
| chr9:105638629 | G | A | 1 | a0001c0001t0042 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3365G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3365 | chr9 | 105638629 | ||||||
| chr9:105638641 | A | G | 2 | a0001c0001t0009 a0001c0001t0034 |
5 | HG02056.hp2 NA18957.hp1 NA18959.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3377A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3377 | chr9 | 105638641 | ||||||
| chr9:105639042 | T | C | 8 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0046 others(5): Show |
15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3778T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3778 | chr9 | 105639042 | ||||||
| chr9:105639130 | C | T | 2 | a0001c0006t0015 a0006c0009t0015 |
2 | HG02723.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3866C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 3866 | chr9 | 105639130 | ||||||
| chr9:105639595 | A | T | 1 | a0001c0001t0033 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4331A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 4331 | chr9 | 105639595 | ||||||
| chr9:105639642 | GA | G | 3 | a0001c0001t0006 a0001c0001t0018 a0001c0001t0047 |
19 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4388delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 4388 | INFO_REALIGN_3_PRIME | chr9 | 105639642 | |||||
| chr9:105639755 | T | C | 1 | a0007c0014t0043 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4491T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 4491 | chr9 | 105639755 | ||||||
| chr9:105639765 | A | G | 1 | a0001c0001t0033 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4501A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 4501 | chr9 | 105639765 | ||||||
| chr9:105640089 | T | C | 3 | a0001c0001t0010 a0001c0001t0012 a0001c0005t0019 |
9 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4825T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 4825 | chr9 | 105640089 | ||||||
| chr9:105640305 | G | A | 6 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0018 others(3): Show |
36 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*5041G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5041 | chr9 | 105640305 | ||||||
| chr9:105640326 | G | A | 3 | a0001c0001t0006 a0001c0001t0018 a0001c0001t0047 |
19 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5062G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5062 | chr9 | 105640326 | ||||||
| chr9:105640348 | C | T | 1 | a0002c0002t0020 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5084C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5084 | chr9 | 105640348 | ||||||
| chr9:105640349 | G | A | 1 | a0001c0001t0044 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5085G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5085 | chr9 | 105640349 | ||||||
| chr9:105640376 | C | A | 1 | a0001c0001t0049 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5112C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5112 | chr9 | 105640376 | ||||||
| chr9:105640516 | G | A | 1 | a0001c0005t0019 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5252G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5252 | chr9 | 105640516 | ||||||
| chr9:105640524 | G | T | 6 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0048 others(3): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*5260G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5260 | chr9 | 105640524 | ||||||
| chr9:105640559 | A | G | 1 | a0001c0001t0046 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5295A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5295 | chr9 | 105640559 | ||||||
| chr9:105640781 | T | C | 1 | a0001c0001t0010 | 4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5517T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5517 | chr9 | 105640781 | ||||||
| chr9:105640882 | T | A | 17 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0016 others(14): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*5618T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5618 | chr9 | 105640882 | ||||||
| chr9:105640905 | A | G | 1 | a0001c0001t0032 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5641A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5641 | chr9 | 105640905 | ||||||
| chr9:105640938 | C | T | 1 | a0001c0001t0031 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5674C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5674 | chr9 | 105640938 | ||||||
| chr9:105640945 | A | T | 1 | a0001c0001t0031 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5681A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5681 | chr9 | 105640945 | ||||||
| chr9:105640947 | A | T | 1 | a0001c0001t0031 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5683A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5683 | chr9 | 105640947 | ||||||
| chr9:105640951 | T | TTTCTGTT others(29): Show |
1 | a0001c0001t0031 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5687_*5688insTTCT others(32): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 11/11 | 5688 | chr9 | 105640951 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:105558205 | T | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+40T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558205 | |||||||
| chr9:105558400 | G | A | 1 | a0001c0001t0006g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-181+235G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558400 | |||||||
| chr9:105558585 | T | G | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-181+420T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558585 | |||||||
| chr9:105558630 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+465G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558630 | |||||||
| chr9:105558636 | GA | G | 12 | a0001c0001t0001g0309 a0001c0001t0006g0015 a0001c0001t0006g0308 others(9): Show |
14 | HG01255.hp2 HG02257.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.-181+485delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105558636 | ||||||
| chr9:105558650 | A | C | 1 | a0001c0001t0001g0309 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-181+485A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558650 | |||||||
| chr9:105558707 | G | A | 195 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(192): Show |
227 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-181+542G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558707 | |||||||
| chr9:105558793 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
5 | HG00099.hp1 HG00280.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.-181+628G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558793 | |||||||
| chr9:105558874 | C | T | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+709C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105558874 | |||||||
| chr9:105559084 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+919A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559084 | |||||||
| chr9:105559302 | G | C | 1 | a0001c0001t0010g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-181+1137G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559302 | |||||||
| chr9:105559483 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+1318A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559483 | |||||||
| chr9:105559541 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+1376G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559541 | |||||||
| chr9:105559603 | G | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+1438G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559603 | |||||||
| chr9:105559684 | C | CA | 10 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(7): Show |
10 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-181+1533dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105559684 | ||||||
| chr9:105559743 | G | A | 2 | a0002c0002t0004g0067 a0002c0002t0004g0068 |
2 | HG01243.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-181+1578G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559743 | |||||||
| chr9:105559755 | T | C | 1 | a0001c0001t0006g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-181+1590T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559755 | |||||||
| chr9:105559836 | G | C | 240 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0219 others(237): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.-181+1671G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105559836 | |||||||
| chr9:105560109 | C | G | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+1944C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560109 | |||||||
| chr9:105560254 | C | T | 5 | a0004c0004t0005g0042 a0004c0004t0005g0043 a0004c0004t0005g0044 others(2): Show |
8 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-181+2089C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560254 | |||||||
| chr9:105560274 | T | G | 1 | a0001c0001t0002g0069 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-181+2109T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560274 | |||||||
| chr9:105560330 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-181+2165G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560330 | |||||||
| chr9:105560518 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+2353T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560518 | |||||||
| chr9:105560522 | C | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+2357C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560522 | |||||||
| chr9:105560809 | C | G | 1 | a0001c0001t0003g0214 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-181+2644C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560809 | |||||||
| chr9:105560828 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+2663T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560828 | |||||||
| chr9:105560845 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0219 |
3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-181+2680T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560845 | |||||||
| chr9:105560870 | C | T | 42 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(39): Show |
48 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-181+2705C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560870 | |||||||
| chr9:105560920 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+2755C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105560920 | |||||||
| chr9:105561046 | A | G | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+2881A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561046 | |||||||
| chr9:105561084 | CAAAAAAC others(5): Show |
C | 1 | a0004c0004t0005g0250 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-181+2931_-181+294 others(16): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105561084 | ||||||
| chr9:105561091 | CA | C | 10 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(7): Show |
10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-181+2937delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105561091 | ||||||
| chr9:105561282 | A | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+3117A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561282 | |||||||
| chr9:105561327 | TAC | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+3164_-181+316 others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105561327 | ||||||
| chr9:105561566 | T | A | 1 | a0002c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-181+3401T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561566 | |||||||
| chr9:105561569 | T | A | 1 | a0002c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-181+3404T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561569 | |||||||
| chr9:105561570 | T | C | 1 | a0002c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-181+3405T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561570 | |||||||
| chr9:105561571 | C | A | 1 | a0002c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-181+3406C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561571 | |||||||
| chr9:105561641 | A | C | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+3476A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561641 | |||||||
| chr9:105561783 | A | G | 1 | a0002c0002t0020g0213 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-181+3618A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561783 | |||||||
| chr9:105561828 | T | G | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+3663T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105561828 | |||||||
| chr9:105561925 | A | AT | 9 | a0001c0001t0001g0304 a0001c0001t0001g0306 a0001c0001t0002g0031 others(6): Show |
10 | HG01258.hp1 HG02523.hp1 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.-181+3775dupT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105561925 | ||||||
| chr9:105561925 | AT | A | 10 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(7): Show |
10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-181+3775delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105561925 | ||||||
| chr9:105562004 | ATCTC | A | 4 | a0001c0001t0006g0038 a0001c0001t0006g0220 a0001c0001t0018g0038 others(1): Show |
4 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+3843_-181+384 others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105562004 | ||||||
| chr9:105562033 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+3868C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562033 | |||||||
| chr9:105562149 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-181+3984C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562149 | |||||||
| chr9:105562169 | T | C | 63 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0252 others(60): Show |
81 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.-181+4004T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562169 | |||||||
| chr9:105562399 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4234G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562399 | |||||||
| chr9:105562543 | G | C | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-181+4378G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562543 | |||||||
| chr9:105562601 | C | A | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-181+4436C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562601 | |||||||
| chr9:105562619 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4454C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562619 | |||||||
| chr9:105562624 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4459T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562624 | |||||||
| chr9:105562649 | G | A | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-181+4484G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562649 | |||||||
| chr9:105562746 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4581C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562746 | |||||||
| chr9:105562831 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4666T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562831 | |||||||
| chr9:105562853 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0301 a0001c0001t0001g0302 |
5 | HG01109.hp1 HG02615.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-181+4688A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562853 | |||||||
| chr9:105562903 | C | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4738C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562903 | |||||||
| chr9:105562904 | T | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+4739T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562904 | |||||||
| chr9:105562961 | C | A | 1 | a0002c0002t0004g0182 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-181+4796C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562961 | |||||||
| chr9:105562999 | A | G | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-181+4834A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105562999 | |||||||
| chr9:105563113 | C | G | 1 | a0002c0002t0004g0211 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-181+4948C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563113 | |||||||
| chr9:105563172 | G | T | 1 | a0001c0001t0003g0006 | 3 | NA18951.hp1 NA19056.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-181+5007G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563172 | |||||||
| chr9:105563181 | A | G | 1 | a0001c0001t0002g0069 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-181+5016A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563181 | |||||||
| chr9:105563199 | C | T | 19 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0023 others(16): Show |
24 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.-181+5034C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563199 | |||||||
| chr9:105563201 | C | A | 8 | a0002c0002t0004g0032 a0002c0002t0004g0033 a0002c0002t0004g0183 others(5): Show |
10 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.-181+5036C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563201 | |||||||
| chr9:105563237 | C | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5072C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563237 | |||||||
| chr9:105563238 | G | A | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+5073G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563238 | |||||||
| chr9:105563239 | G | A | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-181+5074G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563239 | |||||||
| chr9:105563302 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-181+5137G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563302 | |||||||
| chr9:105563322 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5157C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563322 | |||||||
| chr9:105563328 | G | A | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-181+5163G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563328 | |||||||
| chr9:105563332 | G | A | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+5167G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563332 | |||||||
| chr9:105563382 | CAG | C | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-181+5218_-181+521 others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563382 | |||||||
| chr9:105563418 | C | G | 5 | a0004c0004t0005g0042 a0004c0004t0005g0043 a0004c0004t0005g0044 others(2): Show |
8 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-181+5253C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563418 | |||||||
| chr9:105563446 | C | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5281C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563446 | |||||||
| chr9:105563508 | C | A | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-181+5343C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563508 | |||||||
| chr9:105563593 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0219 a0001c0001t0012g0062 others(3): Show |
7 | HG01081.hp2 HG01255.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+5428G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563593 | |||||||
| chr9:105563598 | T | TG | 26 | a0001c0001t0001g0045 a0001c0001t0001g0299 a0001c0001t0001g0300 others(23): Show |
31 | HG00280.hp1 HG00741.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.-181+5444dupG | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105563598 | ||||||
| chr9:105563598 | TG | T | 152 | a0001c0001t0001g0106 a0001c0001t0001g0255 a0001c0001t0002g0003 others(149): Show |
177 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.-181+5444delG | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105563598 | ||||||
| chr9:105563601 | G | T | 2 | a0002c0002t0004g0179 a0002c0002t0021g0210 |
2 | HG01516.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-181+5436G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563601 | |||||||
| chr9:105563602 | G | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5437G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563602 | |||||||
| chr9:105563603 | G | GT | 5 | a0004c0004t0005g0042 a0004c0004t0005g0043 a0004c0004t0005g0044 others(2): Show |
8 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-181+5438_-181+543 others(5): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563603 | |||||||
| chr9:105563604 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0309 |
2 | NA18979.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-181+5439G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563604 | |||||||
| chr9:105563605 | G | C | 1 | a0001c0001t0007g0102 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-181+5440G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563605 | |||||||
| chr9:105563606 | G | C | 1 | a0001c0001t0029g0103 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-181+5441G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563606 | |||||||
| chr9:105563614 | C | T | 3 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 |
4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+5449C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563614 | |||||||
| chr9:105563644 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5479G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563644 | |||||||
| chr9:105563714 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-181+5549T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563714 | |||||||
| chr9:105563760 | T | A | 1 | a0002c0002t0004g0187 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-181+5595T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563760 | |||||||
| chr9:105563827 | GA | G | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5663delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563827 | |||||||
| chr9:105563853 | C | T | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+5688C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563853 | |||||||
| chr9:105563916 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+5751T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563916 | |||||||
| chr9:105563933 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-181+5768G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105563933 | |||||||
| chr9:105564051 | A | C | 2 | a0005c0007t0005g0039 a0005c0007t0005g0239 |
3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-181+5886A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564051 | |||||||
| chr9:105564051 | A | T | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+5886A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564051 | |||||||
| chr9:105564078 | A | G | 2 | a0002c0002t0004g0206 a0002c0002t0020g0213 |
2 | HG01884.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-181+5913A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564078 | |||||||
| chr9:105564298 | G | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+6133G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564298 | |||||||
| chr9:105564307 | C | T | 196 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(193): Show |
228 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-181+6142C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564307 | |||||||
| chr9:105564327 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0219 a0004c0004t0005g0250 |
4 | HG00735.hp1 HG01081.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+6162G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564327 | |||||||
| chr9:105564335 | C | T | 3 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 |
3 | HG01069.hp2 HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-181+6170C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564335 | |||||||
| chr9:105564349 | C | T | 3 | a0003c0003t0001g0235 a0003c0003t0001g0236 a0003c0003t0001g0237 |
3 | HG02886.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-181+6184C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564349 | |||||||
| chr9:105564370 | A | G | 45 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(42): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-181+6205A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564370 | |||||||
| chr9:105564436 | T | C | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+6271T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564436 | |||||||
| chr9:105564496 | A | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+6331A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564496 | |||||||
| chr9:105564508 | C | G | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+6343C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564508 | |||||||
| chr9:105564558 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+6393A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564558 | |||||||
| chr9:105564665 | C | T | 1 | a0001c0001t0003g0022 | 2 | HG00741.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-181+6500C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564665 | |||||||
| chr9:105564666 | G | A | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-181+6501G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564666 | |||||||
| chr9:105564670 | G | A | 3 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 |
3 | HG01255.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-181+6505G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564670 | |||||||
| chr9:105564686 | A | T | 2 | a0001c0006t0015g0054 a0006c0009t0015g0053 |
2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-181+6521A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564686 | |||||||
| chr9:105564736 | C | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+6571C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564736 | |||||||
| chr9:105564915 | A | T | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-181+6750A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105564915 | |||||||
| chr9:105565045 | A | T | 3 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 |
4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+6880A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565045 | |||||||
| chr9:105565096 | G | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+6931G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565096 | |||||||
| chr9:105565125 | C | A | 1 | a0002c0002t0004g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-181+6960C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565125 | |||||||
| chr9:105565146 | G | A | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+6981G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565146 | |||||||
| chr9:105565170 | G | A | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7005G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565170 | |||||||
| chr9:105565174 | A | G | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7009A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565174 | |||||||
| chr9:105565182 | C | T | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7017C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565182 | |||||||
| chr9:105565183 | T | G | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7018T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565183 | |||||||
| chr9:105565187 | C | A | 2 | a0001c0001t0003g0089 a0001c0001t0003g0090 |
2 | NA18954.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-181+7022C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565187 | |||||||
| chr9:105565192 | A | T | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7027A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565192 | |||||||
| chr9:105565200 | G | A | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7035G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565200 | |||||||
| chr9:105565202 | T | A | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7037T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565202 | |||||||
| chr9:105565204 | C | G | 15 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(12): Show |
15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-181+7039C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565204 | |||||||
| chr9:105565213 | A | G | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7048A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565213 | |||||||
| chr9:105565215 | G | C | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7050G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565215 | |||||||
| chr9:105565218 | T | G | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7053T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565218 | |||||||
| chr9:105565219 | G | A | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7054G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565219 | |||||||
| chr9:105565225 | C | A | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7060C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565225 | |||||||
| chr9:105565235 | A | G | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7070A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565235 | |||||||
| chr9:105565256 | G | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+7091G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565256 | |||||||
| chr9:105565300 | G | A | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7135G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565300 | |||||||
| chr9:105565306 | C | T | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7141C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565306 | |||||||
| chr9:105565321 | G | A | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7156G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565321 | |||||||
| chr9:105565328 | G | T | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7163G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565328 | |||||||
| chr9:105565330 | C | T | 2 | a0001c0001t0001g0298 a0001c0005t0019g0189 |
2 | HG01433.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-181+7165C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565330 | |||||||
| chr9:105565335 | G | T | 5 | a0001c0005t0019g0189 a0001c0006t0014g0051 a0001c0006t0014g0052 others(2): Show |
5 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-181+7170G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565335 | |||||||
| chr9:105565384 | G | A | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7219G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565384 | |||||||
| chr9:105565411 | A | G | 5 | a0001c0005t0019g0189 a0001c0006t0014g0051 a0001c0006t0014g0052 others(2): Show |
5 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-181+7246A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565411 | |||||||
| chr9:105565416 | A | G | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7251A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565416 | |||||||
| chr9:105565441 | G | A | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7276G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565441 | |||||||
| chr9:105565485 | T | C | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-181+7320T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565485 | |||||||
| chr9:105565509 | A | T | 1 | a0001c0001t0001g0295 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-181+7344A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565509 | |||||||
| chr9:105565554 | G | T | 30 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(27): Show |
38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-181+7389G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565554 | |||||||
| chr9:105565555 | C | T | 30 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(27): Show |
38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-181+7390C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565555 | |||||||
| chr9:105565601 | G | A | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-181+7436G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565601 | |||||||
| chr9:105565602 | T | G | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-181+7437T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565602 | |||||||
| chr9:105565604 | T | C | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-181+7439T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565604 | |||||||
| chr9:105565654 | C | A | 1 | a0004c0004t0005g0042 | 2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-181+7489C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565654 | |||||||
| chr9:105565814 | A | G | 1 | a0001c0001t0029g0103 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-181+7649A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565814 | |||||||
| chr9:105565892 | T | A | 1 | a0001c0001t0002g0105 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-181+7727T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565892 | |||||||
| chr9:105565893 | A | T | 1 | a0001c0001t0002g0105 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-181+7728A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565893 | |||||||
| chr9:105565912 | C | G | 1 | a0003c0003t0001g0230 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-180-7743C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565912 | |||||||
| chr9:105565921 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-7734C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565921 | |||||||
| chr9:105565947 | G | A | 16 | a0002c0002t0004g0032 a0002c0002t0004g0033 a0002c0002t0004g0067 others(13): Show |
18 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.-180-7708G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565947 | |||||||
| chr9:105565987 | T | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-7668T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105565987 | |||||||
| chr9:105566063 | A | G | 21 | a0001c0001t0002g0003 a0001c0001t0002g0031 a0001c0001t0002g0164 others(18): Show |
25 | HG00609.hp2 HG00642.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.-180-7592A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566063 | |||||||
| chr9:105566120 | T | C | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-7535T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566120 | |||||||
| chr9:105566305 | G | A | 225 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(222): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.-180-7350G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566305 | |||||||
| chr9:105566307 | A | C | 42 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(39): Show |
48 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-180-7348A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566307 | |||||||
| chr9:105566355 | T | C | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-180-7300T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566355 | |||||||
| chr9:105566390 | G | C | 3 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0065 |
3 | HG01255.hp2 HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-7265G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566390 | |||||||
| chr9:105566435 | G | C | 10 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(7): Show |
10 | HG01884.hp1 HG02723.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-180-7220G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566435 | |||||||
| chr9:105566443 | C | T | 2 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
2 | NA18962.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-180-7212C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566443 | |||||||
| chr9:105566485 | C | T | 1 | a0001c0001t0029g0103 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-180-7170C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566485 | |||||||
| chr9:105566541 | C | T | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-180-7114C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566541 | |||||||
| chr9:105566571 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-7084C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566571 | |||||||
| chr9:105566606 | A | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(42): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-180-7049A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566606 | |||||||
| chr9:105566754 | C | T | 42 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(39): Show |
48 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-180-6901C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566754 | |||||||
| chr9:105566761 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-180-6894C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566761 | |||||||
| chr9:105566771 | G | A | 3 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 |
4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-6884G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566771 | |||||||
| chr9:105566778 | C | T | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-180-6877C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566778 | |||||||
| chr9:105566947 | A | G | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-180-6708A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566947 | |||||||
| chr9:105566993 | A | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-6662A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566993 | |||||||
| chr9:105566995 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-6660A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105566995 | |||||||
| chr9:105567076 | G | A | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-180-6579G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567076 | |||||||
| chr9:105567142 | G | A | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-6513G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567142 | |||||||
| chr9:105567158 | A | G | 1 | a0001c0001t0003g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-180-6497A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567158 | |||||||
| chr9:105567163 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(42): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-180-6492C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567163 | |||||||
| chr9:105567183 | C | A | 34 | a0002c0002t0004g0032 a0002c0002t0004g0033 a0002c0002t0004g0034 others(31): Show |
39 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-180-6472C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567183 | |||||||
| chr9:105567345 | A | G | 5 | a0004c0004t0005g0042 a0004c0004t0005g0043 a0004c0004t0005g0044 others(2): Show |
8 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-6310A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567345 | |||||||
| chr9:105567373 | T | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-6282T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567373 | |||||||
| chr9:105567401 | A | G | 2 | a0002c0002t0022g0202 a0002c0002t0023g0203 |
2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-180-6254A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567401 | |||||||
| chr9:105567455 | G | A | 1 | a0001c0001t0006g0240 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-180-6200G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567455 | |||||||
| chr9:105567598 | C | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-6057C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567598 | |||||||
| chr9:105567631 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-6024G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567631 | |||||||
| chr9:105567760 | A | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-5895A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567760 | |||||||
| chr9:105567790 | ACTT | A | 3 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 |
3 | HG02083.hp2 NA18990.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-180-5864_-180-586 others(7): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567790 | |||||||
| chr9:105567810 | G | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-5845G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567810 | |||||||
| chr9:105567829 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-180-5826G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567829 | |||||||
| chr9:105567863 | G | C | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-180-5792G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567863 | |||||||
| chr9:105567871 | A | G | 235 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0219 others(232): Show |
276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.-180-5784A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567871 | |||||||
| chr9:105567872 | C | T | 2 | a0001c0001t0005g0248 a0001c0001t0006g0218 |
2 | HG03453.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-180-5783C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567872 | |||||||
| chr9:105567873 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-5782G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567873 | |||||||
| chr9:105567951 | A | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-5704A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567951 | |||||||
| chr9:105567951 | A | T | 42 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(39): Show |
48 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-180-5704A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567951 | |||||||
| chr9:105567966 | G | A | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-180-5689G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105567966 | |||||||
| chr9:105568164 | T | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | NA18970.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-180-5491T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568164 | |||||||
| chr9:105568376 | T | A | 1 | a0001c0001t0012g0062 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-180-5279T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568376 | |||||||
| chr9:105568411 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-180-5244C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568411 | |||||||
| chr9:105568425 | A | T | 2 | a0001c0001t0038g0159 a0001c0001t0039g0158 |
2 | NA18945.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-180-5230A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568425 | |||||||
| chr9:105568466 | C | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-5189C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568466 | |||||||
| chr9:105568523 | C | G | 5 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-180-5132C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568523 | |||||||
| chr9:105568606 | T | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-5049T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568606 | |||||||
| chr9:105568616 | G | A | 1 | a0002c0002t0004g0190 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-180-5039G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568616 | |||||||
| chr9:105568666 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-4989T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568666 | |||||||
| chr9:105568678 | T | C | 45 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(42): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-180-4977T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568678 | |||||||
| chr9:105568694 | C | G | 1 | a0001c0001t0003g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-180-4961C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568694 | |||||||
| chr9:105568731 | C | T | 1 | a0001c0001t0003g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-180-4924C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568731 | |||||||
| chr9:105568740 | T | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-4915T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568740 | |||||||
| chr9:105568927 | G | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(42): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-180-4728G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568927 | |||||||
| chr9:105568953 | G | A | 42 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(39): Show |
48 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-180-4702G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105568953 | |||||||
| chr9:105569056 | G | T | 2 | a0001c0001t0011g0208 a0001c0001t0011g0209 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-180-4599G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569056 | |||||||
| chr9:105569150 | C | G | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-180-4505C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569150 | |||||||
| chr9:105569161 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-180-4494C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569161 | |||||||
| chr9:105569204 | G | T | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-4451G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569204 | |||||||
| chr9:105569253 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-4402T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569253 | |||||||
| chr9:105569525 | T | G | 1 | a0001c0001t0029g0103 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-180-4130T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569525 | |||||||
| chr9:105569555 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-4100A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569555 | |||||||
| chr9:105569591 | A | C | 2 | a0001c0001t0017g0021 a0001c0001t0048g0087 |
3 | HG02071.hp1 HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-180-4064A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569591 | |||||||
| chr9:105569599 | G | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-4056G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569599 | |||||||
| chr9:105569796 | T | C | 91 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(88): Show |
102 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.-180-3859T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105569796 | |||||||
| chr9:105570052 | A | G | 45 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(42): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-180-3603A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570052 | |||||||
| chr9:105570142 | C | CT | 8 | a0001c0001t0001g0293 a0001c0006t0014g0051 a0001c0006t0014g0052 others(5): Show |
10 | HG00597.hp1 HG02004.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-180-3503dupT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105570142 | ||||||
| chr9:105570221 | G | C | 3 | a0001c0001t0003g0023 a0001c0001t0003g0091 a0001c0001t0003g0092 |
4 | HG00597.hp2 HG02074.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-3434G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570221 | |||||||
| chr9:105570333 | C | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-3322C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570333 | |||||||
| chr9:105570431 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-3224T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570431 | |||||||
| chr9:105570742 | T | G | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-2913T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570742 | |||||||
| chr9:105570823 | G | A | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-2832G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570823 | |||||||
| chr9:105570922 | G | A | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-180-2733G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570922 | |||||||
| chr9:105570956 | C | A | 1 | a0001c0001t0001g0046 | 2 | HG01106.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.-180-2699C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570956 | |||||||
| chr9:105570973 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-2682G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105570973 | |||||||
| chr9:105571038 | A | G | 14 | a0001c0001t0002g0003 a0001c0001t0002g0168 a0001c0001t0002g0170 others(11): Show |
17 | HG00642.hp2 HG01358.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.-180-2617A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571038 | |||||||
| chr9:105571057 | A | G | 3 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 |
4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-2598A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571057 | |||||||
| chr9:105571076 | G | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-2579G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571076 | |||||||
| chr9:105571103 | G | A | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-2552G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571103 | |||||||
| chr9:105571167 | A | G | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-180-2488A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571167 | |||||||
| chr9:105571284 | C | T | 3 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 |
4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-2371C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571284 | |||||||
| chr9:105571309 | G | A | 225 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(222): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.-180-2346G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571309 | |||||||
| chr9:105571355 | C | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-2300C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571355 | |||||||
| chr9:105571420 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-2235T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571420 | |||||||
| chr9:105571478 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-2177G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571478 | |||||||
| chr9:105571509 | G | T | 1 | a0001c0001t0002g0069 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-180-2146G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571509 | |||||||
| chr9:105571616 | C | T | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-2039C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571616 | |||||||
| chr9:105571924 | A | G | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-180-1731A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571924 | |||||||
| chr9:105571971 | G | A | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-180-1684G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105571971 | |||||||
| chr9:105572046 | T | C | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-1609T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572046 | |||||||
| chr9:105572064 | A | C | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-180-1591A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572064 | |||||||
| chr9:105572121 | C | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-1534C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572121 | |||||||
| chr9:105572121 | C | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-1534C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572121 | |||||||
| chr9:105572149 | T | G | 2 | a0001c0001t0003g0016 a0001c0001t0003g0088 |
3 | HG00323.hp1 HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-180-1506T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572149 | |||||||
| chr9:105572228 | CTG | C | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-1425_-180-142 others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105572228 | ||||||
| chr9:105572230 | GTA | G | 169 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(166): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.-180-1405_-180-140 others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105572230 | ||||||
| chr9:105572230 | GTATA | G | 18 | a0001c0001t0005g0232 a0001c0001t0005g0242 a0001c0001t0005g0243 others(15): Show |
18 | HG00280.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-180-1407_-180-140 others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105572230 | ||||||
| chr9:105572255 | A | T | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-1400A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572255 | |||||||
| chr9:105572279 | G | T | 1 | a0001c0001t0001g0306 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-180-1376G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572279 | |||||||
| chr9:105572317 | C | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-1338C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572317 | |||||||
| chr9:105572338 | G | A | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-180-1317G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572338 | |||||||
| chr9:105572342 | A | G | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-1313A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572342 | |||||||
| chr9:105572406 | T | C | 1 | a0001c0001t0002g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-180-1249T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572406 | |||||||
| chr9:105572439 | G | T | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-1216G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572439 | |||||||
| chr9:105572480 | T | C | 4 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 others(1): Show |
5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-180-1175T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572480 | |||||||
| chr9:105572537 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-180-1118C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572537 | |||||||
| chr9:105572601 | C | G | 1 | a0001c0001t0003g0086 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-180-1054C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572601 | |||||||
| chr9:105572728 | T | C | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG02040.hp1 HG02071.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-180-927T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572728 | |||||||
| chr9:105572813 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-842C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572813 | |||||||
| chr9:105572867 | A | C | 2 | a0002c0002t0004g0190 a0002c0002t0004g0207 |
2 | HG00735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-180-788A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572867 | |||||||
| chr9:105572895 | ATTTC | A | 11 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0071 others(8): Show |
14 | HG00673.hp2 HG02071.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.-180-753_-180-750d others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105572895 | ||||||
| chr9:105572933 | C | T | 34 | a0002c0002t0004g0032 a0002c0002t0004g0033 a0002c0002t0004g0034 others(31): Show |
39 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-180-722C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572933 | |||||||
| chr9:105572934 | G | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(42): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-180-721G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572934 | |||||||
| chr9:105572948 | A | G | 60 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(57): Show |
75 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.-180-707A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572948 | |||||||
| chr9:105572971 | A | T | 1 | a0001c0001t0002g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-180-684A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105572971 | |||||||
| chr9:105573063 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-592C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573063 | |||||||
| chr9:105573077 | A | G | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-578A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573077 | |||||||
| chr9:105573215 | A | C | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-180-440A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573215 | |||||||
| chr9:105573219 | A | G | 6 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(3): Show |
6 | HG01884.hp1 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-180-436A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573219 | |||||||
| chr9:105573238 | C | CA | 217 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(214): Show |
255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.-180-406dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105573238 | ||||||
| chr9:105573238 | C | CAA | 6 | a0001c0001t0002g0069 a0001c0001t0002g0108 a0001c0001t0003g0093 others(3): Show |
8 | HG03098.hp2 NA18747.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-407_-180-406d others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105573238 | ||||||
| chr9:105573260 | T | C | 3 | a0001c0001t0003g0016 a0001c0001t0003g0086 a0001c0001t0003g0088 |
4 | HG00323.hp1 HG01361.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-395T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573260 | |||||||
| chr9:105573312 | A | G | 1 | a0001c0001t0016g0155 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-180-343A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573312 | |||||||
| chr9:105573413 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-242T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573413 | |||||||
| chr9:105573427 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-228C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573427 | |||||||
| chr9:105573463 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-180-192A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573463 | |||||||
| chr9:105573495 | G | C | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-180-160G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573495 | |||||||
| chr9:105573550 | T | C | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-180-105T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573550 | |||||||
| chr9:105573553 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-102G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573553 | |||||||
| chr9:105573553 | G | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-102G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573553 | |||||||
| chr9:105573554 | G | C | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-101G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573554 | |||||||
| chr9:105573589 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-180-66T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573589 | |||||||
| chr9:105573606 | C | T | 1 | a0002c0002t0004g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-180-49C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573606 | |||||||
| chr9:105573627 | C | CA | 11 | a0001c0001t0006g0240 a0001c0001t0010g0056 a0001c0001t0010g0057 others(8): Show |
11 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-180-15dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 105573627 | ||||||
| chr9:105573629 | A | G | 2 | a0001c0001t0001g0291 a0001c0001t0001g0303 |
2 | NA19068.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-180-26A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 1/10 | chr9 | 105573629 | |||||||
| chr9:105573789 | T | C | 47 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(44): Show |
62 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89+43T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105573789 | |||||||
| chr9:105573866 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0256 a0001c0001t0001g0257 others(7): Show |
13 | HG02080.hp1 NA18940.hp2 NA18954.hp1 others(10): Show |
intron_variant | MODIFIER | c.-89+120G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105573866 | |||||||
| chr9:105573867 | T | C | 30 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(27): Show |
38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-89+121T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105573867 | |||||||
| chr9:105573989 | A | G | 1 | a0001c0001t0047g0234 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-89+243A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105573989 | |||||||
| chr9:105574395 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-88-550A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574395 | |||||||
| chr9:105574466 | A | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-88-479A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574466 | |||||||
| chr9:105574601 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-88-344C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574601 | |||||||
| chr9:105574698 | T | A | 1 | a0001c0001t0001g0215 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-88-247T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574698 | |||||||
| chr9:105574752 | A | G | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-88-193A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574752 | |||||||
| chr9:105574813 | T | G | 1 | a0001c0001t0006g0241 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-88-132T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574813 | |||||||
| chr9:105574835 | T | A | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-88-110T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574835 | |||||||
| chr9:105574939 | T | C | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | splice_region_variant&intron_variant | LOW | c.-88-6T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 2/10 | chr9 | 105574939 | |||||||
| chr9:105575169 | CCTTT | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+36_105+39delTC others(2): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105575169 | ||||||
| chr9:105575265 | GC | G | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+129delC | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575265 | |||||||
| chr9:105575563 | A | C | 1 | a0001c0001t0001g0302 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.105+426A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575563 | |||||||
| chr9:105575672 | T | G | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+535T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575672 | |||||||
| chr9:105575694 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+557G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575694 | |||||||
| chr9:105575711 | C | T | 1 | a0001c0005t0026g0181 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+574C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575711 | |||||||
| chr9:105575759 | A | AT | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+622_105+623ins others(1): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575759 | |||||||
| chr9:105575760 | A | T | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+623A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575760 | |||||||
| chr9:105575822 | C | T | 1 | a0001c0001t0001g0050 | 2 | NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.105+685C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575822 | |||||||
| chr9:105575876 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+739T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575876 | |||||||
| chr9:105575920 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+783T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105575920 | |||||||
| chr9:105576038 | A | T | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+901A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576038 | |||||||
| chr9:105576090 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+953T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576090 | |||||||
| chr9:105576101 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+964A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576101 | |||||||
| chr9:105576132 | A | G | 19 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0023 others(16): Show |
24 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.105+995A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576132 | |||||||
| chr9:105576145 | CT | C | 51 | a0001c0001t0002g0031 a0001c0001t0002g0109 a0001c0001t0002g0110 others(48): Show |
63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.105+1024delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105576145 | ||||||
| chr9:105576149 | T | C | 2 | a0001c0001t0003g0023 a0001c0001t0003g0091 |
3 | HG00597.hp2 NA18999.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.105+1012T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576149 | |||||||
| chr9:105576170 | T | A | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1033T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576170 | |||||||
| chr9:105576192 | G | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
5 | HG00099.hp1 HG00280.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.105+1055G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576192 | |||||||
| chr9:105576206 | T | G | 5 | a0001c0001t0001g0256 a0001c0006t0014g0051 a0001c0006t0014g0052 others(2): Show |
5 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.105+1069T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576206 | |||||||
| chr9:105576300 | A | G | 1 | a0002c0002t0023g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.105+1163A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576300 | |||||||
| chr9:105576337 | T | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1200T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576337 | |||||||
| chr9:105576388 | T | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1251T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576388 | |||||||
| chr9:105576413 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0219 |
3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.105+1276C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576413 | |||||||
| chr9:105576435 | A | G | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+1298A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576435 | |||||||
| chr9:105576616 | C | T | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1479C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576616 | |||||||
| chr9:105576626 | A | G | 1 | a0002c0002t0004g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.105+1489A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576626 | |||||||
| chr9:105576631 | T | G | 5 | a0001c0001t0003g0089 a0001c0001t0012g0062 a0001c0001t0012g0063 others(2): Show |
5 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.105+1494T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576631 | |||||||
| chr9:105576667 | A | C | 5 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(2): Show |
5 | HG02723.hp2 HG03130.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+1530A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576667 | |||||||
| chr9:105576735 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0219 |
3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.105+1598A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576735 | |||||||
| chr9:105576886 | T | A | 3 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0006c0009t0015g0053 |
3 | HG03471.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.105+1749T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576886 | |||||||
| chr9:105576946 | T | G | 28 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(25): Show |
35 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.105+1809T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576946 | |||||||
| chr9:105576994 | C | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1857C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576994 | |||||||
| chr9:105576995 | G | A | 1 | a0001c0001t0045g0231 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.105+1858G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105576995 | |||||||
| chr9:105577014 | G | T | 133 | a0001c0001t0002g0153 a0001c0001t0003g0001 a0001c0001t0003g0005 others(130): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.105+1877G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577014 | |||||||
| chr9:105577048 | A | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1911A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577048 | |||||||
| chr9:105577093 | A | G | 8 | a0001c0001t0006g0038 a0001c0001t0006g0220 a0001c0001t0018g0038 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+1956A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577093 | |||||||
| chr9:105577109 | T | G | 4 | a0001c0001t0006g0038 a0001c0001t0006g0220 a0001c0001t0018g0038 others(1): Show |
4 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+1972T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577109 | |||||||
| chr9:105577206 | C | T | 1 | a0001c0001t0002g0176 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.105+2069C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577206 | |||||||
| chr9:105577207 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2070T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577207 | |||||||
| chr9:105577211 | G | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2074G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577211 | |||||||
| chr9:105577217 | G | A | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.105+2080G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577217 | |||||||
| chr9:105577225 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2088G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577225 | |||||||
| chr9:105577308 | C | T | 2 | a0001c0001t0002g0152 a0001c0001t0002g0176 |
2 | NA18965.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.105+2171C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577308 | |||||||
| chr9:105577339 | T | C | 1 | a0001c0001t0032g0111 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.105+2202T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577339 | |||||||
| chr9:105577410 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2273A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577410 | |||||||
| chr9:105577414 | A | G | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.105+2277A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577414 | |||||||
| chr9:105577440 | T | G | 15 | a0001c0001t0005g0248 a0001c0001t0010g0056 a0001c0001t0010g0057 others(12): Show |
15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.105+2303T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577440 | |||||||
| chr9:105577481 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2344G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577481 | |||||||
| chr9:105577486 | C | T | 30 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(27): Show |
38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.105+2349C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577486 | |||||||
| chr9:105577487 | G | A | 1 | a0003c0003t0001g0222 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.105+2350G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577487 | |||||||
| chr9:105577497 | C | G | 1 | a0003c0003t0028g0229 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.105+2360C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577497 | |||||||
| chr9:105577565 | A | C | 46 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(43): Show |
52 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.105+2428A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577565 | |||||||
| chr9:105577577 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2440T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577577 | |||||||
| chr9:105577591 | G | C | 2 | a0001c0001t0002g0109 a0001c0001t0002g0112 |
2 | HG00140.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.105+2454G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577591 | |||||||
| chr9:105577600 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2463C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577600 | |||||||
| chr9:105577668 | C | A | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+2531C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577668 | |||||||
| chr9:105577728 | G | C | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.105+2591G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577728 | |||||||
| chr9:105577787 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2650C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577787 | |||||||
| chr9:105577810 | G | A | 1 | a0001c0001t0006g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.105+2673G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577810 | |||||||
| chr9:105577843 | C | G | 1 | a0002c0002t0020g0213 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.105+2706C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577843 | |||||||
| chr9:105577853 | G | C | 1 | a0001c0001t0001g0252 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.105+2716G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577853 | |||||||
| chr9:105577934 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2797A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577934 | |||||||
| chr9:105577940 | A | G | 226 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(223): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.105+2803A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577940 | |||||||
| chr9:105577949 | C | G | 1 | a0002c0002t0001g0290 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.105+2812C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105577949 | |||||||
| chr9:105578025 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2888T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578025 | |||||||
| chr9:105578062 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.105+2925A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578062 | |||||||
| chr9:105578107 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.105+2970G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578107 | |||||||
| chr9:105578124 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+2987G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578124 | |||||||
| chr9:105578339 | G | A | 1 | a0001c0001t0033g0169 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.105+3202G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578339 | |||||||
| chr9:105578384 | T | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+3247T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578384 | |||||||
| chr9:105578488 | A | C | 39 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0019g0189 others(36): Show |
45 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.105+3351A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578488 | |||||||
| chr9:105578509 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+3372A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578509 | |||||||
| chr9:105578612 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.105+3475A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578612 | |||||||
| chr9:105578730 | G | A | 1 | a0001c0001t0034g0113 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.105+3593G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578730 | |||||||
| chr9:105578778 | C | T | 4 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(1): Show |
4 | HG02040.hp1 NA18612.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+3641C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578778 | |||||||
| chr9:105578842 | T | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(42): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.105+3705T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578842 | |||||||
| chr9:105578871 | A | T | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.105+3734A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578871 | |||||||
| chr9:105578907 | A | G | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+3770A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578907 | |||||||
| chr9:105578936 | A | C | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | NA18969.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.105+3799A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578936 | |||||||
| chr9:105578947 | T | C | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.105+3810T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578947 | |||||||
| chr9:105578993 | A | G | 38 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(35): Show |
43 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.105+3856A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578993 | |||||||
| chr9:105578995 | T | G | 2 | a0001c0001t0001g0291 a0001c0001t0001g0303 |
2 | NA19068.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.105+3858T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105578995 | |||||||
| chr9:105579023 | G | A | 1 | a0001c0001t0003g0071 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.105+3886G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579023 | |||||||
| chr9:105579034 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(42): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.105+3897C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579034 | |||||||
| chr9:105579035 | G | A | 3 | a0001c0001t0002g0114 a0001c0001t0016g0115 a0001c0001t0016g0155 |
3 | HG02602.hp2 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.105+3898G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579035 | |||||||
| chr9:105579037 | C | G | 3 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0030g0150 |
3 | NA18970.hp2 NA18999.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.105+3900C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579037 | |||||||
| chr9:105579043 | C | G | 6 | a0001c0001t0046g0060 a0001c0006t0014g0051 a0001c0006t0014g0052 others(3): Show |
6 | HG02723.hp2 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.105+3906C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579043 | |||||||
| chr9:105579142 | T | G | 226 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(223): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.105+4005T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579142 | |||||||
| chr9:105579235 | C | G | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4098C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579235 | |||||||
| chr9:105579237 | A | C | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+4100A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579237 | |||||||
| chr9:105579338 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4201C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579338 | |||||||
| chr9:105579339 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4202A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579339 | |||||||
| chr9:105579362 | C | T | 1 | a0001c0001t0001g0287 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.105+4225C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579362 | |||||||
| chr9:105579376 | C | T | 3 | a0003c0003t0001g0235 a0003c0003t0001g0236 a0003c0003t0001g0237 |
3 | HG02886.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.105+4239C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579376 | |||||||
| chr9:105579415 | C | T | 1 | a0001c0001t0003g0016 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.105+4278C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579415 | |||||||
| chr9:105579471 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4334C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579471 | |||||||
| chr9:105579485 | T | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4348T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579485 | |||||||
| chr9:105579492 | A | C | 2 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
2 | NA18962.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.105+4355A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579492 | |||||||
| chr9:105579588 | A | T | 1 | a0001c0001t0006g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.105+4451A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579588 | |||||||
| chr9:105579737 | C | T | 4 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 others(1): Show |
5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+4600C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579737 | |||||||
| chr9:105579756 | G | A | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.105+4619G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579756 | |||||||
| chr9:105579767 | G | A | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.105+4630G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579767 | |||||||
| chr9:105579799 | C | G | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4662C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579799 | |||||||
| chr9:105579820 | A | T | 1 | a0002c0002t0020g0213 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.105+4683A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579820 | |||||||
| chr9:105579821 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(42): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.105+4684C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579821 | |||||||
| chr9:105579845 | T | G | 1 | a0002c0002t0001g0269 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.105+4708T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579845 | |||||||
| chr9:105579869 | A | G | 5 | a0002c0002t0001g0269 a0002c0002t0001g0283 a0002c0002t0001g0284 others(2): Show |
5 | NA18747.hp2 NA18966.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+4732A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105579869 | |||||||
| chr9:105580072 | G | C | 3 | a0001c0001t0011g0204 a0001c0001t0011g0208 a0001c0001t0011g0209 |
3 | HG02486.hp1 HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.105+4935G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580072 | |||||||
| chr9:105580094 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4957T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580094 | |||||||
| chr9:105580099 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+4962G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580099 | |||||||
| chr9:105580121 | A | G | 4 | a0001c0001t0002g0029 a0001c0001t0002g0147 a0001c0001t0046g0060 others(1): Show |
5 | HG00323.hp2 HG01255.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+4984A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580121 | |||||||
| chr9:105580126 | C | A | 12 | a0003c0003t0001g0222 a0003c0003t0001g0223 a0003c0003t0001g0224 others(9): Show |
12 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.105+4989C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580126 | |||||||
| chr9:105580170 | A | G | 1 | a0001c0001t0047g0234 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.105+5033A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580170 | |||||||
| chr9:105580265 | C | T | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+5128C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580265 | |||||||
| chr9:105580332 | T | C | 2 | a0002c0002t0004g0190 a0002c0002t0004g0207 |
2 | HG00735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.105+5195T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580332 | |||||||
| chr9:105580406 | A | T | 91 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(88): Show |
102 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.105+5269A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580406 | |||||||
| chr9:105580534 | C | T | 2 | a0005c0007t0005g0039 a0005c0007t0005g0239 |
3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.105+5397C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580534 | |||||||
| chr9:105580542 | A | G | 47 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(44): Show |
62 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.105+5405A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580542 | |||||||
| chr9:105580576 | C | G | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+5439C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580576 | |||||||
| chr9:105580596 | A | C | 2 | a0001c0001t0001g0282 a0001c0001t0001g0300 |
2 | HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.105+5459A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580596 | |||||||
| chr9:105580662 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.105+5525G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580662 | |||||||
| chr9:105580668 | T | G | 3 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0006c0009t0015g0053 |
4 | HG02109.hp2 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+5531T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580668 | |||||||
| chr9:105580689 | A | G | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.105+5552A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580689 | |||||||
| chr9:105580787 | A | G | 1 | a0001c0001t0002g0029 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.105+5650A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580787 | |||||||
| chr9:105580859 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+5722C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580859 | |||||||
| chr9:105580900 | G | A | 1 | a0001c0001t0042g0258 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.105+5763G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580900 | |||||||
| chr9:105580954 | C | T | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+5817C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105580954 | |||||||
| chr9:105581016 | A | G | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+5879A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581016 | |||||||
| chr9:105581031 | T | C | 30 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(27): Show |
38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.105+5894T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581031 | |||||||
| chr9:105581036 | C | T | 1 | a0001c0001t0027g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.105+5899C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581036 | |||||||
| chr9:105581081 | A | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+5944A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581081 | |||||||
| chr9:105581089 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+5952T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581089 | |||||||
| chr9:105581143 | G | T | 55 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(52): Show |
70 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.105+6006G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581143 | |||||||
| chr9:105581168 | G | A | 47 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(44): Show |
63 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.105+6031G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581168 | |||||||
| chr9:105581177 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6040A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581177 | |||||||
| chr9:105581197 | C | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6060C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581197 | |||||||
| chr9:105581198 | C | T | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+6061C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581198 | |||||||
| chr9:105581227 | T | G | 1 | a0001c0005t0026g0181 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+6090T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581227 | |||||||
| chr9:105581240 | G | A | 58 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(55): Show |
72 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.105+6103G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581240 | |||||||
| chr9:105581240 | G | C | 2 | a0001c0001t0003g0020 a0001c0001t0003g0085 |
3 | HG02155.hp1 NA18953.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.105+6103G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581240 | |||||||
| chr9:105581241 | C | G | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6104C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581241 | |||||||
| chr9:105581312 | T | A | 1 | a0001c0001t0003g0081 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.105+6175T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581312 | |||||||
| chr9:105581331 | A | T | 42 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(39): Show |
48 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.105+6194A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581331 | |||||||
| chr9:105581391 | G | C | 1 | a0001c0001t0003g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.105+6254G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581391 | |||||||
| chr9:105581402 | G | T | 1 | a0001c0001t0027g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.105+6265G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581402 | |||||||
| chr9:105581416 | G | A | 30 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(27): Show |
38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.105+6279G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581416 | |||||||
| chr9:105581418 | A | G | 30 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(27): Show |
38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.105+6281A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581418 | |||||||
| chr9:105581426 | T | G | 1 | a0001c0001t0003g0086 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.105+6289T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581426 | |||||||
| chr9:105581445 | C | T | 3 | a0002c0002t0004g0184 a0002c0002t0004g0186 a0002c0002t0004g0211 |
3 | HG00741.hp2 HG01257.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.105+6308C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581445 | |||||||
| chr9:105581453 | C | G | 35 | a0001c0001t0002g0146 a0001c0001t0003g0006 a0001c0001t0003g0099 others(32): Show |
45 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.105+6316C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581453 | |||||||
| chr9:105581512 | C | T | 1 | a0001c0001t0016g0155 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.105+6375C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581512 | |||||||
| chr9:105581521 | G | C | 7 | a0001c0001t0002g0116 a0001c0001t0032g0111 a0001c0006t0014g0051 others(4): Show |
7 | HG00621.hp1 HG02148.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+6384G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581521 | |||||||
| chr9:105581521 | G | T | 4 | a0001c0001t0003g0020 a0001c0001t0003g0085 a0001c0001t0038g0159 others(1): Show |
5 | HG02155.hp1 NA18945.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+6384G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581521 | |||||||
| chr9:105581584 | G | T | 1 | a0001c0001t0042g0258 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.105+6447G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581584 | |||||||
| chr9:105581678 | A | G | 5 | a0002c0002t0001g0269 a0002c0002t0001g0283 a0002c0002t0001g0284 others(2): Show |
5 | NA18747.hp2 NA18966.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+6541A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581678 | |||||||
| chr9:105581680 | T | C | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+6543T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581680 | |||||||
| chr9:105581694 | T | C | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+6557T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581694 | |||||||
| chr9:105581710 | C | A | 1 | a0002c0002t0004g0187 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.105+6573C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581710 | |||||||
| chr9:105581710 | C | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6573C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581710 | |||||||
| chr9:105581747 | C | T | 1 | a0002c0002t0004g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.105+6610C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581747 | |||||||
| chr9:105581763 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.105+6626A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581763 | |||||||
| chr9:105581770 | C | T | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.105+6633C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581770 | |||||||
| chr9:105581790 | C | A | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.105+6653C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581790 | |||||||
| chr9:105581794 | G | C | 1 | a0001c0005t0026g0181 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+6657G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581794 | |||||||
| chr9:105581802 | G | T | 13 | a0003c0003t0001g0222 a0003c0003t0001g0223 a0003c0003t0001g0224 others(10): Show |
13 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.105+6665G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581802 | |||||||
| chr9:105581823 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.105+6686C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581823 | |||||||
| chr9:105581846 | C | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6709C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581846 | |||||||
| chr9:105581854 | G | A | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.105+6717G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581854 | |||||||
| chr9:105581875 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6738T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105581875 | |||||||
| chr9:105582008 | C | T | 1 | a0001c0001t0012g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.105+6871C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582008 | |||||||
| chr9:105582038 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.105+6901G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582038 | |||||||
| chr9:105582039 | C | T | 1 | a0001c0001t0003g0097 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.105+6902C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582039 | |||||||
| chr9:105582044 | C | A | 8 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(5): Show |
8 | HG01255.hp2 HG02257.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+6907C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582044 | |||||||
| chr9:105582049 | A | G | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+6912A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582049 | |||||||
| chr9:105582055 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.105+6918C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582055 | |||||||
| chr9:105582085 | G | T | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.105+6948G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582085 | |||||||
| chr9:105582095 | C | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+6958C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582095 | |||||||
| chr9:105582122 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0287 |
2 | HG00621.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.105+6985G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582122 | |||||||
| chr9:105582139 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7002T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582139 | |||||||
| chr9:105582159 | A | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0279 a0001c0001t0001g0288 others(1): Show |
5 | NA18969.hp2 NA18982.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+7022A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582159 | |||||||
| chr9:105582228 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7091G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582228 | |||||||
| chr9:105582247 | A | G | 3 | a0003c0003t0001g0235 a0003c0003t0001g0236 a0003c0003t0001g0237 |
3 | HG02886.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.105+7110A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582247 | |||||||
| chr9:105582269 | G | A | 1 | a0002c0002t0025g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.105+7132G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582269 | |||||||
| chr9:105582279 | A | AC | 195 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(192): Show |
227 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.105+7142_105+7143i others(3): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582279 | |||||||
| chr9:105582321 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.105+7184G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582321 | |||||||
| chr9:105582333 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7196A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582333 | |||||||
| chr9:105582335 | A | T | 1 | a0001c0001t0003g0085 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.105+7198A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582335 | |||||||
| chr9:105582350 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7213C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582350 | |||||||
| chr9:105582351 | G | A | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.105+7214G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582351 | |||||||
| chr9:105582471 | C | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7334C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582471 | |||||||
| chr9:105582482 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7345T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582482 | |||||||
| chr9:105582538 | C | A | 2 | a0001c0005t0013g0035 a0001c0005t0013g0180 |
3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.105+7401C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582538 | |||||||
| chr9:105582538 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7401C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582538 | |||||||
| chr9:105582638 | A | G | 1 | a0001c0001t0003g0080 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.105+7501A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582638 | |||||||
| chr9:105582737 | A | G | 1 | a0001c0001t0001g0280 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.105+7600A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582737 | |||||||
| chr9:105582739 | T | A | 1 | a0001c0001t0011g0204 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.105+7602T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582739 | |||||||
| chr9:105582829 | C | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7692C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582829 | |||||||
| chr9:105582931 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+7794A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105582931 | |||||||
| chr9:105583213 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+8076C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583213 | |||||||
| chr9:105583388 | C | G | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+8251C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583388 | |||||||
| chr9:105583413 | A | G | 9 | a0003c0003t0001g0222 a0003c0003t0001g0223 a0003c0003t0001g0224 others(6): Show |
9 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.105+8276A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583413 | |||||||
| chr9:105583493 | G | C | 1 | a0001c0001t0003g0083 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.105+8356G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583493 | |||||||
| chr9:105583594 | T | C | 1 | a0001c0001t0003g0083 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.105+8457T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583594 | |||||||
| chr9:105583641 | G | A | 2 | a0005c0007t0005g0039 a0005c0007t0005g0239 |
3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.105+8504G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583641 | |||||||
| chr9:105583726 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+8589A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583726 | |||||||
| chr9:105583849 | A | G | 2 | a0001c0001t0012g0062 a0001c0001t0012g0063 |
2 | HG01255.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.105+8712A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583849 | |||||||
| chr9:105583885 | C | G | 1 | a0001c0006t0014g0052 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.105+8748C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583885 | |||||||
| chr9:105583890 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+8753T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583890 | |||||||
| chr9:105583900 | A | G | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.105+8763A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583900 | |||||||
| chr9:105583984 | G | A | 1 | a0001c0001t0029g0103 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.105+8847G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105583984 | |||||||
| chr9:105584098 | A | G | 1 | a0001c0001t0016g0155 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.105+8961A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584098 | |||||||
| chr9:105584162 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+9025A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584162 | |||||||
| chr9:105584460 | A | G | 1 | a0003c0003t0004g0238 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.105+9323A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584460 | |||||||
| chr9:105584649 | A | C | 1 | a0002c0011t0004g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.105+9512A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584649 | |||||||
| chr9:105584789 | C | G | 1 | a0001c0001t0001g0266 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.105+9652C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584789 | |||||||
| chr9:105584794 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.105+9657C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584794 | |||||||
| chr9:105584858 | C | T | 2 | a0001c0001t0002g0152 a0001c0001t0002g0176 |
2 | NA18965.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.105+9721C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584858 | |||||||
| chr9:105584859 | G | A | 1 | a0003c0003t0001g0223 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.105+9722G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584859 | |||||||
| chr9:105584868 | C | G | 1 | a0001c0001t0002g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.105+9731C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584868 | |||||||
| chr9:105584869 | C | T | 1 | a0001c0001t0030g0150 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.105+9732C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584869 | |||||||
| chr9:105584891 | G | T | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.105+9754G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584891 | |||||||
| chr9:105584932 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.105+9795A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584932 | |||||||
| chr9:105584984 | G | C | 1 | a0001c0001t0002g0118 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.105+9847G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105584984 | |||||||
| chr9:105585117 | G | GA | 43 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(40): Show |
49 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.105+9989dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105585117 | ||||||
| chr9:105585238 | A | G | 1 | a0001c0001t0010g0059 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.105+10101A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105585238 | |||||||
| chr9:105585433 | T | G | 2 | a0001c0001t0002g0170 a0001c0001t0002g0178 |
2 | NA19004.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.105+10296T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105585433 | |||||||
| chr9:105585613 | A | G | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.105+10476A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105585613 | |||||||
| chr9:105585857 | G | A | 34 | a0002c0002t0004g0032 a0002c0002t0004g0033 a0002c0002t0004g0034 others(31): Show |
39 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.105+10720G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105585857 | |||||||
| chr9:105585858 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.105+10721C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105585858 | |||||||
| chr9:105585919 | A | G | 1 | a0001c0001t0033g0169 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.106-10679A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105585919 | |||||||
| chr9:105586023 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.106-10575G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586023 | |||||||
| chr9:105586056 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10542C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586056 | |||||||
| chr9:105586127 | C | A | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-10471C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586127 | |||||||
| chr9:105586142 | G | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10456G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586142 | |||||||
| chr9:105586145 | G | A | 1 | a0003c0003t0001g0224 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.106-10453G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586145 | |||||||
| chr9:105586176 | C | T | 2 | a0001c0001t0011g0208 a0001c0001t0011g0209 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.106-10422C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586176 | |||||||
| chr9:105586201 | TATC | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10394_106-1039 others(7): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105586201 | ||||||
| chr9:105586229 | T | TAGTA | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10368_106-1036 others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105586229 | ||||||
| chr9:105586233 | A | G | 2 | a0001c0001t0003g0096 a0001c0001t0003g0097 |
2 | HG00558.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.106-10365A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586233 | |||||||
| chr9:105586253 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10345A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586253 | |||||||
| chr9:105586524 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.106-10074G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586524 | |||||||
| chr9:105586578 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10020A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586578 | |||||||
| chr9:105586608 | C | T | 313 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(310): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.106-9990C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586608 | |||||||
| chr9:105586632 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-9966A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586632 | |||||||
| chr9:105586659 | G | A | 5 | a0004c0004t0005g0042 a0004c0004t0005g0043 a0004c0004t0005g0044 others(2): Show |
8 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-9939G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586659 | |||||||
| chr9:105586790 | A | T | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.106-9808A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586790 | |||||||
| chr9:105586950 | G | C | 45 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(42): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.106-9648G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105586950 | |||||||
| chr9:105587071 | A | T | 1 | a0003c0003t0001g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.106-9527A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587071 | |||||||
| chr9:105587353 | G | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-9245G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587353 | |||||||
| chr9:105587773 | C | T | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.106-8825C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587773 | |||||||
| chr9:105587809 | T | C | 4 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0119 others(1): Show |
5 | NA18953.hp1 NA18968.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-8789T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587809 | |||||||
| chr9:105587835 | G | A | 1 | a0002c0002t0004g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.106-8763G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587835 | |||||||
| chr9:105587890 | G | A | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-8708G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587890 | |||||||
| chr9:105587900 | G | A | 225 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(222): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.106-8698G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105587900 | |||||||
| chr9:105588002 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-8596A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588002 | |||||||
| chr9:105588047 | T | A | 42 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(39): Show |
48 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.106-8551T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588047 | |||||||
| chr9:105588113 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.106-8485C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588113 | |||||||
| chr9:105588360 | AT | A | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-8229delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105588360 | ||||||
| chr9:105588373 | C | G | 1 | a0001c0001t0003g0077 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.106-8225C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588373 | |||||||
| chr9:105588446 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-8152G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588446 | |||||||
| chr9:105588549 | G | C | 3 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 |
4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-8049G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588549 | |||||||
| chr9:105588799 | C | G | 2 | a0001c0001t0012g0062 a0001c0001t0012g0063 |
2 | HG01255.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.106-7799C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588799 | |||||||
| chr9:105588952 | C | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-7646C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105588952 | |||||||
| chr9:105589082 | A | G | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-7516A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589082 | |||||||
| chr9:105589215 | C | T | 1 | a0001c0001t0006g0247 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.106-7383C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589215 | |||||||
| chr9:105589459 | G | A | 10 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(7): Show |
10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.106-7139G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589459 | |||||||
| chr9:105589521 | C | CG | 7 | a0001c0001t0002g0117 a0001c0001t0002g0128 a0001c0001t0006g0038 others(4): Show |
7 | HG00735.hp1 HG01243.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-7074dupG | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105589521 | ||||||
| chr9:105589521 | C | G | 2 | a0001c0001t0012g0065 a0002c0002t0004g0182 |
2 | HG02027.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.106-7077C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589521 | |||||||
| chr9:105589521 | C | T | 3 | a0004c0004t0005g0042 a0004c0004t0005g0043 a0004c0004t0005g0249 |
5 | HG01099.hp2 HG01167.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-7077C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589521 | |||||||
| chr9:105589529 | A | G | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-7069A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589529 | |||||||
| chr9:105589535 | A | T | 38 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0019g0189 others(35): Show |
44 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.106-7063A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589535 | |||||||
| chr9:105589631 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-6967G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589631 | |||||||
| chr9:105589696 | G | T | 2 | a0001c0005t0013g0035 a0001c0005t0013g0180 |
3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.106-6902G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589696 | |||||||
| chr9:105589858 | G | C | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-6740G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589858 | |||||||
| chr9:105589934 | G | A | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-6664G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589934 | |||||||
| chr9:105589934 | G | C | 3 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 |
4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-6664G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589934 | |||||||
| chr9:105589969 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-6629G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589969 | |||||||
| chr9:105589974 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-6624A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105589974 | |||||||
| chr9:105590067 | C | T | 238 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(235): Show |
278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.106-6531C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590067 | |||||||
| chr9:105590093 | G | A | 3 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 |
3 | NA18973.hp2 NA19056.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.106-6505G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590093 | |||||||
| chr9:105590106 | C | T | 2 | a0002c0002t0022g0202 a0002c0002t0023g0203 |
2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.106-6492C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590106 | |||||||
| chr9:105590142 | C | G | 1 | a0002c0002t0008g0201 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.106-6456C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590142 | |||||||
| chr9:105590151 | G | A | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-6447G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590151 | |||||||
| chr9:105590192 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-6406C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590192 | |||||||
| chr9:105590319 | T | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0256 a0001c0001t0001g0257 others(6): Show |
12 | HG02080.hp1 NA18954.hp1 NA18970.hp1 others(9): Show |
intron_variant | MODIFIER | c.106-6279T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590319 | |||||||
| chr9:105590568 | A | C | 2 | a0001c0006t0015g0054 a0006c0009t0015g0053 |
2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.106-6030A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590568 | |||||||
| chr9:105590716 | GT | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-5875delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105590716 | ||||||
| chr9:105590727 | C | T | 1 | a0001c0001t0042g0258 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.106-5871C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590727 | |||||||
| chr9:105590883 | G | A | 1 | a0002c0002t0004g0067 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.106-5715G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590883 | |||||||
| chr9:105590898 | AC | A | 42 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(39): Show |
48 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.106-5699delC | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590898 | |||||||
| chr9:105590922 | G | A | 31 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(28): Show |
39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.106-5676G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590922 | |||||||
| chr9:105590929 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-5669G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590929 | |||||||
| chr9:105590932 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.106-5666C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105590932 | |||||||
| chr9:105591217 | A | G | 194 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(191): Show |
226 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.106-5381A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591217 | |||||||
| chr9:105591237 | C | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-5361C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591237 | |||||||
| chr9:105591311 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-5287C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591311 | |||||||
| chr9:105591373 | G | A | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.106-5225G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591373 | |||||||
| chr9:105591433 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-5165G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591433 | |||||||
| chr9:105591586 | C | G | 5 | a0002c0002t0001g0269 a0002c0002t0001g0283 a0002c0002t0001g0284 others(2): Show |
5 | NA18747.hp2 NA18966.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-5012C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591586 | |||||||
| chr9:105591647 | G | C | 13 | a0003c0003t0001g0222 a0003c0003t0001g0223 a0003c0003t0001g0224 others(10): Show |
13 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.106-4951G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591647 | |||||||
| chr9:105591896 | C | T | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-4702C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591896 | |||||||
| chr9:105591949 | C | T | 207 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(204): Show |
239 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.106-4649C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105591949 | |||||||
| chr9:105592031 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-4567A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592031 | |||||||
| chr9:105592120 | G | T | 314 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(311): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.106-4478G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592120 | |||||||
| chr9:105592136 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.106-4462C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592136 | |||||||
| chr9:105592215 | A | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-4383A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592215 | |||||||
| chr9:105592216 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-4382A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592216 | |||||||
| chr9:105592404 | C | T | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.106-4194C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592404 | |||||||
| chr9:105592405 | G | T | 2 | a0005c0007t0005g0039 a0005c0007t0005g0239 |
3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.106-4193G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592405 | |||||||
| chr9:105592439 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-4159T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592439 | |||||||
| chr9:105592519 | C | A | 1 | a0001c0001t0006g0241 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.106-4079C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592519 | |||||||
| chr9:105592653 | G | T | 1 | a0001c0001t0003g0099 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.106-3945G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592653 | |||||||
| chr9:105592688 | C | G | 1 | a0003c0003t0001g0227 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.106-3910C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592688 | |||||||
| chr9:105592749 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-3849A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592749 | |||||||
| chr9:105592767 | CT | C | 13 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(10): Show |
13 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.106-3826delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 105592767 | ||||||
| chr9:105592941 | T | C | 207 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(204): Show |
239 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.106-3657T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592941 | |||||||
| chr9:105592954 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.106-3644A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105592954 | |||||||
| chr9:105593014 | A | C | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.106-3584A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593014 | |||||||
| chr9:105593040 | A | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-3558A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593040 | |||||||
| chr9:105593130 | A | C | 2 | a0001c0001t0003g0075 a0001c0001t0003g0076 |
2 | NA19004.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.106-3468A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593130 | |||||||
| chr9:105593333 | C | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-3265C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593333 | |||||||
| chr9:105593333 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(42): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.106-3265C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593333 | |||||||
| chr9:105593352 | C | G | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-3246C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593352 | |||||||
| chr9:105593470 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0219 |
3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.106-3128A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593470 | |||||||
| chr9:105593556 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-3042C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593556 | |||||||
| chr9:105593804 | A | G | 1 | a0001c0001t0002g0143 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.106-2794A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593804 | |||||||
| chr9:105593814 | A | C | 6 | a0001c0001t0006g0015 a0001c0001t0006g0041 a0001c0001t0006g0055 others(3): Show |
9 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.106-2784A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593814 | |||||||
| chr9:105593818 | T | C | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.106-2780T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105593818 | |||||||
| chr9:105594109 | C | A | 9 | a0003c0003t0001g0222 a0003c0003t0001g0223 a0003c0003t0001g0224 others(6): Show |
9 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.106-2489C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594109 | |||||||
| chr9:105594341 | G | A | 5 | a0001c0001t0006g0246 a0001c0006t0014g0051 a0001c0006t0014g0052 others(2): Show |
5 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.106-2257G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594341 | |||||||
| chr9:105594437 | C | A | 1 | a0002c0002t0024g0199 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.106-2161C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594437 | |||||||
| chr9:105594522 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-2076C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594522 | |||||||
| chr9:105594695 | G | A | 3 | a0002c0002t0022g0202 a0002c0002t0023g0203 a0007c0014t0043g0070 |
3 | HG02280.hp2 HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.106-1903G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594695 | |||||||
| chr9:105594840 | G | A | 2 | a0001c0006t0015g0054 a0006c0009t0015g0053 |
2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.106-1758G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594840 | |||||||
| chr9:105594955 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-1643A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594955 | |||||||
| chr9:105594969 | T | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-1629T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105594969 | |||||||
| chr9:105595086 | C | T | 1 | a0001c0001t0003g0095 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.106-1512C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595086 | |||||||
| chr9:105595143 | A | G | 4 | a0001c0001t0003g0019 a0001c0001t0003g0022 a0001c0001t0003g0079 others(1): Show |
6 | HG00741.hp1 HG01099.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-1455A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595143 | |||||||
| chr9:105595231 | T | C | 59 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 others(56): Show |
65 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.106-1367T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595231 | |||||||
| chr9:105595425 | G | C | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.106-1173G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595425 | |||||||
| chr9:105595634 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-964C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595634 | |||||||
| chr9:105595702 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-896A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595702 | |||||||
| chr9:105595718 | G | A | 1 | a0001c0001t0003g0072 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.106-880G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595718 | |||||||
| chr9:105595729 | T | C | 1 | a0002c0002t0001g0267 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.106-869T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595729 | |||||||
| chr9:105595730 | C | T | 1 | a0002c0002t0001g0267 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.106-868C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595730 | |||||||
| chr9:105595850 | C | A | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.106-748C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105595850 | |||||||
| chr9:105596004 | C | T | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.106-594C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596004 | |||||||
| chr9:105596040 | A | C | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-558A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596040 | |||||||
| chr9:105596051 | CG | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-546delG | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596051 | |||||||
| chr9:105596065 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-533C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596065 | |||||||
| chr9:105596071 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.106-527G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596071 | |||||||
| chr9:105596079 | T | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-519T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596079 | |||||||
| chr9:105596117 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-481C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596117 | |||||||
| chr9:105596137 | A | C | 1 | a0001c0001t0002g0143 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.106-461A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596137 | |||||||
| chr9:105596249 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-349A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596249 | |||||||
| chr9:105596353 | C | T | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.106-245C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596353 | |||||||
| chr9:105596429 | A | G | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-169A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596429 | |||||||
| chr9:105596558 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-40A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596558 | |||||||
| chr9:105596588 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-10G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 3/10 | chr9 | 105596588 | |||||||
| chr9:105596686 | A | G | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.165+29A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105596686 | |||||||
| chr9:105596720 | G | T | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.165+63G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105596720 | |||||||
| chr9:105596776 | G | A | 1 | a0001c0005t0026g0181 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.165+119G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105596776 | |||||||
| chr9:105596871 | T | A | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.165+214T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105596871 | |||||||
| chr9:105597084 | A | T | 1 | a0002c0002t0025g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.165+427A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597084 | |||||||
| chr9:105597193 | C | T | 2 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
2 | NA18962.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.165+536C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597193 | |||||||
| chr9:105597258 | C | A | 95 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(92): Show |
106 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.165+601C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597258 | |||||||
| chr9:105597461 | A | C | 3 | a0001c0001t0002g0026 a0001c0001t0002g0119 a0001c0015t0002g0026 |
3 | NA18953.hp1 NA18979.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.165+804A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597461 | |||||||
| chr9:105597659 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+1002C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597659 | |||||||
| chr9:105597668 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.165+1011C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597668 | |||||||
| chr9:105597919 | G | A | 13 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(10): Show |
13 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+1262G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597919 | |||||||
| chr9:105597920 | G | A | 1 | a0002c0002t0025g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.165+1263G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597920 | |||||||
| chr9:105597975 | G | A | 1 | a0001c0001t0035g0123 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.165+1318G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597975 | |||||||
| chr9:105597976 | C | G | 1 | a0001c0001t0035g0123 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.165+1319C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105597976 | |||||||
| chr9:105598069 | T | C | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.165+1412T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598069 | |||||||
| chr9:105598284 | A | G | 2 | a0005c0007t0005g0039 a0005c0007t0005g0239 |
3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.165+1627A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598284 | |||||||
| chr9:105598423 | A | G | 3 | a0001c0001t0002g0142 a0001c0001t0038g0159 a0001c0001t0039g0158 |
3 | NA18945.hp1 NA18957.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.165+1766A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598423 | |||||||
| chr9:105598466 | G | T | 2 | a0005c0007t0005g0039 a0005c0007t0005g0239 |
3 | HG02615.hp2 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.165+1809G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598466 | |||||||
| chr9:105598537 | A | T | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+1880A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598537 | |||||||
| chr9:105598816 | T | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+2159T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598816 | |||||||
| chr9:105598839 | T | G | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2182T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105598839 | |||||||
| chr9:105598932 | G | GAC | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0010g0056 others(4): Show |
7 | HG01884.hp1 HG02818.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-2193_166-2192d others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105598932 | ||||||
| chr9:105598932 | GAC | G | 145 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(142): Show |
162 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.166-2193_166-2192d others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105598932 | ||||||
| chr9:105599091 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.166-2054T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599091 | |||||||
| chr9:105599215 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0276 a0001c0001t0001g0301 others(1): Show |
6 | HG01109.hp1 HG01952.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-1930T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599215 | |||||||
| chr9:105599475 | C | CT | 49 | a0001c0001t0001g0037 a0001c0001t0001g0219 a0001c0001t0002g0119 others(46): Show |
57 | HG00323.hp1 HG00673.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.166-1652dupT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105599475 | ||||||
| chr9:105599475 | C | CTT | 25 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(22): Show |
33 | HG00558.hp1 HG00609.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.166-1653_166-1652d others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105599475 | ||||||
| chr9:105599475 | CT | C | 6 | a0001c0001t0002g0117 a0001c0001t0002g0120 a0001c0001t0002g0176 others(3): Show |
6 | HG03130.hp2 HG03453.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-1652delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105599475 | ||||||
| chr9:105599533 | ATGTGATC others(23): Show |
A | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.166-1581_166-1552d others(32): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105599533 | ||||||
| chr9:105599568 | A | T | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.166-1577A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599568 | |||||||
| chr9:105599661 | G | A | 2 | a0001c0001t0003g0020 a0001c0001t0003g0085 |
3 | HG02155.hp1 NA18953.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.166-1484G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599661 | |||||||
| chr9:105599689 | A | C | 1 | a0001c0001t0007g0102 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.166-1456A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599689 | |||||||
| chr9:105599712 | C | T | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-1433C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599712 | |||||||
| chr9:105599790 | A | C | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.166-1355A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105599790 | |||||||
| chr9:105599923 | C | CT | 2 | a0001c0001t0001g0050 a0001c0001t0001g0279 |
3 | NA18992.hp2 NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.166-1221dupT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 105599923 | ||||||
| chr9:105600008 | T | C | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.166-1137T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600008 | |||||||
| chr9:105600026 | T | C | 1 | a0002c0002t0008g0008 | 3 | NA18948.hp1 NA18951.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.166-1119T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600026 | |||||||
| chr9:105600106 | C | T | 1 | a0001c0001t0012g0062 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.166-1039C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600106 | |||||||
| chr9:105600371 | A | G | 1 | a0002c0002t0004g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-774A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600371 | |||||||
| chr9:105600414 | A | T | 1 | a0002c0002t0004g0185 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.166-731A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600414 | |||||||
| chr9:105600508 | T | G | 25 | a0002c0002t0001g0267 a0002c0002t0001g0269 a0002c0002t0001g0274 others(22): Show |
27 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-637T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600508 | |||||||
| chr9:105600564 | A | G | 247 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(244): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.166-581A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600564 | |||||||
| chr9:105600637 | A | G | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.166-508A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600637 | |||||||
| chr9:105600817 | T | A | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-328T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600817 | |||||||
| chr9:105600853 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.166-292G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105600853 | |||||||
| chr9:105601041 | G | A | 1 | a0003c0003t0001g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.166-104G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105601041 | |||||||
| chr9:105601139 | A | G | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | splice_region_variant&intron_variant | LOW | c.166-6A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 4/10 | chr9 | 105601139 | |||||||
| chr9:105601391 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.369+43C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601391 | |||||||
| chr9:105601434 | A | C | 2 | a0001c0001t0001g0254 a0001c0001t0001g0309 |
2 | NA18979.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.369+86A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601434 | |||||||
| chr9:105601453 | T | C | 1 | a0002c0002t0004g0185 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.369+105T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601453 | |||||||
| chr9:105601654 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.369+306C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601654 | |||||||
| chr9:105601740 | C | T | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.369+392C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601740 | |||||||
| chr9:105601752 | G | T | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+404G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601752 | |||||||
| chr9:105601813 | A | T | 13 | a0003c0003t0001g0222 a0003c0003t0001g0223 a0003c0003t0001g0224 others(10): Show |
13 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.369+465A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105601813 | |||||||
| chr9:105602173 | G | A | 2 | a0001c0005t0013g0035 a0001c0005t0013g0180 |
3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.369+825G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602173 | |||||||
| chr9:105602306 | G | A | 1 | a0001c0001t0002g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.369+958G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602306 | |||||||
| chr9:105602587 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.369+1239G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602587 | |||||||
| chr9:105602633 | G | T | 1 | a0002c0002t0004g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.369+1285G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602633 | |||||||
| chr9:105602891 | T | A | 5 | a0001c0001t0002g0116 a0001c0001t0002g0124 a0001c0001t0002g0125 others(2): Show |
5 | HG00621.hp1 HG02027.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.370-1324T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602891 | |||||||
| chr9:105602918 | C | A | 6 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(3): Show |
6 | NA18963.hp1 NA18991.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-1297C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602918 | |||||||
| chr9:105602944 | A | G | 1 | a0001c0001t0027g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.370-1271A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105602944 | |||||||
| chr9:105603180 | C | T | 1 | a0001c0001t0002g0151 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.370-1035C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603180 | |||||||
| chr9:105603181 | G | A | 15 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(12): Show |
15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.370-1034G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603181 | |||||||
| chr9:105603200 | C | T | 4 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 others(1): Show |
5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.370-1015C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603200 | |||||||
| chr9:105603234 | A | G | 5 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(2): Show |
5 | NA18963.hp1 NA18991.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-981A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603234 | |||||||
| chr9:105603281 | G | A | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.370-934G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603281 | |||||||
| chr9:105603297 | G | C | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.370-918G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603297 | |||||||
| chr9:105603435 | T | C | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.370-780T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603435 | |||||||
| chr9:105603462 | T | C | 1 | a0002c0002t0004g0196 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.370-753T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603462 | |||||||
| chr9:105603582 | AT | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-632delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603582 | |||||||
| chr9:105603679 | G | T | 4 | a0001c0001t0006g0038 a0001c0001t0006g0220 a0001c0001t0018g0038 others(1): Show |
4 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-536G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603679 | |||||||
| chr9:105603679 | GT | G | 15 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(12): Show |
15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.370-524delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 105603679 | ||||||
| chr9:105603799 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.370-416A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603799 | |||||||
| chr9:105603902 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.370-313A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603902 | |||||||
| chr9:105603954 | T | C | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.370-261T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 5/10 | chr9 | 105603954 | |||||||
| chr9:105604528 | G | A | 4 | a0001c0001t0006g0038 a0001c0001t0006g0220 a0001c0001t0018g0038 others(1): Show |
4 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+36G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105604528 | |||||||
| chr9:105604703 | C | T | 1 | a0008c0012t0004g0212 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.647+211C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105604703 | |||||||
| chr9:105604812 | C | T | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.647+320C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105604812 | |||||||
| chr9:105604870 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.647+378T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105604870 | |||||||
| chr9:105604896 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.647+404T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105604896 | |||||||
| chr9:105604955 | C | A | 46 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 others(43): Show |
52 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.647+463C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105604955 | |||||||
| chr9:105604955 | C | CA | 15 | a0001c0001t0001g0288 a0001c0001t0001g0303 a0001c0001t0002g0025 others(12): Show |
16 | HG01261.hp1 HG02165.hp1 HG03098.hp2 others(13): Show |
intron_variant | MODIFIER | c.647+479dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 105604955 | ||||||
| chr9:105605128 | A | T | 5 | a0001c0001t0002g0139 a0001c0001t0012g0062 a0001c0001t0012g0063 others(2): Show |
5 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.647+636A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105605128 | |||||||
| chr9:105605163 | A | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
5 | HG00099.hp1 HG00280.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.647+671A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105605163 | |||||||
| chr9:105605166 | AAC | A | 3 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 |
4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+676_647+677del others(2): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 105605166 | ||||||
| chr9:105605225 | A | G | 1 | a0001c0001t0003g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.647+733A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105605225 | |||||||
| chr9:105605416 | G | A | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.647+924G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105605416 | |||||||
| chr9:105605692 | T | A | 1 | a0001c0001t0002g0143 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.647+1200T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105605692 | |||||||
| chr9:105605882 | TA | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.647+1394delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 105605882 | ||||||
| chr9:105605990 | G | A | 46 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 others(43): Show |
52 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.647+1498G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105605990 | |||||||
| chr9:105606070 | A | T | 4 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0119 others(1): Show |
5 | NA18953.hp1 NA18968.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.647+1578A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606070 | |||||||
| chr9:105606103 | A | T | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+1611A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606103 | |||||||
| chr9:105606202 | C | G | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.648-1617C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606202 | |||||||
| chr9:105606257 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0254 a0001c0001t0001g0309 others(3): Show |
7 | NA18949.hp1 NA18957.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.648-1562A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606257 | |||||||
| chr9:105606415 | C | T | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.648-1404C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606415 | |||||||
| chr9:105606481 | T | C | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.648-1338T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606481 | |||||||
| chr9:105606515 | A | G | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.648-1304A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606515 | |||||||
| chr9:105606541 | A | C | 2 | a0001c0001t0006g0233 a0001c0001t0006g0245 |
2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.648-1278A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606541 | |||||||
| chr9:105606673 | T | G | 6 | a0002c0002t0004g0196 a0002c0002t0008g0008 a0002c0002t0008g0200 others(3): Show |
8 | HG00597.hp1 HG01074.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.648-1146T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606673 | |||||||
| chr9:105606680 | AAT | A | 30 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(27): Show |
38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.648-1126_648-1125d others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 105606680 | ||||||
| chr9:105606682 | T | A | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.648-1137T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606682 | |||||||
| chr9:105606694 | TTA | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-1115_648-1114d others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 105606694 | ||||||
| chr9:105606702 | A | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-1117A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606702 | |||||||
| chr9:105606704 | A | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-1115A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606704 | |||||||
| chr9:105606706 | G | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-1113G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606706 | |||||||
| chr9:105606707 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-1112T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606707 | |||||||
| chr9:105606709 | T | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-1110T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606709 | |||||||
| chr9:105606709 | T | TTCTC | 245 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0219 others(242): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.648-1106_648-1103d others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 105606709 | ||||||
| chr9:105606779 | G | A | 46 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 others(43): Show |
52 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.648-1040G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606779 | |||||||
| chr9:105606803 | C | G | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.648-1016C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606803 | |||||||
| chr9:105606816 | T | G | 10 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(7): Show |
10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.648-1003T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606816 | |||||||
| chr9:105606869 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.648-950A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606869 | |||||||
| chr9:105606950 | A | G | 1 | a0001c0006t0014g0052 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.648-869A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105606950 | |||||||
| chr9:105607093 | G | C | 234 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(231): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.648-726G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105607093 | |||||||
| chr9:105607338 | A | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.648-481A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105607338 | |||||||
| chr9:105607561 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.648-258G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105607561 | |||||||
| chr9:105607690 | T | A | 1 | a0001c0001t0001g0294 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.648-129T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 6/10 | chr9 | 105607690 | |||||||
| chr9:105608023 | T | C | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.780+72T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608023 | |||||||
| chr9:105608063 | C | G | 1 | a0001c0001t0002g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.780+112C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608063 | |||||||
| chr9:105608080 | T | C | 30 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(27): Show |
38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.780+129T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608080 | |||||||
| chr9:105608102 | T | G | 2 | a0002c0002t0004g0187 a0002c0002t0025g0194 |
2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.780+151T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608102 | |||||||
| chr9:105608117 | A | G | 1 | a0001c0001t0002g0104 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.780+166A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608117 | |||||||
| chr9:105608244 | T | G | 1 | a0001c0001t0001g0251 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.780+293T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608244 | |||||||
| chr9:105608264 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0219 |
3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.780+313C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608264 | |||||||
| chr9:105608301 | C | G | 1 | a0001c0013t0002g0307 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.780+350C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608301 | |||||||
| chr9:105608393 | G | T | 1 | a0003c0003t0001g0230 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.780+442G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608393 | |||||||
| chr9:105608638 | C | T | 2 | a0001c0001t0002g0152 a0001c0001t0002g0176 |
2 | NA18965.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.780+687C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608638 | |||||||
| chr9:105608689 | G | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+738G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608689 | |||||||
| chr9:105608778 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+827C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608778 | |||||||
| chr9:105608857 | CAT | C | 16 | a0001c0001t0006g0015 a0001c0001t0006g0038 a0001c0001t0006g0041 others(13): Show |
19 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.780+907_780+908del others(2): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105608857 | |||||||
| chr9:105609040 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+1089C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609040 | |||||||
| chr9:105609056 | A | G | 8 | a0001c0001t0003g0016 a0001c0001t0003g0019 a0001c0001t0003g0022 others(5): Show |
11 | HG00323.hp1 HG00741.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.780+1105A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609056 | |||||||
| chr9:105609217 | G | A | 1 | a0002c0002t0004g0211 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.780+1266G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609217 | |||||||
| chr9:105609217 | G | T | 2 | a0002c0002t0001g0283 a0002c0002t0001g0286 |
2 | NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.780+1266G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609217 | |||||||
| chr9:105609230 | T | G | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.780+1279T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609230 | |||||||
| chr9:105609268 | C | T | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.780+1317C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609268 | |||||||
| chr9:105609338 | G | A | 1 | a0001c0001t0002g0031 | 2 | HG02523.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.780+1387G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609338 | |||||||
| chr9:105609353 | T | C | 5 | a0001c0001t0001g0106 a0001c0001t0002g0027 a0001c0001t0002g0130 others(2): Show |
6 | HG02148.hp1 HG02273.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+1402T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609353 | |||||||
| chr9:105609509 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(42): Show |
60 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.780+1558C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609509 | |||||||
| chr9:105609535 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.780+1584A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609535 | |||||||
| chr9:105609646 | T | A | 1 | a0001c0005t0026g0181 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.780+1695T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609646 | |||||||
| chr9:105609758 | AT | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+1809delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105609758 | ||||||
| chr9:105609843 | G | A | 3 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 |
4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+1892G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105609843 | |||||||
| chr9:105610003 | T | C | 13 | a0003c0003t0001g0222 a0003c0003t0001g0223 a0003c0003t0001g0224 others(10): Show |
13 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.780+2052T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610003 | |||||||
| chr9:105610075 | A | G | 2 | a0002c0002t0001g0275 a0002c0002t0001g0290 |
2 | HG02004.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.780+2124A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610075 | |||||||
| chr9:105610755 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+2804C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610755 | |||||||
| chr9:105610757 | T | C | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.780+2806T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610757 | |||||||
| chr9:105610773 | G | A | 313 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(310): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.780+2822G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610773 | |||||||
| chr9:105610854 | C | T | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.780+2903C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610854 | |||||||
| chr9:105610903 | C | A | 97 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(94): Show |
108 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.780+2952C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610903 | |||||||
| chr9:105610980 | C | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+3029C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105610980 | |||||||
| chr9:105611063 | A | G | 2 | a0004c0004t0005g0044 a0004c0004t0005g0250 |
3 | HG00140.hp1 HG00735.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.780+3112A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611063 | |||||||
| chr9:105611223 | C | T | 5 | a0002c0002t0001g0269 a0002c0002t0001g0283 a0002c0002t0001g0284 others(2): Show |
5 | NA18747.hp2 NA18966.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+3272C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611223 | |||||||
| chr9:105611328 | A | T | 16 | a0001c0001t0006g0015 a0001c0001t0006g0038 a0001c0001t0006g0041 others(13): Show |
19 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.780+3377A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611328 | |||||||
| chr9:105611500 | C | A | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+3549C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611500 | |||||||
| chr9:105611601 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0219 |
3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.780+3650G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611601 | |||||||
| chr9:105611704 | C | T | 4 | a0001c0001t0005g0232 a0001c0001t0005g0242 a0001c0001t0005g0243 others(1): Show |
4 | HG00280.hp1 HG03654.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-3574C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611704 | |||||||
| chr9:105611817 | G | A | 1 | a0001c0001t0006g0240 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.781-3461G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611817 | |||||||
| chr9:105611935 | C | T | 30 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(27): Show |
38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.781-3343C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105611935 | |||||||
| chr9:105612015 | G | GTTTAT | 5 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(2): Show |
5 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-3236_781-3232d others(7): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105612015 | ||||||
| chr9:105612241 | A | T | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.781-3037A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105612241 | |||||||
| chr9:105612357 | T | C | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0264 others(1): Show |
4 | NA18970.hp1 NA18977.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-2921T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105612357 | |||||||
| chr9:105612503 | G | GT | 235 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(232): Show |
275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.781-2771dupT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105612503 | ||||||
| chr9:105612556 | A | T | 1 | a0001c0008t0003g0094 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.781-2722A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105612556 | |||||||
| chr9:105612690 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.781-2588C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105612690 | |||||||
| chr9:105613080 | T | C | 12 | a0003c0003t0001g0222 a0003c0003t0001g0223 a0003c0003t0001g0224 others(9): Show |
12 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.781-2198T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613080 | |||||||
| chr9:105613113 | T | C | 1 | a0002c0002t0025g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.781-2165T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613113 | |||||||
| chr9:105613195 | T | A | 3 | a0001c0001t0002g0118 a0001c0001t0002g0132 a0001c0001t0002g0145 |
3 | HG00408.hp1 HG02040.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.781-2083T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613195 | |||||||
| chr9:105613352 | T | C | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.781-1926T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613352 | |||||||
| chr9:105613424 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-1854G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613424 | |||||||
| chr9:105613465 | A | G | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.781-1813A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613465 | |||||||
| chr9:105613577 | G | T | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-1701G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613577 | |||||||
| chr9:105613755 | T | C | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-1523T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613755 | |||||||
| chr9:105613829 | A | G | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-1449A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613829 | |||||||
| chr9:105613980 | G | A | 4 | a0002c0002t0004g0034 a0002c0002t0004g0195 a0002c0002t0004g0197 others(1): Show |
5 | HG02559.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-1298G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105613980 | |||||||
| chr9:105614103 | A | AC | 3 | a0001c0001t0001g0012 a0001c0001t0001g0253 a0001c0001t0001g0299 |
5 | HG00639.hp1 HG00642.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-1173dupC | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105614103 | ||||||
| chr9:105614155 | A | G | 30 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(27): Show |
38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.781-1123A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614155 | |||||||
| chr9:105614366 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.781-912A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614366 | |||||||
| chr9:105614383 | TTTCA | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-886_781-883del others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105614383 | ||||||
| chr9:105614480 | T | C | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.781-798T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614480 | |||||||
| chr9:105614600 | T | A | 1 | a0002c0002t0004g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.781-678T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614600 | |||||||
| chr9:105614816 | G | A | 61 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(58): Show |
67 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.781-462G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614816 | |||||||
| chr9:105614884 | C | CT | 49 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(46): Show |
64 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.781-382dupT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105614884 | ||||||
| chr9:105614888 | T | C | 1 | a0002c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.781-390T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614888 | |||||||
| chr9:105614976 | C | T | 1 | a0002c0002t0001g0286 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.781-302C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105614976 | |||||||
| chr9:105615015 | C | T | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-263C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105615015 | |||||||
| chr9:105615025 | AG | A | 93 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.781-251delG | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105615025 | ||||||
| chr9:105615055 | T | TA | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-222dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 105615055 | ||||||
| chr9:105615115 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.781-163C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 7/10 | chr9 | 105615115 | |||||||
| chr9:105615421 | G | A | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.910+14G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615421 | |||||||
| chr9:105615452 | C | T | 2 | a0001c0001t0003g0020 a0001c0001t0003g0085 |
3 | HG02155.hp1 NA18953.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.910+45C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615452 | |||||||
| chr9:105615466 | A | G | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.910+59A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615466 | |||||||
| chr9:105615697 | T | G | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.910+290T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615697 | |||||||
| chr9:105615740 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.910+333C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615740 | |||||||
| chr9:105615743 | T | C | 48 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0019g0189 others(45): Show |
54 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.910+336T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615743 | |||||||
| chr9:105615762 | C | T | 43 | a0002c0002t0001g0267 a0002c0002t0001g0269 a0002c0002t0001g0274 others(40): Show |
48 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.910+355C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615762 | |||||||
| chr9:105615770 | T | C | 2 | a0001c0001t0002g0069 a0001c0001t0002g0108 |
2 | NA18747.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.910+363T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615770 | |||||||
| chr9:105615832 | A | G | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.910+425A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615832 | |||||||
| chr9:105615918 | A | T | 1 | a0003c0003t0001g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.910+511A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105615918 | |||||||
| chr9:105616145 | C | A | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.910+738C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105616145 | |||||||
| chr9:105616190 | G | T | 8 | a0003c0003t0001g0222 a0003c0003t0001g0223 a0003c0003t0001g0224 others(5): Show |
8 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.910+783G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105616190 | |||||||
| chr9:105616236 | A | G | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.910+829A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105616236 | |||||||
| chr9:105616605 | CTTGA | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.910+1201_910+1204d others(6): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 105616605 | ||||||
| chr9:105616660 | A | G | 4 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 others(1): Show |
5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.910+1253A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105616660 | |||||||
| chr9:105616861 | C | G | 1 | a0001c0001t0001g0049 | 2 | NA19001.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.911-1098C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105616861 | |||||||
| chr9:105616879 | C | CA | 51 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0277 others(48): Show |
59 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.911-1065dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 105616879 | ||||||
| chr9:105616881 | A | G | 4 | a0001c0001t0006g0038 a0001c0001t0006g0220 a0001c0001t0018g0038 others(1): Show |
4 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.911-1078A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105616881 | |||||||
| chr9:105617107 | A | G | 10 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(7): Show |
10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.911-852A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105617107 | |||||||
| chr9:105617316 | T | A | 1 | a0001c0001t0001g0295 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.911-643T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105617316 | |||||||
| chr9:105617547 | C | T | 1 | a0001c0001t0002g0142 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.911-412C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105617547 | |||||||
| chr9:105617673 | TCAAA | T | 10 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(7): Show |
10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.911-281_911-278del others(4): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 105617673 | ||||||
| chr9:105617699 | T | C | 1 | a0001c0001t0002g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.911-260T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105617699 | |||||||
| chr9:105617723 | G | A | 157 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(154): Show |
174 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.911-236G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 8/10 | chr9 | 105617723 | |||||||
| chr9:105618150 | C | T | 15 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(12): Show |
15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1044+58C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618150 | |||||||
| chr9:105618176 | A | C | 1 | a0001c0001t0001g0262 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1044+84A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618176 | |||||||
| chr9:105618241 | A | T | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1044+149A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618241 | |||||||
| chr9:105618440 | A | G | 47 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0019g0189 others(44): Show |
53 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1044+348A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618440 | |||||||
| chr9:105618464 | C | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0219 |
3 | HG01081.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1044+372C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618464 | |||||||
| chr9:105618465 | C | T | 1 | a0001c0013t0002g0307 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1044+373C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618465 | |||||||
| chr9:105618508 | G | A | 2 | a0001c0006t0014g0051 a0001c0006t0014g0052 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1044+416G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618508 | |||||||
| chr9:105618761 | T | C | 2 | a0001c0001t0003g0020 a0001c0001t0003g0085 |
3 | HG02155.hp1 NA18953.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1044+669T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618761 | |||||||
| chr9:105618848 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1044+756T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618848 | |||||||
| chr9:105618916 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1044+824G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105618916 | |||||||
| chr9:105619053 | C | T | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1045-881C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105619053 | |||||||
| chr9:105619058 | T | TA | 6 | a0001c0001t0001g0106 a0001c0001t0002g0128 a0001c0001t0002g0133 others(3): Show |
6 | HG03098.hp2 HG03130.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-859dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 105619058 | ||||||
| chr9:105619058 | TA | T | 50 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0002g0142 others(47): Show |
56 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1045-859delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 105619058 | ||||||
| chr9:105619156 | G | T | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045-778G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105619156 | |||||||
| chr9:105619482 | G | T | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1045-452G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105619482 | |||||||
| chr9:105619639 | G | C | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1045-295G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105619639 | |||||||
| chr9:105619744 | T | G | 1 | a0001c0001t0006g0233 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1045-190T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105619744 | |||||||
| chr9:105619894 | C | A | 1 | a0001c0001t0006g0241 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1045-40C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 9/10 | chr9 | 105619894 | |||||||
| chr9:105620147 | C | A | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1172+86C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105620147 | |||||||
| chr9:105620659 | A | G | 1 | a0001c0001t0002g0105 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1172+598A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105620659 | |||||||
| chr9:105620711 | C | G | 1 | a0001c0001t0003g0101 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1172+650C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105620711 | |||||||
| chr9:105620775 | A | ATAG | 44 | a0001c0001t0001g0011 a0001c0001t0002g0029 a0001c0001t0002g0105 others(41): Show |
52 | HG00099.hp2 HG00323.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1172+759_1172+761d others(5): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | ||||||
| chr9:105620775 | A | ATAGTAG | 85 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0219 others(82): Show |
98 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.1172+756_1172+761d others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | ||||||
| chr9:105620775 | A | ATAGTAGT others(2): Show |
35 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0069 others(32): Show |
38 | HG00408.hp1 HG00558.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1172+753_1172+761d others(11): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | ||||||
| chr9:105620775 | A | ATAGTAGT others(5): Show |
11 | a0001c0001t0002g0109 a0001c0001t0002g0142 a0001c0001t0002g0148 others(8): Show |
11 | HG00140.hp2 HG01074.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.1172+750_1172+761d others(14): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | ||||||
| chr9:105620775 | A | ATAGTAGT others(8): Show |
1 | a0001c0001t0002g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1172+747_1172+761d others(17): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | ||||||
| chr9:105620775 | ATAG | A | 100 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0012 others(97): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1172+759_1172+761d others(5): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | ||||||
| chr9:105620775 | ATAGTAG | A | 7 | a0001c0001t0001g0306 a0001c0001t0003g0072 a0001c0001t0003g0095 others(4): Show |
8 | HG01099.hp2 HG01192.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1172+756_1172+761d others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105620775 | ||||||
| chr9:105621124 | C | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1172+1063C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621124 | |||||||
| chr9:105621147 | G | A | 98 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(95): Show |
109 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1172+1086G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621147 | |||||||
| chr9:105621517 | T | A | 235 | a0001c0001t0001g0106 a0001c0001t0001g0253 a0001c0001t0002g0003 others(232): Show |
275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.1172+1456T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621517 | |||||||
| chr9:105621522 | T | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0045 |
5 | NA18967.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.1172+1461T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621522 | |||||||
| chr9:105621682 | C | T | 91 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(88): Show |
102 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1172+1621C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621682 | |||||||
| chr9:105621793 | A | G | 98 | a0001c0001t0001g0106 a0001c0001t0002g0003 a0001c0001t0002g0007 others(95): Show |
109 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1172+1732A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621793 | |||||||
| chr9:105621911 | G | A | 2 | a0001c0001t0017g0021 a0001c0001t0048g0087 |
3 | HG02071.hp1 HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1172+1850G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105621911 | |||||||
| chr9:105622204 | C | A | 1 | a0001c0001t0027g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1172+2143C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622204 | |||||||
| chr9:105622222 | G | A | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1172+2161G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622222 | |||||||
| chr9:105622515 | T | G | 1 | a0001c0005t0019g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1172+2454T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622515 | |||||||
| chr9:105622901 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1172+2840G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622901 | |||||||
| chr9:105622910 | A | G | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1172+2849A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622910 | |||||||
| chr9:105622923 | G | A | 46 | a0001c0001t0001g0253 a0001c0001t0003g0001 a0001c0001t0003g0005 others(43): Show |
61 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1172+2862G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622923 | |||||||
| chr9:105622941 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0304 |
5 | NA18942.hp2 NA19001.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1172+2880C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622941 | |||||||
| chr9:105622956 | G | A | 46 | a0001c0001t0001g0253 a0001c0001t0003g0001 a0001c0001t0003g0005 others(43): Show |
61 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1172+2895G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105622956 | |||||||
| chr9:105623150 | G | T | 2 | a0002c0002t0022g0202 a0002c0002t0023g0203 |
2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1172+3089G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105623150 | |||||||
| chr9:105623194 | G | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1172+3133G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105623194 | |||||||
| chr9:105623248 | ATACT | A | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1172+3192_1172+319 others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105623248 | ||||||
| chr9:105623442 | A | C | 1 | a0002c0002t0001g0290 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1172+3381A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105623442 | |||||||
| chr9:105623645 | G | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1172+3584G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105623645 | |||||||
| chr9:105623790 | C | T | 6 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(3): Show |
6 | NA18963.hp1 NA18991.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1172+3729C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105623790 | |||||||
| chr9:105624075 | A | G | 10 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0001g0049 others(7): Show |
13 | HG00673.hp1 NA18942.hp2 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.1172+4014A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624075 | |||||||
| chr9:105624096 | T | C | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1172+4035T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624096 | |||||||
| chr9:105624400 | A | G | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1172+4339A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624400 | |||||||
| chr9:105624417 | C | T | 1 | a0001c0001t0006g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1172+4356C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624417 | |||||||
| chr9:105624452 | C | T | 1 | a0002c0002t0004g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1172+4391C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624452 | |||||||
| chr9:105624515 | C | T | 7 | a0001c0001t0002g0104 a0001c0001t0002g0137 a0001c0001t0002g0138 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1172+4454C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624515 | |||||||
| chr9:105624599 | C | T | 4 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 others(1): Show |
5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1172+4538C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624599 | |||||||
| chr9:105624623 | C | CA | 12 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0279 others(9): Show |
14 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(11): Show |
intron_variant | MODIFIER | c.1172+4580dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105624623 | ||||||
| chr9:105624623 | CA | C | 6 | a0001c0001t0001g0297 a0001c0001t0002g0120 a0001c0001t0002g0142 others(3): Show |
7 | HG01975.hp1 HG02735.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1172+4580delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105624623 | ||||||
| chr9:105624640 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1172+4579A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624640 | |||||||
| chr9:105624894 | T | C | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1172+4833T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624894 | |||||||
| chr9:105624966 | C | A | 1 | a0001c0001t0001g0292 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1172+4905C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105624966 | |||||||
| chr9:105625100 | T | C | 8 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(5): Show |
8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1172+5039T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105625100 | |||||||
| chr9:105625836 | TA | T | 9 | a0003c0003t0001g0222 a0003c0003t0001g0223 a0003c0003t0001g0224 others(6): Show |
9 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1172+5787delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105625836 | ||||||
| chr9:105625923 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1172+5862C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105625923 | |||||||
| chr9:105626048 | T | C | 1 | a0001c0001t0016g0115 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1172+5987T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626048 | |||||||
| chr9:105626113 | T | C | 2 | a0001c0005t0013g0035 a0001c0005t0013g0180 |
3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1172+6052T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626113 | |||||||
| chr9:105626166 | G | A | 2 | a0001c0006t0014g0051 a0001c0006t0014g0052 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1172+6105G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626166 | |||||||
| chr9:105626180 | A | G | 1 | a0001c0001t0003g0024 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1172+6119A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626180 | |||||||
| chr9:105626356 | C | T | 2 | a0001c0001t0009g0278 a0001c0001t0009g0305 |
2 | NA18957.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1172+6295C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626356 | |||||||
| chr9:105626423 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1172+6362G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626423 | |||||||
| chr9:105626627 | T | C | 1 | a0001c0001t0016g0155 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1172+6566T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626627 | |||||||
| chr9:105626698 | C | T | 89 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0025 others(86): Show |
100 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1172+6637C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626698 | |||||||
| chr9:105626971 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0293 |
2 | NA18983.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1172+6910C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105626971 | |||||||
| chr9:105626981 | C | CTTTTTTT | 8 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(5): Show |
8 | HG01255.hp2 HG02257.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1172+6930_1172+693 others(11): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105626981 | ||||||
| chr9:105626981 | CT | C | 200 | a0001c0001t0001g0251 a0001c0001t0001g0257 a0001c0001t0002g0003 others(197): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1172+6936delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105626981 | ||||||
| chr9:105627220 | C | A | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1172+7159C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105627220 | |||||||
| chr9:105627625 | A | G | 9 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(6): Show |
9 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173-7426A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105627625 | |||||||
| chr9:105627722 | T | G | 1 | a0003c0003t0001g0223 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1173-7329T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105627722 | |||||||
| chr9:105627934 | C | A | 1 | a0002c0002t0008g0200 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1173-7117C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105627934 | |||||||
| chr9:105627972 | A | G | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-7079A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105627972 | |||||||
| chr9:105627979 | A | G | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-7072A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105627979 | |||||||
| chr9:105628090 | T | C | 1 | a0001c0001t0002g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1173-6961T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628090 | |||||||
| chr9:105628252 | G | T | 4 | a0001c0001t0003g0019 a0001c0001t0003g0022 a0001c0001t0003g0079 others(1): Show |
6 | HG00741.hp1 HG01099.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173-6799G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628252 | |||||||
| chr9:105628311 | G | T | 15 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(12): Show |
15 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1173-6740G>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628311 | |||||||
| chr9:105628323 | C | T | 3 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 |
4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173-6728C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628323 | |||||||
| chr9:105628419 | T | C | 1 | a0002c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1173-6632T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628419 | |||||||
| chr9:105628448 | A | AG | 30 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(27): Show |
38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1173-6602dupG | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105628448 | ||||||
| chr9:105628615 | A | G | 2 | a0001c0005t0013g0035 a0001c0005t0013g0180 |
3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1173-6436A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628615 | |||||||
| chr9:105628645 | C | A | 1 | a0001c0001t0002g0177 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1173-6406C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628645 | |||||||
| chr9:105628663 | C | T | 4 | a0001c0001t0011g0204 a0001c0001t0011g0205 a0001c0001t0011g0208 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-6388C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628663 | |||||||
| chr9:105628846 | G | A | 4 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173-6205G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105628846 | |||||||
| chr9:105629028 | TAAGA | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-6022_1173-601 others(8): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629028 | |||||||
| chr9:105629056 | C | G | 14 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(11): Show |
14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1173-5995C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629056 | |||||||
| chr9:105629084 | A | T | 1 | a0001c0001t0002g0117 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1173-5967A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629084 | |||||||
| chr9:105629130 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1173-5921G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629130 | |||||||
| chr9:105629179 | T | C | 1 | a0001c0001t0002g0130 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1173-5872T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629179 | |||||||
| chr9:105629184 | A | G | 2 | a0002c0002t0004g0032 a0002c0002t0004g0033 |
4 | HG00099.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-5867A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629184 | |||||||
| chr9:105629218 | T | C | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-5833T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629218 | |||||||
| chr9:105629287 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1173-5764G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629287 | |||||||
| chr9:105629292 | C | G | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1173-5759C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629292 | |||||||
| chr9:105629295 | A | G | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-5756A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629295 | |||||||
| chr9:105629311 | A | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-5740A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629311 | |||||||
| chr9:105629425 | G | C | 1 | a0001c0001t0002g0117 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1173-5626G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629425 | |||||||
| chr9:105629456 | A | T | 1 | a0001c0001t0002g0117 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1173-5595A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629456 | |||||||
| chr9:105629581 | G | C | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-5470G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629581 | |||||||
| chr9:105629704 | G | A | 233 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0025 others(230): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.1173-5347G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629704 | |||||||
| chr9:105629934 | A | G | 101 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0025 others(98): Show |
112 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1173-5117A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105629934 | |||||||
| chr9:105630042 | G | A | 1 | a0001c0001t0001g0287 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1173-5009G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630042 | |||||||
| chr9:105630165 | C | T | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-4886C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630165 | |||||||
| chr9:105630201 | TA | T | 8 | a0001c0001t0002g0117 a0001c0001t0003g0018 a0001c0001t0003g0071 others(5): Show |
9 | HG00673.hp2 HG03927.hp1 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173-4842delA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105630201 | ||||||
| chr9:105630280 | A | C | 1 | a0001c0001t0002g0117 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1173-4771A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630280 | |||||||
| chr9:105630326 | A | T | 1 | a0001c0001t0002g0117 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1173-4725A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630326 | |||||||
| chr9:105630403 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1173-4648C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630403 | |||||||
| chr9:105630424 | C | T | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1173-4627C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630424 | |||||||
| chr9:105630455 | C | T | 1 | a0001c0001t0002g0151 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1173-4596C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630455 | |||||||
| chr9:105630543 | A | C | 1 | a0001c0001t0001g0304 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1173-4508A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630543 | |||||||
| chr9:105630548 | A | T | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1173-4503A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630548 | |||||||
| chr9:105630624 | T | G | 1 | a0001c0001t0027g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1173-4427T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630624 | |||||||
| chr9:105630807 | A | G | 1 | a0001c0001t0012g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1173-4244A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105630807 | |||||||
| chr9:105631061 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1173-3990A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631061 | |||||||
| chr9:105631191 | C | T | 1 | a0002c0002t0022g0202 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1173-3860C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631191 | |||||||
| chr9:105631540 | C | G | 1 | a0002c0002t0004g0034 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1173-3511C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631540 | |||||||
| chr9:105631622 | C | A | 11 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0071 others(8): Show |
14 | HG00673.hp2 HG02071.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1173-3429C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631622 | |||||||
| chr9:105631779 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1173-3272A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631779 | |||||||
| chr9:105631883 | G | A | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1173-3168G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631883 | |||||||
| chr9:105631904 | C | G | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-3147C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631904 | |||||||
| chr9:105631967 | C | A | 8 | a0001c0001t0006g0015 a0001c0001t0006g0041 a0001c0001t0006g0055 others(5): Show |
11 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1173-3084C>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631967 | |||||||
| chr9:105631969 | G | A | 12 | a0001c0001t0006g0015 a0001c0001t0006g0041 a0001c0001t0006g0055 others(9): Show |
15 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1173-3082G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105631969 | |||||||
| chr9:105632082 | G | C | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1173-2969G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632082 | |||||||
| chr9:105632157 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | NA18969.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1173-2894C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632157 | |||||||
| chr9:105632185 | G | A | 1 | a0001c0001t0012g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1173-2866G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632185 | |||||||
| chr9:105632187 | A | G | 46 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(43): Show |
61 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1173-2864A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632187 | |||||||
| chr9:105632233 | A | C | 47 | a0001c0005t0013g0035 a0001c0005t0013g0180 a0001c0005t0026g0181 others(44): Show |
53 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1173-2818A>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632233 | |||||||
| chr9:105632294 | G | C | 1 | a0001c0001t0010g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1173-2757G>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632294 | |||||||
| chr9:105632419 | T | TA | 64 | a0001c0001t0005g0040 a0001c0001t0005g0232 a0001c0001t0005g0242 others(61): Show |
75 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1173-2623dupA | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 105632419 | ||||||
| chr9:105632425 | A | T | 1 | a0001c0001t0012g0064 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1173-2626A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632425 | |||||||
| chr9:105632427 | A | AT | 9 | a0001c0001t0040g0244 a0002c0002t0001g0267 a0002c0002t0004g0187 others(6): Show |
12 | HG00140.hp1 HG00735.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1173-2624_1173-262 others(5): Show |
FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632427 | |||||||
| chr9:105632427 | A | T | 31 | a0001c0001t0002g0153 a0001c0001t0010g0056 a0001c0001t0010g0057 others(28): Show |
31 | HG01255.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1173-2624A>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632427 | |||||||
| chr9:105632429 | T | A | 46 | a0001c0001t0001g0270 a0001c0001t0001g0287 a0001c0001t0003g0001 others(43): Show |
59 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1173-2622T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632429 | |||||||
| chr9:105632438 | AT | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-2612delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632438 | |||||||
| chr9:105632440 | AT | A | 10 | a0001c0001t0010g0056 a0001c0001t0010g0057 a0001c0001t0010g0058 others(7): Show |
10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1173-2610delT | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632440 | |||||||
| chr9:105632441 | T | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-2610T>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632441 | |||||||
| chr9:105632577 | G | A | 1 | a0001c0001t0003g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1173-2474G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632577 | |||||||
| chr9:105632612 | A | G | 43 | a0002c0002t0001g0267 a0002c0002t0001g0269 a0002c0002t0001g0274 others(40): Show |
48 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1173-2439A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632612 | |||||||
| chr9:105632616 | G | A | 4 | a0001c0006t0014g0051 a0001c0006t0014g0052 a0001c0006t0015g0054 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173-2435G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632616 | |||||||
| chr9:105632656 | T | G | 1 | a0004c0010t0041g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1173-2395T>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632656 | |||||||
| chr9:105632747 | A | G | 1 | a0001c0001t0006g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1173-2304A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632747 | |||||||
| chr9:105632799 | T | C | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1173-2252T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632799 | |||||||
| chr9:105632914 | A | G | 313 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(310): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1173-2137A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105632914 | |||||||
| chr9:105633651 | A | G | 246 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0025 others(243): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1173-1400A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105633651 | |||||||
| chr9:105633753 | G | A | 89 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0025 others(86): Show |
100 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1173-1298G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105633753 | |||||||
| chr9:105633770 | G | A | 2 | a0001c0001t0046g0060 a0004c0010t0041g0061 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1173-1281G>A | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105633770 | |||||||
| chr9:105634282 | C | G | 93 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0025 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1173-769C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634282 | |||||||
| chr9:105634353 | C | T | 103 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0025 others(100): Show |
114 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1173-698C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634353 | |||||||
| chr9:105634635 | C | G | 1 | a0007c0014t0043g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1173-416C>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634635 | |||||||
| chr9:105634735 | C | T | 89 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0025 others(86): Show |
100 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1173-316C>T | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634735 | |||||||
| chr9:105634737 | A | G | 1 | a0001c0006t0014g0052 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1173-314A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634737 | |||||||
| chr9:105634824 | T | C | 1 | a0001c0001t0003g0080 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1173-227T>C | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634824 | |||||||
| chr9:105634891 | A | G | 1 | a0001c0001t0046g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1173-160A>G | FKTN | ENSG00000106692.15 | transcript | ENST00000357998.10 | protein_coding | 10/10 | chr9 | 105634891 |