Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 26259 |
|---|---|
| ensemblid | ENSG00000174989.13 |
| hgncid | 13597 |
| symbol | FBXW8 |
| name | F-box and WD repeat domain containing 8 |
| refseq_nuc | NM_153348.3 |
| refseq_prot | NP_699179.2 |
| ensembl_nuc | ENST00000652555.1 |
| ensembl_prot | ENSP00000498999.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 116910950 |
| end | 117031148 |
| strand | + |
| ver | v1.2 |
| region | chr12:116910950-117031148 |
| region5000 | chr12:116905950-117036148 |
| regionname0 | FBXW8_chr12_116910950_117031148 |
| regionname5000 | FBXW8_chr12_116905950_117036148 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 598 | 138 | 20 | 23 | 62 | 4 | 28 | 39 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002 | 1/0 | 598 | 93 | 35 | 9 | 39 | 2 | 7 | 32 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003 | 0/0 | 598 | 32 | 29 | 1 | 0 | 0 | 2 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0004 | 0/0 | 598 | 12 | 0 | 0 | 12 | 0 | 0 | 8 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0005 | 0/0 | 598 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0006 | 0/0 | 598 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0007 | 0/0 | 72 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0008 | 0/0 | 598 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0009 | 0/0 | 598 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0010 | 0/0 | 598 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0011 | 0/0 | 598 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0012 | 0/0 | 598 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1797 | 129 | 20 | 18 | 62 | 4 | 24 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0002 | 0/0 | 1797 | 86 | 34 | 7 | 37 | 1 | 7 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0003 | 0/0 | 1797 | 24 | 21 | 1 | 0 | 0 | 2 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0004 | 0/0 | 1797 | 12 | 0 | 0 | 12 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0005 | 0/0 | 1797 | 6 | 6 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0006 | 0/0 | 1797 | 6 | 0 | 5 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0007 | 0/0 | 1797 | 6 | 6 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0008 | 0/0 | 1797 | 4 | 1 | 2 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0009 | 0/0 | 1797 | 3 | 0 | 0 | 0 | 0 | 3 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0010 | 0/0 | 1797 | 2 | 1 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0011 | 0/0 | 1797 | 2 | 0 | 0 | 2 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0012 | 0/0 | 1778 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0013 | 1/0 | 1797 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0014 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0015 | 0/0 | 1797 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0016 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0017 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0018 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0019 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0020 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| c0021 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 3065 | 93 | 10 | 15 | 50 | 3 | 13 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0002 | 0/0 | 3065 | 68 | 28 | 5 | 32 | 1 | 2 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0003 | 0/0 | 3065 | 39 | 12 | 6 | 15 | 1 | 5 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0004 | 0/0 | 3063 | 16 | 0 | 0 | 8 | 0 | 8 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0005 | 0/0 | 3063 | 10 | 0 | 2 | 3 | 1 | 4 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0006 | 0/0 | 3065 | 8 | 8 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0007 | 0/0 | 3065 | 6 | 6 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0008 | 0/0 | 3065 | 6 | 5 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0009 | 0/0 | 3075 | 6 | 6 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0010 | 0/0 | 3065 | 5 | 3 | 0 | 0 | 0 | 2 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0011 | 0/0 | 3062 | 4 | 4 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0012 | 0/0 | 3065 | 3 | 3 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0013 | 0/0 | 3065 | 2 | 1 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0014 | 0/0 | 3065 | 2 | 0 | 0 | 0 | 0 | 2 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0015 | 0/0 | 3065 | 2 | 0 | 1 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0016 | 0/0 | 3065 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0017 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0018 | 0/0 | 3062 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0019 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0020 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0021 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0022 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0023 | 0/0 | 3065 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0024 | 0/0 | 3065 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0025 | 0/0 | 3065 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0026 | 0/0 | 3065 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0027 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0028 | 0/0 | 3065 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0029 | 0/0 | 3065 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0030 | 0/0 | 3065 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0031 | 0/0 | 3065 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0032 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0033 | 0/0 | 3062 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0034 | 0/0 | 3065 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| t0035 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1797 | 129 | 20 | 18 | 62 | 4 | 24 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0006 | 0/0 | 1797 | 6 | 0 | 5 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0009 | 0/0 | 1797 | 3 | 0 | 0 | 0 | 0 | 3 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002 | 0/0 | 1797 | 86 | 34 | 7 | 37 | 1 | 7 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0008 | 0/0 | 1797 | 4 | 1 | 2 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0011 | 0/0 | 1797 | 2 | 0 | 0 | 2 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0013 | 1/0 | 1797 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0003 | 0/0 | 1797 | 24 | 21 | 1 | 0 | 0 | 2 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0005 | 0/0 | 1797 | 6 | 6 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0020 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0021 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0004c0004 | 0/0 | 1797 | 12 | 0 | 0 | 12 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0005c0007 | 0/0 | 1797 | 6 | 6 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0005c0017 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0006c0010 | 0/0 | 1797 | 2 | 1 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0007c0012 | 0/0 | 1778 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0008c0016 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0009c0015 | 0/0 | 1797 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0010c0019 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0011c0018 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0012c0014 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4861 | 69 | 9 | 10 | 37 | 3 | 9 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0001t0003 | 0/0 | 4861 | 34 | 8 | 6 | 15 | 1 | 4 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0001t0004 | 0/0 | 4859 | 16 | 0 | 0 | 8 | 0 | 8 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0001t0014 | 0/0 | 4861 | 2 | 0 | 0 | 0 | 0 | 2 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0001t0015 | 0/0 | 4861 | 2 | 0 | 1 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0001t0025 | 0/0 | 4861 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0001t0031 | 0/0 | 4861 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0001t0032 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0001t0033 | 0/0 | 4858 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0001t0034 | 0/0 | 4861 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0001t0035 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0006t0001 | 0/0 | 4861 | 6 | 0 | 5 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0001c0009t0001 | 0/0 | 4861 | 3 | 0 | 0 | 0 | 0 | 3 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002t0001 | 0/0 | 4861 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002t0002 | 0/0 | 4861 | 54 | 19 | 3 | 30 | 0 | 2 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002t0005 | 0/0 | 4859 | 10 | 0 | 2 | 3 | 1 | 4 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002t0008 | 0/0 | 4861 | 6 | 5 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002t0009 | 0/0 | 4871 | 6 | 6 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002t0011 | 0/0 | 4858 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002t0016 | 0/0 | 4861 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002t0022 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002t0024 | 0/0 | 4861 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002t0026 | 0/0 | 4861 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002t0027 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002t0028 | 0/0 | 4861 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0002t0030 | 0/0 | 4861 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0008t0002 | 0/0 | 4861 | 4 | 1 | 2 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0011t0002 | 0/0 | 4861 | 2 | 0 | 0 | 2 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0002c0013t0001 | 1/0 | 4861 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0003t0001 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0003t0003 | 0/0 | 4861 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0003t0006 | 0/0 | 4861 | 8 | 8 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0003t0010 | 0/0 | 4861 | 5 | 3 | 0 | 0 | 0 | 2 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0003t0011 | 0/0 | 4858 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0003t0012 | 0/0 | 4861 | 3 | 3 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0003t0019 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0003t0021 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0003t0029 | 0/0 | 4861 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0005t0002 | 0/0 | 4861 | 6 | 6 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0020t0020 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0003c0021t0017 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0004c0004t0001 | 0/0 | 4861 | 12 | 0 | 0 | 12 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0005c0007t0002 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0005c0007t0007 | 0/0 | 4861 | 5 | 5 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0005c0017t0007 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0006c0010t0013 | 0/0 | 4861 | 2 | 1 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0007c0012t0018 | 0/0 | 4839 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0008c0016t0003 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0009c0015t0003 | 0/0 | 4861 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0010c0019t0003 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0011c0018t0002 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| a0012c0014t0023 | 0/0 | 4861 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | copy fasta | chr12 | 116905950 | 117036148 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0014g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0014g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0015g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0015g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0025g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0031g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0032g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0033g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0034g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0001t0035g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0006t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0006t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0006t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0006t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0006t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0006t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0009t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0009t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0001c0009t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0005g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0008g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0008g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0009g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0011g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0011g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0016g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0022g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0024g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0026g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0027g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0028g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0002t0030g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0008t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0008t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0008t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0008t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0011t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0011t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0002c0013t0001g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0010g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0010g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0019g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0021g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0003t0029g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0005t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0005t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0005t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0005t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0005t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0005t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0020t0020g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0003c0021t0017g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0004c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0005c0007t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0005c0007t0007g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0005c0007t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0005c0007t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0005c0007t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0005c0017t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0006c0010t0013g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0006c0010t0013g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0007c0012t0018g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0008c0016t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0009c0015t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0010c0019t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0011c0018t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| a0012c0014t0023g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | GBR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0195 | EUR | GBR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00323 | hp1 | a0002 | c0002 | t0005 | g0147 | EUR | FIN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00423 | hp2 | a0004 | c0004 | t0001 | g0245 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00438 | hp1 | a0004 | c0004 | t0001 | g0246 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | CHS | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00642 | hp1 | a0001 | c0006 | t0001 | g0181 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00642 | hp2 | a0002 | c0002 | t0005 | g0098 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00741 | hp1 | a0003 | c0003 | t0029 | g0021 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG00741 | hp2 | a0001 | c0006 | t0001 | g0236 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01074 | hp1 | a0006 | c0010 | t0013 | g0104 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01106 | hp1 | a0002 | c0002 | t0008 | g0130 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01106 | hp2 | a0001 | c0006 | t0001 | g0260 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01168 | hp1 | a0001 | c0006 | t0001 | g0217 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01175 | hp1 | a0002 | c0002 | t0024 | g0066 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0093 | AMR | PUR | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01256 | hp2 | a0002 | c0002 | t0005 | g0097 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01258 | hp2 | a0001 | c0001 | t0015 | g0213 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01261 | hp1 | a0002 | c0008 | t0002 | g0071 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01261 | hp2 | a0001 | c0001 | t0031 | g0046 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0126 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01358 | hp2 | a0001 | c0006 | t0001 | g0284 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | CLM | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01884 | hp1 | a0003 | c0003 | t0012 | g0013 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01884 | hp2 | a0005 | c0017 | t0007 | g0027 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0128 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01891 | hp2 | a0003 | c0003 | t0011 | g0012 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0055 | AMR | PEL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02027 | hp1 | a0004 | c0004 | t0001 | g0257 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02055 | hp1 | a0001 | c0001 | t0032 | g0044 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02055 | hp2 | a0007 | c0012 | t0018 | g0005 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02135 | hp2 | a0004 | c0004 | t0001 | g0269 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02145 | hp1 | a0003 | c0003 | t0019 | g0024 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02145 | hp2 | a0005 | c0007 | t0007 | g0023 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02148 | hp1 | a0002 | c0008 | t0002 | g0068 | AMR | PEL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | CDX | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | CDX | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02257 | hp1 | a0002 | c0002 | t0008 | g0070 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02257 | hp2 | a0003 | c0005 | t0002 | g0063 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02258 | hp1 | a0001 | c0001 | t0033 | g0239 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02258 | hp2 | a0002 | c0002 | t0011 | g0080 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02280 | hp1 | a0002 | c0002 | t0009 | g0143 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02280 | hp2 | a0005 | c0007 | t0007 | g0002 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | KHV | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02572 | hp1 | a0003 | c0003 | t0010 | g0019 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02572 | hp2 | a0003 | c0003 | t0010 | g0016 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0090 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02602 | hp2 | a0001 | c0006 | t0001 | g0261 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02615 | hp1 | a0003 | c0003 | t0006 | g0006 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02615 | hp2 | a0003 | c0021 | t0017 | g0007 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02622 | hp2 | a0002 | c0002 | t0008 | g0129 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0095 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02647 | hp1 | a0005 | c0007 | t0007 | g0025 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0138 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0202 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02698 | hp1 | a0001 | c0009 | t0001 | g0237 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02698 | hp2 | a0001 | c0001 | t0014 | g0162 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0086 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0085 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0053 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02723 | hp2 | a0003 | c0003 | t0006 | g0004 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02738 | hp1 | a0002 | c0002 | t0005 | g0065 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02738 | hp2 | a0002 | c0002 | t0028 | g0064 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02886 | hp1 | a0003 | c0003 | t0006 | g0008 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02886 | hp2 | a0002 | c0002 | t0009 | g0001 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0087 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02897 | hp2 | a0003 | c0003 | t0010 | g0017 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02922 | hp1 | a0003 | c0005 | t0002 | g0062 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02965 | hp2 | a0002 | c0002 | t0009 | g0141 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02970 | hp1 | a0002 | c0002 | t0027 | g0133 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02970 | hp2 | a0003 | c0003 | t0012 | g0014 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0125 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03017 | hp1 | a0001 | c0001 | t0014 | g0161 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03017 | hp2 | a0001 | c0001 | t0025 | g0263 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03041 | hp2 | a0005 | c0007 | t0007 | g0002 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0102 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03130 | hp2 | a0002 | c0002 | t0009 | g0001 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0150 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03195 | hp1 | a0003 | c0005 | t0002 | g0059 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03195 | hp2 | a0002 | c0002 | t0009 | g0142 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03209 | hp1 | a0003 | c0003 | t0006 | g0004 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03209 | hp2 | a0003 | c0020 | t0020 | g0079 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0283 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03225 | hp2 | a0003 | c0003 | t0012 | g0015 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03239 | hp2 | a0003 | c0003 | t0010 | g0020 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03453 | hp1 | a0003 | c0003 | t0003 | g0186 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0096 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03486 | hp1 | a0001 | c0001 | t0035 | g0175 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03486 | hp2 | a0003 | c0003 | t0021 | g0009 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03490 | hp1 | a0002 | c0002 | t0005 | g0127 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0033 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0205 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03516 | hp1 | a0008 | c0016 | t0003 | g0029 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03516 | hp2 | a0002 | c0002 | t0011 | g0140 | AFR | ESN | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03540 | hp1 | a0002 | c0002 | t0008 | g0105 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03540 | hp2 | a0003 | c0003 | t0006 | g0152 | AFR | GWD | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03579 | hp1 | a0010 | c0019 | t0003 | g0187 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0038 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0030 | SAS | STU | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0117 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0040 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03710 | hp2 | a0003 | c0003 | t0010 | g0022 | SAS | PJL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0042 | SAS | BEB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03942 | hp1 | a0002 | c0002 | t0005 | g0099 | SAS | BEB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03942 | hp2 | a0001 | c0009 | t0001 | g0275 | SAS | BEB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0035 | SAS | BEB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0163 | SAS | STU | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG04228 | hp1 | a0009 | c0015 | t0003 | g0190 | SAS | STU | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0032 | SAS | STU | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18522 | hp1 | a0005 | c0007 | t0002 | g0026 | AFR | YRI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18522 | hp2 | a0002 | c0002 | t0009 | g0001 | AFR | YRI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | CHB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18906 | hp1 | a0003 | c0003 | t0003 | g0166 | AFR | YRI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18906 | hp2 | a0006 | c0010 | t0013 | g0103 | AFR | YRI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18949 | hp2 | a0012 | c0014 | t0023 | g0077 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18956 | hp2 | a0004 | c0004 | t0001 | g0178 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18965 | hp2 | a0004 | c0004 | t0001 | g0250 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18967 | hp1 | a0002 | c0011 | t0002 | g0123 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18967 | hp2 | a0004 | c0004 | t0001 | g0159 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18975 | hp1 | a0002 | c0002 | t0005 | g0089 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18980 | hp1 | a0002 | c0002 | t0005 | g0148 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18993 | hp1 | a0001 | c0001 | t0034 | g0172 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18994 | hp1 | a0002 | c0002 | t0030 | g0121 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18994 | hp2 | a0004 | c0004 | t0001 | g0244 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18997 | hp2 | a0004 | c0004 | t0001 | g0270 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19005 | hp1 | a0004 | c0004 | t0001 | g0240 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19005 | hp2 | a0002 | c0011 | t0002 | g0135 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19030 | hp1 | a0005 | c0007 | t0007 | g0028 | AFR | LWK | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19030 | hp2 | a0002 | c0002 | t0022 | g0094 | AFR | LWK | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0100 | AFR | LWK | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0092 | AFR | LWK | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19058 | hp2 | a0002 | c0002 | t0026 | g0072 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19068 | hp2 | a0004 | c0004 | t0001 | g0248 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19080 | hp1 | a0002 | c0002 | t0016 | g0107 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19080 | hp2 | a0002 | c0002 | t0005 | g0118 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19090 | hp1 | a0004 | c0004 | t0001 | g0183 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19240 | hp1 | a0003 | c0003 | t0006 | g0153 | AFR | YRI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | YRI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20129 | hp1 | a0003 | c0003 | t0011 | g0011 | AFR | ASW | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20129 | hp2 | a0003 | c0005 | t0002 | g0060 | AFR | ASW | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0266 | EUR | TSI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20805 | hp2 | a0002 | c0008 | t0002 | g0069 | EUR | TSI | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20905 | hp1 | a0001 | c0009 | t0001 | g0281 | SAS | GIH | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20905 | hp2 | a0002 | c0002 | t0005 | g0149 | SAS | GIH | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02109 | hp1 | a0011 | c0018 | t0002 | g0018 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0088 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02486 | hp1 | a0003 | c0005 | t0002 | g0058 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0084 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG02559 | hp2 | a0002 | c0002 | t0008 | g0081 | AFR | ACB | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03471 | hp1 | a0003 | c0003 | t0006 | g0151 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG03471 | hp2 | a0002 | c0002 | t0008 | g0106 | AFR | MSL | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | USA | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0101 | AFR | USA | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA18955 | hp2 | a0001 | c0001 | t0015 | g0251 | EAS | JPT | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | USA | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA20300 | hp2 | a0003 | c0003 | t0006 | g0010 | AFR | USA | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA21309 | hp1 | a0003 | c0005 | t0002 | g0061 | AFR | LWK | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| NA21309 | hp2 | a0002 | c0008 | t0002 | g0067 | AFR | LWK | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0160 | REF | REF | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| homoSapiens_grch38 | hp1 | a0002 | c0013 | t0001 | g0091 | REF | REF | FBXW8_chr12_116905950_117036148 | FBXW8 | chr12 | 116905950 | 117036148 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116911140
|
CGGGCTCG others(12): Show |
C | 1 | a0007 | 1 | HG02055.hp2 | frameshift_variant | HIGH | c.110_128delGGCGGCCG others(11): Show |
p.Arg37fs | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/11 | 198/4861 | 110/1797 | 37/598 | INFO_REALIGN_3_PRIME | chr12 | 116911140 | |
| chr12:116911209
|
C | G | 9 | a0001a0003a0004others(6): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(191): Show |
missense_variant | MODERATE | c.172C>G | p.Arg58Gly | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/11 | 260/4861 | 172/1797 | 58/598 | chr12 | 116911209 | ||
| chr12:116945515
|
G | A | 6 | a0001a0004a0005others(3): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(158): Show |
missense_variant | MODERATE | c.575G>A | p.Arg192Gln | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/11 | 663/4861 | 575/1797 | 192/598 | chr12 | 116945515 | ||
| chr12:116949660
|
A | G | 1 | a0005 | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
missense_variant | MODERATE | c.631A>G | p.Thr211Ala | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/11 | 719/4861 | 631/1797 | 211/598 | chr12 | 116949660 | ||
| chr12:116985235
|
G | A | 1 | a0011 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.865G>A | p.Gly289Arg | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/11 | 953/4861 | 865/1797 | 289/598 | chr12 | 116985235 | ||
| chr12:117010353
|
C | T | 1 | a0008 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.1270C>T | p.Arg424Cys | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/11 | 1358/4861 | 1270/1797 | 424/598 | chr12 | 117010353 | ||
| chr12:117027419
|
A | G | 2 | a0006a0010 | 3 | HG01074.hp1 HG03579.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.1567A>G | p.Ser523Gly | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/11 | 1655/4861 | 1567/1797 | 523/598 | chr12 | 117027419 | ||
| chr12:117027459
|
C | T | 1 | a0004 | 12 | HG00423.hp2 HG00438.hp1 HG02027.hp1 others(9): Show |
missense_variant | MODERATE | c.1607C>T | p.Thr536Met | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/11 | 1695/4861 | 1607/1797 | 536/598 | chr12 | 117027459 | ||
| chr12:117027468
|
G | A | 1 | a0009 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1616G>A | p.Arg539Gln | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/11 | 1704/4861 | 1616/1797 | 539/598 | chr12 | 117027468 | ||
| chr12:117028032
|
C | T | 1 | a0012 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1657C>T | p.Arg553Trp | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1745/4861 | 1657/1797 | 553/598 | chr12 | 117028032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116911163
|
C | A | 1 | a0002c0008 | 4 | HG01261.hp1 HG02148.hp1 NA20805.hp2 others(1): Show |
synonymous_variant | LOW | c.126C>A | p.Gly42Gly | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/11 | 214/4861 | 126/1797 | 42/598 | chr12 | 116911163 | ||
| chr12:116911271
|
C | T | 1 | a0003c0021 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.234C>T | p.Asp78Asp | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/11 | 322/4861 | 234/1797 | 78/598 | chr12 | 116911271 | ||
| chr12:116911340
|
G | A | 1 | a0003c0005 | 6 | HG02257.hp2 HG02486.hp1 HG02922.hp1 others(3): Show |
synonymous_variant | LOW | c.303G>A | p.Gln101Gln | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/11 | 391/4861 | 303/1797 | 101/598 | chr12 | 116911340 | ||
| chr12:116985264
|
C | T | 1 | a0003c0020 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.894C>T | p.His298His | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/11 | 982/4861 | 894/1797 | 298/598 | chr12 | 116985264 | ||
| chr12:116985400
|
C | T | 1 | a0005c0017 | 1 | HG01884.hp2 | splice_region_variant&synonymous_variant | LOW | c.1030C>T | p.Leu344Leu | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/11 | 1118/4861 | 1030/1797 | 344/598 | chr12 | 116985400 | ||
| chr12:117024273
|
C | T | 1 | a0002c0011 | 2 | NA18967.hp1 NA19005.hp2 |
synonymous_variant | LOW | c.1494C>T | p.Ser498Ser | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/11 | 1582/4861 | 1494/1797 | 498/598 | chr12 | 117024273 | ||
| chr12:117028046
|
C | T | 1 | a0001c0009 | 3 | HG02698.hp1 HG03942.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.1671C>T | p.Arg557Arg | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1759/4861 | 1671/1797 | 557/598 | chr12 | 117028046 | ||
| chr12:117028052
|
T | C | 19 | a0001c0001a0001c0009a0002c0002others(16): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
synonymous_variant | LOW | c.1677T>C | p.Tyr559Tyr | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1765/4861 | 1677/1797 | 559/598 | chr12 | 117028052 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116910966
|
C | T | 1 | a0002c0002t0009 | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-72C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/11 | 72 | chr12 | 116910966 | |||||
| chr12:117028176
|
T | C | 38 | a0001c0001t0003a0001c0001t0004a0001c0001t0025others(35): Show | 188 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*4T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 4 | chr12 | 117028176 | |||||
| chr12:117028307
|
C | T | 1 | a0002c0002t0030 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*135C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 135 | chr12 | 117028307 | |||||
| chr12:117028462
|
G | A | 1 | a0002c0002t0016 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 290 | chr12 | 117028462 | |||||
| chr12:117028466
|
C | T | 2 | a0003c0003t0010a0003c0003t0029 | 6 | HG00741.hp1 HG02572.hp1 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*294C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 294 | chr12 | 117028466 | |||||
| chr12:117028468
|
C | T | 1 | a0002c0002t0028 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*296C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 296 | chr12 | 117028468 | |||||
| chr12:117028695
|
G | A | 2 | a0001c0001t0031a0001c0001t0032 | 2 | HG01261.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*523G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 523 | chr12 | 117028695 | |||||
| chr12:117028757
|
T | C | 4 | a0002c0002t0011a0003c0003t0011a0003c0021t0017others(1): Show | 6 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*585T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 585 | chr12 | 117028757 | |||||
| chr12:117029004
|
A | G | 1 | a0003c0003t0029 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*832A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 832 | chr12 | 117029004 | |||||
| chr12:117029116
|
A | G | 1 | a0002c0002t0027 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*944A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 944 | chr12 | 117029116 | |||||
| chr12:117029162
|
C | G | 1 | a0001c0001t0035 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*990C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 990 | chr12 | 117029162 | |||||
| chr12:117029212
|
C | G | 1 | a0001c0001t0032 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1040C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1040 | chr12 | 117029212 | |||||
| chr12:117029255
|
C | T | 1 | a0007c0012t0018 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1083C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1083 | chr12 | 117029255 | |||||
| chr12:117029311
|
T | A | 2 | a0003c0003t0019a0003c0020t0020 | 2 | HG02145.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1139T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1139 | chr12 | 117029311 | |||||
| chr12:117029320
|
G | A | 4 | a0003c0003t0006a0003c0003t0010a0003c0003t0021others(1): Show | 15 | HG00741.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1148G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1148 | chr12 | 117029320 | |||||
| chr12:117029394
|
A | G | 5 | a0002c0002t0011a0003c0003t0011a0003c0003t0012others(2): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1222A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1222 | chr12 | 117029394 | |||||
| chr12:117029409
|
ACT | A | 1 | a0002c0002t0005 | 10 | HG00323.hp1 HG00642.hp2 HG01256.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1242_*1243delCT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1242 | INFO_REALIGN_3_PRIME | chr12 | 117029409 | ||||
| chr12:117029460
|
T | TGGGGCTG others(3): Show |
1 | a0002c0002t0009 | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1296_*1305dupGGAG others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1306 | INFO_REALIGN_3_PRIME | chr12 | 117029460 | ||||
| chr12:117029478
|
T | G | 1 | a0001c0001t0014 | 2 | HG02698.hp2 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1306T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1306 | chr12 | 117029478 | |||||
| chr12:117029567
|
G | A | 29 | a0002c0002t0002a0002c0002t0005a0002c0002t0008others(26): Show | 129 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1395G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1395 | chr12 | 117029567 | |||||
| chr12:117029635
|
C | T | 1 | a0002c0002t0008 | 6 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1463C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1463 | chr12 | 117029635 | |||||
| chr12:117029700
|
C | T | 1 | a0002c0002t0024 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1528C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1528 | chr12 | 117029700 | |||||
| chr12:117030136
|
C | T | 1 | a0003c0020t0020 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1964C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 1964 | chr12 | 117030136 | |||||
| chr12:117030260
|
C | T | 1 | a0012c0014t0023 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2088C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2088 | chr12 | 117030260 | |||||
| chr12:117030306
|
G | A | 1 | a0006c0010t0013 | 2 | HG01074.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2134G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2134 | chr12 | 117030306 | |||||
| chr12:117030463
|
TTC | T | 1 | a0001c0001t0004 | 16 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2298_*2299delTC | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2298 | INFO_REALIGN_3_PRIME | chr12 | 117030463 | ||||
| chr12:117030534
|
A | G | 1 | a0002c0002t0022 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2362A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2362 | chr12 | 117030534 | |||||
| chr12:117030541
|
G | A | 1 | a0002c0002t0030 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2369G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2369 | chr12 | 117030541 | |||||
| chr12:117030547
|
A | T | 1 | a0001c0001t0034 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2375A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2375 | chr12 | 117030547 | |||||
| chr12:117030562
|
C | G | 29 | a0002c0002t0002a0002c0002t0005a0002c0002t0008others(26): Show | 129 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*2390C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2390 | chr12 | 117030562 | |||||
| chr12:117030600
|
C | T | 1 | a0001c0001t0015 | 2 | HG01258.hp2 NA18955.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2428C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2428 | chr12 | 117030600 | |||||
| chr12:117030630
|
G | C | 1 | a0003c0003t0021 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2458G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2458 | chr12 | 117030630 | |||||
| chr12:117030668
|
G | A | 1 | a0003c0020t0020 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2496G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2496 | chr12 | 117030668 | |||||
| chr12:117030751
|
T | G | 2 | a0003c0003t0010a0003c0003t0029 | 6 | HG00741.hp1 HG02572.hp1 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2579T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2579 | chr12 | 117030751 | |||||
| chr12:117030958
|
CCTT | C | 4 | a0001c0001t0033a0002c0002t0011a0003c0003t0011others(1): Show | 6 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2790_*2792delCTT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2790 | INFO_REALIGN_3_PRIME | chr12 | 117030958 | ||||
| chr12:117030993
|
C | T | 3 | a0002c0002t0008a0005c0007t0007a0005c0017t0007 | 12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2821C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2821 | chr12 | 117030993 | |||||
| chr12:117031068
|
A | G | 37 | a0001c0001t0003a0001c0001t0004a0002c0002t0002others(34): Show | 187 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*2896A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 11/11 | 2896 | chr12 | 117031068 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116911670
|
A | G | 132 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0160others(129): Show | 132 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.318+315A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116911670 | ||||||
| chr12:116912052
|
A | G | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+697A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912052 | ||||||
| chr12:116912062
|
G | C | 22 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(19): Show | 23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+707G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912062 | ||||||
| chr12:116912171
|
GT | G | 162 | a0001c0001t0001g0045a0001c0001t0001g0158a0001c0001t0001g0160others(159): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.318+831delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116912171 | |||||
| chr12:116912171
|
GTT | G | 11 | a0001c0001t0001g0156a0001c0001t0003g0154a0001c0001t0003g0155others(8): Show | 12 | HG01884.hp2 HG02040.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.318+830_318+831del others(2): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116912171 | |||||
| chr12:116912183
|
T | C | 22 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(19): Show | 23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+828T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912183 | ||||||
| chr12:116912336
|
C | G | 1 | a0003c0003t0001g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.318+981C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912336 | ||||||
| chr12:116912377
|
A | G | 1 | a0002c0002t0002g0150 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.318+1022A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912377 | ||||||
| chr12:116912432
|
C | T | 1 | a0002c0002t0005g0149 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.318+1077C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912432 | ||||||
| chr12:116912450
|
TC | T | 3 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051 | 3 | HG02630.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.318+1096delC | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912450 | ||||||
| chr12:116912451
|
C | CT | 13 | a0002c0002t0002g0144a0002c0002t0002g0145a0002c0002t0002g0146others(10): Show | 15 | HG00323.hp1 HG01884.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.318+1117dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116912451 | |||||
| chr12:116912451
|
C | CTT | 13 | a0003c0003t0006g0008a0003c0003t0006g0010a0003c0003t0010g0016others(10): Show | 13 | HG00741.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.318+1116_318+1117d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116912451 | |||||
| chr12:116912451
|
C | T | 1 | a0001c0001t0003g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.318+1096C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912451 | ||||||
| chr12:116912451
|
CT | C | 149 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(146): Show | 150 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.318+1117delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116912451 | |||||
| chr12:116912615
|
C | A | 1 | a0001c0001t0001g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.318+1260C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912615 | ||||||
| chr12:116912664
|
T | C | 1 | a0008c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.318+1309T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912664 | ||||||
| chr12:116912714
|
C | T | 156 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.318+1359C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912714 | ||||||
| chr12:116912724
|
A | G | 1 | a0002c0002t0011g0140 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.318+1369A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912724 | ||||||
| chr12:116912755
|
G | T | 3 | a0003c0003t0011g0011a0003c0003t0011g0012a0007c0012t0018g0005 | 3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.318+1400G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912755 | ||||||
| chr12:116912777
|
T | A | 1 | a0004c0004t0001g0159 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+1422T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912777 | ||||||
| chr12:116912778
|
A | C | 1 | a0004c0004t0001g0159 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+1423A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116912778 | ||||||
| chr12:116913020
|
G | A | 7 | a0003c0003t0010g0016a0003c0003t0010g0017a0003c0003t0010g0019others(4): Show | 7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+1665G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913020 | ||||||
| chr12:116913045
|
T | C | 1 | a0001c0001t0001g0160 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.318+1690T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913045 | ||||||
| chr12:116913118
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.318+1763C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913118 | ||||||
| chr12:116913170
|
T | C | 22 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(19): Show | 23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+1815T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913170 | ||||||
| chr12:116913180
|
C | CA | 22 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(19): Show | 23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+1827dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116913180 | |||||
| chr12:116913458
|
T | C | 1 | a0002c0002t0002g0057 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.318+2103T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913458 | ||||||
| chr12:116913722
|
C | G | 1 | a0002c0002t0001g0139 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.318+2367C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913722 | ||||||
| chr12:116913744
|
G | A | 1 | a0003c0005t0002g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.318+2389G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913744 | ||||||
| chr12:116913769
|
T | C | 22 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(19): Show | 23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+2414T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913769 | ||||||
| chr12:116913828
|
G | C | 1 | a0004c0004t0001g0159 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2473G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913828 | ||||||
| chr12:116913830
|
A | C | 1 | a0004c0004t0001g0159 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2475A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913830 | ||||||
| chr12:116913832
|
C | A | 1 | a0004c0004t0001g0159 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2477C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913832 | ||||||
| chr12:116913833
|
T | G | 1 | a0004c0004t0001g0159 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2478T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913833 | ||||||
| chr12:116913836
|
T | G | 1 | a0004c0004t0001g0159 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2481T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913836 | ||||||
| chr12:116913838
|
C | G | 1 | a0004c0004t0001g0159 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2483C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913838 | ||||||
| chr12:116913839
|
A | T | 1 | a0004c0004t0001g0159 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+2484A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116913839 | ||||||
| chr12:116914034
|
G | A | 22 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(19): Show | 23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+2679G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914034 | ||||||
| chr12:116914293
|
T | C | 6 | a0003c0005t0002g0058a0003c0005t0002g0059a0003c0005t0002g0060others(3): Show | 6 | HG02257.hp2 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+2938T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914293 | ||||||
| chr12:116914342
|
G | A | 7 | a0003c0003t0019g0024a0005c0007t0002g0026a0005c0007t0007g0002others(4): Show | 8 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+2987G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914342 | ||||||
| chr12:116914484
|
G | A | 2 | a0001c0001t0014g0161a0001c0001t0014g0162 | 2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.318+3129G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914484 | ||||||
| chr12:116914542
|
C | T | 7 | a0003c0003t0019g0024a0005c0007t0002g0026a0005c0007t0007g0002others(4): Show | 8 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+3187C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914542 | ||||||
| chr12:116914572
|
C | CA | 139 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0164others(136): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.318+3238dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116914572 | |||||
| chr12:116914572
|
C | CAA | 44 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0169others(41): Show | 44 | HG00544.hp2 HG00642.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.318+3237_318+3238d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116914572 | |||||
| chr12:116914572
|
C | CAAA | 8 | a0001c0001t0003g0163a0001c0001t0004g0030a0001c0001t0004g0031others(5): Show | 8 | HG00544.hp1 HG03491.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+3236_318+3238d others(5): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116914572 | |||||
| chr12:116914594
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.318+3239G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914594 | ||||||
| chr12:116914752
|
G | A | 156 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.318+3397G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914752 | ||||||
| chr12:116914779
|
G | T | 7 | a0003c0003t0019g0024a0005c0007t0002g0026a0005c0007t0007g0002others(4): Show | 8 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+3424G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116914779 | ||||||
| chr12:116915041
|
A | G | 1 | a0002c0002t0002g0138 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.318+3686A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915041 | ||||||
| chr12:116915105
|
C | T | 1 | a0004c0004t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.318+3750C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915105 | ||||||
| chr12:116915214
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.318+3859G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915214 | ||||||
| chr12:116915432
|
A | G | 163 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(160): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.318+4077A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915432 | ||||||
| chr12:116915640
|
C | CT | 42 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(39): Show | 43 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.318+4313dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | |||||
| chr12:116915640
|
C | CTT | 18 | a0002c0002t0002g0134a0002c0002t0002g0136a0002c0002t0002g0137others(15): Show | 18 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.318+4312_318+4313d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | |||||
| chr12:116915640
|
C | CTTT | 7 | a0003c0003t0006g0006a0003c0003t0006g0010a0003c0005t0002g0058others(4): Show | 7 | HG02257.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+4311_318+4313d others(5): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | |||||
| chr12:116915640
|
CTTTT | C | 10 | a0001c0001t0001g0182a0001c0001t0001g0274a0001c0001t0001g0276others(7): Show | 10 | HG01261.hp2 HG02135.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.318+4310_318+4313d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | |||||
| chr12:116915640
|
CTTTTT | C | 78 | a0001c0001t0001g0045a0001c0001t0001g0158a0001c0001t0001g0160others(75): Show | 78 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.318+4309_318+4313d others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | |||||
| chr12:116915640
|
CTTTTTT | C | 20 | a0001c0001t0001g0156a0001c0001t0001g0169a0001c0001t0001g0170others(17): Show | 20 | HG00423.hp1 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.318+4308_318+4313d others(8): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | |||||
| chr12:116915640
|
CTTTTTTT | C | 55 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(52): Show | 56 | HG00140.hp2 HG00544.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.318+4307_318+4313d others(9): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | |||||
| chr12:116915640
|
CTTTTTTT others(5): Show |
C | 1 | a0003c0003t0012g0013 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.318+4302_318+4313d others(14): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | |||||
| chr12:116915640
|
CTTTTTTT others(9): Show |
C | 1 | a0002c0002t0002g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.318+4298_318+4313d others(18): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915640 | |||||
| chr12:116915675
|
T | TA | 22 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(19): Show | 23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+4321dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116915675 | |||||
| chr12:116915689
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.318+4334G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915689 | ||||||
| chr12:116915737
|
T | C | 22 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(19): Show | 23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.318+4382T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915737 | ||||||
| chr12:116915911
|
G | A | 198 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(195): Show | 202 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.318+4556G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116915911 | ||||||
| chr12:116916099
|
A | C | 7 | a0003c0003t0019g0024a0005c0007t0002g0026a0005c0007t0007g0002others(4): Show | 8 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+4744A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916099 | ||||||
| chr12:116916229
|
G | A | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG00323.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.318+4874G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916229 | ||||||
| chr12:116916288
|
A | T | 1 | a0002c0002t0016g0107 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.318+4933A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916288 | ||||||
| chr12:116916462
|
G | C | 1 | a0003c0020t0020g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.318+5107G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916462 | ||||||
| chr12:116916534
|
G | T | 1 | a0003c0003t0001g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.318+5179G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916534 | ||||||
| chr12:116916627
|
G | C | 16 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(13): Show | 16 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.318+5272G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916627 | ||||||
| chr12:116916630
|
G | C | 1 | a0001c0001t0004g0037 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.318+5275G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916630 | ||||||
| chr12:116916889
|
C | CGT | 8 | a0001c0001t0001g0174a0002c0002t0002g0137a0002c0002t0002g0146others(5): Show | 8 | HG02257.hp2 HG02922.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+5556_318+5557d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916889 | |||||
| chr12:116916889
|
C | T | 1 | a0003c0003t0006g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.318+5534C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916889 | ||||||
| chr12:116916889
|
CGT | C | 4 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(1): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.318+5556_318+5557d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916889 | |||||
| chr12:116916907
|
T | TGA | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.318+5553_318+5554i others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916907 | |||||
| chr12:116916909
|
T | A | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.318+5554T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916909 | ||||||
| chr12:116916909
|
T | TGA | 10 | a0003c0003t0010g0020a0003c0003t0010g0022a0003c0003t0019g0024others(7): Show | 11 | HG00741.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.318+5555_318+5556i others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916909 | |||||
| chr12:116916911
|
T | A | 25 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(22): Show | 27 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.318+5556T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916911 | ||||||
| chr12:116916911
|
T | TGAGA | 54 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(51): Show | 54 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.318+5569_318+5572d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916911 | |||||
| chr12:116916911
|
T | TGTGA | 3 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015 | 3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.318+5557_318+5558i others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916911 | |||||
| chr12:116916911
|
T | TGTGAGAG others(1): Show |
14 | a0001c0001t0001g0045a0001c0001t0001g0171a0001c0001t0001g0173others(11): Show | 14 | HG00621.hp1 HG02071.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+5557_318+5558i others(10): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916911 | |||||
| chr12:116916911
|
T | TGTGTGAG others(1): Show |
76 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0164others(73): Show | 76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.318+5557_318+5558i others(10): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916911 | |||||
| chr12:116916911
|
T | TGTGTGTG others(3): Show |
9 | a0001c0001t0001g0158a0001c0001t0001g0218a0001c0001t0001g0220others(6): Show | 9 | HG00323.hp2 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.318+5557_318+5558i others(12): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116916911 | |||||
| chr12:116916913
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.318+5558A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916913 | ||||||
| chr12:116916954
|
C | T | 1 | a0003c0003t0010g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.318+5599C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916954 | ||||||
| chr12:116916980
|
C | T | 166 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.318+5625C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116916980 | ||||||
| chr12:116917128
|
A | G | 1 | a0001c0001t0003g0206 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.318+5773A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116917128 | ||||||
| chr12:116917405
|
C | T | 4 | a0003c0003t0010g0019a0003c0003t0021g0009a0003c0021t0017g0007others(1): Show | 4 | HG02109.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+6050C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116917405 | ||||||
| chr12:116917662
|
G | A | 4 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(1): Show | 4 | HG02615.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+6307G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116917662 | ||||||
| chr12:116917751
|
G | A | 1 | a0001c0001t0003g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.318+6396G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116917751 | ||||||
| chr12:116917863
|
G | A | 2 | a0003c0003t0010g0016a0003c0003t0010g0017 | 2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.318+6508G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116917863 | ||||||
| chr12:116917890
|
G | T | 1 | a0002c0002t0002g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.318+6535G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116917890 | ||||||
| chr12:116917991
|
C | CA | 147 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(144): Show | 147 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.318+6649dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116917991 | |||||
| chr12:116918005
|
C | A | 3 | a0001c0001t0001g0224a0002c0002t0028g0064a0003c0021t0017g0007 | 3 | HG02132.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.318+6650C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918005 | ||||||
| chr12:116918013
|
A | C | 1 | a0001c0001t0001g0262 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.318+6658A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918013 | ||||||
| chr12:116918231
|
C | A | 3 | a0002c0002t0002g0053a0002c0002t0002g0084a0002c0002t0002g0085 | 3 | HG02486.hp2 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.318+6876C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918231 | ||||||
| chr12:116918474
|
G | A | 7 | a0003c0003t0019g0024a0005c0007t0002g0026a0005c0007t0007g0002others(4): Show | 8 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+7119G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918474 | ||||||
| chr12:116918508
|
C | T | 1 | a0002c0002t0008g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.318+7153C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918508 | ||||||
| chr12:116918535
|
G | T | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+7180G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918535 | ||||||
| chr12:116918580
|
A | C | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.318+7225A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918580 | ||||||
| chr12:116918739
|
C | G | 1 | a0002c0002t0008g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.318+7384C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918739 | ||||||
| chr12:116918787
|
T | G | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.318+7432T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918787 | ||||||
| chr12:116918799
|
A | G | 1 | a0002c0008t0002g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.318+7444A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918799 | ||||||
| chr12:116918963
|
A | G | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.318+7608A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116918963 | ||||||
| chr12:116918965
|
G | GT | 7 | a0002c0002t0005g0065a0002c0002t0008g0070a0002c0002t0008g0081others(4): Show | 7 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+7619dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116918965 | |||||
| chr12:116919054
|
A | G | 1 | a0002c0008t0002g0069 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.318+7699A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116919054 | ||||||
| chr12:116919640
|
G | A | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.318+8285G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116919640 | ||||||
| chr12:116919686
|
GT | G | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.318+8334delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116919686 | |||||
| chr12:116919819
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.319-8204A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116919819 | ||||||
| chr12:116920128
|
G | A | 2 | a0003c0003t0011g0011a0003c0003t0011g0012 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.319-7895G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920128 | ||||||
| chr12:116920177
|
T | C | 1 | a0001c0001t0003g0188 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.319-7846T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920177 | ||||||
| chr12:116920223
|
G | T | 2 | a0001c0006t0001g0261a0001c0006t0001g0284 | 2 | HG01358.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.319-7800G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920223 | ||||||
| chr12:116920402
|
G | C | 1 | a0001c0001t0025g0263 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.319-7621G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920402 | ||||||
| chr12:116920412
|
A | G | 2 | a0006c0010t0013g0103a0006c0010t0013g0104 | 2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.319-7611A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920412 | ||||||
| chr12:116920485
|
T | G | 1 | a0001c0001t0001g0264 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.319-7538T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920485 | ||||||
| chr12:116920576
|
T | A | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.319-7447T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920576 | ||||||
| chr12:116920619
|
C | T | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.319-7404C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920619 | ||||||
| chr12:116920698
|
G | C | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-7325G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920698 | ||||||
| chr12:116920714
|
G | A | 4 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(1): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-7309G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920714 | ||||||
| chr12:116920720
|
A | G | 2 | a0006c0010t0013g0103a0006c0010t0013g0104 | 2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.319-7303A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116920720 | ||||||
| chr12:116921139
|
G | A | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.319-6884G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921139 | ||||||
| chr12:116921227
|
A | G | 2 | a0001c0006t0001g0181a0001c0006t0001g0260 | 2 | HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.319-6796A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921227 | ||||||
| chr12:116921278
|
G | A | 1 | a0008c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.319-6745G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921278 | ||||||
| chr12:116921399
|
G | A | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.319-6624G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921399 | ||||||
| chr12:116921586
|
T | C | 1 | a0001c0001t0003g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.319-6437T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921586 | ||||||
| chr12:116921631
|
C | T | 1 | a0001c0001t0001g0259 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.319-6392C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921631 | ||||||
| chr12:116921692
|
G | T | 1 | a0001c0001t0001g0268 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.319-6331G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921692 | ||||||
| chr12:116921710
|
T | C | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.319-6313T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116921710 | ||||||
| chr12:116921822
|
C | CT | 53 | a0001c0001t0001g0156a0001c0001t0001g0169a0001c0001t0001g0179others(50): Show | 56 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.319-6177dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116921822 | |||||
| chr12:116921822
|
CT | C | 22 | a0001c0001t0001g0182a0001c0001t0001g0209a0001c0001t0001g0265others(19): Show | 23 | HG01433.hp1 HG01884.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.319-6177delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116921822 | |||||
| chr12:116921822
|
CTT | C | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.319-6178_319-6177d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116921822 | |||||
| chr12:116922654
|
T | G | 1 | a0001c0001t0004g0037 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.319-5369T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922654 | ||||||
| chr12:116922810
|
G | GT | 9 | a0001c0001t0003g0206a0001c0009t0001g0275a0003c0003t0006g0010others(6): Show | 10 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.319-5212dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116922810 | |||||
| chr12:116922812
|
G | GT | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0282others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.319-5203dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116922812 | |||||
| chr12:116922812
|
G | T | 184 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(181): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.319-5211G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922812 | ||||||
| chr12:116922814
|
T | G | 5 | a0002c0002t0002g0003a0002c0002t0002g0086a0002c0002t0002g0087others(2): Show | 6 | HG01175.hp1 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-5209T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922814 | ||||||
| chr12:116922835
|
A | T | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-5188A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922835 | ||||||
| chr12:116922861
|
T | C | 3 | a0002c0002t0005g0089a0002c0002t0005g0148a0002c0002t0016g0107 | 3 | NA18975.hp1 NA18980.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.319-5162T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922861 | ||||||
| chr12:116922874
|
T | G | 233 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(230): Show | 235 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.319-5149T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922874 | ||||||
| chr12:116922892
|
T | C | 1 | a0003c0003t0021g0009 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.319-5131T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922892 | ||||||
| chr12:116922935
|
G | A | 2 | a0001c0001t0003g0056a0008c0016t0003g0029 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.319-5088G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116922935 | ||||||
| chr12:116923153
|
C | G | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.319-4870C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923153 | ||||||
| chr12:116923261
|
G | T | 2 | a0001c0001t0004g0036a0001c0001t0004g0043 | 2 | NA18947.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.319-4762G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923261 | ||||||
| chr12:116923276
|
A | AT | 13 | a0001c0001t0001g0265a0001c0001t0001g0267a0002c0002t0002g0053others(10): Show | 14 | HG01884.hp1 HG02083.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.319-4736dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116923276 | |||||
| chr12:116923287
|
TA | T | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.319-4733delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116923287 | |||||
| chr12:116923288
|
A | T | 147 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(144): Show | 148 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.319-4735A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923288 | ||||||
| chr12:116923517
|
T | G | 1 | a0002c0002t0008g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.319-4506T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923517 | ||||||
| chr12:116923542
|
CAG | C | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-4478_319-4477d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116923542 | |||||
| chr12:116923551
|
G | T | 1 | a0001c0001t0003g0051 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.319-4472G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923551 | ||||||
| chr12:116923717
|
A | T | 12 | a0001c0001t0001g0256a0002c0002t0002g0088a0002c0002t0002g0124others(9): Show | 12 | HG00609.hp1 HG01261.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.319-4306A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923717 | ||||||
| chr12:116923717
|
AATTT | A | 6 | a0001c0001t0003g0050a0001c0001t0003g0051a0003c0003t0006g0006others(3): Show | 6 | HG02615.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-4289_319-4286d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116923717 | |||||
| chr12:116923721
|
T | A | 79 | a0001c0001t0001g0158a0001c0001t0001g0210a0001c0001t0001g0211others(76): Show | 80 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.319-4302T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923721 | ||||||
| chr12:116923725
|
T | A | 10 | a0002c0002t0011g0080a0002c0002t0011g0140a0003c0003t0003g0186others(7): Show | 10 | HG00741.hp1 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.319-4298T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923725 | ||||||
| chr12:116923729
|
T | A | 5 | a0003c0003t0010g0016a0003c0003t0010g0017a0003c0003t0010g0019others(2): Show | 5 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.319-4294T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923729 | ||||||
| chr12:116923796
|
C | G | 1 | a0001c0001t0001g0259 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.319-4227C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923796 | ||||||
| chr12:116923936
|
A | G | 1 | a0002c0002t0002g0108 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.319-4087A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116923936 | ||||||
| chr12:116924117
|
C | G | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-3906C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924117 | ||||||
| chr12:116924143
|
A | C | 185 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(182): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.319-3880A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924143 | ||||||
| chr12:116924146
|
GGTTGTCC others(22): Show |
G | 162 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(159): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.319-3845_319-3817d others(31): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116924146 | |||||
| chr12:116924210
|
G | A | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-3813G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924210 | ||||||
| chr12:116924285
|
C | CTTTTA | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.319-3735_319-3734i others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116924285 | |||||
| chr12:116924340
|
G | A | 1 | a0002c0002t0002g0109 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.319-3683G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924340 | ||||||
| chr12:116924407
|
G | A | 185 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(182): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.319-3616G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924407 | ||||||
| chr12:116924574
|
T | C | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-3449T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924574 | ||||||
| chr12:116924648
|
G | A | 182 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(179): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.319-3375G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924648 | ||||||
| chr12:116924864
|
C | T | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.319-3159C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924864 | ||||||
| chr12:116924893
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.319-3130A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116924893 | ||||||
| chr12:116925076
|
TA | T | 6 | a0003c0003t0010g0019a0003c0003t0010g0020a0003c0003t0010g0022others(3): Show | 6 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-2935delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116925076 | |||||
| chr12:116925137
|
G | A | 1 | a0003c0005t0002g0060 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.319-2886G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925137 | ||||||
| chr12:116925239
|
T | G | 185 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(182): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.319-2784T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925239 | ||||||
| chr12:116925245
|
G | A | 159 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(156): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.319-2778G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925245 | ||||||
| chr12:116925361
|
G | T | 134 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.319-2662G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925361 | ||||||
| chr12:116925398
|
G | A | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-2625G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925398 | ||||||
| chr12:116925502
|
G | C | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.319-2521G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925502 | ||||||
| chr12:116925505
|
A | G | 284 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(281): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.319-2518A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925505 | ||||||
| chr12:116925640
|
G | A | 2 | a0002c0002t0011g0080a0002c0002t0011g0140 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.319-2383G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925640 | ||||||
| chr12:116925652
|
T | A | 153 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.319-2371T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925652 | ||||||
| chr12:116925693
|
A | G | 1 | a0002c0008t0002g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.319-2330A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925693 | ||||||
| chr12:116925775
|
C | A | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-2248C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925775 | ||||||
| chr12:116925903
|
GTA | G | 3 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015 | 3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.319-2118_319-2117d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116925903 | |||||
| chr12:116925929
|
C | T | 1 | a0002c0008t0002g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.319-2094C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116925929 | ||||||
| chr12:116926007
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.319-2016G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926007 | ||||||
| chr12:116926026
|
A | G | 155 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.319-1997A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926026 | ||||||
| chr12:116926050
|
G | A | 187 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(184): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.319-1973G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926050 | ||||||
| chr12:116926474
|
G | T | 187 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(184): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.319-1549G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926474 | ||||||
| chr12:116926630
|
C | G | 5 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(2): Show | 5 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-1393C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926630 | ||||||
| chr12:116926760
|
T | A | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.319-1263T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926760 | ||||||
| chr12:116926845
|
C | A | 2 | a0001c0006t0001g0181a0001c0006t0001g0260 | 2 | HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.319-1178C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926845 | ||||||
| chr12:116926895
|
T | C | 161 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(158): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.319-1128T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116926895 | ||||||
| chr12:116927025
|
G | A | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.319-998G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116927025 | ||||||
| chr12:116927098
|
A | C | 284 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(281): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.319-925A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116927098 | ||||||
| chr12:116927174
|
A | G | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-849A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116927174 | ||||||
| chr12:116927701
|
G | A | 233 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(230): Show | 235 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.319-322G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116927701 | ||||||
| chr12:116927960
|
G | A | 1 | a0001c0001t0003g0199 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.319-63G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | chr12 | 116927960 | ||||||
| chr12:116928004
|
CTT | C | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.319-10_319-9delTT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116928004 | |||||
| chr12:116928195
|
G | A | 2 | a0001c0001t0003g0056a0002c0002t0002g0092 | 2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.423+68G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928195 | ||||||
| chr12:116928416
|
A | G | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.423+289A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928416 | ||||||
| chr12:116928494
|
A | G | 239 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(236): Show | 243 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.423+367A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928494 | ||||||
| chr12:116928500
|
T | G | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.423+373T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928500 | ||||||
| chr12:116928533
|
C | A | 153 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.423+406C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928533 | ||||||
| chr12:116928589
|
T | C | 19 | a0001c0001t0003g0163a0001c0001t0003g0185a0001c0001t0003g0191others(16): Show | 19 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.423+462T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928589 | ||||||
| chr12:116928664
|
G | A | 3 | a0002c0002t0005g0089a0002c0002t0005g0148a0002c0002t0016g0107 | 3 | NA18975.hp1 NA18980.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.423+537G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928664 | ||||||
| chr12:116928726
|
C | T | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.423+599C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928726 | ||||||
| chr12:116928976
|
A | G | 1 | a0001c0001t0004g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.423+849A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116928976 | ||||||
| chr12:116929017
|
C | G | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.423+890C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929017 | ||||||
| chr12:116929084
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.423+957G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929084 | ||||||
| chr12:116929116
|
T | A | 7 | a0003c0003t0010g0016a0003c0003t0010g0017a0003c0003t0010g0019others(4): Show | 7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.423+989T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929116 | ||||||
| chr12:116929216
|
G | A | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+1089G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929216 | ||||||
| chr12:116929303
|
C | T | 1 | a0003c0003t0006g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.423+1176C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929303 | ||||||
| chr12:116929425
|
C | T | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+1298C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929425 | ||||||
| chr12:116929494
|
C | T | 3 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0208 | 3 | HG01168.hp2 HG01169.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.423+1367C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929494 | ||||||
| chr12:116929517
|
G | T | 2 | a0006c0010t0013g0103a0006c0010t0013g0104 | 2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.423+1390G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929517 | ||||||
| chr12:116929543
|
CT | C | 233 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(230): Show | 235 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.423+1423delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116929543 | |||||
| chr12:116929591
|
A | G | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.423+1464A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929591 | ||||||
| chr12:116929679
|
C | T | 1 | a0002c0002t0002g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.423+1552C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929679 | ||||||
| chr12:116929813
|
T | C | 3 | a0003c0003t0011g0011a0003c0003t0011g0012a0007c0012t0018g0005 | 3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.423+1686T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116929813 | ||||||
| chr12:116930621
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.423+2494C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116930621 | ||||||
| chr12:116930753
|
C | T | 187 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(184): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.423+2626C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116930753 | ||||||
| chr12:116930814
|
A | C | 1 | a0007c0012t0018g0005 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.423+2687A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116930814 | ||||||
| chr12:116930855
|
T | C | 127 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(124): Show | 128 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.423+2728T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116930855 | ||||||
| chr12:116931011
|
T | C | 2 | a0001c0001t0003g0056a0008c0016t0003g0029 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.423+2884T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931011 | ||||||
| chr12:116931028
|
G | A | 1 | a0002c0002t0008g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.423+2901G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931028 | ||||||
| chr12:116931079
|
G | T | 5 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(2): Show | 5 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+2952G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931079 | ||||||
| chr12:116931123
|
C | T | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+2996C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931123 | ||||||
| chr12:116931458
|
C | CT | 4 | a0002c0002t0002g0122a0002c0002t0002g0131a0002c0011t0002g0123others(1): Show | 4 | NA18956.hp1 NA18965.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+3334dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116931458 | |||||
| chr12:116931480
|
G | A | 5 | a0001c0006t0001g0181a0001c0006t0001g0236a0001c0006t0001g0260others(2): Show | 5 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+3353G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931480 | ||||||
| chr12:116931536
|
C | T | 134 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.423+3409C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931536 | ||||||
| chr12:116931640
|
G | A | 237 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(234): Show | 241 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.423+3513G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931640 | ||||||
| chr12:116931667
|
A | G | 1 | a0001c0001t0001g0259 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.423+3540A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931667 | ||||||
| chr12:116931943
|
C | G | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0282others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+3816C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931943 | ||||||
| chr12:116931998
|
G | C | 2 | a0003c0003t0011g0011a0003c0003t0011g0012 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.423+3871G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116931998 | ||||||
| chr12:116932163
|
G | T | 4 | a0002c0002t0002g0100a0002c0002t0002g0101a0002c0002t0002g0102others(1): Show | 4 | HG01891.hp1 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+4036G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932163 | ||||||
| chr12:116932174
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.423+4047G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932174 | ||||||
| chr12:116932277
|
A | G | 187 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(184): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.423+4150A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932277 | ||||||
| chr12:116932430
|
T | C | 1 | a0003c0003t0006g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.423+4303T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932430 | ||||||
| chr12:116932598
|
C | T | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+4471C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932598 | ||||||
| chr12:116932605
|
G | A | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+4478G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932605 | ||||||
| chr12:116932610
|
A | G | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.423+4483A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932610 | ||||||
| chr12:116932637
|
G | A | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.423+4510G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932637 | ||||||
| chr12:116932766
|
T | G | 8 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(5): Show | 9 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.423+4639T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932766 | ||||||
| chr12:116932783
|
C | T | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+4656C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932783 | ||||||
| chr12:116932852
|
A | G | 7 | a0003c0003t0010g0016a0003c0003t0010g0017a0003c0003t0010g0019others(4): Show | 7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.423+4725A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116932852 | ||||||
| chr12:116933021
|
T | TA | 59 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0271others(56): Show | 59 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.423+4902dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116933021 | |||||
| chr12:116933021
|
T | TAA | 96 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.423+4901_423+4902d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116933021 | |||||
| chr12:116933021
|
TA | T | 10 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(7): Show | 13 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.423+4902delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116933021 | |||||
| chr12:116933149
|
C | T | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+5022C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933149 | ||||||
| chr12:116933166
|
C | T | 1 | a0003c0005t0002g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.423+5039C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933166 | ||||||
| chr12:116933169
|
G | C | 7 | a0003c0003t0010g0016a0003c0003t0010g0017a0003c0003t0010g0019others(4): Show | 7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.423+5042G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933169 | ||||||
| chr12:116933282
|
A | G | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.423+5155A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933282 | ||||||
| chr12:116933669
|
G | A | 1 | a0001c0001t0004g0030 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.423+5542G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933669 | ||||||
| chr12:116933713
|
A | T | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+5586A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933713 | ||||||
| chr12:116933774
|
C | A | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.423+5647C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933774 | ||||||
| chr12:116933961
|
T | C | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.423+5834T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116933961 | ||||||
| chr12:116934012
|
A | T | 30 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(27): Show | 30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.423+5885A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934012 | ||||||
| chr12:116934178
|
C | T | 1 | a0001c0001t0003g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.423+6051C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934178 | ||||||
| chr12:116934301
|
G | A | 1 | a0002c0002t0002g0076 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.423+6174G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934301 | ||||||
| chr12:116934315
|
C | G | 2 | a0001c0001t0001g0272a0001c0001t0001g0274 | 2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.423+6188C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934315 | ||||||
| chr12:116934321
|
G | A | 1 | a0003c0003t0006g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.423+6194G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934321 | ||||||
| chr12:116934401
|
A | T | 2 | a0003c0003t0010g0016a0003c0003t0010g0017 | 2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.423+6274A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934401 | ||||||
| chr12:116934438
|
CT | C | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.423+6318delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116934438 | |||||
| chr12:116934575
|
A | C | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.423+6448A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934575 | ||||||
| chr12:116934889
|
G | A | 6 | a0001c0006t0001g0181a0001c0006t0001g0217a0001c0006t0001g0236others(3): Show | 6 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+6762G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116934889 | ||||||
| chr12:116934955
|
CCTTT | C | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.423+6830_423+6833d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116934955 | |||||
| chr12:116935032
|
T | C | 3 | a0003c0003t0011g0011a0003c0003t0011g0012a0007c0012t0018g0005 | 3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.423+6905T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935032 | ||||||
| chr12:116935033
|
T | C | 1 | a0002c0002t0002g0128 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.423+6906T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935033 | ||||||
| chr12:116935249
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.423+7122T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935249 | ||||||
| chr12:116935785
|
A | G | 39 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(36): Show | 39 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.423+7658A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935785 | ||||||
| chr12:116935789
|
C | T | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.423+7662C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935789 | ||||||
| chr12:116935813
|
G | A | 184 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(181): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.423+7686G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935813 | ||||||
| chr12:116935843
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.423+7716G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935843 | ||||||
| chr12:116935851
|
G | T | 2 | a0006c0010t0013g0103a0006c0010t0013g0104 | 2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.423+7724G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935851 | ||||||
| chr12:116935892
|
A | T | 2 | a0002c0002t0002g0137a0002c0002t0002g0146 | 2 | NA18963.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.423+7765A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935892 | ||||||
| chr12:116935926
|
G | A | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.423+7799G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935926 | ||||||
| chr12:116935934
|
A | C | 2 | a0003c0003t0010g0019a0011c0018t0002g0018 | 2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.423+7807A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935934 | ||||||
| chr12:116935953
|
T | C | 100 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.423+7826T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116935953 | ||||||
| chr12:116936031
|
GTA | G | 274 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(271): Show | 279 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.423+7909_423+7910d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116936031 | |||||
| chr12:116936354
|
A | G | 2 | a0003c0003t0011g0011a0003c0003t0011g0012 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.423+8227A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936354 | ||||||
| chr12:116936470
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.423+8343T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936470 | ||||||
| chr12:116936492
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.423+8365C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936492 | ||||||
| chr12:116936518
|
G | A | 161 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(158): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.423+8391G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936518 | ||||||
| chr12:116936563
|
G | A | 3 | a0005c0007t0007g0002a0005c0007t0007g0023a0005c0007t0007g0028 | 4 | HG02145.hp2 HG02280.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+8436G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936563 | ||||||
| chr12:116936677
|
C | T | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.423+8550C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936677 | ||||||
| chr12:116936690
|
C | T | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+8563C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936690 | ||||||
| chr12:116936703
|
G | A | 155 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.423+8576G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936703 | ||||||
| chr12:116936829
|
G | A | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-8535G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936829 | ||||||
| chr12:116936990
|
G | C | 1 | a0002c0002t0026g0072 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.424-8374G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116936990 | ||||||
| chr12:116937166
|
C | A | 2 | a0003c0003t0010g0019a0011c0018t0002g0018 | 2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.424-8198C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116937166 | ||||||
| chr12:116937386
|
C | T | 1 | a0001c0001t0004g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.424-7978C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116937386 | ||||||
| chr12:116937413
|
G | A | 1 | a0001c0009t0001g0237 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.424-7951G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116937413 | ||||||
| chr12:116937469
|
A | G | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-7895A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116937469 | ||||||
| chr12:116937675
|
T | A | 2 | a0001c0001t0003g0163a0009c0015t0003g0190 | 2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.424-7689T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116937675 | ||||||
| chr12:116937700
|
G | A | 2 | a0001c0001t0003g0056a0008c0016t0003g0029 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424-7664G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116937700 | ||||||
| chr12:116937720
|
CTA | C | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.424-7642_424-7641d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116937720 | |||||
| chr12:116937732
|
T | TCCTC | 22 | a0001c0001t0003g0184a0002c0002t0011g0080a0002c0002t0011g0140others(19): Show | 23 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.424-7629_424-7626d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116937732 | |||||
| chr12:116937853
|
C | CT | 161 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.424-7499dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116937853 | |||||
| chr12:116938025
|
C | A | 2 | a0001c0001t0003g0185a0001c0001t0003g0223 | 2 | NA19055.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.424-7339C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116938025 | ||||||
| chr12:116938612
|
T | G | 4 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(1): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-6752T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116938612 | ||||||
| chr12:116938856
|
G | A | 1 | a0008c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.424-6508G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116938856 | ||||||
| chr12:116938974
|
G | C | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-6390G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116938974 | ||||||
| chr12:116939167
|
A | G | 4 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(1): Show | 4 | HG02615.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-6197A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116939167 | ||||||
| chr12:116939293
|
T | C | 1 | a0008c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.424-6071T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116939293 | ||||||
| chr12:116939299
|
C | T | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.424-6065C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116939299 | ||||||
| chr12:116939300
|
G | A | 1 | a0007c0012t0018g0005 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.424-6064G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116939300 | ||||||
| chr12:116939466
|
T | C | 1 | a0001c0001t0014g0162 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.424-5898T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116939466 | ||||||
| chr12:116940030
|
G | A | 2 | a0003c0003t0006g0006a0003c0003t0006g0008 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.424-5334G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940030 | ||||||
| chr12:116940192
|
G | C | 1 | a0001c0001t0001g0230 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424-5172G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940192 | ||||||
| chr12:116940255
|
C | CT | 27 | a0001c0001t0001g0216a0001c0001t0003g0193a0001c0001t0003g0194others(24): Show | 28 | HG00423.hp1 HG00741.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.424-5096dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116940255 | |||||
| chr12:116940269
|
A | T | 1 | a0001c0001t0003g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.424-5095A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940269 | ||||||
| chr12:116940408
|
C | T | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-4956C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940408 | ||||||
| chr12:116940493
|
C | CT | 96 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.424-4858dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116940493 | |||||
| chr12:116940506
|
T | C | 7 | a0003c0003t0010g0016a0003c0003t0010g0017a0003c0003t0010g0019others(4): Show | 7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.424-4858T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940506 | ||||||
| chr12:116940523
|
TA | T | 19 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(16): Show | 19 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.424-4830delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116940523 | |||||
| chr12:116940607
|
A | T | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.424-4757A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940607 | ||||||
| chr12:116940797
|
C | T | 1 | a0002c0002t0002g0096 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.424-4567C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940797 | ||||||
| chr12:116940856
|
T | C | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.424-4508T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940856 | ||||||
| chr12:116940893
|
C | T | 1 | a0001c0001t0003g0155 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.424-4471C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116940893 | ||||||
| chr12:116941139
|
C | T | 11 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(8): Show | 11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.424-4225C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116941139 | ||||||
| chr12:116941245
|
G | A | 1 | a0002c0008t0002g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424-4119G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116941245 | ||||||
| chr12:116941293
|
T | C | 1 | a0002c0002t0002g0145 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.424-4071T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116941293 | ||||||
| chr12:116941320
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424-4044G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116941320 | ||||||
| chr12:116941368
|
A | G | 2 | a0003c0003t0010g0019a0011c0018t0002g0018 | 2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.424-3996A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116941368 | ||||||
| chr12:116941880
|
C | G | 7 | a0001c0001t0001g0164a0001c0001t0001g0209a0001c0001t0001g0252others(4): Show | 7 | HG01192.hp1 HG01433.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.424-3484C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116941880 | ||||||
| chr12:116942085
|
A | G | 23 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(20): Show | 24 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.424-3279A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942085 | ||||||
| chr12:116942155
|
A | G | 4 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(1): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-3209A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942155 | ||||||
| chr12:116942188
|
C | A | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.424-3176C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942188 | ||||||
| chr12:116942195
|
A | AT | 16 | a0001c0001t0001g0212a0001c0001t0015g0251a0002c0002t0011g0080others(13): Show | 18 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.424-3155dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942195 | |||||
| chr12:116942233
|
A | C | 3 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010 | 3 | HG02615.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.424-3131A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942233 | ||||||
| chr12:116942351
|
A | G | 1 | a0003c0003t0011g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.424-3013A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942351 | ||||||
| chr12:116942374
|
A | AT | 170 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(167): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.424-2974dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942374 | |||||
| chr12:116942374
|
A | ATT | 16 | a0001c0001t0001g0176a0001c0001t0001g0212a0003c0003t0010g0016others(13): Show | 17 | HG00741.hp1 HG01884.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.424-2975_424-2974d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942374 | |||||
| chr12:116942770
|
A | AT | 43 | a0002c0002t0001g0139a0002c0002t0002g0047a0002c0002t0002g0054others(40): Show | 44 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.424-2569dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942770 | |||||
| chr12:116942770
|
A | ATT | 12 | a0002c0002t0002g0132a0002c0002t0002g0134a0002c0002t0002g0136others(9): Show | 14 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.424-2570_424-2569d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942770 | |||||
| chr12:116942770
|
AT | A | 64 | a0001c0001t0001g0169a0001c0001t0001g0180a0001c0001t0001g0215others(61): Show | 64 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.424-2569delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942770 | |||||
| chr12:116942770
|
ATT | A | 105 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(102): Show | 105 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.424-2570_424-2569d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 116942770 | |||||
| chr12:116942800
|
C | T | 7 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(4): Show | 7 | HG02486.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.424-2564C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942800 | ||||||
| chr12:116942864
|
G | A | 1 | a0004c0004t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.424-2500G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116942864 | ||||||
| chr12:116943156
|
G | A | 232 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(229): Show | 234 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.424-2208G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116943156 | ||||||
| chr12:116943228
|
T | A | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.424-2136T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116943228 | ||||||
| chr12:116943255
|
C | G | 8 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0003t0012g0013others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.424-2109C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116943255 | ||||||
| chr12:116943320
|
T | C | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.424-2044T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116943320 | ||||||
| chr12:116943564
|
T | C | 100 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.424-1800T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116943564 | ||||||
| chr12:116943841
|
C | T | 2 | a0001c0001t0031g0046a0001c0001t0032g0044 | 2 | HG01261.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.424-1523C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116943841 | ||||||
| chr12:116944056
|
G | A | 30 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(27): Show | 30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.424-1308G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944056 | ||||||
| chr12:116944241
|
G | A | 1 | a0002c0002t0002g0131 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.424-1123G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944241 | ||||||
| chr12:116944309
|
C | G | 2 | a0003c0003t0010g0019a0011c0018t0002g0018 | 2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.424-1055C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944309 | ||||||
| chr12:116944485
|
C | T | 160 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(157): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.424-879C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944485 | ||||||
| chr12:116944598
|
C | T | 1 | a0002c0002t0002g0150 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.424-766C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944598 | ||||||
| chr12:116944599
|
G | A | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.424-765G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944599 | ||||||
| chr12:116944691
|
A | C | 3 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015 | 3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.424-673A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116944691 | ||||||
| chr12:116945174
|
T | C | 1 | a0002c0002t0026g0072 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.424-190T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116945174 | ||||||
| chr12:116945258
|
A | G | 2 | a0002c0002t0002g0055a0002c0002t0027g0133 | 2 | HG01975.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.424-106A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 2/10 | chr12 | 116945258 | ||||||
| chr12:116945786
|
C | G | 1 | a0001c0001t0001g0238 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.588+258C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116945786 | ||||||
| chr12:116945910
|
A | G | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.588+382A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116945910 | ||||||
| chr12:116946311
|
A | C | 1 | a0002c0002t0002g0120 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.588+783A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946311 | ||||||
| chr12:116946357
|
T | C | 30 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(27): Show | 30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.588+829T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946357 | ||||||
| chr12:116946443
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.588+915G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946443 | ||||||
| chr12:116946599
|
T | A | 4 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(1): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+1071T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946599 | ||||||
| chr12:116946604
|
G | C | 154 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.588+1076G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946604 | ||||||
| chr12:116946716
|
G | A | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.588+1188G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946716 | ||||||
| chr12:116946773
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.588+1245G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116946773 | ||||||
| chr12:116947076
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.588+1548G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947076 | ||||||
| chr12:116947230
|
G | C | 90 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(87): Show | 90 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.588+1702G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947230 | ||||||
| chr12:116947273
|
T | C | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+1745T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947273 | ||||||
| chr12:116947346
|
G | C | 187 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(184): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.588+1818G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947346 | ||||||
| chr12:116947360
|
A | G | 1 | a0008c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.588+1832A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947360 | ||||||
| chr12:116947362
|
T | G | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.588+1834T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947362 | ||||||
| chr12:116947472
|
G | A | 2 | a0002c0002t0011g0080a0002c0002t0011g0140 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.588+1944G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947472 | ||||||
| chr12:116947736
|
C | CA | 11 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(8): Show | 11 | HG01106.hp1 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.589-1864dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116947736 | |||||
| chr12:116947750
|
A | AAAAAG | 90 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(87): Show | 90 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.589-1859_589-1855d others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116947750 | |||||
| chr12:116947750
|
A | AAAAG | 66 | a0001c0001t0001g0243a0001c0001t0001g0279a0001c0001t0001g0280others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.589-1865_589-1864i others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116947750 | |||||
| chr12:116947750
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.589-1868A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947750 | ||||||
| chr12:116947751
|
A | G | 1 | a0002c0002t0002g0119 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.589-1867A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947751 | ||||||
| chr12:116947768
|
G | GAA | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-1848_589-1847d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116947768 | |||||
| chr12:116947798
|
T | G | 1 | a0002c0002t0001g0139 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.589-1820T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947798 | ||||||
| chr12:116947807
|
G | A | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.589-1811G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947807 | ||||||
| chr12:116947863
|
C | T | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-1755C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947863 | ||||||
| chr12:116947882
|
G | A | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.589-1736G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116947882 | ||||||
| chr12:116948025
|
G | A | 39 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(36): Show | 39 | HG00140.hp2 HG00423.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.589-1593G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116948025 | ||||||
| chr12:116948037
|
T | C | 1 | a0001c0001t0003g0193 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.589-1581T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116948037 | ||||||
| chr12:116948233
|
A | G | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-1385A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116948233 | ||||||
| chr12:116948280
|
A | C | 187 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(184): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.589-1338A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116948280 | ||||||
| chr12:116948365
|
G | A | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.589-1253G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116948365 | ||||||
| chr12:116949121
|
C | T | 2 | a0002c0002t0009g0141a0002c0002t0009g0143 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.589-497C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116949121 | ||||||
| chr12:116949336
|
T | G | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.589-282T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116949336 | ||||||
| chr12:116949338
|
T | C | 1 | a0001c0001t0014g0162 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.589-280T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116949338 | ||||||
| chr12:116949614
|
G | A | 1 | a0007c0012t0018g0005 | 1 | HG02055.hp2 | splice_region_variant&intron_variant | LOW | c.589-4G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 3/10 | chr12 | 116949614 | ||||||
| chr12:116949765
|
A | G | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.677+59A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116949765 | ||||||
| chr12:116949840
|
A | G | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.677+134A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116949840 | ||||||
| chr12:116949881
|
G | A | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.677+175G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116949881 | ||||||
| chr12:116949881
|
G | T | 1 | a0002c0008t0002g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.677+175G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116949881 | ||||||
| chr12:116949906
|
G | T | 1 | a0005c0017t0007g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.677+200G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116949906 | ||||||
| chr12:116950182
|
G | GT | 23 | a0001c0001t0003g0049a0001c0001t0003g0051a0001c0001t0003g0052others(20): Show | 24 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.677+487dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116950182 | |||||
| chr12:116950182
|
GT | G | 5 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(2): Show | 7 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+487delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116950182 | |||||
| chr12:116950558
|
T | C | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+852T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950558 | ||||||
| chr12:116950576
|
T | C | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+870T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950576 | ||||||
| chr12:116950620
|
C | G | 1 | a0001c0001t0031g0046 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.677+914C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950620 | ||||||
| chr12:116950723
|
C | T | 1 | a0001c0009t0001g0237 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.677+1017C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950723 | ||||||
| chr12:116950759
|
G | A | 187 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(184): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.677+1053G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950759 | ||||||
| chr12:116950844
|
A | C | 1 | a0002c0011t0002g0123 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.677+1138A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950844 | ||||||
| chr12:116950887
|
G | A | 2 | a0001c0001t0003g0223a0002c0002t0002g0057 | 2 | HG02155.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.677+1181G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950887 | ||||||
| chr12:116950984
|
A | G | 1 | a0002c0008t0002g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.677+1278A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116950984 | ||||||
| chr12:116951309
|
A | C | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+1603A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951309 | ||||||
| chr12:116951322
|
G | A | 7 | a0003c0003t0010g0016a0003c0003t0010g0017a0003c0003t0010g0019others(4): Show | 7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.677+1616G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951322 | ||||||
| chr12:116951373
|
A | G | 5 | a0001c0001t0004g0030a0001c0001t0004g0032a0001c0001t0004g0033others(2): Show | 5 | HG03491.hp2 HG03492.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.677+1667A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951373 | ||||||
| chr12:116951568
|
G | T | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.677+1862G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951568 | ||||||
| chr12:116951592
|
C | G | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+1886C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951592 | ||||||
| chr12:116951835
|
G | A | 1 | a0002c0002t0005g0149 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.677+2129G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951835 | ||||||
| chr12:116951836
|
T | C | 1 | a0001c0001t0004g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.677+2130T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951836 | ||||||
| chr12:116951857
|
C | G | 1 | a0001c0001t0001g0255 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.677+2151C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116951857 | ||||||
| chr12:116952140
|
T | A | 1 | a0002c0002t0002g0150 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.677+2434T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952140 | ||||||
| chr12:116952174
|
T | C | 164 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(161): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.677+2468T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952174 | ||||||
| chr12:116952313
|
G | C | 7 | a0001c0001t0001g0272a0001c0001t0001g0274a0001c0001t0001g0279others(4): Show | 7 | HG01109.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+2607G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952313 | ||||||
| chr12:116952327
|
C | T | 4 | a0002c0002t0002g0076a0002c0002t0002g0082a0002c0002t0002g0134others(1): Show | 4 | NA18959.hp1 NA18997.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+2621C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952327 | ||||||
| chr12:116952344
|
G | A | 100 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.677+2638G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952344 | ||||||
| chr12:116952534
|
T | C | 164 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(161): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.677+2828T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952534 | ||||||
| chr12:116952543
|
G | A | 2 | a0002c0002t0011g0080a0002c0002t0011g0140 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.677+2837G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952543 | ||||||
| chr12:116952550
|
T | C | 283 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(280): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.677+2844T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952550 | ||||||
| chr12:116952572
|
C | T | 7 | a0003c0003t0010g0016a0003c0003t0010g0017a0003c0003t0010g0019others(4): Show | 7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.677+2866C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952572 | ||||||
| chr12:116952605
|
G | A | 164 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(161): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.677+2899G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952605 | ||||||
| chr12:116952611
|
C | T | 1 | a0001c0009t0001g0237 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.677+2905C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952611 | ||||||
| chr12:116952628
|
A | G | 2 | a0003c0003t0010g0016a0003c0003t0010g0017 | 2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.677+2922A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952628 | ||||||
| chr12:116952748
|
A | C | 1 | a0001c0001t0004g0039 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.677+3042A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952748 | ||||||
| chr12:116952820
|
C | T | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+3114C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952820 | ||||||
| chr12:116952883
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.677+3177G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116952883 | ||||||
| chr12:116953022
|
G | A | 5 | a0005c0007t0007g0002a0005c0007t0007g0023a0005c0007t0007g0025others(2): Show | 6 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.677+3316G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953022 | ||||||
| chr12:116953154
|
T | C | 12 | a0002c0002t0002g0073a0002c0002t0002g0109a0002c0002t0002g0110others(9): Show | 12 | HG02071.hp2 HG02738.hp2 NA18954.hp2 others(9): Show |
intron_variant | MODIFIER | c.677+3448T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953154 | ||||||
| chr12:116953378
|
C | G | 164 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(161): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.677+3672C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953378 | ||||||
| chr12:116953383
|
G | T | 1 | a0001c0001t0001g0262 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.677+3677G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953383 | ||||||
| chr12:116953416
|
T | G | 1 | a0003c0003t0001g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.677+3710T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953416 | ||||||
| chr12:116953485
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.677+3779C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953485 | ||||||
| chr12:116953500
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.677+3794G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953500 | ||||||
| chr12:116953792
|
AC | A | 3 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015 | 3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.677+4087delC | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953792 | ||||||
| chr12:116953982
|
C | T | 10 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0278others(7): Show | 11 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.677+4276C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116953982 | ||||||
| chr12:116954111
|
CA | C | 182 | a0001c0001t0001g0045a0001c0001t0001g0158a0001c0001t0001g0160others(179): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.677+4428delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116954111 | |||||
| chr12:116954111
|
CAA | C | 18 | a0002c0002t0002g0111a0002c0002t0002g0124a0003c0003t0006g0004others(15): Show | 19 | HG00609.hp1 HG00741.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.677+4427_677+4428d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116954111 | |||||
| chr12:116954129
|
A | G | 3 | a0002c0002t0002g0053a0002c0002t0002g0084a0002c0002t0002g0085 | 3 | HG02486.hp2 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.677+4423A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954129 | ||||||
| chr12:116954133
|
A | AT | 20 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(17): Show | 20 | HG00544.hp1 HG02080.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.677+4427_677+4428i others(3): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954133 | ||||||
| chr12:116954133
|
A | T | 217 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(214): Show | 221 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.677+4427A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954133 | ||||||
| chr12:116954300
|
G | A | 187 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(184): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.677+4594G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954300 | ||||||
| chr12:116954483
|
T | C | 1 | a0001c0001t0003g0154 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.677+4777T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954483 | ||||||
| chr12:116954494
|
T | A | 2 | a0002c0002t0002g0086a0002c0002t0002g0088 | 2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.677+4788T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954494 | ||||||
| chr12:116954666
|
C | G | 5 | a0002c0002t0002g0076a0002c0002t0002g0082a0002c0002t0002g0124others(2): Show | 5 | HG00609.hp1 NA18959.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.677+4960C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954666 | ||||||
| chr12:116954710
|
G | T | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.677+5004G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954710 | ||||||
| chr12:116954887
|
C | G | 4 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(1): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.677+5181C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954887 | ||||||
| chr12:116954970
|
T | C | 1 | a0002c0002t0002g0090 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.677+5264T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954970 | ||||||
| chr12:116954981
|
C | T | 3 | a0003c0003t0011g0011a0003c0003t0011g0012a0007c0012t0018g0005 | 3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.677+5275C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116954981 | ||||||
| chr12:116955036
|
T | TG | 106 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0160others(103): Show | 106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.677+5342dupG | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116955036 | |||||
| chr12:116955036
|
T | TGG | 42 | a0001c0001t0001g0158a0001c0001t0001g0169a0001c0001t0001g0170others(39): Show | 42 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.677+5341_677+5342d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116955036 | |||||
| chr12:116955036
|
TGG | T | 33 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(30): Show | 33 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.677+5341_677+5342d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116955036 | |||||
| chr12:116955039
|
G | C | 18 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(15): Show | 19 | HG01175.hp1 HG01261.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.677+5333G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955039 | ||||||
| chr12:116955041
|
G | T | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+5335G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955041 | ||||||
| chr12:116955048
|
G | C | 5 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(2): Show | 6 | HG02723.hp2 HG03209.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.677+5342G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955048 | ||||||
| chr12:116955049
|
C | G | 11 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(8): Show | 11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.677+5343C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955049 | ||||||
| chr12:116955181
|
G | T | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.677+5475G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955181 | ||||||
| chr12:116955319
|
C | T | 1 | a0008c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.677+5613C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955319 | ||||||
| chr12:116955853
|
A | G | 7 | a0001c0001t0003g0191a0001c0001t0003g0200a0001c0001t0003g0201others(4): Show | 7 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.677+6147A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116955853 | ||||||
| chr12:116956190
|
C | T | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+6484C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956190 | ||||||
| chr12:116956219
|
G | A | 176 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(173): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.677+6513G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956219 | ||||||
| chr12:116956281
|
C | G | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.677+6575C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956281 | ||||||
| chr12:116956452
|
A | G | 1 | a0002c0002t0008g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.677+6746A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956452 | ||||||
| chr12:116956517
|
G | C | 4 | a0002c0002t0002g0100a0002c0002t0002g0101a0002c0002t0002g0102others(1): Show | 4 | HG01891.hp1 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+6811G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956517 | ||||||
| chr12:116956542
|
G | A | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+6836G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956542 | ||||||
| chr12:116956549
|
A | C | 2 | a0001c0001t0003g0185a0001c0001t0003g0223 | 2 | NA19055.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.677+6843A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116956549 | ||||||
| chr12:116956725
|
T | TGGGAGGC others(20): Show |
1 | a0002c0008t0002g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.677+7023_677+7049d others(29): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116956725 | |||||
| chr12:116957049
|
C | A | 8 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0003t0012g0013others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.677+7343C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116957049 | ||||||
| chr12:116957517
|
A | G | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.678-7180A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116957517 | ||||||
| chr12:116957808
|
AATTT | A | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.678-6880_678-6877d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116957808 | |||||
| chr12:116958036
|
C | T | 1 | a0003c0020t0020g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.678-6661C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958036 | ||||||
| chr12:116958149
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.678-6548A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958149 | ||||||
| chr12:116958153
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.678-6544G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958153 | ||||||
| chr12:116958155
|
C | A | 1 | a0003c0003t0010g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.678-6542C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958155 | ||||||
| chr12:116958237
|
C | T | 30 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(27): Show | 30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.678-6460C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958237 | ||||||
| chr12:116958292
|
G | C | 136 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.678-6405G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958292 | ||||||
| chr12:116958307
|
A | G | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.678-6390A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958307 | ||||||
| chr12:116958712
|
T | G | 1 | a0002c0002t0002g0112 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.678-5985T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958712 | ||||||
| chr12:116958716
|
G | A | 1 | a0002c0002t0002g0112 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.678-5981G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958716 | ||||||
| chr12:116958775
|
T | C | 1 | a0003c0003t0021g0009 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.678-5922T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958775 | ||||||
| chr12:116958816
|
T | C | 1 | a0002c0002t0011g0140 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.678-5881T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958816 | ||||||
| chr12:116958822
|
T | G | 100 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.678-5875T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116958822 | ||||||
| chr12:116959008
|
T | A | 100 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.678-5689T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959008 | ||||||
| chr12:116959017
|
C | T | 172 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(169): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.678-5680C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959017 | ||||||
| chr12:116959596
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.678-5101T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959596 | ||||||
| chr12:116959674
|
T | G | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.678-5023T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959674 | ||||||
| chr12:116959825
|
G | A | 2 | a0006c0010t0013g0103a0006c0010t0013g0104 | 2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.678-4872G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959825 | ||||||
| chr12:116959845
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.678-4852T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959845 | ||||||
| chr12:116959949
|
G | C | 1 | a0001c0001t0004g0032 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.678-4748G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116959949 | ||||||
| chr12:116960241
|
A | G | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.678-4456A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960241 | ||||||
| chr12:116960245
|
A | C | 1 | a0002c0008t0002g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.678-4452A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960245 | ||||||
| chr12:116960250
|
G | C | 11 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(8): Show | 11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.678-4447G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960250 | ||||||
| chr12:116960338
|
G | A | 6 | a0001c0001t0001g0158a0001c0001t0001g0218a0001c0001t0001g0220others(3): Show | 6 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.678-4359G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960338 | ||||||
| chr12:116960404
|
C | T | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.678-4293C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960404 | ||||||
| chr12:116960576
|
G | T | 2 | a0006c0010t0013g0103a0006c0010t0013g0104 | 2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.678-4121G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960576 | ||||||
| chr12:116960643
|
T | C | 166 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.678-4054T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960643 | ||||||
| chr12:116960848
|
A | AT | 5 | a0003c0003t0010g0019a0003c0003t0010g0020a0003c0003t0010g0022others(2): Show | 5 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.678-3849_678-3848i others(3): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960848 | ||||||
| chr12:116960943
|
A | T | 3 | a0002c0002t0002g0047a0002c0002t0002g0095a0002c0002t0022g0094 | 3 | HG02630.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.678-3754A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960943 | ||||||
| chr12:116960970
|
A | G | 9 | a0001c0001t0001g0254a0003c0003t0011g0011a0003c0003t0011g0012others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.678-3727A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116960970 | ||||||
| chr12:116961098
|
C | T | 8 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0003t0012g0013others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.678-3599C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961098 | ||||||
| chr12:116961117
|
TC | T | 3 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0120 | 3 | NA19010.hp2 NA19068.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.678-3577delC | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116961117 | |||||
| chr12:116961274
|
C | A | 11 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(8): Show | 11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.678-3423C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961274 | ||||||
| chr12:116961325
|
A | T | 1 | a0001c0001t0004g0165 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.678-3372A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961325 | ||||||
| chr12:116961437
|
G | A | 2 | a0002c0002t0005g0065a0002c0002t0005g0097 | 2 | HG01256.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.678-3260G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961437 | ||||||
| chr12:116961454
|
C | T | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.678-3243C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961454 | ||||||
| chr12:116961508
|
G | A | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.678-3189G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961508 | ||||||
| chr12:116961607
|
C | A | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.678-3090C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961607 | ||||||
| chr12:116961676
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.678-3021G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961676 | ||||||
| chr12:116961715
|
C | G | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.678-2982C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961715 | ||||||
| chr12:116961899
|
C | T | 32 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(29): Show | 32 | HG00140.hp2 HG00423.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.678-2798C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116961899 | ||||||
| chr12:116962256
|
G | A | 4 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(1): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.678-2441G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116962256 | ||||||
| chr12:116962324
|
C | T | 1 | a0003c0020t0020g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.678-2373C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116962324 | ||||||
| chr12:116962565
|
C | T | 1 | a0001c0001t0003g0193 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.678-2132C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116962565 | ||||||
| chr12:116962594
|
T | C | 1 | a0001c0001t0003g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.678-2103T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116962594 | ||||||
| chr12:116962888
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.678-1809C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116962888 | ||||||
| chr12:116963014
|
C | T | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.678-1683C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963014 | ||||||
| chr12:116963044
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.678-1653G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963044 | ||||||
| chr12:116963084
|
C | T | 1 | a0002c0002t0002g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.678-1613C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963084 | ||||||
| chr12:116963373
|
G | A | 2 | a0002c0002t0002g0047a0002c0002t0022g0094 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.678-1324G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963373 | ||||||
| chr12:116963496
|
T | G | 2 | a0001c0001t0001g0272a0001c0001t0001g0274 | 2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.678-1201T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963496 | ||||||
| chr12:116963534
|
A | C | 2 | a0001c0001t0003g0056a0008c0016t0003g0029 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.678-1163A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963534 | ||||||
| chr12:116963822
|
A | G | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.678-875A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116963822 | ||||||
| chr12:116964496
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.678-201G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116964496 | ||||||
| chr12:116964678
|
G | A | 1 | a0001c0001t0025g0263 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.678-19G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 4/10 | chr12 | 116964678 | ||||||
| chr12:116964906
|
A | T | 5 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(2): Show | 5 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+52A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116964906 | ||||||
| chr12:116964950
|
T | C | 270 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(267): Show | 275 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.835+96T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116964950 | ||||||
| chr12:116965070
|
T | G | 1 | a0001c0001t0001g0214 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.835+216T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965070 | ||||||
| chr12:116965215
|
A | G | 1 | a0001c0001t0003g0191 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.835+361A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965215 | ||||||
| chr12:116965224
|
T | C | 4 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(1): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.835+370T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965224 | ||||||
| chr12:116965419
|
A | T | 1 | a0002c0008t0002g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.835+565A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965419 | ||||||
| chr12:116965535
|
TGTGAA | T | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+685_835+689del others(5): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116965535 | |||||
| chr12:116965629
|
C | G | 3 | a0003c0003t0011g0011a0003c0003t0011g0012a0007c0012t0018g0005 | 3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.835+775C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965629 | ||||||
| chr12:116965769
|
A | G | 2 | a0005c0007t0007g0002a0005c0007t0007g0023 | 3 | HG02145.hp2 HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.835+915A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965769 | ||||||
| chr12:116965904
|
G | A | 1 | a0001c0006t0001g0236 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.835+1050G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116965904 | ||||||
| chr12:116965925
|
A | AT | 62 | a0001c0001t0003g0056a0001c0001t0003g0189a0001c0001t0003g0191others(59): Show | 63 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.835+1090dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116965925 | |||||
| chr12:116965925
|
A | ATT | 158 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(155): Show | 159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.835+1089_835+1090d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116965925 | |||||
| chr12:116966092
|
A | G | 1 | a0001c0001t0003g0188 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.835+1238A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966092 | ||||||
| chr12:116966133
|
C | T | 183 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(180): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.835+1279C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966133 | ||||||
| chr12:116966378
|
G | A | 2 | a0002c0002t0005g0065a0002c0002t0005g0097 | 2 | HG01256.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.835+1524G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966378 | ||||||
| chr12:116966417
|
G | C | 3 | a0003c0003t0011g0011a0003c0003t0011g0012a0007c0012t0018g0005 | 3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.835+1563G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966417 | ||||||
| chr12:116966580
|
C | T | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+1726C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966580 | ||||||
| chr12:116966655
|
A | G | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+1801A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966655 | ||||||
| chr12:116966700
|
G | A | 4 | a0002c0002t0002g0100a0002c0002t0002g0101a0002c0002t0002g0102others(1): Show | 4 | HG01891.hp1 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+1846G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966700 | ||||||
| chr12:116966819
|
A | G | 5 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(2): Show | 6 | HG02723.hp2 HG03209.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.835+1965A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966819 | ||||||
| chr12:116966861
|
A | G | 9 | a0003c0003t0003g0166a0003c0003t0003g0186a0005c0007t0002g0026others(6): Show | 10 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.835+2007A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966861 | ||||||
| chr12:116966900
|
C | G | 1 | a0001c0001t0001g0256 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.835+2046C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966900 | ||||||
| chr12:116966962
|
C | A | 172 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(169): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.835+2108C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116966962 | ||||||
| chr12:116967138
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.835+2284G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967138 | ||||||
| chr12:116967153
|
C | T | 1 | a0001c0001t0003g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.835+2299C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967153 | ||||||
| chr12:116967159
|
C | CT | 8 | a0001c0001t0003g0050a0003c0005t0002g0063a0005c0007t0002g0026others(5): Show | 9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.835+2320dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116967159 | |||||
| chr12:116967159
|
CT | C | 7 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(4): Show | 7 | HG00423.hp2 HG02523.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+2320delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116967159 | |||||
| chr12:116967593
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.835+2739G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967593 | ||||||
| chr12:116967763
|
C | T | 17 | a0003c0003t0003g0166a0003c0003t0003g0186a0003c0003t0011g0011others(14): Show | 18 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.835+2909C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967763 | ||||||
| chr12:116967792
|
A | C | 1 | a0004c0004t0001g0244 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.835+2938A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967792 | ||||||
| chr12:116967816
|
G | C | 2 | a0001c0001t0014g0161a0001c0001t0014g0162 | 2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.835+2962G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967816 | ||||||
| chr12:116967850
|
T | C | 2 | a0002c0002t0011g0080a0002c0002t0011g0140 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835+2996T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116967850 | ||||||
| chr12:116968060
|
C | T | 1 | a0003c0020t0020g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.835+3206C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968060 | ||||||
| chr12:116968065
|
G | A | 1 | a0002c0002t0005g0149 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.835+3211G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968065 | ||||||
| chr12:116968131
|
AT | A | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+3283delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116968131 | |||||
| chr12:116968196
|
G | C | 157 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.835+3342G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968196 | ||||||
| chr12:116968246
|
C | T | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.835+3392C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968246 | ||||||
| chr12:116968282
|
T | C | 1 | a0002c0002t0005g0098 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.835+3428T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968282 | ||||||
| chr12:116968464
|
G | A | 4 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(1): Show | 4 | HG02615.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+3610G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968464 | ||||||
| chr12:116968475
|
A | C | 1 | a0002c0002t0002g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.835+3621A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968475 | ||||||
| chr12:116968497
|
G | C | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+3643G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968497 | ||||||
| chr12:116968644
|
A | G | 1 | a0008c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.835+3790A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968644 | ||||||
| chr12:116968676
|
C | G | 1 | a0005c0007t0002g0026 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.835+3822C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116968676 | ||||||
| chr12:116969099
|
A | G | 1 | a0002c0002t0005g0098 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.835+4245A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116969099 | ||||||
| chr12:116969220
|
C | A | 1 | a0007c0012t0018g0005 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.835+4366C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116969220 | ||||||
| chr12:116969451
|
G | A | 1 | a0002c0002t0002g0096 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.835+4597G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116969451 | ||||||
| chr12:116969695
|
C | T | 154 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.835+4841C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116969695 | ||||||
| chr12:116969805
|
C | T | 1 | a0003c0020t0020g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.835+4951C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116969805 | ||||||
| chr12:116969840
|
AT | A | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+4989delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116969840 | |||||
| chr12:116970235
|
G | A | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.835+5381G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970235 | ||||||
| chr12:116970284
|
G | A | 2 | a0002c0002t0011g0080a0002c0002t0011g0140 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835+5430G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970284 | ||||||
| chr12:116970317
|
C | T | 8 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0003t0012g0013others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.835+5463C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970317 | ||||||
| chr12:116970320
|
G | A | 1 | a0008c0016t0003g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.835+5466G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970320 | ||||||
| chr12:116970343
|
T | C | 182 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(179): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.835+5489T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970343 | ||||||
| chr12:116970410
|
G | A | 184 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(181): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.835+5556G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970410 | ||||||
| chr12:116970477
|
T | C | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.835+5623T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970477 | ||||||
| chr12:116970495
|
C | T | 1 | a0001c0001t0003g0168 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.835+5641C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970495 | ||||||
| chr12:116970638
|
G | A | 161 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(158): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.835+5784G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116970638 | ||||||
| chr12:116971053
|
A | G | 100 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.835+6199A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116971053 | ||||||
| chr12:116971116
|
C | T | 32 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(29): Show | 32 | HG00140.hp2 HG00423.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.835+6262C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116971116 | ||||||
| chr12:116971326
|
T | C | 157 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.835+6472T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116971326 | ||||||
| chr12:116971357
|
C | CA | 55 | a0001c0001t0001g0164a0001c0001t0003g0052a0001c0001t0004g0033others(52): Show | 55 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.835+6517dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116971357 | |||||
| chr12:116971845
|
G | A | 8 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0003t0012g0013others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.835+6991G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116971845 | ||||||
| chr12:116971935
|
T | C | 6 | a0001c0006t0001g0181a0001c0006t0001g0217a0001c0006t0001g0236others(3): Show | 6 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.835+7081T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116971935 | ||||||
| chr12:116971947
|
A | G | 5 | a0002c0002t0002g0096a0002c0008t0002g0067a0002c0008t0002g0068others(2): Show | 5 | HG01261.hp1 HG02148.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+7093A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116971947 | ||||||
| chr12:116972228
|
A | G | 4 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(1): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.835+7374A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972228 | ||||||
| chr12:116972354
|
G | T | 136 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.835+7500G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972354 | ||||||
| chr12:116972610
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.835+7756C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972610 | ||||||
| chr12:116972630
|
G | C | 174 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(171): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.835+7776G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972630 | ||||||
| chr12:116972695
|
C | T | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.835+7841C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972695 | ||||||
| chr12:116972830
|
G | A | 2 | a0002c0002t0011g0080a0002c0002t0011g0140 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835+7976G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972830 | ||||||
| chr12:116972837
|
C | A | 1 | a0001c0001t0003g0155 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.835+7983C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972837 | ||||||
| chr12:116972898
|
A | G | 1 | a0001c0001t0004g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.835+8044A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116972898 | ||||||
| chr12:116973275
|
C | T | 100 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.835+8421C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973275 | ||||||
| chr12:116973382
|
C | T | 3 | a0001c0001t0003g0049a0001c0001t0003g0051a0001c0001t0003g0052 | 3 | HG02622.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.835+8528C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973382 | ||||||
| chr12:116973483
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.835+8629G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973483 | ||||||
| chr12:116973656
|
C | T | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+8802C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973656 | ||||||
| chr12:116973663
|
G | A | 1 | a0004c0004t0001g0245 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.835+8809G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973663 | ||||||
| chr12:116973852
|
T | G | 7 | a0003c0003t0010g0016a0003c0003t0010g0017a0003c0003t0010g0019others(4): Show | 7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.835+8998T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973852 | ||||||
| chr12:116973861
|
C | A | 58 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(55): Show | 58 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.835+9007C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973861 | ||||||
| chr12:116973898
|
A | C | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.835+9044A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116973898 | ||||||
| chr12:116974059
|
C | T | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.835+9205C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974059 | ||||||
| chr12:116974100
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.835+9246C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974100 | ||||||
| chr12:116974152
|
G | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0271 | 3 | HG02818.hp1 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.835+9298G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974152 | ||||||
| chr12:116974261
|
C | T | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+9407C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974261 | ||||||
| chr12:116974267
|
T | C | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+9413T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974267 | ||||||
| chr12:116974798
|
A | G | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.835+9944A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974798 | ||||||
| chr12:116974822
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.835+9968A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116974822 | ||||||
| chr12:116975208
|
G | A | 2 | a0001c0009t0001g0237a0001c0009t0001g0275 | 2 | HG02698.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.836-9998G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116975208 | ||||||
| chr12:116975281
|
TTA | T | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.836-9922_836-9921d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116975281 | |||||
| chr12:116975355
|
A | G | 4 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(1): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.836-9851A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116975355 | ||||||
| chr12:116975520
|
G | C | 2 | a0003c0003t0010g0020a0003c0003t0010g0022 | 2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.836-9686G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116975520 | ||||||
| chr12:116975544
|
A | G | 2 | a0006c0010t0013g0103a0006c0010t0013g0104 | 2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.836-9662A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116975544 | ||||||
| chr12:116975545
|
A | G | 139 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(136): Show | 139 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.836-9661A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116975545 | ||||||
| chr12:116975622
|
T | C | 13 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(10): Show | 13 | HG01433.hp2 HG02027.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.836-9584T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116975622 | ||||||
| chr12:116976153
|
C | T | 187 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(184): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.836-9053C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976153 | ||||||
| chr12:116976167
|
T | C | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.836-9039T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976167 | ||||||
| chr12:116976195
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.836-9011G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976195 | ||||||
| chr12:116976232
|
T | C | 6 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(3): Show | 6 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.836-8974T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976232 | ||||||
| chr12:116976386
|
TA | T | 79 | a0001c0001t0001g0268a0001c0001t0003g0163a0001c0001t0003g0191others(76): Show | 80 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.836-8805delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116976386 | |||||
| chr12:116976450
|
C | CT | 31 | a0001c0001t0004g0042a0002c0002t0002g0047a0002c0002t0002g0092others(28): Show | 32 | HG01106.hp1 HG01358.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.836-8734dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116976450 | |||||
| chr12:116976450
|
CT | C | 113 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(110): Show | 113 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.836-8734delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116976450 | |||||
| chr12:116976472
|
T | C | 1 | a0003c0003t0006g0010 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.836-8734T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976472 | ||||||
| chr12:116976558
|
C | T | 3 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015 | 3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.836-8648C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976558 | ||||||
| chr12:116976621
|
AT | A | 166 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(163): Show | 170 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.836-8569delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116976621 | |||||
| chr12:116976692
|
C | T | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.836-8514C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976692 | ||||||
| chr12:116976756
|
C | T | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.836-8450C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976756 | ||||||
| chr12:116976779
|
T | C | 1 | a0001c0006t0001g0236 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.836-8427T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976779 | ||||||
| chr12:116976894
|
C | T | 1 | a0002c0002t0026g0072 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.836-8312C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976894 | ||||||
| chr12:116976985
|
C | G | 4 | a0002c0008t0002g0067a0002c0008t0002g0068a0002c0008t0002g0069others(1): Show | 4 | HG01261.hp1 HG02148.hp1 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-8221C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116976985 | ||||||
| chr12:116977072
|
T | C | 10 | a0002c0002t0002g0073a0002c0002t0002g0109a0002c0002t0002g0111others(7): Show | 10 | HG02071.hp2 NA18954.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.836-8134T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977072 | ||||||
| chr12:116977169
|
C | T | 6 | a0001c0001t0001g0158a0001c0001t0001g0218a0001c0001t0001g0220others(3): Show | 6 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.836-8037C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977169 | ||||||
| chr12:116977280
|
C | A | 2 | a0002c0002t0005g0065a0002c0002t0005g0097 | 2 | HG01256.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.836-7926C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977280 | ||||||
| chr12:116977337
|
G | A | 4 | a0001c0001t0003g0050a0003c0003t0003g0166a0003c0003t0003g0186others(1): Show | 4 | HG02818.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.836-7869G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977337 | ||||||
| chr12:116977345
|
G | C | 1 | a0001c0001t0001g0218 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.836-7861G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977345 | ||||||
| chr12:116977357
|
A | G | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-7849A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977357 | ||||||
| chr12:116977488
|
G | A | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.836-7718G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977488 | ||||||
| chr12:116977538
|
G | A | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.836-7668G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977538 | ||||||
| chr12:116977763
|
A | G | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.836-7443A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977763 | ||||||
| chr12:116977997
|
C | T | 2 | a0003c0003t0011g0011a0003c0003t0011g0012 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.836-7209C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116977997 | ||||||
| chr12:116978064
|
A | G | 1 | a0001c0001t0003g0189 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.836-7142A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978064 | ||||||
| chr12:116978080
|
C | T | 2 | a0003c0003t0010g0016a0003c0003t0010g0017 | 2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.836-7126C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978080 | ||||||
| chr12:116978188
|
A | C | 8 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0086others(5): Show | 9 | HG01175.hp1 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.836-7018A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978188 | ||||||
| chr12:116978349
|
T | G | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.836-6857T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978349 | ||||||
| chr12:116978506
|
T | A | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-6700T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978506 | ||||||
| chr12:116978536
|
A | C | 1 | a0002c0002t0002g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.836-6670A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978536 | ||||||
| chr12:116978541
|
A | C | 1 | a0001c0001t0032g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.836-6665A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978541 | ||||||
| chr12:116978753
|
G | A | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.836-6453G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978753 | ||||||
| chr12:116978864
|
T | C | 1 | a0003c0020t0020g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.836-6342T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116978864 | ||||||
| chr12:116979361
|
G | A | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.836-5845G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116979361 | ||||||
| chr12:116979727
|
T | C | 11 | a0003c0005t0002g0059a0003c0005t0002g0060a0003c0005t0002g0061others(8): Show | 12 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.836-5479T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116979727 | ||||||
| chr12:116979777
|
C | CA | 66 | a0001c0001t0001g0045a0001c0001t0001g0158a0001c0001t0001g0160others(63): Show | 66 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.836-5410dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116979777 | |||||
| chr12:116979777
|
C | CAA | 24 | a0001c0001t0001g0177a0001c0001t0003g0049a0001c0001t0003g0050others(21): Show | 24 | HG01891.hp2 HG02055.hp2 HG02135.hp1 others(21): Show |
intron_variant | MODIFIER | c.836-5411_836-5410d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116979777 | |||||
| chr12:116979777
|
CA | C | 18 | a0001c0001t0001g0280a0003c0003t0006g0010a0003c0003t0010g0016others(15): Show | 19 | HG00741.hp1 HG01884.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.836-5410delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116979777 | |||||
| chr12:116979814
|
A | G | 1 | a0003c0005t0002g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.836-5392A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116979814 | ||||||
| chr12:116980034
|
G | C | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.836-5172G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116980034 | ||||||
| chr12:116980454
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.836-4752T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116980454 | ||||||
| chr12:116980664
|
C | T | 1 | a0001c0001t0004g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.836-4542C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116980664 | ||||||
| chr12:116981002
|
C | T | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.836-4204C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116981002 | ||||||
| chr12:116981060
|
T | C | 5 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(2): Show | 6 | HG02723.hp2 HG03209.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.836-4146T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116981060 | ||||||
| chr12:116981349
|
T | C | 13 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(10): Show | 14 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.836-3857T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116981349 | ||||||
| chr12:116981589
|
A | G | 15 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(12): Show | 16 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.836-3617A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116981589 | ||||||
| chr12:116981613
|
CT | C | 144 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(141): Show | 144 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.836-3579delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116981613 | |||||
| chr12:116981770
|
T | C | 2 | a0003c0003t0011g0011a0003c0003t0011g0012 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.836-3436T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116981770 | ||||||
| chr12:116982112
|
A | T | 1 | a0002c0008t0002g0069 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.836-3094A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982112 | ||||||
| chr12:116982290
|
C | T | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-2916C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982290 | ||||||
| chr12:116982308
|
T | A | 11 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(8): Show | 11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.836-2898T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982308 | ||||||
| chr12:116982333
|
C | G | 158 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.836-2873C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982333 | ||||||
| chr12:116982374
|
A | T | 17 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(14): Show | 18 | HG00741.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.836-2832A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982374 | ||||||
| chr12:116982623
|
A | AT | 99 | a0002c0002t0001g0139a0002c0002t0002g0003a0002c0002t0002g0047others(96): Show | 103 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.836-2566dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116982623 | |||||
| chr12:116982623
|
A | ATT | 9 | a0002c0002t0002g0093a0002c0002t0002g0134a0002c0011t0002g0123others(6): Show | 10 | HG01192.hp2 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.836-2567_836-2566d others(4): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116982623 | |||||
| chr12:116982623
|
AT | A | 157 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(154): Show | 157 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.836-2566delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116982623 | |||||
| chr12:116982900
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.836-2306C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982900 | ||||||
| chr12:116982957
|
G | A | 2 | a0006c0010t0013g0103a0006c0010t0013g0104 | 2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.836-2249G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982957 | ||||||
| chr12:116982975
|
A | C | 179 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(176): Show | 181 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.836-2231A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116982975 | ||||||
| chr12:116983142
|
T | G | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.836-2064T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983142 | ||||||
| chr12:116983284
|
A | G | 4 | a0001c0001t0001g0216a0001c0001t0001g0241a0001c0001t0015g0213others(1): Show | 4 | HG01258.hp2 HG02293.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-1922A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983284 | ||||||
| chr12:116983336
|
G | C | 1 | a0002c0002t0008g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.836-1870G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983336 | ||||||
| chr12:116983366
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.836-1840C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983366 | ||||||
| chr12:116983375
|
C | T | 30 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(27): Show | 30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.836-1831C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983375 | ||||||
| chr12:116983408
|
T | C | 1 | a0002c0002t0002g0150 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.836-1798T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983408 | ||||||
| chr12:116983527
|
C | T | 11 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(8): Show | 11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.836-1679C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983527 | ||||||
| chr12:116983847
|
G | A | 18 | a0001c0001t0001g0226a0001c0001t0004g0030a0001c0001t0004g0031others(15): Show | 18 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.836-1359G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983847 | ||||||
| chr12:116983933
|
A | T | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.836-1273A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983933 | ||||||
| chr12:116983937
|
A | G | 99 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(96): Show | 99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.836-1269A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116983937 | ||||||
| chr12:116984050
|
A | G | 1 | a0002c0002t0002g0138 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.836-1156A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984050 | ||||||
| chr12:116984117
|
G | A | 158 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.836-1089G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984117 | ||||||
| chr12:116984187
|
T | G | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.836-1019T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984187 | ||||||
| chr12:116984310
|
C | T | 153 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.836-896C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984310 | ||||||
| chr12:116984561
|
C | T | 1 | a0002c0002t0005g0097 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.836-645C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984561 | ||||||
| chr12:116984587
|
G | T | 153 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.836-619G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984587 | ||||||
| chr12:116984844
|
G | C | 1 | a0001c0001t0003g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.836-362G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984844 | ||||||
| chr12:116984845
|
C | T | 7 | a0003c0003t0010g0016a0003c0003t0010g0017a0003c0003t0010g0019others(4): Show | 7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.836-361C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984845 | ||||||
| chr12:116984863
|
G | A | 3 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015 | 3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.836-343G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984863 | ||||||
| chr12:116984867
|
G | A | 6 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.836-339G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984867 | ||||||
| chr12:116984922
|
C | T | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-284C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984922 | ||||||
| chr12:116984983
|
T | C | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-223T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116984983 | ||||||
| chr12:116985063
|
G | A | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.836-143G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116985063 | ||||||
| chr12:116985140
|
T | A | 2 | a0003c0003t0010g0016a0003c0003t0010g0017 | 2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.836-66T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 5/10 | chr12 | 116985140 | ||||||
| chr12:116985459
|
G | A | 171 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.1032+57G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116985459 | ||||||
| chr12:116985466
|
C | T | 4 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(1): Show | 4 | HG01433.hp2 HG02040.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+64C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116985466 | ||||||
| chr12:116985617
|
G | A | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+215G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116985617 | ||||||
| chr12:116985663
|
G | A | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+261G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116985663 | ||||||
| chr12:116985984
|
T | A | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+582T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116985984 | ||||||
| chr12:116986357
|
C | A | 1 | a0004c0004t0001g0183 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1032+955C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986357 | ||||||
| chr12:116986500
|
C | T | 1 | a0002c0002t0005g0148 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1032+1098C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986500 | ||||||
| chr12:116986577
|
G | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0271 | 3 | HG02818.hp1 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1032+1175G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986577 | ||||||
| chr12:116986596
|
A | C | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1032+1194A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986596 | ||||||
| chr12:116986625
|
C | CA | 30 | a0001c0001t0001g0226a0001c0001t0004g0030a0001c0001t0004g0036others(27): Show | 32 | HG00609.hp1 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1032+1236dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116986625 | |||||
| chr12:116986631
|
AAAAAAAA others(3): Show |
A | 1 | a0005c0017t0007g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1032+1237_1032+124 others(14): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116986631 | |||||
| chr12:116986649
|
C | A | 1 | a0005c0017t0007g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1032+1247C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986649 | ||||||
| chr12:116986650
|
A | G | 1 | a0005c0017t0007g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1032+1248A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986650 | ||||||
| chr12:116986661
|
G | A | 1 | a0002c0008t0002g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1032+1259G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986661 | ||||||
| chr12:116986701
|
T | A | 142 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1032+1299T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116986701 | ||||||
| chr12:116987169
|
C | T | 160 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1033-1494C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987169 | ||||||
| chr12:116987189
|
A | T | 1 | a0002c0002t0030g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1033-1474A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987189 | ||||||
| chr12:116987207
|
T | A | 2 | a0002c0002t0002g0087a0002c0002t0024g0066 | 2 | HG01175.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1033-1456T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987207 | ||||||
| chr12:116987212
|
G | A | 1 | a0001c0001t0004g0039 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1033-1451G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987212 | ||||||
| chr12:116987235
|
G | A | 158 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1033-1428G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987235 | ||||||
| chr12:116987267
|
A | G | 160 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1033-1396A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987267 | ||||||
| chr12:116987349
|
T | G | 11 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(8): Show | 11 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1033-1314T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987349 | ||||||
| chr12:116987376
|
G | T | 1 | a0004c0004t0001g0250 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1033-1287G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987376 | ||||||
| chr12:116987451
|
C | G | 105 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(102): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1033-1212C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987451 | ||||||
| chr12:116987631
|
A | G | 189 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1033-1032A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987631 | ||||||
| chr12:116987645
|
A | T | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1033-1018A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987645 | ||||||
| chr12:116987692
|
TAAAC | T | 6 | a0002c0002t0002g0100a0002c0002t0002g0101a0005c0007t0007g0002others(3): Show | 7 | HG02145.hp2 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033-955_1033-952d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116987692 | |||||
| chr12:116987708
|
CAAAA | C | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1033-952_1033-949d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116987708 | |||||
| chr12:116987726
|
C | CA | 6 | a0001c0001t0003g0185a0001c0001t0003g0192a0001c0001t0003g0193others(3): Show | 6 | HG00423.hp1 HG02083.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1033-930dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116987726 | |||||
| chr12:116987733
|
A | C | 1 | a0001c0001t0001g0226 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1033-930A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987733 | ||||||
| chr12:116987761
|
A | G | 1 | a0003c0003t0010g0020 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1033-902A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987761 | ||||||
| chr12:116987864
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1033-799G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987864 | ||||||
| chr12:116987890
|
C | T | 8 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0003t0012g0013others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1033-773C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987890 | ||||||
| chr12:116987948
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1033-715A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116987948 | ||||||
| chr12:116988311
|
C | T | 18 | a0001c0001t0001g0226a0001c0001t0004g0030a0001c0001t0004g0031others(15): Show | 18 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.1033-352C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116988311 | ||||||
| chr12:116988312
|
C | G | 2 | a0004c0004t0001g0244a0004c0004t0001g0248 | 2 | NA18994.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1033-351C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116988312 | ||||||
| chr12:116988601
|
T | C | 1 | a0001c0001t0004g0039 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1033-62T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 6/10 | chr12 | 116988601 | ||||||
| chr12:116989409
|
A | G | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1239+540A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116989409 | ||||||
| chr12:116989550
|
A | G | 9 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(6): Show | 9 | HG02040.hp2 NA18954.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.1239+681A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116989550 | ||||||
| chr12:116989843
|
A | G | 3 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0208 | 3 | HG01168.hp2 HG01169.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1239+974A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116989843 | ||||||
| chr12:116989898
|
G | A | 1 | a0002c0002t0002g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1239+1029G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116989898 | ||||||
| chr12:116990052
|
T | C | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1239+1183T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990052 | ||||||
| chr12:116990180
|
C | T | 4 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(1): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239+1311C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990180 | ||||||
| chr12:116990321
|
G | A | 2 | a0004c0004t0001g0246a0004c0004t0001g0257 | 2 | HG00438.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1239+1452G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990321 | ||||||
| chr12:116990481
|
G | C | 4 | a0001c0001t0003g0050a0003c0003t0003g0166a0003c0003t0003g0186others(1): Show | 4 | HG02818.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239+1612G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990481 | ||||||
| chr12:116990613
|
CT | C | 44 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(41): Show | 44 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1239+1749delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116990613 | |||||
| chr12:116990666
|
A | G | 1 | a0003c0003t0029g0021 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1239+1797A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990666 | ||||||
| chr12:116990792
|
A | G | 8 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(5): Show | 9 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1239+1923A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990792 | ||||||
| chr12:116990997
|
C | A | 2 | a0001c0001t0003g0199a0001c0001t0003g0206 | 2 | NA18747.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1239+2128C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116990997 | ||||||
| chr12:116991035
|
G | A | 7 | a0003c0003t0010g0016a0003c0003t0010g0017a0003c0003t0010g0019others(4): Show | 7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+2166G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116991035 | ||||||
| chr12:116991161
|
CAT | C | 7 | a0001c0001t0001g0164a0001c0001t0001g0209a0001c0001t0001g0252others(4): Show | 7 | HG01192.hp1 HG01433.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+2293_1239+229 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116991161 | ||||||
| chr12:116991273
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1239+2404A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116991273 | ||||||
| chr12:116991490
|
G | A | 1 | a0004c0004t0001g0269 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1239+2621G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116991490 | ||||||
| chr12:116991936
|
T | A | 1 | a0003c0020t0020g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1239+3067T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116991936 | ||||||
| chr12:116991994
|
A | T | 1 | a0001c0001t0003g0155 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1239+3125A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116991994 | ||||||
| chr12:116992163
|
C | T | 3 | a0001c0001t0004g0032a0001c0001t0004g0033a0001c0001t0004g0034 | 3 | HG03491.hp2 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1239+3294C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992163 | ||||||
| chr12:116992262
|
A | T | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1239+3393A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992262 | ||||||
| chr12:116992399
|
CT | C | 35 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(32): Show | 37 | HG00741.hp1 HG01106.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1239+3540delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992399 | |||||
| chr12:116992418
|
G | C | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239+3549G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992418 | ||||||
| chr12:116992420
|
G | GT | 25 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(22): Show | 27 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1239+3555dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992420 | |||||
| chr12:116992425
|
G | GT | 25 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(22): Show | 25 | HG00140.hp2 HG00423.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1239+3566dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992425 | |||||
| chr12:116992425
|
G | GTT | 12 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(9): Show | 12 | HG01433.hp2 HG02027.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.1239+3565_1239+356 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992425 | |||||
| chr12:116992425
|
G | T | 35 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(32): Show | 37 | HG00741.hp1 HG01106.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1239+3556G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992425 | ||||||
| chr12:116992441
|
G | A | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.1239+3572G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992441 | ||||||
| chr12:116992595
|
C | G | 1 | a0007c0012t0018g0005 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1239+3726C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992595 | ||||||
| chr12:116992761
|
G | GGT | 29 | a0001c0001t0001g0156a0001c0001t0001g0220a0001c0001t0001g0221others(26): Show | 30 | HG00323.hp2 HG01175.hp2 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.1239+3927_1239+392 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | |||||
| chr12:116992761
|
G | GGTGT | 45 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0001g0177others(42): Show | 45 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1239+3925_1239+392 others(8): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | |||||
| chr12:116992761
|
G | GGTGTGT | 91 | a0001c0001t0001g0045a0001c0001t0001g0158a0001c0001t0001g0164others(88): Show | 94 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1239+3923_1239+392 others(10): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | |||||
| chr12:116992761
|
G | GGTGTGTG others(1): Show |
29 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0210others(26): Show | 29 | HG00642.hp1 HG01106.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.1239+3921_1239+392 others(12): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | |||||
| chr12:116992761
|
G | GGTGTGTG others(3): Show |
16 | a0001c0001t0001g0216a0001c0001t0001g0229a0001c0001t0001g0241others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.1239+3919_1239+392 others(14): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | |||||
| chr12:116992761
|
G | GGTGTGTG others(5): Show |
3 | a0001c0001t0001g0262a0001c0001t0003g0163a0002c0008t0002g0068 | 3 | HG02148.hp1 HG02293.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1239+3917_1239+392 others(16): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | |||||
| chr12:116992761
|
GGT | G | 41 | a0002c0002t0002g0054a0002c0002t0002g0055a0002c0002t0002g0073others(38): Show | 41 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.1239+3927_1239+392 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | |||||
| chr12:116992761
|
GGTGTGTG others(9): Show |
G | 3 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010 | 3 | HG02615.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1239+3913_1239+392 others(20): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116992761 | |||||
| chr12:116992867
|
T | A | 1 | a0003c0020t0020g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1239+3998T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116992867 | ||||||
| chr12:116993044
|
A | G | 139 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(136): Show | 139 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1239+4175A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993044 | ||||||
| chr12:116993098
|
C | CT | 154 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0160others(151): Show | 155 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1239+4252dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116993098 | |||||
| chr12:116993098
|
C | CTT | 25 | a0001c0001t0001g0158a0001c0001t0001g0169a0001c0001t0001g0173others(22): Show | 25 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.1239+4251_1239+425 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116993098 | |||||
| chr12:116993129
|
C | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0252a0001c0001t0001g0256others(1): Show | 4 | HG01192.hp1 HG01433.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239+4260C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993129 | ||||||
| chr12:116993208
|
G | A | 25 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(22): Show | 26 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1239+4339G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993208 | ||||||
| chr12:116993276
|
G | A | 2 | a0002c0002t0002g0055a0002c0002t0027g0133 | 2 | HG01975.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1239+4407G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993276 | ||||||
| chr12:116993392
|
G | A | 5 | a0003c0005t0002g0059a0003c0005t0002g0060a0003c0005t0002g0061others(2): Show | 5 | HG02257.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1239+4523G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993392 | ||||||
| chr12:116993398
|
G | A | 25 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(22): Show | 26 | HG01175.hp1 HG01192.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1239+4529G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993398 | ||||||
| chr12:116993657
|
A | G | 2 | a0001c0001t0001g0272a0001c0001t0001g0274 | 2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1239+4788A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993657 | ||||||
| chr12:116993664
|
G | C | 1 | a0004c0004t0001g0183 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1239+4795G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993664 | ||||||
| chr12:116993799
|
C | T | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1239+4930C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993799 | ||||||
| chr12:116993898
|
T | G | 39 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(36): Show | 39 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.1239+5029T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993898 | ||||||
| chr12:116993955
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1239+5086A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116993955 | ||||||
| chr12:116994199
|
A | G | 235 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(232): Show | 237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.1239+5330A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994199 | ||||||
| chr12:116994220
|
GGTACTGG others(7): Show |
G | 1 | a0001c0001t0003g0189 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1239+5369_1239+538 others(18): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116994220 | |||||
| chr12:116994312
|
A | C | 4 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(1): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239+5443A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994312 | ||||||
| chr12:116994429
|
G | A | 264 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(261): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.1239+5560G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994429 | ||||||
| chr12:116994457
|
G | C | 1 | a0003c0020t0020g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1239+5588G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994457 | ||||||
| chr12:116994562
|
T | C | 1 | a0003c0003t0006g0151 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1239+5693T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994562 | ||||||
| chr12:116994707
|
T | C | 2 | a0003c0003t0010g0019a0011c0018t0002g0018 | 2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1239+5838T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994707 | ||||||
| chr12:116994802
|
T | G | 1 | a0002c0002t0002g0076 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1239+5933T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994802 | ||||||
| chr12:116994822
|
T | TTG | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1239+5955_1239+595 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116994822 | |||||
| chr12:116994873
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1239+6004A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994873 | ||||||
| chr12:116994922
|
A | G | 1 | a0002c0002t0002g0128 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1239+6053A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116994922 | ||||||
| chr12:116995003
|
T | G | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1239+6134T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116995003 | ||||||
| chr12:116995292
|
C | T | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1239+6423C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116995292 | ||||||
| chr12:116995471
|
T | G | 1 | a0005c0007t0002g0026 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1239+6602T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116995471 | ||||||
| chr12:116995854
|
G | A | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0282others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239+6985G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116995854 | ||||||
| chr12:116996004
|
G | A | 23 | a0002c0002t0001g0139a0002c0002t0002g0073a0002c0002t0002g0108others(20): Show | 23 | HG00408.hp2 HG00621.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1239+7135G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996004 | ||||||
| chr12:116996008
|
G | A | 1 | a0002c0002t0002g0145 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1239+7139G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996008 | ||||||
| chr12:116996106
|
A | G | 1 | a0004c0004t0001g0183 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1239+7237A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996106 | ||||||
| chr12:116996308
|
G | A | 2 | a0003c0003t0006g0006a0003c0003t0006g0008 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1239+7439G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996308 | ||||||
| chr12:116996340
|
C | T | 30 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(27): Show | 30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1239+7471C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996340 | ||||||
| chr12:116996407
|
A | T | 189 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1239+7538A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996407 | ||||||
| chr12:116996497
|
T | A | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1239+7628T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996497 | ||||||
| chr12:116996501
|
AGT | A | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239+7633_1239+763 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996501 | ||||||
| chr12:116996512
|
C | CA | 160 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1239+7653dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116996512 | |||||
| chr12:116996527
|
G | A | 1 | a0001c0001t0004g0036 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1239+7658G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996527 | ||||||
| chr12:116996589
|
A | T | 1 | a0003c0003t0006g0010 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1239+7720A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996589 | ||||||
| chr12:116996784
|
G | A | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1239+7915G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996784 | ||||||
| chr12:116996906
|
C | T | 1 | a0001c0001t0004g0037 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1239+8037C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116996906 | ||||||
| chr12:116997211
|
T | C | 241 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(238): Show | 243 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.1239+8342T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997211 | ||||||
| chr12:116997268
|
A | C | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1239+8399A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997268 | ||||||
| chr12:116997303
|
C | G | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1239+8434C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997303 | ||||||
| chr12:116997307
|
G | A | 1 | a0002c0002t0030g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1239+8438G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997307 | ||||||
| chr12:116997504
|
G | A | 1 | a0002c0002t0005g0098 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1239+8635G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997504 | ||||||
| chr12:116997566
|
C | T | 160 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1239+8697C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997566 | ||||||
| chr12:116997670
|
C | T | 2 | a0006c0010t0013g0103a0006c0010t0013g0104 | 2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1239+8801C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997670 | ||||||
| chr12:116997877
|
G | A | 5 | a0003c0005t0002g0059a0003c0005t0002g0060a0003c0005t0002g0061others(2): Show | 5 | HG02257.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1239+9008G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997877 | ||||||
| chr12:116997959
|
G | T | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1239+9090G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997959 | ||||||
| chr12:116997961
|
G | A | 1 | a0003c0005t0002g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1239+9092G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997961 | ||||||
| chr12:116997964
|
T | C | 27 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(24): Show | 29 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1239+9095T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116997964 | ||||||
| chr12:116998074
|
C | G | 5 | a0001c0001t0001g0219a0001c0001t0001g0224a0001c0001t0001g0226others(2): Show | 5 | HG02132.hp2 NA18964.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1239+9205C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998074 | ||||||
| chr12:116998164
|
G | C | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1239+9295G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998164 | ||||||
| chr12:116998194
|
G | C | 181 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(178): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.1239+9325G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998194 | ||||||
| chr12:116998380
|
C | CT | 160 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1239+9512dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116998380 | |||||
| chr12:116998581
|
C | G | 1 | a0002c0002t0002g0115 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1239+9712C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998581 | ||||||
| chr12:116998721
|
TC | T | 139 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(136): Show | 139 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1239+9854delC | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116998721 | |||||
| chr12:116998780
|
A | G | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239+9911A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998780 | ||||||
| chr12:116998880
|
C | G | 1 | a0002c0002t0002g0122 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1239+10011C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998880 | ||||||
| chr12:116998906
|
C | T | 1 | a0001c0001t0003g0199 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1239+10037C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116998906 | ||||||
| chr12:116999056
|
C | T | 272 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(269): Show | 277 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.1239+10187C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999056 | ||||||
| chr12:116999067
|
A | G | 160 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1239+10198A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999067 | ||||||
| chr12:116999085
|
C | T | 7 | a0003c0003t0010g0016a0003c0003t0010g0017a0003c0003t0010g0019others(4): Show | 7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+10216C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999085 | ||||||
| chr12:116999204
|
C | G | 1 | a0001c0001t0001g0285 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1239+10335C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999204 | ||||||
| chr12:116999361
|
A | G | 8 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0003t0012g0013others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1239+10492A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999361 | ||||||
| chr12:116999531
|
C | T | 1 | a0002c0002t0005g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1239+10662C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999531 | ||||||
| chr12:116999566
|
C | T | 1 | a0003c0020t0020g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1239+10697C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999566 | ||||||
| chr12:116999583
|
G | A | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239+10714G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999583 | ||||||
| chr12:116999613
|
C | T | 2 | a0001c0009t0001g0237a0001c0009t0001g0275 | 2 | HG02698.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1240-10710C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999613 | ||||||
| chr12:116999624
|
CT | C | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-10697delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116999624 | |||||
| chr12:116999646
|
G | A | 160 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1240-10677G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999646 | ||||||
| chr12:116999672
|
G | C | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1240-10651G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 116999672 | ||||||
| chr12:116999981
|
A | AT | 157 | a0001c0001t0001g0045a0001c0001t0001g0158a0001c0001t0001g0160others(154): Show | 158 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1240-10322dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116999981 | |||||
| chr12:116999981
|
A | ATT | 8 | a0001c0001t0001g0182a0001c0001t0001g0226a0001c0001t0031g0046others(5): Show | 8 | HG00438.hp1 HG01261.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240-10323_1240-10 others(8): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116999981 | |||||
| chr12:117000008
|
G | A | 1 | a0001c0001t0003g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1240-10315G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000008 | ||||||
| chr12:117000015
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1240-10308G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000015 | ||||||
| chr12:117000045
|
G | A | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-10278G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000045 | ||||||
| chr12:117000054
|
T | C | 16 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(13): Show | 17 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1240-10269T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000054 | ||||||
| chr12:117000255
|
C | T | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-10068C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000255 | ||||||
| chr12:117000327
|
T | C | 8 | a0001c0001t0004g0031a0001c0001t0004g0036a0001c0001t0004g0037others(5): Show | 8 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240-9996T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000327 | ||||||
| chr12:117000358
|
C | T | 100 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(97): Show | 100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1240-9965C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000358 | ||||||
| chr12:117000501
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1240-9822C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000501 | ||||||
| chr12:117000518
|
C | T | 2 | a0001c0001t0003g0185a0001c0001t0003g0223 | 2 | NA19055.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1240-9805C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000518 | ||||||
| chr12:117000519
|
G | C | 5 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0001t0001g0179others(2): Show | 5 | HG02258.hp1 HG03491.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240-9804G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000519 | ||||||
| chr12:117000531
|
C | G | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-9792C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000531 | ||||||
| chr12:117000717
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1240-9606G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000717 | ||||||
| chr12:117000833
|
A | G | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-9490A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000833 | ||||||
| chr12:117000893
|
A | G | 1 | a0001c0001t0003g0184 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1240-9430A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117000893 | ||||||
| chr12:117001134
|
T | C | 160 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1240-9189T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001134 | ||||||
| chr12:117001342
|
GCTGCCTG others(1): Show |
G | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240-8975_1240-896 others(12): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 117001342 | |||||
| chr12:117001360
|
T | G | 1 | a0001c0001t0004g0040 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1240-8963T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001360 | ||||||
| chr12:117001376
|
C | G | 1 | a0001c0001t0003g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240-8947C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001376 | ||||||
| chr12:117001410
|
G | C | 2 | a0001c0001t0003g0056a0008c0016t0003g0029 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1240-8913G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001410 | ||||||
| chr12:117001611
|
A | T | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-8712A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001611 | ||||||
| chr12:117001649
|
G | A | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-8674G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001649 | ||||||
| chr12:117001767
|
G | A | 1 | a0002c0008t0002g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1240-8556G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001767 | ||||||
| chr12:117001903
|
C | A | 1 | a0001c0001t0001g0176 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1240-8420C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001903 | ||||||
| chr12:117001974
|
G | A | 2 | a0002c0002t0002g0108a0002c0002t0002g0144 | 2 | NA18953.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1240-8349G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117001974 | ||||||
| chr12:117002315
|
C | T | 3 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010 | 3 | HG02615.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1240-8008C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002315 | ||||||
| chr12:117002415
|
G | A | 45 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(42): Show | 46 | HG00323.hp1 HG00642.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.1240-7908G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002415 | ||||||
| chr12:117002468
|
T | G | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1240-7855T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002468 | ||||||
| chr12:117002598
|
C | G | 6 | a0002c0002t0011g0080a0002c0002t0011g0140a0003c0003t0011g0011others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240-7725C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002598 | ||||||
| chr12:117002603
|
G | A | 30 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(27): Show | 30 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1240-7720G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002603 | ||||||
| chr12:117002631
|
T | G | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-7692T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002631 | ||||||
| chr12:117002742
|
A | T | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-7581A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002742 | ||||||
| chr12:117002828
|
T | C | 282 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0158others(279): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1240-7495T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002828 | ||||||
| chr12:117002877
|
C | T | 1 | a0002c0008t0002g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1240-7446C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002877 | ||||||
| chr12:117002898
|
G | A | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-7425G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117002898 | ||||||
| chr12:117003153
|
T | C | 4 | a0002c0008t0002g0067a0002c0008t0002g0068a0002c0008t0002g0069others(1): Show | 4 | HG01261.hp1 HG02148.hp1 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-7170T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117003153 | ||||||
| chr12:117003218
|
C | T | 2 | a0006c0010t0013g0103a0006c0010t0013g0104 | 2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1240-7105C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117003218 | ||||||
| chr12:117003364
|
C | T | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.1240-6959C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117003364 | ||||||
| chr12:117003367
|
A | T | 45 | a0002c0002t0001g0139a0002c0002t0002g0054a0002c0002t0002g0055others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1240-6956A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117003367 | ||||||
| chr12:117003484
|
A | ATTG | 126 | a0002c0002t0001g0139a0002c0002t0002g0003a0002c0002t0002g0047others(123): Show | 131 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1240-6836_1240-683 others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 117003484 | |||||
| chr12:117003538
|
T | C | 7 | a0001c0001t0001g0272a0001c0001t0001g0274a0001c0001t0001g0279others(4): Show | 7 | HG01109.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240-6785T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117003538 | ||||||
| chr12:117003668
|
C | G | 1 | a0002c0002t0005g0098 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1240-6655C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117003668 | ||||||
| chr12:117004012
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1240-6311T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004012 | ||||||
| chr12:117004189
|
T | C | 3 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010 | 3 | HG02615.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1240-6134T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004189 | ||||||
| chr12:117004367
|
T | C | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-5956T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004367 | ||||||
| chr12:117004402
|
T | C | 1 | a0002c0002t0002g0138 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1240-5921T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004402 | ||||||
| chr12:117004499
|
G | A | 45 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(42): Show | 46 | HG00323.hp1 HG00642.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.1240-5824G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004499 | ||||||
| chr12:117004767
|
GTCTCCTG others(10): Show |
G | 184 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(181): Show | 189 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1240-5533_1240-551 others(21): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 117004767 | |||||
| chr12:117004774
|
G | A | 24 | a0001c0001t0001g0169a0001c0001t0001g0173a0001c0001t0001g0176others(21): Show | 24 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.1240-5549G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004774 | ||||||
| chr12:117004831
|
T | C | 184 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(181): Show | 189 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1240-5492T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004831 | ||||||
| chr12:117004900
|
A | G | 1 | a0002c0002t0008g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1240-5423A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117004900 | ||||||
| chr12:117005016
|
G | T | 2 | a0002c0002t0009g0141a0002c0002t0009g0143 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1240-5307G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005016 | ||||||
| chr12:117005097
|
A | G | 49 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(46): Show | 52 | HG00323.hp1 HG00642.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.1240-5226A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005097 | ||||||
| chr12:117005203
|
G | A | 2 | a0001c0001t0003g0201a0001c0001t0003g0205 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1240-5120G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005203 | ||||||
| chr12:117005277
|
C | T | 6 | a0005c0007t0002g0026a0005c0007t0007g0002a0005c0007t0007g0023others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240-5046C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005277 | ||||||
| chr12:117005329
|
C | T | 4 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(1): Show | 4 | HG00423.hp1 HG02083.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240-4994C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005329 | ||||||
| chr12:117005754
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1240-4569C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005754 | ||||||
| chr12:117005786
|
C | T | 143 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(140): Show | 148 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1240-4537C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005786 | ||||||
| chr12:117005945
|
C | T | 1 | a0002c0002t0008g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1240-4378C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005945 | ||||||
| chr12:117005965
|
C | G | 6 | a0001c0001t0001g0158a0001c0001t0001g0218a0001c0001t0001g0220others(3): Show | 6 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240-4358C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117005965 | ||||||
| chr12:117006039
|
T | C | 2 | a0002c0002t0005g0065a0002c0002t0005g0097 | 2 | HG01256.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1240-4284T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006039 | ||||||
| chr12:117006232
|
T | C | 3 | a0002c0002t0002g0003a0002c0002t0002g0086a0002c0002t0002g0088 | 4 | HG02109.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-4091T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006232 | ||||||
| chr12:117006295
|
A | G | 2 | a0001c0001t0003g0056a0008c0016t0003g0029 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1240-4028A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006295 | ||||||
| chr12:117006385
|
T | C | 1 | a0003c0003t0010g0020 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1240-3938T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006385 | ||||||
| chr12:117006442
|
C | T | 4 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(1): Show | 4 | HG02615.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-3881C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006442 | ||||||
| chr12:117006519
|
C | T | 1 | a0003c0003t0021g0009 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1240-3804C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006519 | ||||||
| chr12:117006544
|
G | A | 1 | a0002c0002t0008g0070 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1240-3779G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006544 | ||||||
| chr12:117006662
|
G | A | 3 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0278 | 3 | NA18969.hp1 NA18975.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1240-3661G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006662 | ||||||
| chr12:117006731
|
A | G | 11 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(8): Show | 12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1240-3592A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006731 | ||||||
| chr12:117006980
|
T | C | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1240-3343T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117006980 | ||||||
| chr12:117007154
|
C | G | 1 | a0001c0001t0003g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240-3169C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007154 | ||||||
| chr12:117007174
|
T | C | 2 | a0002c0002t0009g0141a0002c0002t0009g0143 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1240-3149T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007174 | ||||||
| chr12:117007240
|
G | T | 14 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(11): Show | 15 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240-3083G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007240 | ||||||
| chr12:117007252
|
G | T | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.1240-3071G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007252 | ||||||
| chr12:117007261
|
GA | G | 21 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(18): Show | 22 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1240-3051delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 117007261 | |||||
| chr12:117007377
|
C | A | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-2946C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007377 | ||||||
| chr12:117007525
|
A | G | 1 | a0002c0002t0002g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1240-2798A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007525 | ||||||
| chr12:117007725
|
A | G | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-2598A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007725 | ||||||
| chr12:117007753
|
A | G | 1 | a0003c0005t0002g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1240-2570A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007753 | ||||||
| chr12:117007784
|
A | C | 1 | a0001c0001t0001g0255 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1240-2539A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007784 | ||||||
| chr12:117007832
|
G | A | 43 | a0002c0002t0002g0054a0002c0002t0002g0055a0002c0002t0002g0073others(40): Show | 43 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.1240-2491G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007832 | ||||||
| chr12:117007867
|
C | G | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1240-2456C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007867 | ||||||
| chr12:117007874
|
C | A | 2 | a0003c0003t0010g0016a0003c0003t0010g0017 | 2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1240-2449C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117007874 | ||||||
| chr12:117008173
|
C | T | 1 | a0001c0006t0001g0260 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1240-2150C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117008173 | ||||||
| chr12:117008758
|
CAT | C | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240-1564_1240-156 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117008758 | ||||||
| chr12:117008829
|
G | T | 1 | a0003c0005t0002g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1240-1494G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117008829 | ||||||
| chr12:117008959
|
C | G | 1 | a0003c0020t0020g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1240-1364C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117008959 | ||||||
| chr12:117009021
|
C | T | 1 | a0002c0002t0002g0117 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1240-1302C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009021 | ||||||
| chr12:117009207
|
A | C | 4 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010others(1): Show | 4 | HG02615.hp1 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-1116A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009207 | ||||||
| chr12:117009286
|
G | A | 1 | a0001c0001t0032g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1240-1037G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009286 | ||||||
| chr12:117009395
|
A | G | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1240-928A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009395 | ||||||
| chr12:117009502
|
G | C | 2 | a0001c0001t0003g0056a0008c0016t0003g0029 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1240-821G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009502 | ||||||
| chr12:117009606
|
GTTGAA | G | 6 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(3): Show | 6 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240-709_1240-705d others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 117009606 | |||||
| chr12:117009695
|
T | C | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240-628T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009695 | ||||||
| chr12:117009739
|
A | G | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240-584A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009739 | ||||||
| chr12:117009852
|
A | C | 1 | a0003c0003t0006g0008 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1240-471A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117009852 | ||||||
| chr12:117010092
|
A | G | 10 | a0002c0002t0011g0080a0002c0002t0011g0140a0003c0003t0011g0011others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240-231A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 7/10 | chr12 | 117010092 | ||||||
| chr12:117010667
|
G | C | 2 | a0004c0004t0001g0244a0004c0004t0001g0248 | 2 | NA18994.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1367+217G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117010667 | ||||||
| chr12:117010698
|
G | A | 24 | a0002c0002t0002g0073a0002c0002t0002g0075a0002c0002t0002g0108others(21): Show | 24 | HG00408.hp2 HG00621.hp2 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1367+248G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117010698 | ||||||
| chr12:117010756
|
ATTTG | A | 5 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0001t0001g0179others(2): Show | 5 | HG02258.hp1 HG03491.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+311_1367+314d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117010756 | |||||
| chr12:117010843
|
C | T | 1 | a0002c0002t0002g0124 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1367+393C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117010843 | ||||||
| chr12:117010983
|
C | T | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+533C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117010983 | ||||||
| chr12:117010993
|
C | T | 10 | a0002c0002t0005g0065a0002c0002t0005g0089a0002c0002t0005g0097others(7): Show | 10 | HG00323.hp1 HG00642.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1367+543C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117010993 | ||||||
| chr12:117011017
|
C | T | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1367+567C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011017 | ||||||
| chr12:117011031
|
A | T | 6 | a0002c0002t0011g0080a0002c0002t0011g0140a0003c0003t0011g0011others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367+581A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011031 | ||||||
| chr12:117011127
|
C | CTTTTT | 43 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(40): Show | 44 | HG00544.hp1 HG00741.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.1367+688_1367+692d others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117011127 | |||||
| chr12:117011127
|
C | CTTTTTT | 35 | a0001c0001t0003g0155a0001c0001t0003g0157a0001c0001t0003g0163others(32): Show | 35 | HG00140.hp2 HG00423.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1367+687_1367+692d others(8): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117011127 | |||||
| chr12:117011127
|
C | CTTTTTTT | 53 | a0001c0001t0003g0198a0002c0002t0002g0003a0002c0002t0002g0047others(50): Show | 57 | HG00323.hp1 HG00642.hp2 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.1367+686_1367+692d others(9): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117011127 | |||||
| chr12:117011127
|
C | CTTTTTTT others(1): Show |
42 | a0002c0002t0002g0055a0002c0002t0002g0073a0002c0002t0002g0074others(39): Show | 42 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1367+685_1367+692d others(10): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117011127 | |||||
| chr12:117011148
|
G | A | 2 | a0006c0010t0013g0103a0006c0010t0013g0104 | 2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1367+698G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011148 | ||||||
| chr12:117011240
|
G | A | 1 | a0002c0002t0002g0117 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1367+790G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011240 | ||||||
| chr12:117011280
|
C | T | 5 | a0002c0002t0002g0003a0002c0002t0002g0086a0002c0002t0002g0087others(2): Show | 6 | HG01175.hp1 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1367+830C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011280 | ||||||
| chr12:117011358
|
G | A | 3 | a0002c0002t0002g0090a0002c0002t0002g0093a0002c0002t0002g0126 | 3 | HG01192.hp2 HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1367+908G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011358 | ||||||
| chr12:117011375
|
C | A | 182 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(179): Show | 187 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.1367+925C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011375 | ||||||
| chr12:117011406
|
C | G | 17 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(14): Show | 17 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.1367+956C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011406 | ||||||
| chr12:117011449
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1367+999A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011449 | ||||||
| chr12:117011472
|
G | A | 3 | a0001c0009t0001g0237a0001c0009t0001g0275a0001c0009t0001g0281 | 3 | HG02698.hp1 HG03942.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1367+1022G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011472 | ||||||
| chr12:117011514
|
G | C | 1 | a0002c0002t0005g0098 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1367+1064G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011514 | ||||||
| chr12:117011555
|
C | T | 2 | a0001c0001t0003g0056a0008c0016t0003g0029 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1367+1105C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011555 | ||||||
| chr12:117011594
|
A | G | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+1144A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011594 | ||||||
| chr12:117011659
|
T | G | 1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1367+1209T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011659 | ||||||
| chr12:117011664
|
T | C | 1 | a0001c0001t0004g0030 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1367+1214T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011664 | ||||||
| chr12:117011876
|
T | C | 1 | a0012c0014t0023g0077 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1367+1426T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011876 | ||||||
| chr12:117011925
|
C | A | 1 | a0001c0001t0001g0231 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1367+1475C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011925 | ||||||
| chr12:117011947
|
G | A | 1 | a0001c0001t0003g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1367+1497G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117011947 | ||||||
| chr12:117012190
|
C | CTCATT | 87 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(84): Show | 90 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1367+1740_1367+174 others(9): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012190 | ||||||
| chr12:117012192
|
G | T | 87 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(84): Show | 90 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1367+1742G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012192 | ||||||
| chr12:117012194
|
G | T | 87 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(84): Show | 90 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1367+1744G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012194 | ||||||
| chr12:117012196
|
G | C | 87 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(84): Show | 90 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1367+1746G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012196 | ||||||
| chr12:117012197
|
G | GCACTA | 87 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(84): Show | 90 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1367+1747_1367+174 others(9): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012197 | ||||||
| chr12:117012236
|
T | A | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1367+1786T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012236 | ||||||
| chr12:117012298
|
T | A | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+1848T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012298 | ||||||
| chr12:117012375
|
T | C | 1 | a0001c0001t0003g0194 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1367+1925T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012375 | ||||||
| chr12:117012683
|
A | T | 114 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(111): Show | 119 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1367+2233A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012683 | ||||||
| chr12:117012803
|
A | G | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+2353A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012803 | ||||||
| chr12:117012959
|
G | T | 2 | a0003c0003t0010g0019a0011c0018t0002g0018 | 2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1367+2509G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117012959 | ||||||
| chr12:117013025
|
G | A | 1 | a0002c0002t0002g0054 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1367+2575G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013025 | ||||||
| chr12:117013110
|
A | G | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+2660A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013110 | ||||||
| chr12:117013137
|
G | T | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1367+2687G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013137 | ||||||
| chr12:117013235
|
CCAT | C | 141 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(138): Show | 146 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1367+2790_1367+279 others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117013235 | |||||
| chr12:117013343
|
C | T | 1 | a0001c0006t0001g0181 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1367+2893C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013343 | ||||||
| chr12:117013375
|
G | A | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+2925G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013375 | ||||||
| chr12:117013411
|
A | G | 1 | a0001c0001t0003g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1367+2961A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013411 | ||||||
| chr12:117013440
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1367+2990A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013440 | ||||||
| chr12:117013508
|
G | A | 1 | a0009c0015t0003g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1367+3058G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013508 | ||||||
| chr12:117013610
|
T | A | 2 | a0003c0003t0010g0016a0003c0003t0010g0017 | 2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1367+3160T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013610 | ||||||
| chr12:117013624
|
A | T | 4 | a0001c0001t0003g0189a0003c0003t0003g0166a0003c0003t0003g0186others(1): Show | 4 | HG02976.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+3174A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013624 | ||||||
| chr12:117013625
|
T | A | 1 | a0001c0001t0003g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1367+3175T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013625 | ||||||
| chr12:117013736
|
T | TTTTA | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+3306_1367+330 others(8): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117013736 | |||||
| chr12:117013790
|
A | G | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1367+3340A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117013790 | ||||||
| chr12:117014098
|
C | T | 1 | a0002c0002t0002g0131 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1367+3648C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014098 | ||||||
| chr12:117014146
|
G | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0225a0002c0002t0001g0139 | 3 | HG00621.hp1 HG02071.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1367+3696G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014146 | ||||||
| chr12:117014263
|
T | TA | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1367+3818dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117014263 | |||||
| chr12:117014339
|
T | C | 1 | a0003c0003t0006g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1367+3889T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014339 | ||||||
| chr12:117014344
|
T | A | 4 | a0003c0003t0006g0004a0003c0003t0006g0151a0003c0003t0006g0152others(1): Show | 5 | HG02723.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+3894T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014344 | ||||||
| chr12:117014361
|
G | A | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+3911G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014361 | ||||||
| chr12:117014471
|
C | T | 16 | a0001c0001t0001g0264a0003c0003t0006g0004a0003c0003t0006g0006others(13): Show | 17 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1367+4021C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014471 | ||||||
| chr12:117014472
|
G | A | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+4022G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014472 | ||||||
| chr12:117014538
|
G | A | 1 | a0001c0001t0003g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1367+4088G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014538 | ||||||
| chr12:117014634
|
C | T | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+4184C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014634 | ||||||
| chr12:117014644
|
T | G | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1367+4194T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014644 | ||||||
| chr12:117014649
|
A | C | 2 | a0003c0003t0011g0011a0003c0003t0011g0012 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1367+4199A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014649 | ||||||
| chr12:117014655
|
T | G | 2 | a0003c0003t0011g0011a0003c0003t0011g0012 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1367+4205T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014655 | ||||||
| chr12:117014724
|
G | A | 4 | a0001c0001t0001g0218a0001c0001t0001g0220a0001c0001t0001g0221others(1): Show | 4 | HG00323.hp2 HG01074.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+4274G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014724 | ||||||
| chr12:117014735
|
A | G | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+4285A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014735 | ||||||
| chr12:117014778
|
T | A | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4328T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014778 | ||||||
| chr12:117014780
|
G | T | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4330G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014780 | ||||||
| chr12:117014782
|
C | A | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4332C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014782 | ||||||
| chr12:117014782
|
C | T | 9 | a0002c0002t0002g0003a0002c0002t0002g0086a0002c0002t0002g0087others(6): Show | 10 | HG00642.hp2 HG01175.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1367+4332C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014782 | ||||||
| chr12:117014792
|
T | A | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4342T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014792 | ||||||
| chr12:117014794
|
A | G | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4344A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014794 | ||||||
| chr12:117014814
|
GGGATGAG others(44): Show |
G | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4365_1367+441 others(55): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014814 | ||||||
| chr12:117014892
|
T | A | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4442T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014892 | ||||||
| chr12:117014898
|
T | A | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4448T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014898 | ||||||
| chr12:117014901
|
C | T | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4451C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014901 | ||||||
| chr12:117014907
|
T | A | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4457T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014907 | ||||||
| chr12:117014919
|
T | C | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4469T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014919 | ||||||
| chr12:117014922
|
C | G | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4472C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014922 | ||||||
| chr12:117014927
|
A | T | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4477A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014927 | ||||||
| chr12:117014928
|
C | G | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4478C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014928 | ||||||
| chr12:117014930
|
G | A | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4480G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014930 | ||||||
| chr12:117014936
|
T | C | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4486T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014936 | ||||||
| chr12:117014937
|
G | T | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4487G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014937 | ||||||
| chr12:117014938
|
G | C | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4488G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014938 | ||||||
| chr12:117014942
|
G | C | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4492G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014942 | ||||||
| chr12:117014944
|
A | ATCTCACT others(3): Show |
1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4494_1367+449 others(14): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014944 | ||||||
| chr12:117014947
|
A | T | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4497A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014947 | ||||||
| chr12:117014948
|
T | C | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4498T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014948 | ||||||
| chr12:117014949
|
G | A | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4499G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014949 | ||||||
| chr12:117014953
|
T | C | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4503T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014953 | ||||||
| chr12:117014955
|
T | C | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4505T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014955 | ||||||
| chr12:117014959
|
T | C | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4509T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014959 | ||||||
| chr12:117014960
|
C | T | 3 | a0003c0003t0010g0020a0003c0003t0010g0022a0003c0003t0029g0021 | 3 | HG00741.hp1 HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1367+4510C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014960 | ||||||
| chr12:117014961
|
A | C | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4511A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014961 | ||||||
| chr12:117014980
|
T | A | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1367+4530T>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014980 | ||||||
| chr12:117014985
|
G | A | 1 | a0009c0015t0003g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1367+4535G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117014985 | ||||||
| chr12:117015090
|
C | T | 1 | a0002c0002t0030g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1367+4640C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015090 | ||||||
| chr12:117015117
|
A | G | 44 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(41): Show | 47 | HG00323.hp1 HG00642.hp2 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.1367+4667A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015117 | ||||||
| chr12:117015417
|
A | G | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+4967A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015417 | ||||||
| chr12:117015494
|
G | C | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+5044G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015494 | ||||||
| chr12:117015726
|
T | C | 1 | a0003c0020t0020g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1367+5276T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015726 | ||||||
| chr12:117015752
|
TC | T | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+5304delC | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117015752 | |||||
| chr12:117015777
|
A | G | 2 | a0001c0001t0004g0036a0001c0001t0004g0043 | 2 | NA18947.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1367+5327A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015777 | ||||||
| chr12:117015778
|
C | T | 1 | a0001c0001t0003g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1367+5328C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015778 | ||||||
| chr12:117015788
|
T | G | 8 | a0002c0002t0002g0003a0002c0002t0002g0086a0002c0002t0002g0087others(5): Show | 9 | HG01175.hp1 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1367+5338T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117015788 | ||||||
| chr12:117016110
|
A | G | 1 | a0002c0002t0005g0089 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1367+5660A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117016110 | ||||||
| chr12:117016165
|
A | G | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+5715A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117016165 | ||||||
| chr12:117016336
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1367+5886C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117016336 | ||||||
| chr12:117016383
|
C | T | 2 | a0006c0010t0013g0103a0006c0010t0013g0104 | 2 | HG01074.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1367+5933C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117016383 | ||||||
| chr12:117016492
|
A | AT | 88 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(85): Show | 91 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1367+6049dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117016492 | |||||
| chr12:117016642
|
G | GT | 23 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0004g0030others(20): Show | 23 | HG00423.hp2 HG00544.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1367+6207dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117016642 | |||||
| chr12:117016642
|
GT | G | 19 | a0001c0001t0001g0169a0002c0002t0002g0090a0002c0002t0002g0093others(16): Show | 20 | HG00741.hp1 HG01192.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1367+6207delT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117016642 | |||||
| chr12:117016646
|
T | G | 1 | a0005c0007t0007g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1367+6196T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117016646 | ||||||
| chr12:117016672
|
T | C | 8 | a0001c0001t0004g0031a0001c0001t0004g0036a0001c0001t0004g0037others(5): Show | 8 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1367+6222T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117016672 | ||||||
| chr12:117017560
|
A | G | 157 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(154): Show | 162 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1368-6587A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117017560 | ||||||
| chr12:117017678
|
A | T | 3 | a0002c0002t0002g0083a0002c0002t0002g0114a0002c0002t0002g0116 | 3 | NA18950.hp1 NA18955.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1368-6469A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117017678 | ||||||
| chr12:117017987
|
C | T | 4 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-6160C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117017987 | ||||||
| chr12:117018129
|
T | C | 1 | a0001c0001t0003g0202 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1368-6018T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117018129 | ||||||
| chr12:117018303
|
A | G | 1 | a0001c0006t0001g0236 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1368-5844A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117018303 | ||||||
| chr12:117018606
|
A | AGCTT | 120 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(117): Show | 123 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1368-5541_1368-554 others(8): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117018606 | ||||||
| chr12:117018633
|
A | C | 1 | a0001c0001t0001g0219 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1368-5514A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117018633 | ||||||
| chr12:117018954
|
G | GA | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-5189dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117018954 | |||||
| chr12:117019015
|
T | C | 2 | a0002c0002t0011g0080a0002c0002t0011g0140 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1368-5132T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019015 | ||||||
| chr12:117019018
|
A | C | 145 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(142): Show | 150 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1368-5129A>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019018 | ||||||
| chr12:117019030
|
G | A | 1 | a0002c0002t0002g0096 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1368-5117G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019030 | ||||||
| chr12:117019219
|
T | G | 1 | a0001c0001t0001g0171 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1368-4928T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019219 | ||||||
| chr12:117019258
|
G | A | 1 | a0002c0002t0024g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1368-4889G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019258 | ||||||
| chr12:117019302
|
C | T | 1 | a0002c0002t0002g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1368-4845C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019302 | ||||||
| chr12:117019420
|
C | T | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1368-4727C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019420 | ||||||
| chr12:117019434
|
T | C | 1 | a0002c0002t0002g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1368-4713T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019434 | ||||||
| chr12:117019474
|
T | C | 1 | a0001c0001t0003g0189 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1368-4673T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019474 | ||||||
| chr12:117019667
|
G | T | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-4480G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019667 | ||||||
| chr12:117019698
|
C | T | 2 | a0003c0020t0020g0079a0008c0016t0003g0029 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1368-4449C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019698 | ||||||
| chr12:117019736
|
T | C | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-4411T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019736 | ||||||
| chr12:117019958
|
A | G | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-4189A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117019958 | ||||||
| chr12:117020091
|
G | A | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1368-4056G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020091 | ||||||
| chr12:117020106
|
A | G | 1 | a0002c0002t0002g0075 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1368-4041A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020106 | ||||||
| chr12:117020220
|
A | G | 1 | a0002c0002t0002g0145 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1368-3927A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020220 | ||||||
| chr12:117020289
|
C | G | 3 | a0003c0003t0003g0166a0003c0003t0003g0186a0010c0019t0003g0187 | 3 | HG03453.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1368-3858C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020289 | ||||||
| chr12:117020328
|
A | AT | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-3813dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117020328 | |||||
| chr12:117020426
|
T | C | 1 | a0003c0020t0020g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1368-3721T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020426 | ||||||
| chr12:117020451
|
C | T | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1368-3696C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020451 | ||||||
| chr12:117020456
|
G | A | 1 | a0002c0002t0005g0098 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1368-3691G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020456 | ||||||
| chr12:117020503
|
T | C | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-3644T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020503 | ||||||
| chr12:117020508
|
C | A | 1 | a0009c0015t0003g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1368-3639C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020508 | ||||||
| chr12:117020584
|
C | T | 11 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(8): Show | 12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1368-3563C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020584 | ||||||
| chr12:117020636
|
A | G | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1368-3511A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020636 | ||||||
| chr12:117020679
|
C | T | 1 | a0001c0001t0003g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1368-3468C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020679 | ||||||
| chr12:117020997
|
C | T | 17 | a0002c0002t0002g0084a0002c0002t0002g0085a0003c0003t0006g0004others(14): Show | 18 | HG00741.hp1 HG02109.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1368-3150C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020997 | ||||||
| chr12:117020999
|
G | T | 2 | a0001c0001t0004g0036a0001c0001t0004g0043 | 2 | NA18947.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1368-3148G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117020999 | ||||||
| chr12:117021054
|
G | A | 142 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(139): Show | 147 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.1368-3093G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021054 | ||||||
| chr12:117021158
|
G | C | 13 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(10): Show | 14 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1368-2989G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021158 | ||||||
| chr12:117021240
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1368-2907C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021240 | ||||||
| chr12:117021393
|
G | A | 3 | a0003c0003t0011g0011a0003c0003t0011g0012a0007c0012t0018g0005 | 3 | HG01891.hp2 HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1368-2754G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021393 | ||||||
| chr12:117021489
|
AAT | A | 3 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015 | 3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1368-2655_1368-265 others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117021489 | |||||
| chr12:117021496
|
T | C | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-2651T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021496 | ||||||
| chr12:117021581
|
ATAGAG | A | 3 | a0001c0001t0003g0049a0001c0001t0003g0051a0001c0001t0003g0052 | 3 | HG02622.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1368-2563_1368-255 others(9): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117021581 | |||||
| chr12:117021583
|
A | AGAG | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-2563_1368-256 others(7): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117021583 | |||||
| chr12:117021592
|
T | C | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-2555T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021592 | ||||||
| chr12:117021639
|
A | AT | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1368-2503dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117021639 | |||||
| chr12:117021640
|
T | C | 31 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(28): Show | 31 | HG00140.hp2 HG00423.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1368-2507T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021640 | ||||||
| chr12:117021676
|
G | A | 1 | a0001c0001t0004g0042 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1368-2471G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021676 | ||||||
| chr12:117021745
|
A | AT | 13 | a0002c0002t0002g0150a0002c0002t0008g0070a0002c0002t0008g0081others(10): Show | 14 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1368-2394dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117021745 | |||||
| chr12:117021805
|
T | C | 9 | a0002c0002t0011g0080a0002c0002t0011g0140a0003c0003t0011g0011others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1368-2342T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117021805 | ||||||
| chr12:117022003
|
C | T | 1 | a0002c0002t0001g0139 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1368-2144C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022003 | ||||||
| chr12:117022134
|
A | G | 13 | a0002c0002t0002g0150a0002c0002t0008g0070a0002c0002t0008g0081others(10): Show | 14 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1368-2013A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022134 | ||||||
| chr12:117022272
|
T | C | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1368-1875T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022272 | ||||||
| chr12:117022355
|
T | TA | 20 | a0001c0001t0003g0056a0001c0001t0004g0030a0001c0001t0004g0031others(17): Show | 20 | HG00544.hp1 HG02080.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1368-1777dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117022355 | |||||
| chr12:117022355
|
TA | T | 20 | a0001c0001t0001g0233a0002c0002t0008g0070a0002c0002t0008g0081others(17): Show | 21 | HG00741.hp1 HG01074.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1368-1777delA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117022355 | |||||
| chr12:117022357
|
A | T | 15 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(12): Show | 16 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1368-1790A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022357 | ||||||
| chr12:117022358
|
A | T | 1 | a0003c0003t0021g0009 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1368-1789A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022358 | ||||||
| chr12:117022424
|
G | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0271 | 3 | HG02818.hp1 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1368-1723G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022424 | ||||||
| chr12:117022442
|
C | T | 4 | a0002c0002t0009g0001a0002c0002t0009g0141a0002c0002t0009g0142others(1): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368-1705C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022442 | ||||||
| chr12:117022451
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1368-1696C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022451 | ||||||
| chr12:117022548
|
G | A | 16 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0032others(13): Show | 16 | HG00544.hp1 HG02080.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.1368-1599G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022548 | ||||||
| chr12:117022614
|
C | T | 1 | a0002c0002t0002g0116 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1368-1533C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022614 | ||||||
| chr12:117022656
|
T | TA | 7 | a0003c0003t0010g0016a0003c0003t0010g0017a0003c0003t0010g0019others(4): Show | 7 | HG00741.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1368-1483dupA | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117022656 | |||||
| chr12:117022998
|
C | T | 1 | a0002c0002t0002g0096 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1368-1149C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117022998 | ||||||
| chr12:117023036
|
C | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0259 | 2 | HG02040.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1368-1111C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023036 | ||||||
| chr12:117023204
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1368-943A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023204 | ||||||
| chr12:117023247
|
G | A | 1 | a0003c0021t0017g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1368-900G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023247 | ||||||
| chr12:117023279
|
C | T | 1 | a0002c0002t0005g0147 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1368-868C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023279 | ||||||
| chr12:117023545
|
T | TG | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-598dupG | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 117023545 | |||||
| chr12:117023613
|
C | T | 1 | a0001c0001t0003g0184 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1368-534C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023613 | ||||||
| chr12:117023668
|
C | T | 1 | a0002c0002t0002g0057 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1368-479C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023668 | ||||||
| chr12:117023970
|
G | A | 2 | a0003c0003t0011g0011a0003c0003t0011g0012 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1368-177G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117023970 | ||||||
| chr12:117024109
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1368-38C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117024109 | ||||||
| chr12:117024112
|
C | T | 2 | a0001c0001t0003g0192a0001c0001t0003g0207 | 2 | HG00423.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1368-35C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117024112 | ||||||
| chr12:117024133
|
C | T | 27 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(24): Show | 29 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1368-14C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 8/10 | chr12 | 117024133 | ||||||
| chr12:117024325
|
G | C | 1 | a0003c0003t0011g0011 | 1 | NA20129.hp1 | splice_region_variant&intron_variant | LOW | c.1541+5G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024325 | ||||||
| chr12:117024363
|
C | G | 3 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015 | 3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1541+43C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024363 | ||||||
| chr12:117024479
|
C | T | 1 | a0002c0002t0002g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1541+159C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024479 | ||||||
| chr12:117024718
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1541+398C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024718 | ||||||
| chr12:117024734
|
G | T | 1 | a0001c0001t0003g0193 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1541+414G>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024734 | ||||||
| chr12:117024777
|
C | T | 39 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(36): Show | 40 | HG00323.hp1 HG00642.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.1541+457C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024777 | ||||||
| chr12:117024847
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1541+527G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024847 | ||||||
| chr12:117024939
|
C | T | 2 | a0003c0003t0012g0014a0003c0003t0012g0015 | 2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1541+619C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024939 | ||||||
| chr12:117024980
|
G | A | 122 | a0001c0001t0001g0224a0002c0002t0002g0003a0002c0002t0002g0047others(119): Show | 127 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1541+660G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117024980 | ||||||
| chr12:117024986
|
C | CCTAA | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1541+669_1541+672d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117024986 | |||||
| chr12:117025128
|
G | A | 1 | a0001c0006t0001g0217 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1541+808G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025128 | ||||||
| chr12:117025130
|
G | A | 1 | a0002c0002t0008g0070 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1541+810G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025130 | ||||||
| chr12:117025146
|
G | C | 3 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015 | 3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1541+826G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025146 | ||||||
| chr12:117025251
|
G | A | 1 | a0003c0003t0021g0009 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1541+931G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025251 | ||||||
| chr12:117025354
|
G | A | 1 | a0001c0001t0003g0168 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1541+1034G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025354 | ||||||
| chr12:117025393
|
A | T | 12 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(9): Show | 12 | HG01433.hp2 HG02027.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.1541+1073A>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025393 | ||||||
| chr12:117025399
|
G | C | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1541+1079G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025399 | ||||||
| chr12:117025494
|
G | A | 3 | a0003c0003t0006g0006a0003c0003t0006g0008a0003c0003t0006g0010 | 3 | HG02615.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1541+1174G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025494 | ||||||
| chr12:117025512
|
A | G | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1541+1192A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025512 | ||||||
| chr12:117025570
|
T | G | 1 | a0001c0001t0004g0039 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1541+1250T>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025570 | ||||||
| chr12:117025585
|
A | G | 159 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(156): Show | 164 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1541+1265A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025585 | ||||||
| chr12:117025610
|
A | G | 6 | a0002c0002t0011g0080a0002c0002t0011g0140a0003c0003t0011g0011others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1541+1290A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025610 | ||||||
| chr12:117025801
|
C | CCATCCA | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1541+1482_1541+148 others(10): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117025801 | |||||
| chr12:117025965
|
C | T | 2 | a0002c0008t0002g0068a0002c0008t0002g0069 | 2 | HG02148.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1542-1429C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117025965 | ||||||
| chr12:117026101
|
T | C | 96 | a0001c0001t0034g0172a0002c0002t0002g0003a0002c0002t0002g0047others(93): Show | 99 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1542-1293T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026101 | ||||||
| chr12:117026127
|
C | T | 13 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(10): Show | 13 | HG01433.hp2 HG02027.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1542-1267C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026127 | ||||||
| chr12:117026181
|
GTCAGTCC others(90): Show |
G | 20 | a0001c0001t0001g0277a0002c0002t0001g0139a0002c0002t0002g0138others(17): Show | 21 | HG00741.hp1 HG01074.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.1542-1072_1542-976 others(100): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117026181 | |||||
| chr12:117026246
|
C | T | 3 | a0003c0003t0012g0013a0003c0003t0012g0014a0003c0003t0012g0015 | 3 | HG01884.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1542-1148C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026246 | ||||||
| chr12:117026276
|
C | G | 2 | a0001c0001t0003g0154a0001c0001t0003g0155 | 2 | NA18969.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1542-1118C>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026276 | ||||||
| chr12:117026322
|
CCCCGGGT others(90): Show |
C | 2 | a0003c0003t0011g0011a0003c0003t0011g0012 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1542-1016_1542-920 others(100): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117026322 | |||||
| chr12:117026384
|
C | T | 14 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(11): Show | 15 | HG00741.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-1010C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026384 | ||||||
| chr12:117026419
|
T | C | 3 | a0002c0002t0011g0080a0002c0002t0011g0140a0007c0012t0018g0005 | 3 | HG02055.hp2 HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1542-975T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026419 | ||||||
| chr12:117026509
|
C | CT | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1542-883dupT | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117026509 | |||||
| chr12:117026578
|
A | G | 15 | a0002c0002t0002g0092a0002c0002t0002g0100a0002c0002t0002g0101others(12): Show | 15 | HG00323.hp1 HG00642.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-816A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026578 | ||||||
| chr12:117026608
|
C | CCAACAGA others(6): Show |
182 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(179): Show | 187 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.1542-784_1542-783i others(15): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117026608 | |||||
| chr12:117026638
|
C | CACTT | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1542-754_1542-751d others(6): Show |
FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 117026638 | |||||
| chr12:117026645
|
C | T | 1 | a0005c0017t0007g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1542-749C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026645 | ||||||
| chr12:117026814
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1542-580G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026814 | ||||||
| chr12:117026869
|
A | G | 14 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(11): Show | 15 | HG01106.hp1 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1542-525A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026869 | ||||||
| chr12:117026880
|
A | G | 71 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(68): Show | 76 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.1542-514A>G | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026880 | ||||||
| chr12:117026965
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1542-429G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117026965 | ||||||
| chr12:117027137
|
T | C | 1 | a0002c0002t0002g0057 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1542-257T>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117027137 | ||||||
| chr12:117027164
|
C | T | 12 | a0002c0002t0008g0070a0002c0002t0008g0081a0002c0002t0008g0105others(9): Show | 13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1542-230C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117027164 | ||||||
| chr12:117027165
|
G | A | 46 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157others(43): Show | 46 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1542-229G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117027165 | ||||||
| chr12:117027189
|
G | A | 2 | a0003c0003t0003g0166a0003c0003t0003g0186 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1542-205G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117027189 | ||||||
| chr12:117027335
|
G | A | 4 | a0003c0003t0011g0011a0003c0003t0011g0012a0003c0021t0017g0007others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1542-59G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 9/10 | chr12 | 117027335 | ||||||
| chr12:117027572
|
C | A | 1 | a0003c0003t0019g0024 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1652+68C>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027572 | ||||||
| chr12:117027577
|
G | A | 1 | a0002c0002t0002g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1652+73G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027577 | ||||||
| chr12:117027648
|
G | A | 1 | a0002c0002t0005g0089 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1652+144G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027648 | ||||||
| chr12:117027719
|
G | A | 14 | a0003c0003t0006g0004a0003c0003t0006g0006a0003c0003t0006g0008others(11): Show | 15 | HG00741.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1652+215G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027719 | ||||||
| chr12:117027757
|
G | C | 45 | a0001c0001t0003g0185a0001c0001t0003g0223a0002c0002t0002g0054others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1652+253G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027757 | ||||||
| chr12:117027828
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1653-200C>T | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027828 | ||||||
| chr12:117027907
|
G | A | 3 | a0002c0002t0005g0065a0002c0002t0005g0097a0002c0002t0005g0127 | 3 | HG01256.hp2 HG02738.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1653-121G>A | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027907 | ||||||
| chr12:117027909
|
G | C | 77 | a0002c0002t0002g0003a0002c0002t0002g0047a0002c0002t0002g0053others(74): Show | 82 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.1653-119G>C | FBXW8 | ENSG00000174989.13 | transcript | ENST00000652555.1 | protein_coding | 10/10 | chr12 | 117027909 |