Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 158158 |
|---|---|
| ensemblid | ENSG00000165105.10 |
| hgncid | 26464 |
| symbol | RASEF |
| name | RAS and EF-hand domain containing |
| refseq_nuc | NM_152573.4 |
| refseq_prot | NP_689786.2 |
| ensembl_nuc | ENST00000376447.4 |
| ensembl_prot | ENSP00000365630.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 82979590 |
| end | 83063142 |
| strand | - |
| ver | v1.2 |
| region | chr9:82979590-83063142 |
| region5000 | chr9:82974590-83068142 |
| regionname0 | RASEF_chr9_82979590_83063142 |
| regionname5000 | RASEF_chr9_82974590_83068142 |
| 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 | 740 | 172 | 37 | 28 | 85 | 5 | 16 | 62 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002 | 1/0 | 740 | 146 | 41 | 27 | 58 | 5 | 14 | 50 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0003 | 0/0 | 740 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0004 | 0/0 | 740 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0005 | 0/0 | 740 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0006 | 0/0 | 740 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0007 | 0/0 | 740 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0008 | 0/0 | 740 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0009 | 0/0 | 740 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0010 | 0/0 | 740 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| 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 | 2223 | 172 | 37 | 28 | 85 | 5 | 16 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| c0002 | 1/0 | 2223 | 139 | 36 | 26 | 58 | 5 | 13 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| c0003 | 0/0 | 2223 | 6 | 6 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| c0004 | 0/0 | 2223 | 5 | 3 | 1 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| c0005 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| c0006 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| c0007 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| c0008 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| c0009 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| c0010 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| c0011 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| c0012 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| c0013 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| 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 | 0/1 | 3347 | 139 | 7 | 23 | 91 | 2 | 15 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0002 | 1/0 | 3363 | 82 | 11 | 21 | 34 | 5 | 10 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0003 | 0/0 | 3353 | 24 | 12 | 4 | 3 | 3 | 2 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0004 | 0/0 | 3347 | 14 | 0 | 0 | 11 | 0 | 3 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0005 | 0/0 | 3363 | 8 | 7 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0006 | 0/0 | 3358 | 7 | 7 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0007 | 0/0 | 3353 | 6 | 5 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0008 | 0/0 | 3358 | 5 | 5 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0009 | 0/0 | 3364 | 5 | 5 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0010 | 0/0 | 3357 | 5 | 5 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0011 | 0/0 | 3357 | 3 | 3 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0012 | 0/0 | 3344 | 3 | 2 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0013 | 0/0 | 3363 | 2 | 1 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0014 | 0/0 | 3357 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0015 | 0/0 | 3357 | 2 | 1 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0016 | 0/0 | 3347 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0017 | 0/0 | 3347 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0018 | 0/0 | 3347 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0019 | 0/0 | 3347 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0020 | 0/0 | 3363 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0021 | 0/0 | 3347 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0022 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0023 | 0/0 | 3364 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0024 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0025 | 0/0 | 3363 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0026 | 0/0 | 3363 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0027 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0028 | 0/0 | 3363 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0029 | 0/0 | 3363 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0030 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0031 | 0/0 | 3347 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0032 | 0/0 | 3347 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0033 | 0/0 | 3363 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0034 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0035 | 0/0 | 3347 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0036 | 0/0 | 3363 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0037 | 0/0 | 3363 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| t0038 | 0/0 | 3353 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| 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 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| 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 | 2223 | 172 | 37 | 28 | 85 | 5 | 16 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002 | 1/0 | 2223 | 139 | 36 | 26 | 58 | 5 | 13 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0004 | 0/0 | 2223 | 5 | 3 | 1 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0010 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0011 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0003c0003 | 0/0 | 2223 | 6 | 6 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0004c0005 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0005c0006 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0006c0007 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0007c0008 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0008c0009 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0009c0012 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0010c0013 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5569 | 120 | 6 | 22 | 75 | 2 | 14 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0002 | 0/0 | 5585 | 10 | 5 | 0 | 5 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0003 | 0/0 | 5575 | 21 | 9 | 4 | 3 | 3 | 2 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0005 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0006 | 0/0 | 5580 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0012 | 0/0 | 5566 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0014 | 0/0 | 5579 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0015 | 0/0 | 5579 | 2 | 1 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0016 | 0/0 | 5569 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0017 | 0/0 | 5569 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0018 | 0/0 | 5569 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0021 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0022 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0030 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0031 | 0/0 | 5569 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0033 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0035 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0001c0001t0038 | 0/0 | 5575 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0001 | 0/0 | 5569 | 16 | 0 | 1 | 15 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0002 | 1/0 | 5585 | 70 | 5 | 20 | 29 | 5 | 10 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0003 | 0/0 | 5575 | 3 | 3 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0004 | 0/0 | 5569 | 14 | 0 | 0 | 11 | 0 | 3 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0005 | 0/0 | 5585 | 7 | 6 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0007 | 0/0 | 5575 | 5 | 4 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0008 | 0/0 | 5580 | 5 | 5 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0009 | 0/0 | 5586 | 5 | 5 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0010 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0011 | 0/0 | 5579 | 3 | 3 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0013 | 0/0 | 5585 | 2 | 1 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0020 | 0/0 | 5585 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0023 | 0/0 | 5586 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0024 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0025 | 0/0 | 5585 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0026 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0028 | 0/0 | 5585 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0029 | 0/0 | 5585 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0002t0032 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0004t0001 | 0/0 | 5569 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0004t0010 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0004t0012 | 0/0 | 5566 | 2 | 1 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0004t0027 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0010t0002 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0002c0011t0010 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0003c0003t0006 | 0/0 | 5580 | 5 | 5 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0003c0003t0034 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0004c0005t0019 | 0/0 | 5569 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0005c0006t0036 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0005c0006t0037 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0006c0007t0010 | 0/0 | 5579 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0007c0008t0002 | 0/0 | 5585 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0008c0009t0007 | 0/0 | 5575 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0009c0012t0001 | 0/0 | 5569 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| a0010c0013t0001 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | copy fasta | chr9 | 82974590 | 83068142 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0012g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0014g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0014g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0015g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0015g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0016g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0016g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0017g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0017g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0018g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0018g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0021g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0022g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0030g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0031g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0033g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0035g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0038g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0007g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0008g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0008g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0008g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0009g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0010g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0011g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0011g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0013g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0013g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0020g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0023g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0024g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0025g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0026g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0028g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0029g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0032g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0004t0010g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0004t0012g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0004t0012g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0004t0027g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0010t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0011t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0003c0003t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0003c0003t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0003c0003t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0003c0003t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0003c0003t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0003c0003t0034g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0004c0005t0019g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0004c0005t0019g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0005c0006t0036g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0005c0006t0037g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0006c0007t0010g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0006c0007t0010g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0007c0008t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0008c0009t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0009c0012t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0010c0013t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0088 | EUR | GBR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0214 | EUR | GBR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0099 | EUR | FIN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00408 | hp2 | a0010 | c0013 | t0001 | g0326 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00609 | hp1 | a0001 | c0001 | t0021 | g0004 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00639 | hp1 | a0002 | c0002 | t0028 | g0078 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0089 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00735 | hp2 | a0002 | c0004 | t0012 | g0281 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00738 | hp1 | a0002 | c0002 | t0025 | g0116 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0063 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0059 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0080 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0094 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0096 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01167 | hp2 | a0001 | c0001 | t0015 | g0038 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0104 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0272 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0269 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0103 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0120 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01192 | hp1 | a0002 | c0002 | t0005 | g0321 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0207 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01255 | hp2 | a0002 | c0002 | t0007 | g0199 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0057 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0292 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0115 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0070 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01358 | hp1 | a0001 | c0001 | t0031 | g0220 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01358 | hp2 | a0007 | c0008 | t0002 | g0005 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0095 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0288 | EUR | IBS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0058 | EUR | IBS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0289 | EUR | IBS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0156 | EUR | IBS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01884 | hp1 | a0002 | c0002 | t0009 | g0162 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01891 | hp2 | a0002 | c0002 | t0005 | g0201 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0147 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0131 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02055 | hp1 | a0002 | c0002 | t0008 | g0212 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02055 | hp2 | a0002 | c0002 | t0005 | g0133 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0126 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CDX | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | CDX | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02257 | hp1 | a0002 | c0011 | t0010 | g0041 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02257 | hp2 | a0002 | c0002 | t0008 | g0298 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02258 | hp1 | a0002 | c0002 | t0007 | g0195 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02258 | hp2 | a0005 | c0006 | t0037 | g0330 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0052 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0127 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0125 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02451 | hp1 | a0002 | c0002 | t0007 | g0073 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0300 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02572 | hp1 | a0009 | c0012 | t0001 | g0325 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02572 | hp2 | a0008 | c0009 | t0007 | g0196 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0071 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02615 | hp1 | a0001 | c0001 | t0014 | g0008 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0268 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02622 | hp1 | a0001 | c0001 | t0017 | g0311 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02622 | hp2 | a0002 | c0002 | t0008 | g0309 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02630 | hp1 | a0001 | c0001 | t0012 | g0046 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02630 | hp2 | a0003 | c0003 | t0006 | g0210 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0157 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0053 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02717 | hp1 | a0002 | c0002 | t0009 | g0163 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02717 | hp2 | a0003 | c0003 | t0006 | g0216 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02723 | hp2 | a0001 | c0001 | t0015 | g0037 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0108 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0132 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02809 | hp2 | a0003 | c0003 | t0034 | g0135 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02818 | hp1 | a0002 | c0002 | t0009 | g0204 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02818 | hp2 | a0002 | c0002 | t0011 | g0077 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02886 | hp1 | a0006 | c0007 | t0010 | g0324 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02886 | hp2 | a0001 | c0001 | t0030 | g0228 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02895 | hp1 | a0002 | c0002 | t0003 | g0001 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02895 | hp2 | a0002 | c0002 | t0008 | g0194 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02897 | hp1 | a0002 | c0002 | t0003 | g0001 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02922 | hp1 | a0003 | c0003 | t0006 | g0215 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02970 | hp1 | a0002 | c0002 | t0005 | g0134 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02970 | hp2 | a0002 | c0002 | t0011 | g0075 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02976 | hp1 | a0001 | c0001 | t0017 | g0310 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02976 | hp2 | a0001 | c0001 | t0018 | g0007 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03017 | hp1 | a0002 | c0004 | t0001 | g0278 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03017 | hp2 | a0002 | c0002 | t0004 | g0009 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03041 | hp1 | a0002 | c0002 | t0011 | g0074 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03098 | hp1 | a0002 | c0002 | t0007 | g0197 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03098 | hp2 | a0006 | c0007 | t0010 | g0323 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03130 | hp1 | a0004 | c0005 | t0019 | g0329 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03130 | hp2 | a0001 | c0001 | t0018 | g0006 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03139 | hp2 | a0002 | c0004 | t0027 | g0279 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03195 | hp1 | a0001 | c0001 | t0016 | g0211 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0209 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0030 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03225 | hp1 | a0002 | c0002 | t0026 | g0055 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03225 | hp2 | a0001 | c0001 | t0022 | g0320 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0066 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0079 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03516 | hp1 | a0002 | c0002 | t0003 | g0202 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03516 | hp2 | a0002 | c0002 | t0008 | g0155 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03540 | hp1 | a0003 | c0003 | t0006 | g0217 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03540 | hp2 | a0001 | c0001 | t0033 | g0040 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03579 | hp1 | a0003 | c0003 | t0006 | g0218 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0067 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0291 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0068 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0117 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0308 | SAS | STU | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0128 | SAS | STU | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0081 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03942 | hp1 | a0002 | c0002 | t0004 | g0015 | SAS | BEB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0064 | SAS | STU | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0090 | SAS | STU | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18522 | hp1 | a0002 | c0004 | t0012 | g0208 | AFR | YRI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18522 | hp2 | a0002 | c0002 | t0024 | g0203 | AFR | YRI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CHB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18906 | hp1 | a0004 | c0005 | t0019 | g0328 | AFR | YRI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18906 | hp2 | a0002 | c0002 | t0009 | g0193 | AFR | YRI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18940 | hp1 | a0002 | c0002 | t0004 | g0017 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18956 | hp1 | a0002 | c0002 | t0004 | g0018 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18972 | hp2 | a0002 | c0002 | t0004 | g0023 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18974 | hp1 | a0002 | c0002 | t0032 | g0019 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18975 | hp2 | a0002 | c0002 | t0020 | g0003 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18979 | hp1 | a0001 | c0001 | t0035 | g0327 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18979 | hp2 | a0002 | c0002 | t0004 | g0026 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18982 | hp1 | a0002 | c0002 | t0004 | g0012 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18998 | hp1 | a0002 | c0002 | t0004 | g0025 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19030 | hp1 | a0002 | c0002 | t0005 | g0287 | AFR | LWK | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0305 | AFR | LWK | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19043 | hp1 | a0002 | c0004 | t0010 | g0280 | AFR | LWK | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | LWK | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19057 | hp1 | a0002 | c0002 | t0004 | g0022 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19060 | hp1 | a0002 | c0002 | t0004 | g0013 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19066 | hp2 | a0002 | c0002 | t0029 | g0069 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19079 | hp2 | a0002 | c0002 | t0004 | g0024 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19087 | hp2 | a0002 | c0002 | t0004 | g0021 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19090 | hp2 | a0002 | c0002 | t0004 | g0020 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19240 | hp1 | a0002 | c0002 | t0007 | g0192 | AFR | YRI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | YRI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20129 | hp1 | a0002 | c0002 | t0023 | g0190 | AFR | ASW | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ASW | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | TSI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0138 | EUR | TSI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | GIH | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20905 | hp2 | a0002 | c0002 | t0004 | g0016 | SAS | GIH | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01123 | hp1 | a0002 | c0002 | t0013 | g0198 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02486 | hp1 | a0001 | c0001 | t0016 | g0166 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02486 | hp2 | a0001 | c0001 | t0038 | g0332 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02559 | hp1 | a0002 | c0002 | t0009 | g0200 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02559 | hp2 | a0002 | c0002 | t0010 | g0304 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03471 | hp1 | a0005 | c0006 | t0036 | g0331 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03471 | hp2 | a0002 | c0002 | t0005 | g0124 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG06807 | hp1 | a0002 | c0002 | t0013 | g0205 | AFR | USA | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | USA | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | USA | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20300 | hp2 | a0002 | c0002 | t0005 | g0122 | AFR | USA | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | LWK | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA21309 | hp2 | a0002 | c0010 | t0002 | g0029 | AFR | LWK | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0226 | REF | REF | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0033 | REF | REF | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:83000447
|
C | T | 1 | a0003 | 6 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
missense_variant | MODERATE | c.1561G>A | p.Ala521Thr | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 11/17 | 1836/5585 | 1561/2223 | 521/740 | chr9 | 83000447 | ||
| chr9:83009756
|
C | T | 1 | a0008 | 1 | HG02572.hp2 | missense_variant&splice_region_variant | MODERATE | c.844G>A | p.Glu282Lys | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/17 | 1119/5585 | 844/2223 | 282/740 | chr9 | 83009756 | ||
| chr9:83012458
|
T | G | 2 | a0004a0005 | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.819A>C | p.Lys273Asn | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/17 | 1094/5585 | 819/2223 | 273/740 | chr9 | 83012458 | ||
| chr9:83012493
|
G | A | 3 | a0001a0009a0010 | 174 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(171): Show |
missense_variant | MODERATE | c.784C>T | p.Arg262Cys | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/17 | 1059/5585 | 784/2223 | 262/740 | chr9 | 83012493 | ||
| chr9:83062511
|
G | C | 1 | a0005 | 2 | HG02258.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.357C>G | p.Cys119Trp | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/17 | 632/5585 | 357/2223 | 119/740 | chr9 | 83062511 | ||
| chr9:83062602
|
G | A | 2 | a0006a0009 | 3 | HG02572.hp1 HG02886.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.266C>T | p.Ala89Val | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/17 | 541/5585 | 266/2223 | 89/740 | chr9 | 83062602 | ||
| chr9:83062648
|
A | C | 2 | a0004a0005 | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.220T>G | p.Ser74Ala | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/17 | 495/5585 | 220/2223 | 74/740 | chr9 | 83062648 | ||
| chr9:83062747
|
G | A | 1 | a0010 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.121C>T | p.Arg41Trp | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/17 | 396/5585 | 121/2223 | 41/740 | chr9 | 83062747 | ||
| chr9:83062854
|
C | T | 1 | a0007 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.14G>A | p.Gly5Glu | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/17 | 289/5585 | 14/2223 | 5/740 | chr9 | 83062854 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:82998439
|
A | G | 1 | a0002c0004 | 5 | HG00735.hp2 HG03017.hp1 HG03139.hp2 others(2): Show |
synonymous_variant | LOW | c.1731T>C | p.Asp577Asp | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/17 | 2006/5585 | 1731/2223 | 577/740 | chr9 | 82998439 | ||
| chr9:83000176
|
G | A | 1 | a0003c0003 | 6 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
synonymous_variant | LOW | c.1716C>T | p.Ala572Ala | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/17 | 1991/5585 | 1716/2223 | 572/740 | chr9 | 83000176 | ||
| chr9:83000938
|
G | A | 1 | a0002c0010 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1395C>T | p.His465His | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 10/17 | 1670/5585 | 1395/2223 | 465/740 | chr9 | 83000938 | ||
| chr9:83001025
|
G | A | 2 | a0002c0011a0006c0007 | 3 | HG02257.hp1 HG02886.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.1308C>T | p.Phe436Phe | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 10/17 | 1583/5585 | 1308/2223 | 436/740 | chr9 | 83001025 | ||
| chr9:83062613
|
A | C | 2 | a0004c0005a0005c0006 | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
synonymous_variant | LOW | c.255T>G | p.Pro85Pro | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/17 | 530/5585 | 255/2223 | 85/740 | chr9 | 83062613 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:82979706
|
A | T | 3 | a0001c0001t0017a0001c0001t0022a0002c0002t0011 | 6 | HG02622.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2971T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 2971 | chr9 | 82979706 | |||||
| chr9:82979711
|
A | C | 3 | a0001c0001t0017a0001c0001t0022a0002c0002t0011 | 6 | HG02622.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2966T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 2966 | chr9 | 82979711 | |||||
| chr9:82979892
|
A | C | 1 | a0001c0001t0014 | 2 | HG02615.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2785T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 2785 | chr9 | 82979892 | |||||
| chr9:82980168
|
T | C | 1 | a0002c0002t0026 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2509A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 2509 | chr9 | 82980168 | |||||
| chr9:82980221
|
C | CAAGTT | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0012others(28): Show | 197 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*2455_*2456insAACT others(1): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 2455 | chr9 | 82980221 | |||||
| chr9:82980428
|
C | G | 1 | a0002c0002t0004 | 14 | HG03017.hp2 HG03942.hp1 NA18940.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2249G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 2249 | chr9 | 82980428 | |||||
| chr9:82980443
|
GATTGGTT others(4): Show |
G | 30 | a0001c0001t0001a0001c0001t0006a0001c0001t0012others(27): Show | 196 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*2223_*2233delGGTC others(7): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 2223 | chr9 | 82980443 | |||||
| chr9:82980481
|
A | G | 1 | a0001c0001t0033 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2196T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 2196 | chr9 | 82980481 | |||||
| chr9:82980696
|
A | T | 1 | a0001c0001t0014 | 2 | HG02615.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1981T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1981 | chr9 | 82980696 | |||||
| chr9:82980703
|
G | C | 12 | a0001c0001t0006a0001c0001t0014a0001c0001t0015others(9): Show | 29 | HG01167.hp2 HG02055.hp1 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1974C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1974 | chr9 | 82980703 | |||||
| chr9:82980936
|
T | C | 1 | a0005c0006t0036 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1741A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1741 | chr9 | 82980936 | |||||
| chr9:82981054
|
G | A | 2 | a0001c0001t0005a0002c0002t0005 | 8 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1623C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1623 | chr9 | 82981054 | |||||
| chr9:82981122
|
C | T | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(17): Show | 179 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1555G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1555 | chr9 | 82981122 | |||||
| chr9:82981243
|
C | A | 2 | a0002c0002t0004a0002c0002t0032 | 15 | HG03017.hp2 HG03942.hp1 NA18940.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1434G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1434 | chr9 | 82981243 | |||||
| chr9:82981347
|
G | A | 1 | a0004c0005t0019 | 2 | HG03130.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1330C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1330 | chr9 | 82981347 | |||||
| chr9:82981406
|
T | C | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(36): Show | 232 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*1271A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1271 | chr9 | 82981406 | |||||
| chr9:82981550
|
C | A | 1 | a0002c0002t0028 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1127G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1127 | chr9 | 82981550 | |||||
| chr9:82981552
|
A | G | 1 | a0004c0005t0019 | 2 | HG03130.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1125T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1125 | chr9 | 82981552 | |||||
| chr9:82981582
|
C | T | 1 | a0002c0002t0025 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1095G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1095 | chr9 | 82981582 | |||||
| chr9:82981596
|
A | AT | 2 | a0002c0002t0009a0002c0002t0024 | 6 | HG01884.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1080dupA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1080 | chr9 | 82981596 | |||||
| chr9:82981644
|
G | A | 4 | a0001c0001t0006a0002c0002t0023a0003c0003t0006others(1): Show | 9 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1033C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1033 | chr9 | 82981644 | |||||
| chr9:82981667
|
TACA | T | 2 | a0001c0001t0012a0002c0004t0012 | 3 | HG00735.hp2 HG02630.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1007_*1009delTGT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 1007 | chr9 | 82981667 | |||||
| chr9:82981691
|
T | G | 1 | a0002c0002t0029 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*986A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 986 | chr9 | 82981691 | |||||
| chr9:82982207
|
G | A | 1 | a0001c0001t0031 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*470C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 470 | chr9 | 82982207 | |||||
| chr9:82982217
|
C | T | 17 | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(14): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*460G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 460 | chr9 | 82982217 | |||||
| chr9:82982277
|
G | C | 4 | a0001c0001t0012a0001c0001t0017a0001c0001t0018others(1): Show | 7 | HG00735.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*400C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 400 | chr9 | 82982277 | |||||
| chr9:82982330
|
T | C | 23 | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(20): Show | 201 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*347A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 347 | chr9 | 82982330 | |||||
| chr9:82982385
|
ATTTCTTT others(3): Show |
A | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(19): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*282_*291delAGAAAA others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 282 | chr9 | 82982385 | |||||
| chr9:82982399
|
C | CT | 5 | a0001c0001t0006a0002c0002t0008a0002c0002t0023others(2): Show | 14 | HG02055.hp1 HG02257.hp2 HG02622.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*277dupA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 277 | chr9 | 82982399 | |||||
| chr9:82982461
|
T | C | 5 | a0002c0002t0004a0002c0002t0007a0002c0002t0032others(2): Show | 23 | HG01255.hp2 HG02258.hp1 HG02451.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*216A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 216 | chr9 | 82982461 | |||||
| chr9:82982580
|
G | T | 1 | a0001c0001t0022 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*97C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 97 | chr9 | 82982580 | |||||
| chr9:82982593
|
G | A | 1 | a0001c0001t0033 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*84C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 84 | chr9 | 82982593 | |||||
| chr9:82982671
|
T | C | 1 | a0003c0003t0034 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 17/17 | 6 | chr9 | 82982671 | |||||
| chr9:83062896
|
T | C | 1 | a0001c0001t0035 | 1 | NA18979.hp1 | 5_prime_UTR_variant | MODIFIER | c.-29A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/17 | 29 | chr9 | 83062896 | |||||
| chr9:83062907
|
G | A | 3 | a0004c0005t0019a0005c0006t0036a0005c0006t0037 | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-40C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/17 | 40 | chr9 | 83062907 | |||||
| chr9:83062977
|
C | T | 1 | a0001c0001t0021 | 1 | HG00609.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/17 | 110 | chr9 | 83062977 | |||||
| chr9:83063093
|
G | A | 1 | a0001c0001t0038 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-226C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/17 | 226 | chr9 | 83063093 | |||||
| chr9:83063120
|
G | T | 1 | a0002c0002t0020 | 1 | NA18975.hp2 | 5_prime_UTR_variant | MODIFIER | c.-253C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/17 | 253 | chr9 | 83063120 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:82982805
|
C | CAG | 4 | a0001c0001t0002g0170a0001c0001t0002g0171a0002c0002t0002g0114others(1): Show | 4 | HG01261.hp1 HG02280.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2118-25_2118-24dup others(2): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82982805 | ||||||
| chr9:82982805
|
C | CAGAG | 11 | a0002c0002t0002g0070a0002c0002t0002g0096a0002c0002t0002g0103others(8): Show | 11 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.2118-27_2118-24dup others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82982805 | ||||||
| chr9:82982805
|
CAGAG | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(179): Show | 183 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.2118-27_2118-24del others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82982805 | ||||||
| chr9:82982805
|
CAGAGAG | C | 12 | a0001c0001t0003g0144a0001c0001t0003g0214a0001c0001t0003g0231others(9): Show | 13 | HG00140.hp2 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.2118-29_2118-24del others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82982805 | ||||||
| chr9:82982815
|
G | A | 15 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(12): Show | 15 | HG03017.hp2 HG03942.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.2118-33C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82982815 | ||||||
| chr9:82982834
|
G | A | 14 | a0001c0001t0006g0209a0001c0001t0006g0305a0002c0002t0008g0155others(11): Show | 14 | HG02055.hp1 HG02257.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.2118-52C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82982834 | ||||||
| chr9:82982897
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(173): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.2118-115C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82982897 | ||||||
| chr9:82982978
|
G | A | 6 | a0002c0002t0007g0073a0002c0002t0007g0192a0002c0002t0007g0195others(3): Show | 6 | HG01255.hp2 HG02258.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2118-196C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82982978 | ||||||
| chr9:82983107
|
C | CCA | 50 | a0001c0001t0001g0149a0001c0001t0001g0159a0001c0001t0001g0164others(47): Show | 51 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.2118-327_2118-326d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983107 | ||||||
| chr9:82983107
|
C | CCACA | 18 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0001t0003g0272others(15): Show | 18 | HG00621.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2118-329_2118-326d others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983107 | ||||||
| chr9:82983107
|
C | CCACACA | 10 | a0001c0001t0001g0158a0001c0001t0003g0207a0001c0001t0003g0271others(7): Show | 10 | HG01123.hp1 HG01243.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2118-331_2118-326d others(8): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983107 | ||||||
| chr9:82983107
|
C | CCACACAC others(1): Show |
7 | a0001c0001t0002g0303a0001c0001t0002g0322a0001c0001t0003g0292others(4): Show | 7 | HG00639.hp1 HG01258.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2118-333_2118-326d others(10): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983107 | ||||||
| chr9:82983107
|
C | CCACACAC others(5): Show |
1 | a0005c0006t0037g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2118-337_2118-326d others(14): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983107 | ||||||
| chr9:82983107
|
C | CCACACAC others(9): Show |
1 | a0002c0002t0002g0014 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2118-341_2118-326d others(18): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983107 | ||||||
| chr9:82983107
|
CCA | C | 78 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0050others(75): Show | 78 | HG00558.hp1 HG00733.hp1 HG01106.hp2 others(75): Show |
intron_variant | MODIFIER | c.2118-327_2118-326d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983107 | ||||||
| chr9:82983107
|
CCACA | C | 28 | a0001c0001t0001g0048a0001c0001t0001g0130a0001c0001t0001g0167others(25): Show | 28 | HG00140.hp1 HG00738.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.2118-329_2118-326d others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983107 | ||||||
| chr9:82983107
|
CCACACA | C | 60 | a0001c0001t0001g0051a0001c0001t0001g0123a0001c0001t0001g0140others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.2118-331_2118-326d others(8): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983107 | ||||||
| chr9:82983107
|
CCACACAC others(3): Show |
C | 5 | a0001c0001t0001g0002a0001c0001t0001g0222a0001c0001t0001g0241others(2): Show | 6 | HG01346.hp1 HG01361.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.2118-335_2118-326d others(12): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983107 | ||||||
| chr9:82983107
|
CCACACAC others(11): Show |
C | 1 | a0010c0013t0001g0326 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2118-343_2118-326d others(20): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983107 | ||||||
| chr9:82983107
|
CCACACAC others(13): Show |
C | 7 | a0001c0001t0012g0046a0001c0001t0017g0310a0001c0001t0017g0311others(4): Show | 7 | HG00735.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2118-345_2118-326d others(22): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983107 | ||||||
| chr9:82983153
|
ACAC | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0173a0001c0001t0001g0251others(1): Show | 4 | HG03239.hp2 HG03710.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.2118-374_2118-372d others(5): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983153 | ||||||
| chr9:82983492
|
T | C | 1 | a0002c0002t0002g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2118-710A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983492 | ||||||
| chr9:82983500
|
C | G | 9 | a0001c0001t0006g0209a0001c0001t0006g0305a0002c0002t0023g0190others(6): Show | 9 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2118-718G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983500 | ||||||
| chr9:82983798
|
A | G | 3 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0285 | 3 | HG00642.hp2 HG01081.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2118-1016T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983798 | ||||||
| chr9:82983813
|
C | G | 2 | a0001c0001t0002g0177a0001c0001t0002g0188 | 2 | NA18612.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2118-1031G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983813 | ||||||
| chr9:82983900
|
C | T | 1 | a0001c0001t0003g0231 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2118-1118G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983900 | ||||||
| chr9:82983901
|
G | A | 23 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(20): Show | 23 | HG01255.hp2 HG02258.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.2118-1119C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983901 | ||||||
| chr9:82983966
|
A | T | 2 | a0001c0001t0014g0008a0001c0001t0014g0157 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2118-1184T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82983966 | ||||||
| chr9:82984665
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(173): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.2118-1883G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82984665 | ||||||
| chr9:82984728
|
G | A | 1 | a0002c0004t0012g0281 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2118-1946C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82984728 | ||||||
| chr9:82984788
|
G | A | 2 | a0001c0001t0002g0302a0001c0001t0002g0303 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2118-2006C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82984788 | ||||||
| chr9:82985119
|
T | C | 1 | a0009c0012t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2118-2337A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82985119 | ||||||
| chr9:82985229
|
G | A | 6 | a0001c0001t0001g0039a0001c0001t0001g0072a0001c0001t0001g0149others(3): Show | 6 | HG00438.hp2 NA18952.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.2118-2447C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82985229 | ||||||
| chr9:82985486
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(173): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.2118-2704C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82985486 | ||||||
| chr9:82985661
|
C | T | 23 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(20): Show | 23 | HG01255.hp2 HG02258.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.2118-2879G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82985661 | ||||||
| chr9:82985978
|
A | G | 2 | a0002c0002t0002g0065a0002c0002t0002g0102 | 2 | NA18980.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2118-3196T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82985978 | ||||||
| chr9:82986085
|
A | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(196): Show | 201 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.2118-3303T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82986085 | ||||||
| chr9:82986215
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2118-3433C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82986215 | ||||||
| chr9:82986606
|
A | G | 6 | a0002c0002t0009g0162a0002c0002t0009g0163a0002c0002t0009g0193others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2117+3785T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82986606 | ||||||
| chr9:82986881
|
C | A | 169 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(166): Show | 171 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2117+3510G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82986881 | ||||||
| chr9:82986888
|
C | T | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2117+3503G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82986888 | ||||||
| chr9:82986903
|
A | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(196): Show | 201 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.2117+3488T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82986903 | ||||||
| chr9:82986915
|
C | T | 15 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0139others(12): Show | 15 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.2117+3476G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82986915 | ||||||
| chr9:82987020
|
G | C | 23 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(20): Show | 23 | HG01255.hp2 HG02258.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.2117+3371C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82987020 | ||||||
| chr9:82987193
|
T | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(163): Show | 168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.2117+3198A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82987193 | ||||||
| chr9:82987216
|
C | T | 15 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(12): Show | 15 | HG03017.hp2 HG03942.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.2117+3175G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82987216 | ||||||
| chr9:82987249
|
T | C | 17 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(14): Show | 17 | HG03017.hp2 HG03130.hp1 HG03942.hp1 others(14): Show |
intron_variant | MODIFIER | c.2117+3142A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82987249 | ||||||
| chr9:82987252
|
GTTTGC | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(173): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.2117+3134_2117+313 others(9): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82987252 | ||||||
| chr9:82987333
|
A | C | 1 | a0001c0001t0022g0320 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2117+3058T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82987333 | ||||||
| chr9:82987344
|
A | T | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2117+3047T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82987344 | ||||||
| chr9:82987374
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(173): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.2117+3017A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82987374 | ||||||
| chr9:82987709
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2117+2682A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82987709 | ||||||
| chr9:82987740
|
A | G | 1 | a0001c0001t0022g0320 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2117+2651T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82987740 | ||||||
| chr9:82987937
|
C | T | 1 | a0001c0001t0003g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2117+2454G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82987937 | ||||||
| chr9:82987964
|
C | T | 2 | a0002c0002t0011g0074a0002c0002t0011g0075 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2117+2427G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82987964 | ||||||
| chr9:82987977
|
A | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(196): Show | 201 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.2117+2414T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82987977 | ||||||
| chr9:82988001
|
G | A | 1 | a0001c0001t0033g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2117+2390C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988001 | ||||||
| chr9:82988027
|
G | A | 1 | a0001c0001t0003g0306 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2117+2364C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988027 | ||||||
| chr9:82988055
|
C | T | 6 | a0002c0002t0007g0073a0002c0002t0007g0192a0002c0002t0007g0195others(3): Show | 6 | HG01255.hp2 HG02258.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2117+2336G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988055 | ||||||
| chr9:82988137
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2117+2254A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988137 | ||||||
| chr9:82988173
|
G | T | 1 | a0001c0001t0033g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2117+2218C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988173 | ||||||
| chr9:82988259
|
C | T | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2117+2132G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988259 | ||||||
| chr9:82988300
|
G | T | 2 | a0002c0002t0009g0193a0002c0002t0009g0200 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2117+2091C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988300 | ||||||
| chr9:82988377
|
AAAAC | A | 23 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(20): Show | 23 | HG01255.hp2 HG02258.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.2117+2010_2117+201 others(8): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988377 | ||||||
| chr9:82988410
|
T | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(196): Show | 201 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.2117+1981A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988410 | ||||||
| chr9:82988412
|
A | C | 24 | a0001c0001t0003g0144a0001c0001t0003g0207a0001c0001t0003g0214others(21): Show | 25 | HG00140.hp2 HG00673.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.2117+1979T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988412 | ||||||
| chr9:82988498
|
C | A | 5 | a0002c0002t0010g0304a0002c0004t0010g0280a0002c0011t0010g0041others(2): Show | 5 | HG02257.hp1 HG02559.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2117+1893G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988498 | ||||||
| chr9:82988936
|
T | C | 2 | a0002c0002t0013g0198a0005c0006t0037g0330 | 2 | HG01123.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2117+1455A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988936 | ||||||
| chr9:82988957
|
G | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(173): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.2117+1434C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988957 | ||||||
| chr9:82989143
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2117+1248G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989143 | ||||||
| chr9:82989170
|
T | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(166): Show | 171 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2117+1221A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989170 | ||||||
| chr9:82989222
|
A | ATG | 160 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(157): Show | 162 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.2117+1167_2117+116 others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989222 | ||||||
| chr9:82989222
|
A | ATGTGTG | 5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG00280.hp1 HG01123.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.2117+1163_2117+116 others(10): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989222 | ||||||
| chr9:82989229
|
C | T | 168 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(165): Show | 170 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2117+1162G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989229 | ||||||
| chr9:82989244
|
G | T | 23 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(20): Show | 23 | HG01255.hp2 HG02258.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.2117+1147C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989244 | ||||||
| chr9:82989246
|
A | G | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0185 | 3 | HG00280.hp1 HG01123.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.2117+1145T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989246 | ||||||
| chr9:82989334
|
T | G | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2117+1057A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989334 | ||||||
| chr9:82989717
|
T | C | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2117+674A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989717 | ||||||
| chr9:82989744
|
G | T | 331 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(328): Show | 333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.2117+647C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989744 | ||||||
| chr9:82989791
|
T | C | 1 | a0003c0003t0034g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2117+600A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989791 | ||||||
| chr9:82989987
|
A | T | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2117+404T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989987 | ||||||
| chr9:82989997
|
A | T | 4 | a0001c0001t0001g0312a0001c0001t0014g0008a0001c0001t0014g0157others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2117+394T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989997 | ||||||
| chr9:82990099
|
C | G | 1 | a0001c0001t0003g0231 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2117+292G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82990099 | ||||||
| chr9:82990124
|
C | T | 2 | a0001c0001t0014g0008a0001c0001t0014g0157 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2117+267G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82990124 | ||||||
| chr9:82990125
|
G | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(170): Show | 175 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.2117+266C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82990125 | ||||||
| chr9:82990148
|
C | T | 2 | a0001c0001t0014g0008a0001c0001t0014g0157 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2117+243G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82990148 | ||||||
| chr9:82990293
|
G | A | 1 | a0001c0001t0005g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2117+98C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82990293 | ||||||
| chr9:82990755
|
G | A | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2041-288C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82990755 | ||||||
| chr9:82990862
|
C | T | 26 | a0001c0001t0003g0144a0001c0001t0003g0207a0001c0001t0003g0214others(23): Show | 27 | HG00140.hp2 HG00673.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.2041-395G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82990862 | ||||||
| chr9:82990943
|
T | C | 17 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(14): Show | 17 | HG03017.hp2 HG03130.hp1 HG03942.hp1 others(14): Show |
intron_variant | MODIFIER | c.2041-476A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82990943 | ||||||
| chr9:82991010
|
C | T | 2 | a0002c0002t0011g0074a0002c0002t0011g0075 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2041-543G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82991010 | ||||||
| chr9:82991089
|
C | T | 5 | a0001c0001t0002g0322a0001c0001t0005g0036a0001c0001t0018g0006others(2): Show | 5 | HG01884.hp2 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041-622G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82991089 | ||||||
| chr9:82991116
|
C | A | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2041-649G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82991116 | ||||||
| chr9:82991121
|
A | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(232): Show | 237 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.2041-654T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82991121 | ||||||
| chr9:82991365
|
T | C | 15 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(12): Show | 15 | HG03017.hp2 HG03942.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.2041-898A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82991365 | ||||||
| chr9:82991475
|
G | T | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2041-1008C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82991475 | ||||||
| chr9:82991563
|
G | C | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2041-1096C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82991563 | ||||||
| chr9:82992039
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2040+867A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82992039 | ||||||
| chr9:82992152
|
C | A | 1 | a0002c0004t0027g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2040+754G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82992152 | ||||||
| chr9:82992176
|
AC | A | 14 | a0001c0001t0016g0166a0002c0002t0002g0052a0002c0002t0005g0287others(11): Show | 14 | HG00735.hp2 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2040+729delG | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82992176 | ||||||
| chr9:82992189
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2040+717G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82992189 | ||||||
| chr9:82992359
|
A | G | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG00544.hp2 HG02056.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.2040+547T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82992359 | ||||||
| chr9:82992507
|
T | C | 2 | a0002c0002t0011g0074a0002c0002t0011g0075 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2040+399A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 15/16 | chr9 | 82992507 | ||||||
| chr9:82993036
|
GA | G | 6 | a0001c0001t0001g0295a0002c0002t0005g0287a0002c0004t0010g0280others(3): Show | 6 | HG00735.hp2 HG03139.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1921-12delT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82993036 | ||||||
| chr9:82993060
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02071.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1921-35T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82993060 | ||||||
| chr9:82993189
|
T | C | 1 | a0001c0001t0016g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1921-164A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82993189 | ||||||
| chr9:82993237
|
A | G | 167 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(164): Show | 169 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1921-212T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82993237 | ||||||
| chr9:82993240
|
A | G | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1921-215T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82993240 | ||||||
| chr9:82993335
|
G | A | 1 | a0001c0001t0001g0318 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1921-310C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82993335 | ||||||
| chr9:82993415
|
C | T | 1 | a0002c0002t0011g0075 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1921-390G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82993415 | ||||||
| chr9:82993677
|
T | A | 1 | a0002c0002t0007g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1921-652A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82993677 | ||||||
| chr9:82993788
|
G | T | 192 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(189): Show | 193 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1921-763C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82993788 | ||||||
| chr9:82993862
|
C | T | 1 | a0002c0002t0002g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1921-837G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82993862 | ||||||
| chr9:82993951
|
T | C | 2 | a0001c0001t0017g0310a0001c0001t0017g0311 | 2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1921-926A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82993951 | ||||||
| chr9:82994158
|
G | GA | 173 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(170): Show | 175 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1921-1134dupT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994158 | ||||||
| chr9:82994225
|
C | T | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1921-1200G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994225 | ||||||
| chr9:82994263
|
C | T | 199 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(196): Show | 201 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1921-1238G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994263 | ||||||
| chr9:82994465
|
C | A | 4 | a0001c0001t0002g0028a0001c0001t0002g0174a0001c0001t0002g0177others(1): Show | 4 | NA18612.hp2 NA18977.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1921-1440G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994465 | ||||||
| chr9:82994483
|
G | C | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1921-1458C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994483 | ||||||
| chr9:82994485
|
A | G | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1921-1460T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994485 | ||||||
| chr9:82994543
|
C | A | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1921-1518G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994543 | ||||||
| chr9:82994658
|
A | G | 3 | a0002c0002t0005g0124a0002c0002t0005g0133a0002c0002t0005g0321 | 3 | HG01192.hp1 HG02055.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1921-1633T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994658 | ||||||
| chr9:82994664
|
G | T | 1 | a0002c0002t0002g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1921-1639C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994664 | ||||||
| chr9:82994797
|
A | G | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1921-1772T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994797 | ||||||
| chr9:82994859
|
GT | G | 7 | a0002c0002t0009g0162a0002c0002t0009g0163a0002c0002t0009g0193others(4): Show | 7 | HG01884.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1921-1835delA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994859 | ||||||
| chr9:82994866
|
G | A | 24 | a0001c0001t0003g0144a0001c0001t0003g0207a0001c0001t0003g0214others(21): Show | 24 | HG00140.hp2 HG00673.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.1921-1841C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994866 | ||||||
| chr9:82994902
|
C | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0282 | 2 | HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1921-1877G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994902 | ||||||
| chr9:82994957
|
C | T | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1921-1932G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994957 | ||||||
| chr9:82995107
|
T | C | 2 | a0001c0001t0014g0008a0001c0001t0014g0157 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1920+1905A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82995107 | ||||||
| chr9:82995141
|
T | C | 1 | a0002c0002t0004g0015 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1920+1871A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82995141 | ||||||
| chr9:82995374
|
T | C | 2 | a0002c0002t0011g0074a0002c0002t0011g0075 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1920+1638A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82995374 | ||||||
| chr9:82995573
|
G | C | 5 | a0002c0002t0005g0287a0002c0004t0010g0280a0002c0004t0012g0208others(2): Show | 5 | HG00735.hp2 HG03139.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1920+1439C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82995573 | ||||||
| chr9:82995773
|
C | T | 5 | a0002c0002t0002g0094a0002c0002t0002g0095a0002c0002t0002g0096others(2): Show | 5 | HG01106.hp2 HG01167.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1920+1239G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82995773 | ||||||
| chr9:82996270
|
T | C | 1 | a0002c0002t0002g0100 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1920+742A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82996270 | ||||||
| chr9:82996504
|
G | A | 9 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(6): Show | 9 | HG02258.hp2 HG03017.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.1920+508C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82996504 | ||||||
| chr9:82996566
|
A | G | 1 | a0001c0001t0001g0172 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1920+446T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82996566 | ||||||
| chr9:82996593
|
C | T | 1 | a0002c0002t0002g0110 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1920+419G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82996593 | ||||||
| chr9:82996598
|
G | A | 9 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(6): Show | 9 | HG02258.hp2 HG03017.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.1920+414C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82996598 | ||||||
| chr9:82996621
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0184 | 2 | HG01175.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1920+391G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82996621 | ||||||
| chr9:82997233
|
A | G | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1806-107T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82997233 | ||||||
| chr9:82997513
|
G | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(171): Show | 176 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1806-387C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82997513 | ||||||
| chr9:82997546
|
A | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(191): Show | 196 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1806-420T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82997546 | ||||||
| chr9:82997618
|
T | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(191): Show | 196 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1806-492A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82997618 | ||||||
| chr9:82997781
|
T | C | 1 | a0001c0001t0003g0308 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1805+584A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82997781 | ||||||
| chr9:82997782
|
C | T | 7 | a0002c0002t0002g0052a0002c0002t0008g0155a0002c0002t0008g0212others(4): Show | 7 | HG02055.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1805+583G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82997782 | ||||||
| chr9:82997956
|
A | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(246): Show | 251 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.1805+409T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82997956 | ||||||
| chr9:82998128
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(190): Show | 195 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1805+237T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82998128 | ||||||
| chr9:82998183
|
A | C | 2 | a0001c0001t0001g0312a0001c0001t0033g0040 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1805+182T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82998183 | ||||||
| chr9:82998191
|
G | A | 1 | a0001c0001t0016g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1805+174C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82998191 | ||||||
| chr9:82998197
|
A | G | 21 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0004g0009others(18): Show | 21 | HG01167.hp2 HG02258.hp2 HG02723.hp2 others(18): Show |
intron_variant | MODIFIER | c.1805+168T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82998197 | ||||||
| chr9:82998476
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1724-30C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82998476 | ||||||
| chr9:82998501
|
T | G | 6 | a0002c0002t0001g0011a0002c0002t0001g0061a0002c0002t0001g0085others(3): Show | 6 | HG02155.hp2 NA18939.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1724-55A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82998501 | ||||||
| chr9:82998717
|
C | T | 4 | a0001c0001t0001g0312a0001c0001t0014g0008a0001c0001t0014g0157others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1724-271G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82998717 | ||||||
| chr9:82998737
|
TTG | T | 21 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0004g0009others(18): Show | 21 | HG01167.hp2 HG02258.hp2 HG02723.hp2 others(18): Show |
intron_variant | MODIFIER | c.1724-293_1724-292d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82998737 | ||||||
| chr9:82998853
|
T | C | 1 | a0002c0002t0002g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1724-407A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82998853 | ||||||
| chr9:82999082
|
T | G | 3 | a0002c0002t0005g0287a0002c0002t0011g0074a0002c0002t0011g0075 | 3 | HG02970.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1724-636A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999082 | ||||||
| chr9:82999096
|
A | AC | 210 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(207): Show | 212 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1724-651_1724-650i others(3): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999096 | ||||||
| chr9:82999205
|
C | CTGAT | 193 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(190): Show | 195 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1724-760_1724-759i others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999205 | ||||||
| chr9:82999380
|
C | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(190): Show | 195 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1723+789G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999380 | ||||||
| chr9:82999407
|
C | G | 6 | a0002c0002t0001g0054a0002c0002t0001g0062a0002c0002t0001g0084others(3): Show | 6 | HG00558.hp1 NA18944.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1723+762G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999407 | ||||||
| chr9:82999442
|
T | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(171): Show | 176 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1723+727A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999442 | ||||||
| chr9:82999445
|
A | G | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1723+724T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999445 | ||||||
| chr9:82999578
|
A | G | 1 | a0001c0001t0016g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1723+591T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999578 | ||||||
| chr9:82999902
|
C | G | 15 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(12): Show | 15 | HG03017.hp2 HG03942.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.1723+267G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999902 | ||||||
| chr9:82999984
|
G | GAC | 7 | a0002c0002t0001g0061a0002c0002t0001g0136a0002c0002t0002g0079others(4): Show | 7 | HG00733.hp1 HG02155.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1723+183_1723+184d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:82999984
|
G | GACAC | 4 | a0002c0002t0001g0062a0002c0002t0001g0084a0002c0002t0001g0087others(1): Show | 4 | HG01978.hp1 NA18944.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1723+181_1723+184d others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:82999984
|
G | GACACACA others(1): Show |
3 | a0002c0002t0001g0054a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG00558.hp1 NA19011.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1723+177_1723+184d others(10): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:82999984
|
GAC | G | 23 | a0002c0002t0001g0092a0002c0002t0002g0010a0002c0002t0002g0035others(20): Show | 23 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1723+183_1723+184d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:82999984
|
GACAC | G | 26 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0001g0107others(23): Show | 26 | HG00280.hp2 HG00438.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.1723+181_1723+184d others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:82999984
|
GACACAC | G | 23 | a0002c0002t0001g0085a0002c0002t0001g0086a0002c0002t0001g0097others(20): Show | 23 | HG00673.hp2 HG01081.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1723+179_1723+184d others(8): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:82999984
|
GACACACA others(1): Show |
G | 5 | a0002c0002t0002g0090a0002c0004t0001g0278a0002c0004t0012g0208others(2): Show | 5 | HG00735.hp2 HG03017.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1723+177_1723+184d others(10): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:82999984
|
GACACACA others(3): Show |
G | 11 | a0002c0002t0002g0030a0002c0002t0002g0083a0002c0002t0004g0009others(8): Show | 11 | HG02015.hp2 HG02559.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.1723+175_1723+184d others(12): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:82999984
|
GACACACA others(5): Show |
G | 9 | a0001c0001t0001g0045a0001c0001t0001g0139a0001c0001t0001g0232others(6): Show | 9 | HG01884.hp1 HG02080.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1723+173_1723+184d others(14): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:82999984
|
GACACACA others(7): Show |
G | 41 | a0001c0001t0001g0051a0001c0001t0001g0129a0001c0001t0001g0130others(38): Show | 41 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.1723+171_1723+184d others(16): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:82999984
|
GACACACA others(9): Show |
G | 130 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0048others(127): Show | 132 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1723+169_1723+184d others(18): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:82999984
|
GACACACA others(11): Show |
G | 4 | a0001c0001t0001g0047a0001c0001t0001g0179a0001c0001t0001g0222others(1): Show | 4 | HG01256.hp1 HG02155.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1723+167_1723+184d others(20): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:82999984
|
GACACACA others(13): Show |
G | 6 | a0002c0002t0007g0192a0002c0002t0007g0195a0002c0002t0007g0197others(3): Show | 6 | HG01123.hp1 HG01255.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1723+165_1723+184d others(22): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:82999984
|
GACACACA others(17): Show |
G | 1 | a0005c0006t0037g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1723+161_1723+184d others(26): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 82999984 | ||||||
| chr9:83000028
|
C | A | 2 | a0006c0007t0010g0323a0006c0007t0010g0324 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1723+141G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 12/16 | chr9 | 83000028 | ||||||
| chr9:83000884
|
T | C | 1 | a0001c0001t0016g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1437+12A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 10/16 | chr9 | 83000884 | ||||||
| chr9:83001227
|
C | T | 5 | a0001c0001t0001g0234a0001c0001t0001g0275a0001c0001t0001g0294others(2): Show | 5 | HG00597.hp2 NA18954.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203-97G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83001227 | ||||||
| chr9:83001274
|
G | T | 1 | a0002c0002t0002g0115 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1203-144C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83001274 | ||||||
| chr9:83001397
|
T | C | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1203-267A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83001397 | ||||||
| chr9:83001495
|
C | T | 3 | a0002c0002t0001g0107a0002c0002t0001g0131a0002c0002t0001g0137 | 3 | HG01978.hp1 NA18942.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1203-365G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83001495 | ||||||
| chr9:83001897
|
C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(174): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.1203-767G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83001897 | ||||||
| chr9:83002145
|
A | C | 1 | a0002c0002t0005g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1203-1015T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83002145 | ||||||
| chr9:83002182
|
A | G | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1203-1052T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83002182 | ||||||
| chr9:83002190
|
T | C | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1203-1060A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83002190 | ||||||
| chr9:83002426
|
G | T | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1203-1296C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83002426 | ||||||
| chr9:83002662
|
A | T | 1 | a0002c0002t0002g0117 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1203-1532T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83002662 | ||||||
| chr9:83002693
|
A | G | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1203-1563T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83002693 | ||||||
| chr9:83002753
|
C | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(174): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.1203-1623G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83002753 | ||||||
| chr9:83002850
|
C | G | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1202+1648G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83002850 | ||||||
| chr9:83003012
|
T | G | 8 | a0002c0002t0002g0052a0002c0002t0003g0001a0002c0002t0008g0155others(5): Show | 9 | HG02055.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202+1486A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83003012 | ||||||
| chr9:83003055
|
G | A | 228 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(225): Show | 230 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1202+1443C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83003055 | ||||||
| chr9:83003090
|
C | G | 15 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(12): Show | 15 | HG03017.hp2 HG03942.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.1202+1408G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83003090 | ||||||
| chr9:83003261
|
G | A | 2 | a0002c0002t0011g0074a0002c0002t0011g0075 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1202+1237C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83003261 | ||||||
| chr9:83003298
|
G | A | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1202+1200C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83003298 | ||||||
| chr9:83003583
|
A | G | 1 | a0002c0002t0002g0110 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1202+915T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83003583 | ||||||
| chr9:83003670
|
G | A | 1 | a0002c0002t0002g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1202+828C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83003670 | ||||||
| chr9:83003800
|
A | G | 15 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(12): Show | 15 | HG03017.hp2 HG03942.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.1202+698T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83003800 | ||||||
| chr9:83003804
|
G | A | 1 | a0001c0001t0005g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1202+694C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83003804 | ||||||
| chr9:83003847
|
G | A | 8 | a0002c0002t0002g0052a0002c0002t0003g0001a0002c0002t0008g0155others(5): Show | 9 | HG02055.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202+651C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83003847 | ||||||
| chr9:83003857
|
T | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1202+641A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83003857 | ||||||
| chr9:83004166
|
C | T | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1202+332G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83004166 | ||||||
| chr9:83004180
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0262 | 2 | HG01261.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1202+318G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83004180 | ||||||
| chr9:83004251
|
T | A | 1 | a0001c0001t0001g0319 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1202+247A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83004251 | ||||||
| chr9:83004288
|
T | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+210A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83004288 | ||||||
| chr9:83004374
|
T | A | 1 | a0002c0002t0007g0197 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1202+124A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83004374 | ||||||
| chr9:83004415
|
T | TTTTATTC others(5): Show |
171 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(168): Show | 172 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1202+82_1202+83ins others(12): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83004415 | ||||||
| chr9:83004436
|
ATTTAC | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(170): Show | 174 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1202+57_1202+61del others(5): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83004436 | ||||||
| chr9:83004482
|
A | G | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+16T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83004482 | ||||||
| chr9:83004595
|
T | C | 3 | a0002c0002t0005g0287a0002c0002t0011g0074a0002c0002t0011g0075 | 3 | HG02970.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1114-9A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 8/16 | chr9 | 83004595 | ||||||
| chr9:83004843
|
G | A | 2 | a0002c0002t0007g0073a0002c0002t0026g0055 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1114-257C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 8/16 | chr9 | 83004843 | ||||||
| chr9:83005093
|
C | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(171): Show | 176 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1113+323G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 8/16 | chr9 | 83005093 | ||||||
| chr9:83005209
|
T | C | 6 | a0003c0003t0006g0210a0003c0003t0006g0215a0003c0003t0006g0216others(3): Show | 6 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+207A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 8/16 | chr9 | 83005209 | ||||||
| chr9:83005305
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1113+111A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 8/16 | chr9 | 83005305 | ||||||
| chr9:83005368
|
C | T | 15 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(12): Show | 15 | HG03017.hp2 HG03942.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.1113+48G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 8/16 | chr9 | 83005368 | ||||||
| chr9:83005641
|
A | C | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1029-141T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83005641 | ||||||
| chr9:83005689
|
T | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029-189A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83005689 | ||||||
| chr9:83005820
|
A | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(171): Show | 176 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1029-320T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83005820 | ||||||
| chr9:83006353
|
T | C | 4 | a0001c0001t0001g0051a0001c0001t0001g0245a0001c0001t0001g0266others(1): Show | 4 | HG00597.hp1 HG00609.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029-853A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83006353 | ||||||
| chr9:83006641
|
T | C | 167 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(164): Show | 169 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1028+796A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83006641 | ||||||
| chr9:83006705
|
C | A | 1 | a0002c0002t0002g0031 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1028+732G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83006705 | ||||||
| chr9:83006806
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1028+631C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83006806 | ||||||
| chr9:83006821
|
T | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028+616A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83006821 | ||||||
| chr9:83006822
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1028+615C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83006822 | ||||||
| chr9:83006831
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1028+606A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83006831 | ||||||
| chr9:83006847
|
A | C | 2 | a0001c0001t0003g0267a0001c0001t0003g0268 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1028+590T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83006847 | ||||||
| chr9:83006962
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0257 | 2 | NA18612.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1028+475G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83006962 | ||||||
| chr9:83007072
|
T | C | 225 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(222): Show | 227 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.1028+365A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83007072 | ||||||
| chr9:83007088
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(173): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.1028+349A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83007088 | ||||||
| chr9:83007093
|
C | CA | 205 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1028+343dupT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83007093 | ||||||
| chr9:83007093
|
C | CAA | 25 | a0001c0001t0001g0221a0001c0001t0001g0261a0001c0001t0001g0294others(22): Show | 25 | HG00733.hp2 HG01167.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.1028+342_1028+343d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83007093 | ||||||
| chr9:83007163
|
T | C | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1028+274A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83007163 | ||||||
| chr9:83007564
|
T | C | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.960-59A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83007564 | ||||||
| chr9:83007649
|
T | C | 2 | a0001c0001t0001g0312a0001c0001t0033g0040 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.960-144A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83007649 | ||||||
| chr9:83007748
|
A | T | 1 | a0002c0004t0012g0281 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.960-243T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83007748 | ||||||
| chr9:83007760
|
G | C | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.960-255C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83007760 | ||||||
| chr9:83007790
|
C | A | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.960-285G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83007790 | ||||||
| chr9:83007871
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(174): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.960-366A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83007871 | ||||||
| chr9:83008173
|
T | A | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.960-668A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008173 | ||||||
| chr9:83008433
|
C | T | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.960-928G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008433 | ||||||
| chr9:83008561
|
T | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0123others(81): Show | 85 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.960-1056A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008561 | ||||||
| chr9:83008580
|
G | A | 1 | a0002c0002t0011g0075 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.959+1061C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008580 | ||||||
| chr9:83008645
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(170): Show | 174 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.959+996G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008645 | ||||||
| chr9:83008673
|
C | T | 1 | a0001c0001t0001g0319 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.959+968G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008673 | ||||||
| chr9:83008712
|
C | T | 6 | a0003c0003t0006g0210a0003c0003t0006g0215a0003c0003t0006g0216others(3): Show | 6 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.959+929G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008712 | ||||||
| chr9:83008838
|
T | C | 1 | a0001c0001t0005g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.959+803A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008838 | ||||||
| chr9:83008889
|
A | ATC | 14 | a0001c0001t0001g0169a0001c0001t0001g0226a0001c0001t0001g0229others(11): Show | 14 | HG01168.hp2 HG01169.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.959+750_959+751dup others(2): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008889 | ||||||
| chr9:83008891
|
C | CAT | 38 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0002g0010others(35): Show | 39 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.959+748_959+749dup others(2): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
C | CATAT | 4 | a0002c0002t0002g0076a0002c0002t0002g0127a0002c0002t0009g0200others(1): Show | 4 | HG00735.hp2 HG02293.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+746_959+749dup others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
C | CATATAT | 16 | a0001c0001t0015g0037a0002c0002t0001g0131a0002c0002t0001g0136others(13): Show | 16 | HG01978.hp1 HG02074.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.959+744_959+749dup others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
C | CATATATA others(1): Show |
8 | a0002c0002t0001g0107a0002c0002t0002g0034a0002c0002t0002g0111others(5): Show | 8 | HG01884.hp1 HG03225.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.959+742_959+749dup others(8): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
C | CATATATA others(3): Show |
7 | a0001c0001t0015g0038a0002c0002t0002g0118a0002c0002t0002g0138others(4): Show | 7 | HG01167.hp2 HG02717.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.959+740_959+749dup others(10): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
C | CATATATA others(5): Show |
5 | a0002c0002t0002g0060a0002c0002t0002g0081a0002c0002t0004g0020others(2): Show | 5 | HG00621.hp2 HG02970.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.959+738_959+749dup others(12): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
C | CTCAT | 10 | a0001c0001t0001g0253a0001c0001t0002g0322a0001c0001t0003g0207others(7): Show | 10 | HG01243.hp1 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.959+749_959+750ins others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
C | CTCATAT | 17 | a0001c0001t0001g0176a0001c0001t0001g0187a0001c0001t0001g0240others(14): Show | 17 | HG00673.hp1 HG00735.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.959+749_959+750ins others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
C | CTCATATA others(1): Show |
15 | a0001c0001t0001g0142a0001c0001t0001g0145a0001c0001t0001g0164others(12): Show | 15 | HG00609.hp2 HG00733.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.959+749_959+750ins others(8): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
C | CTCATATA others(3): Show |
32 | a0001c0001t0001g0139a0001c0001t0001g0146a0001c0001t0001g0152others(29): Show | 32 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.959+749_959+750ins others(10): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
C | CTCATATA others(5): Show |
34 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0140others(31): Show | 34 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.959+749_959+750ins others(12): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
C | CTCATATA others(7): Show |
9 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0178others(6): Show | 9 | HG02015.hp1 HG02155.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.959+749_959+750ins others(14): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
C | CTCATATA others(9): Show |
4 | a0001c0001t0001g0123a0001c0001t0001g0173a0001c0001t0001g0230others(1): Show | 4 | HG00738.hp2 HG02602.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+749_959+750ins others(16): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
CAT | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0154others(23): Show | 27 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.959+748_959+749del others(2): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
CATAT | C | 14 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0051others(11): Show | 14 | HG00609.hp1 HG01123.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.959+746_959+749del others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
CATATAT | C | 12 | a0001c0001t0001g0039a0001c0001t0001g0047a0001c0001t0001g0072others(9): Show | 12 | HG00438.hp2 HG02258.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.959+744_959+749del others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
CATATATA others(3): Show |
C | 5 | a0002c0002t0002g0094a0002c0002t0002g0095a0002c0002t0002g0096others(2): Show | 5 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.959+740_959+749del others(10): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
CATATATA others(5): Show |
C | 1 | a0004c0005t0019g0328 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.959+738_959+749del others(12): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
CATATATA others(9): Show |
C | 2 | a0001c0001t0003g0306a0001c0001t0006g0305 | 2 | NA18974.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.959+734_959+749del others(16): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
CATATATA others(11): Show |
C | 3 | a0001c0001t0001g0179a0001c0001t0003g0273a0002c0002t0002g0053 | 3 | HG02698.hp2 HG03139.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.959+732_959+749del others(18): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008891
|
CATATATA others(19): Show |
C | 2 | a0002c0002t0002g0059a0002c0002t0002g0063 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.959+724_959+749del others(26): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008891 | ||||||
| chr9:83008892
|
A | T | 6 | a0001c0001t0001g0049a0001c0001t0001g0242a0001c0001t0001g0283others(3): Show | 6 | HG00140.hp2 HG01256.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.959+749T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008892 | ||||||
| chr9:83008893
|
T | C | 6 | a0001c0001t0001g0049a0001c0001t0001g0242a0001c0001t0001g0283others(3): Show | 6 | HG00140.hp2 HG01256.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.959+748A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008893 | ||||||
| chr9:83008894
|
A | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0154others(9): Show | 13 | HG00408.hp1 HG00544.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.959+747T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008894 | ||||||
| chr9:83008895
|
T | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0154others(9): Show | 13 | HG00408.hp1 HG00544.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.959+746A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008895 | ||||||
| chr9:83008896
|
A | T | 7 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0051others(4): Show | 7 | HG00609.hp1 HG01978.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.959+745T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008896 | ||||||
| chr9:83008897
|
T | C | 7 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0051others(4): Show | 7 | HG00609.hp1 HG01978.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.959+744A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008897 | ||||||
| chr9:83008898
|
A | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0047a0001c0001t0001g0072others(4): Show | 7 | HG00438.hp2 NA18944.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.959+743T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008898 | ||||||
| chr9:83008899
|
T | C | 7 | a0001c0001t0001g0039a0001c0001t0001g0047a0001c0001t0001g0072others(4): Show | 7 | HG00438.hp2 NA18944.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.959+742A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008899 | ||||||
| chr9:83008908
|
A | T | 2 | a0001c0001t0003g0306a0001c0001t0006g0305 | 2 | NA18974.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.959+733T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008908 | ||||||
| chr9:83008909
|
T | C | 2 | a0001c0001t0003g0306a0001c0001t0006g0305 | 2 | NA18974.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.959+732A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008909 | ||||||
| chr9:83008910
|
A | T | 2 | a0001c0001t0001g0179a0001c0001t0003g0273 | 2 | HG03139.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.959+731T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008910 | ||||||
| chr9:83008911
|
T | C | 2 | a0001c0001t0001g0179a0001c0001t0003g0273 | 2 | HG03139.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.959+730A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83008911 | ||||||
| chr9:83009011
|
T | C | 2 | a0001c0001t0001g0312a0001c0001t0033g0040 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.959+630A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83009011 | ||||||
| chr9:83009169
|
T | C | 2 | a0002c0002t0002g0065a0002c0002t0002g0102 | 2 | NA18980.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.959+472A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83009169 | ||||||
| chr9:83009219
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.959+422C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83009219 | ||||||
| chr9:83009239
|
T | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0184 | 2 | HG01175.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.959+402A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83009239 | ||||||
| chr9:83009282
|
C | T | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+359G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83009282 | ||||||
| chr9:83009461
|
T | A | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.959+180A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83009461 | ||||||
| chr9:83010160
|
A | G | 1 | a0002c0002t0002g0079 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.844-404T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83010160 | ||||||
| chr9:83010269
|
C | T | 1 | a0002c0002t0002g0125 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.844-513G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83010269 | ||||||
| chr9:83010320
|
A | G | 1 | a0004c0005t0019g0328 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.844-564T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83010320 | ||||||
| chr9:83010433
|
G | A | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.844-677C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83010433 | ||||||
| chr9:83010530
|
G | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(124): Show | 128 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.844-774C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83010530 | ||||||
| chr9:83010587
|
G | A | 1 | a0002c0002t0002g0109 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.844-831C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83010587 | ||||||
| chr9:83010655
|
A | G | 1 | a0001c0001t0003g0231 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.844-899T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83010655 | ||||||
| chr9:83010816
|
G | C | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.844-1060C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83010816 | ||||||
| chr9:83010853
|
C | T | 8 | a0002c0002t0002g0052a0002c0002t0003g0001a0002c0002t0008g0155others(5): Show | 9 | HG02055.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-1097G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83010853 | ||||||
| chr9:83011020
|
C | A | 3 | a0002c0002t0005g0287a0002c0002t0011g0074a0002c0002t0011g0075 | 3 | HG02970.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.844-1264G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011020 | ||||||
| chr9:83011048
|
T | C | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.844-1292A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011048 | ||||||
| chr9:83011130
|
C | T | 2 | a0001c0001t0014g0008a0001c0001t0014g0157 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.843+1304G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011130 | ||||||
| chr9:83011131
|
G | A | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG00544.hp2 HG02056.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.843+1303C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011131 | ||||||
| chr9:83011261
|
G | A | 15 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(12): Show | 15 | HG03017.hp2 HG03942.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.843+1173C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011261 | ||||||
| chr9:83011357
|
C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(174): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.843+1077G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011357 | ||||||
| chr9:83011363
|
C | T | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.843+1071G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011363 | ||||||
| chr9:83011422
|
C | A | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.843+1012G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011422 | ||||||
| chr9:83011439
|
C | A | 1 | a0002c0002t0002g0060 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.843+995G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011439 | ||||||
| chr9:83011491
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.843+943C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011491 | ||||||
| chr9:83011507
|
G | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(170): Show | 174 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.843+927C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011507 | ||||||
| chr9:83011550
|
C | CA | 37 | a0001c0001t0014g0008a0001c0001t0014g0157a0002c0002t0001g0061others(34): Show | 38 | HG01123.hp1 HG01255.hp2 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.843+883dupT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011550 | ||||||
| chr9:83011550
|
C | CAA | 11 | a0001c0001t0001g0047a0001c0001t0001g0312a0001c0001t0016g0211others(8): Show | 11 | HG00673.hp2 HG01891.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.843+882_843+883dup others(2): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011550 | ||||||
| chr9:83011550
|
C | CAAA | 102 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.843+881_843+883dup others(3): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011550 | ||||||
| chr9:83011550
|
C | CAAAA | 49 | a0001c0001t0001g0050a0001c0001t0001g0140a0001c0001t0001g0143others(46): Show | 49 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.843+880_843+883dup others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011550 | ||||||
| chr9:83011550
|
C | CAAAAA | 13 | a0001c0001t0001g0049a0001c0001t0001g0123a0001c0001t0001g0230others(10): Show | 13 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.843+879_843+883dup others(5): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011550 | ||||||
| chr9:83011550
|
CA | C | 8 | a0002c0002t0002g0108a0002c0002t0002g0111a0002c0004t0001g0278others(5): Show | 8 | HG02257.hp1 HG02735.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.843+883delT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011550 | ||||||
| chr9:83011567
|
A | C | 1 | a0002c0002t0005g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.843+867T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011567 | ||||||
| chr9:83011712
|
CA | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(174): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.843+721delT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011712 | ||||||
| chr9:83011726
|
A | T | 1 | a0005c0006t0037g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.843+708T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011726 | ||||||
| chr9:83012088
|
A | T | 1 | a0002c0002t0002g0102 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.843+346T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83012088 | ||||||
| chr9:83012266
|
G | A | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.843+168C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83012266 | ||||||
| chr9:83012431
|
T | C | 1 | a0002c0002t0002g0104 | 1 | HG01168.hp1 | splice_region_variant&intron_variant | LOW | c.843+3A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83012431 | ||||||
| chr9:83012625
|
A | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(170): Show | 174 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.766-114T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83012625 | ||||||
| chr9:83012639
|
C | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(205): Show | 209 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.766-128G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83012639 | ||||||
| chr9:83012733
|
C | T | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.766-222G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83012733 | ||||||
| chr9:83012818
|
A | G | 1 | a0002c0004t0012g0281 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.766-307T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83012818 | ||||||
| chr9:83013036
|
C | T | 3 | a0002c0002t0002g0098a0002c0002t0002g0119a0002c0002t0020g0003 | 3 | NA18975.hp2 NA18988.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.766-525G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83013036 | ||||||
| chr9:83013154
|
C | T | 8 | a0001c0001t0001g0123a0001c0001t0001g0226a0001c0001t0001g0260others(5): Show | 8 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.766-643G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83013154 | ||||||
| chr9:83013368
|
CCTTGCCA others(8): Show |
C | 1 | a0002c0002t0008g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.766-872_766-858del others(15): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83013368 | ||||||
| chr9:83013460
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.766-949G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83013460 | ||||||
| chr9:83013903
|
C | T | 4 | a0001c0001t0001g0312a0001c0001t0014g0008a0001c0001t0014g0157others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-1392G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83013903 | ||||||
| chr9:83013984
|
T | C | 1 | a0001c0001t0022g0320 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.766-1473A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83013984 | ||||||
| chr9:83013987
|
G | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(174): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.766-1476C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83013987 | ||||||
| chr9:83014025
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.766-1514C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83014025 | ||||||
| chr9:83014130
|
C | T | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.766-1619G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83014130 | ||||||
| chr9:83014198
|
G | T | 3 | a0002c0002t0005g0287a0002c0002t0011g0074a0002c0002t0011g0075 | 3 | HG02970.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.765+1607C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83014198 | ||||||
| chr9:83014368
|
A | G | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.765+1437T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83014368 | ||||||
| chr9:83014607
|
C | A | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.765+1198G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83014607 | ||||||
| chr9:83014668
|
A | G | 1 | a0001c0001t0001g0317 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.765+1137T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83014668 | ||||||
| chr9:83014738
|
A | T | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.765+1067T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83014738 | ||||||
| chr9:83015193
|
C | T | 4 | a0001c0001t0001g0312a0001c0001t0014g0008a0001c0001t0014g0157others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.765+612G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83015193 | ||||||
| chr9:83015297
|
A | T | 1 | a0001c0001t0016g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.765+508T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83015297 | ||||||
| chr9:83015463
|
C | CT | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG01243.hp2 HG03239.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+341dupA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83015463 | ||||||
| chr9:83015517
|
T | A | 2 | a0001c0001t0017g0310a0001c0001t0017g0311 | 2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.765+288A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83015517 | ||||||
| chr9:83015706
|
C | T | 169 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(166): Show | 170 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.765+99G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83015706 | ||||||
| chr9:83015750
|
T | C | 3 | a0001c0001t0001g0219a0001c0001t0001g0282a0001c0001t0022g0320 | 3 | HG02647.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.765+55A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83015750 | ||||||
| chr9:83015952
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.670-52G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83015952 | ||||||
| chr9:83015996
|
C | T | 1 | a0002c0002t0002g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.670-96G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83015996 | ||||||
| chr9:83016040
|
G | A | 1 | a0002c0002t0001g0137 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.670-140C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83016040 | ||||||
| chr9:83016052
|
T | C | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670-152A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83016052 | ||||||
| chr9:83016399
|
T | G | 1 | a0002c0002t0013g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.670-499A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83016399 | ||||||
| chr9:83016411
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0247 | 2 | HG00408.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.670-511C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83016411 | ||||||
| chr9:83016471
|
TG | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(170): Show | 174 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.670-572delC | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83016471 | ||||||
| chr9:83016626
|
A | G | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670-726T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83016626 | ||||||
| chr9:83016654
|
T | C | 15 | a0002c0002t0004g0009a0002c0002t0004g0012a0002c0002t0004g0013others(12): Show | 15 | HG03017.hp2 HG03942.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.670-754A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83016654 | ||||||
| chr9:83016762
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.670-862C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83016762 | ||||||
| chr9:83016900
|
G | A | 3 | a0002c0002t0003g0001a0002c0002t0008g0309a0002c0002t0010g0304 | 4 | HG02559.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-1000C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83016900 | ||||||
| chr9:83017278
|
G | C | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.670-1378C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017278 | ||||||
| chr9:83017321
|
TA | T | 8 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0295others(5): Show | 8 | HG01123.hp1 HG02922.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.670-1422delT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017321 | ||||||
| chr9:83017339
|
A | AG | 3 | a0001c0001t0001g0189a0001c0001t0001g0244a0001c0001t0018g0006 | 3 | HG03130.hp2 HG04228.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.670-1440_670-1439i others(3): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017339 | ||||||
| chr9:83017339
|
A | G | 170 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(167): Show | 171 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.670-1439T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017339 | ||||||
| chr9:83017356
|
C | T | 6 | a0002c0002t0002g0125a0002c0002t0002g0126a0002c0002t0002g0127others(3): Show | 6 | HG01358.hp2 HG01934.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-1456G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017356 | ||||||
| chr9:83017369
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(205): Show | 209 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.670-1469T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017369 | ||||||
| chr9:83017375
|
C | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(168): Show | 172 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.670-1475G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017375 | ||||||
| chr9:83017390
|
C | T | 169 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(166): Show | 170 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.670-1490G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017390 | ||||||
| chr9:83017392
|
C | G | 5 | a0002c0004t0001g0278a0002c0004t0010g0280a0002c0004t0012g0208others(2): Show | 5 | HG00735.hp2 HG03017.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-1492G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017392 | ||||||
| chr9:83017431
|
T | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(205): Show | 209 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.670-1531A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017431 | ||||||
| chr9:83017486
|
C | T | 1 | a0002c0002t0002g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.670-1586G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017486 | ||||||
| chr9:83017499
|
C | CA | 173 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(170): Show | 174 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.670-1600dupT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017499 | ||||||
| chr9:83017706
|
G | T | 59 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0002g0052others(56): Show | 60 | HG00735.hp2 HG01123.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.670-1806C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017706 | ||||||
| chr9:83017723
|
T | C | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.670-1823A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017723 | ||||||
| chr9:83017726
|
C | T | 7 | a0002c0002t0001g0061a0003c0003t0006g0210a0003c0003t0006g0215others(4): Show | 7 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-1826G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017726 | ||||||
| chr9:83017746
|
A | G | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.670-1846T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017746 | ||||||
| chr9:83017848
|
T | C | 31 | a0002c0002t0003g0202a0002c0002t0004g0009a0002c0002t0004g0012others(28): Show | 31 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.670-1948A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017848 | ||||||
| chr9:83017937
|
A | C | 1 | a0002c0002t0025g0116 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.670-2037T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017937 | ||||||
| chr9:83017969
|
T | C | 1 | a0001c0001t0002g0028 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.670-2069A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017969 | ||||||
| chr9:83018071
|
T | C | 1 | a0002c0002t0002g0109 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.670-2171A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018071 | ||||||
| chr9:83018224
|
A | ATC | 234 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(231): Show | 236 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.670-2325_670-2324i others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018224 | ||||||
| chr9:83018286
|
C | T | 1 | a0001c0001t0003g0270 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.670-2386G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018286 | ||||||
| chr9:83018289
|
G | C | 37 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(34): Show | 37 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.670-2389C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018289 | ||||||
| chr9:83018325
|
C | T | 4 | a0002c0002t0002g0071a0002c0002t0002g0088a0002c0002t0002g0089others(1): Show | 4 | HG00140.hp1 HG00733.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-2425G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018325 | ||||||
| chr9:83018488
|
TGTCAATT others(19): Show |
T | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.670-2614_670-2589d others(28): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018488 | ||||||
| chr9:83018501
|
C | T | 23 | a0001c0001t0001g0312a0001c0001t0014g0008a0001c0001t0014g0157others(20): Show | 23 | HG01891.hp1 HG02258.hp2 HG02615.hp1 others(20): Show |
intron_variant | MODIFIER | c.670-2601G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018501 | ||||||
| chr9:83018575
|
T | A | 167 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(164): Show | 168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.670-2675A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018575 | ||||||
| chr9:83018594
|
G | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.670-2694C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018594 | ||||||
| chr9:83018626
|
C | A | 4 | a0001c0001t0001g0312a0001c0001t0014g0008a0001c0001t0014g0157others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-2726G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018626 | ||||||
| chr9:83018686
|
CTTA | C | 167 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(164): Show | 168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.670-2789_670-2787d others(5): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018686 | ||||||
| chr9:83018688
|
T | TATTATAA others(69): Show |
1 | a0002c0002t0002g0114 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.670-2864_670-2789d others(78): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018688 | ||||||
| chr9:83018807
|
A | G | 2 | a0002c0002t0004g0009a0002c0002t0004g0015 | 2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.670-2907T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018807 | ||||||
| chr9:83018955
|
T | G | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670-3055A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018955 | ||||||
| chr9:83019016
|
G | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(205): Show | 209 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.670-3116C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019016 | ||||||
| chr9:83019119
|
G | A | 1 | a0002c0002t0026g0055 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.669+3217C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019119 | ||||||
| chr9:83019166
|
A | C | 1 | a0002c0002t0002g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.669+3170T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019166 | ||||||
| chr9:83019236
|
G | A | 3 | a0002c0002t0002g0098a0002c0002t0002g0119a0002c0002t0020g0003 | 3 | NA18975.hp2 NA18988.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.669+3100C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019236 | ||||||
| chr9:83019271
|
T | A | 47 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0139others(44): Show | 48 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.669+3065A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019271 | ||||||
| chr9:83019272
|
A | T | 3 | a0001c0001t0006g0209a0004c0005t0019g0328a0004c0005t0019g0329 | 3 | HG03130.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.669+3064T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019272 | ||||||
| chr9:83019282
|
G | T | 1 | a0001c0001t0006g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.669+3054C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019282 | ||||||
| chr9:83019328
|
A | AAT | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.669+3006_669+3007d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019328 | ||||||
| chr9:83019328
|
A | T | 1 | a0002c0002t0002g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.669+3008T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019328 | ||||||
| chr9:83019389
|
T | C | 2 | a0002c0002t0003g0202a0002c0002t0005g0201 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.669+2947A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019389 | ||||||
| chr9:83019660
|
C | A | 222 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0123others(219): Show | 224 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.669+2676G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019660 | ||||||
| chr9:83019722
|
G | A | 1 | a0001c0001t0006g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.669+2614C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019722 | ||||||
| chr9:83019789
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.669+2547A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019789 | ||||||
| chr9:83019813
|
G | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.669+2523C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019813 | ||||||
| chr9:83019833
|
A | G | 167 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(164): Show | 168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.669+2503T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83019833 | ||||||
| chr9:83020111
|
T | TA | 5 | a0002c0011t0010g0041a0004c0005t0019g0328a0004c0005t0019g0329others(2): Show | 5 | HG02257.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+2224dupT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83020111 | ||||||
| chr9:83020152
|
T | A | 1 | a0002c0002t0002g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.669+2184A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83020152 | ||||||
| chr9:83020215
|
A | G | 2 | a0002c0002t0009g0204a0002c0002t0024g0203 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.669+2121T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83020215 | ||||||
| chr9:83020220
|
A | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0123others(151): Show | 155 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.669+2116T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83020220 | ||||||
| chr9:83020404
|
A | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0301 | 2 | NA18939.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.669+1932T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83020404 | ||||||
| chr9:83020477
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.669+1859A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83020477 | ||||||
| chr9:83020504
|
C | T | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.669+1832G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83020504 | ||||||
| chr9:83020535
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.669+1801G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83020535 | ||||||
| chr9:83020549
|
G | A | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.669+1787C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83020549 | ||||||
| chr9:83020724
|
A | G | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.669+1612T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83020724 | ||||||
| chr9:83020813
|
A | G | 3 | a0002c0002t0001g0062a0002c0002t0001g0084a0002c0002t0001g0087 | 3 | NA18944.hp1 NA18951.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.669+1523T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83020813 | ||||||
| chr9:83020942
|
T | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+1394A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83020942 | ||||||
| chr9:83021019
|
A | T | 1 | a0001c0001t0006g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.669+1317T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83021019 | ||||||
| chr9:83021228
|
T | C | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.669+1108A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83021228 | ||||||
| chr9:83021258
|
G | T | 3 | a0002c0002t0005g0287a0002c0002t0011g0074a0002c0002t0011g0075 | 3 | HG02970.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.669+1078C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83021258 | ||||||
| chr9:83021338
|
A | G | 3 | a0002c0011t0010g0041a0006c0007t0010g0323a0006c0007t0010g0324 | 3 | HG02257.hp1 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.669+998T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83021338 | ||||||
| chr9:83021456
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.669+880A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83021456 | ||||||
| chr9:83021502
|
A | G | 1 | a0002c0002t0001g0105 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.669+834T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83021502 | ||||||
| chr9:83021725
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.669+611C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83021725 | ||||||
| chr9:83021751
|
T | G | 2 | a0002c0002t0011g0074a0002c0002t0011g0075 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.669+585A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83021751 | ||||||
| chr9:83021815
|
C | T | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.669+521G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83021815 | ||||||
| chr9:83021888
|
A | C | 1 | a0002c0011t0010g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.669+448T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83021888 | ||||||
| chr9:83021937
|
G | C | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.669+399C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83021937 | ||||||
| chr9:83022051
|
T | G | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.669+285A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83022051 | ||||||
| chr9:83022615
|
A | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-189T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83022615 | ||||||
| chr9:83022629
|
T | A | 1 | a0002c0002t0002g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.579-203A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83022629 | ||||||
| chr9:83022664
|
A | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(187): Show | 192 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.579-238T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83022664 | ||||||
| chr9:83022803
|
G | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-377C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83022803 | ||||||
| chr9:83023041
|
G | T | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.579-615C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023041 | ||||||
| chr9:83023092
|
C | A | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.579-666G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023092 | ||||||
| chr9:83023136
|
T | C | 2 | a0001c0001t0003g0290a0001c0001t0003g0293 | 2 | HG00673.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.579-710A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023136 | ||||||
| chr9:83023237
|
G | A | 5 | a0002c0002t0002g0094a0002c0002t0002g0095a0002c0002t0002g0096others(2): Show | 5 | HG01106.hp2 HG01167.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.579-811C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023237 | ||||||
| chr9:83023268
|
A | G | 2 | a0001c0001t0001g0312a0001c0001t0033g0040 | 2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.579-842T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023268 | ||||||
| chr9:83023399
|
C | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-973G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023399 | ||||||
| chr9:83023484
|
TCA | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-1060_579-1059d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023484 | ||||||
| chr9:83023541
|
G | A | 1 | a0002c0002t0002g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.579-1115C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023541 | ||||||
| chr9:83023708
|
C | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-1282G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023708 | ||||||
| chr9:83023734
|
C | T | 20 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0002g0035others(17): Show | 20 | HG00642.hp1 HG01123.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.579-1308G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023734 | ||||||
| chr9:83023801
|
A | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-1375T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023801 | ||||||
| chr9:83023813
|
A | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-1387T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023813 | ||||||
| chr9:83023907
|
G | T | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.579-1481C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023907 | ||||||
| chr9:83023908
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-1482A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023908 | ||||||
| chr9:83023922
|
G | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-1496C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023922 | ||||||
| chr9:83023955
|
C | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-1529G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023955 | ||||||
| chr9:83023970
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-1544A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023970 | ||||||
| chr9:83023994
|
G | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-1568C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83023994 | ||||||
| chr9:83024003
|
T | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-1577A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024003 | ||||||
| chr9:83024027
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-1601A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024027 | ||||||
| chr9:83024043
|
A | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-1617T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024043 | ||||||
| chr9:83024064
|
C | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.579-1638G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024064 | ||||||
| chr9:83024068
|
A | G | 12 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0139others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.579-1642T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024068 | ||||||
| chr9:83024122
|
T | C | 19 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(16): Show | 19 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.578+1653A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024122 | ||||||
| chr9:83024288
|
A | C | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.578+1487T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024288 | ||||||
| chr9:83024339
|
T | TC | 19 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(16): Show | 19 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.578+1435dupG | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024339 | ||||||
| chr9:83024344
|
A | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(188): Show | 193 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.578+1431T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024344 | ||||||
| chr9:83024434
|
T | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+1341A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024434 | ||||||
| chr9:83024509
|
C | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+1266G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024509 | ||||||
| chr9:83024542
|
C | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+1233G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024542 | ||||||
| chr9:83024569
|
C | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+1206G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024569 | ||||||
| chr9:83024579
|
G | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+1196C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024579 | ||||||
| chr9:83024707
|
C | T | 5 | a0002c0004t0001g0278a0002c0004t0010g0280a0002c0004t0012g0208others(2): Show | 5 | HG00735.hp2 HG03017.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.578+1068G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024707 | ||||||
| chr9:83024708
|
G | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(187): Show | 192 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.578+1067C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024708 | ||||||
| chr9:83024762
|
C | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+1013G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024762 | ||||||
| chr9:83024763
|
G | A | 12 | a0002c0002t0002g0052a0002c0002t0008g0155a0002c0002t0008g0212others(9): Show | 12 | HG00735.hp2 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.578+1012C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024763 | ||||||
| chr9:83024764
|
T | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+1011A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024764 | ||||||
| chr9:83024776
|
G | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+999C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024776 | ||||||
| chr9:83024788
|
C | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+987G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024788 | ||||||
| chr9:83024849
|
C | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+926G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024849 | ||||||
| chr9:83024859
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+916A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024859 | ||||||
| chr9:83024929
|
C | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+846G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024929 | ||||||
| chr9:83024943
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(187): Show | 192 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.578+832A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024943 | ||||||
| chr9:83024977
|
T | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+798A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024977 | ||||||
| chr9:83025057
|
G | A | 2 | a0001c0001t0014g0008a0001c0001t0014g0157 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.578+718C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025057 | ||||||
| chr9:83025080
|
C | T | 1 | a0002c0004t0027g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.578+695G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025080 | ||||||
| chr9:83025098
|
G | GT | 10 | a0001c0001t0001g0173a0001c0001t0001g0230a0001c0001t0001g0233others(7): Show | 10 | HG00438.hp1 HG00639.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.578+676dupA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025098 | ||||||
| chr9:83025098
|
G | GTTT | 15 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(12): Show | 15 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.578+674_578+676dup others(3): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025098 | ||||||
| chr9:83025098
|
G | T | 1 | a0002c0002t0009g0163 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.578+677C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025098 | ||||||
| chr9:83025131
|
A | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+644T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025131 | ||||||
| chr9:83025138
|
T | C | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.578+637A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025138 | ||||||
| chr9:83025156
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+619A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025156 | ||||||
| chr9:83025167
|
G | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+608C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025167 | ||||||
| chr9:83025179
|
G | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+596C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025179 | ||||||
| chr9:83025210
|
T | G | 5 | a0002c0002t0002g0053a0002c0002t0002g0068a0002c0002t0002g0079others(2): Show | 5 | HG01081.hp1 HG02698.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.578+565A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025210 | ||||||
| chr9:83025223
|
G | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0213a0001c0001t0001g0221others(12): Show | 16 | HG00408.hp1 HG00544.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.578+552C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025223 | ||||||
| chr9:83025240
|
A | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+535T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025240 | ||||||
| chr9:83025293
|
A | T | 1 | a0001c0001t0001g0266 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.578+482T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025293 | ||||||
| chr9:83025339
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+436A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025339 | ||||||
| chr9:83025459
|
G | T | 1 | a0002c0002t0001g0137 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.578+316C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025459 | ||||||
| chr9:83025472
|
C | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.578+303G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025472 | ||||||
| chr9:83025759
|
G | A | 1 | a0002c0002t0005g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.578+16C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83025759 | ||||||
| chr9:83025984
|
G | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-63C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83025984 | ||||||
| chr9:83026007
|
A | G | 2 | a0002c0002t0011g0074a0002c0002t0011g0075 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.432-86T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026007 | ||||||
| chr9:83026083
|
G | T | 170 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(167): Show | 172 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.432-162C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026083 | ||||||
| chr9:83026239
|
A | T | 166 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(163): Show | 168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.432-318T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026239 | ||||||
| chr9:83026266
|
T | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(207): Show | 212 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.432-345A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026266 | ||||||
| chr9:83026300
|
G | A | 5 | a0001c0001t0003g0269a0001c0001t0003g0272a0001c0001t0003g0273others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.432-379C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026300 | ||||||
| chr9:83026308
|
A | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-387T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026308 | ||||||
| chr9:83026322
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-401A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026322 | ||||||
| chr9:83026392
|
C | T | 7 | a0002c0002t0002g0052a0002c0002t0008g0155a0002c0002t0008g0212others(4): Show | 7 | HG02055.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.432-471G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026392 | ||||||
| chr9:83026415
|
G | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-494C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026415 | ||||||
| chr9:83026416
|
G | T | 5 | a0002c0004t0001g0278a0002c0004t0010g0280a0002c0004t0012g0208others(2): Show | 5 | HG00735.hp2 HG03017.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.432-495C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026416 | ||||||
| chr9:83026447
|
G | C | 2 | a0002c0002t0011g0074a0002c0002t0011g0075 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.432-526C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026447 | ||||||
| chr9:83026624
|
T | G | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.432-703A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026624 | ||||||
| chr9:83026708
|
C | T | 1 | a0002c0002t0001g0105 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.432-787G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026708 | ||||||
| chr9:83026945
|
A | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-1024T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026945 | ||||||
| chr9:83027094
|
T | C | 1 | a0002c0002t0002g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.432-1173A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83027094 | ||||||
| chr9:83027164
|
G | A | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.432-1243C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83027164 | ||||||
| chr9:83027191
|
C | G | 1 | a0002c0002t0005g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.432-1270G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83027191 | ||||||
| chr9:83027334
|
C | G | 3 | a0001c0001t0001g0263a0001c0001t0001g0265a0001c0001t0002g0264 | 3 | HG02056.hp1 NA18945.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.432-1413G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83027334 | ||||||
| chr9:83027397
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(187): Show | 192 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.432-1476A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83027397 | ||||||
| chr9:83027616
|
C | T | 1 | a0002c0002t0002g0138 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.432-1695G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83027616 | ||||||
| chr9:83027703
|
C | T | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.432-1782G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83027703 | ||||||
| chr9:83027742
|
G | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-1821C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83027742 | ||||||
| chr9:83027789
|
C | G | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.432-1868G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83027789 | ||||||
| chr9:83027813
|
T | C | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.432-1892A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83027813 | ||||||
| chr9:83028248
|
T | C | 5 | a0002c0002t0002g0125a0002c0002t0002g0126a0002c0002t0002g0127others(2): Show | 5 | HG01358.hp2 HG01934.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.432-2327A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83028248 | ||||||
| chr9:83028683
|
C | T | 20 | a0001c0001t0001g0229a0001c0001t0015g0037a0001c0001t0015g0038others(17): Show | 20 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.432-2762G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83028683 | ||||||
| chr9:83028688
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0123others(151): Show | 156 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.432-2767G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83028688 | ||||||
| chr9:83028880
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-2959A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83028880 | ||||||
| chr9:83028971
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.432-3050C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83028971 | ||||||
| chr9:83029083
|
C | G | 1 | a0001c0001t0001g0285 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.432-3162G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029083 | ||||||
| chr9:83029162
|
G | A | 6 | a0002c0002t0007g0192a0002c0002t0007g0195a0002c0002t0007g0197others(3): Show | 6 | HG01123.hp1 HG01255.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-3241C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029162 | ||||||
| chr9:83029389
|
C | A | 17 | a0001c0001t0006g0209a0002c0002t0001g0011a0002c0002t0004g0009others(14): Show | 17 | HG03017.hp2 HG03195.hp2 HG03942.hp1 others(14): Show |
intron_variant | MODIFIER | c.432-3468G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029389 | ||||||
| chr9:83029389
|
C | T | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.432-3468G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029389 | ||||||
| chr9:83029393
|
CT | C | 13 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0002g0302others(10): Show | 13 | HG01167.hp1 HG01517.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.432-3473delA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029393 | ||||||
| chr9:83029559
|
AT | A | 211 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0123others(208): Show | 213 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.432-3639delA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029559 | ||||||
| chr9:83029559
|
ATT | A | 7 | a0001c0001t0001g0229a0001c0001t0017g0310a0001c0001t0017g0311others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.432-3640_432-3639d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029559 | ||||||
| chr9:83029623
|
C | G | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-3702G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029623 | ||||||
| chr9:83029658
|
A | G | 1 | a0002c0002t0002g0128 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.432-3737T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029658 | ||||||
| chr9:83029666
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0123others(151): Show | 156 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.432-3745G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029666 | ||||||
| chr9:83029875
|
G | C | 1 | a0001c0001t0016g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.432-3954C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029875 | ||||||
| chr9:83029890
|
G | T | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.432-3969C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029890 | ||||||
| chr9:83029946
|
T | C | 1 | a0002c0002t0002g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.432-4025A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029946 | ||||||
| chr9:83030088
|
G | C | 1 | a0001c0001t0018g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.432-4167C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83030088 | ||||||
| chr9:83030135
|
T | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-4214A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83030135 | ||||||
| chr9:83030310
|
T | C | 2 | a0002c0002t0008g0309a0002c0002t0010g0304 | 2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.432-4389A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83030310 | ||||||
| chr9:83030818
|
C | T | 2 | a0002c0002t0007g0073a0002c0002t0026g0055 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.432-4897G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83030818 | ||||||
| chr9:83030889
|
C | A | 1 | a0001c0001t0016g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.432-4968G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83030889 | ||||||
| chr9:83030968
|
G | A | 167 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(164): Show | 169 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.432-5047C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83030968 | ||||||
| chr9:83031147
|
G | A | 1 | a0002c0002t0002g0082 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.432-5226C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83031147 | ||||||
| chr9:83031226
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG00544.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.432-5305T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83031226 | ||||||
| chr9:83031231
|
C | A | 1 | a0002c0002t0004g0016 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.432-5310G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83031231 | ||||||
| chr9:83031253
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-5332A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83031253 | ||||||
| chr9:83031361
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-5440A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83031361 | ||||||
| chr9:83031432
|
A | G | 1 | a0002c0002t0001g0061 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.432-5511T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83031432 | ||||||
| chr9:83031485
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.432-5564G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83031485 | ||||||
| chr9:83031643
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-5722A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83031643 | ||||||
| chr9:83031864
|
T | G | 1 | a0001c0001t0016g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.432-5943A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83031864 | ||||||
| chr9:83031958
|
T | C | 4 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0025others(1): Show | 4 | NA18972.hp2 NA18979.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-6037A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83031958 | ||||||
| chr9:83032072
|
T | G | 226 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(223): Show | 228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.432-6151A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83032072 | ||||||
| chr9:83032154
|
T | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-6233A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83032154 | ||||||
| chr9:83032187
|
G | A | 167 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(164): Show | 169 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.432-6266C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83032187 | ||||||
| chr9:83032227
|
C | T | 3 | a0002c0002t0002g0010a0002c0002t0002g0014a0002c0002t0002g0027 | 3 | HG02135.hp1 NA18994.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.432-6306G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83032227 | ||||||
| chr9:83032272
|
C | T | 12 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0139others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.432-6351G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83032272 | ||||||
| chr9:83032287
|
T | G | 3 | a0002c0011t0010g0041a0006c0007t0010g0323a0006c0007t0010g0324 | 3 | HG02257.hp1 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.432-6366A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83032287 | ||||||
| chr9:83032391
|
A | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(164): Show | 169 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.432-6470T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83032391 | ||||||
| chr9:83032418
|
T | C | 3 | a0002c0002t0004g0017a0002c0002t0004g0021a0002c0002t0004g0022 | 3 | NA18940.hp1 NA19057.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.432-6497A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83032418 | ||||||
| chr9:83032672
|
G | A | 1 | a0002c0002t0002g0128 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.432-6751C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83032672 | ||||||
| chr9:83032739
|
T | C | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.432-6818A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83032739 | ||||||
| chr9:83032746
|
T | A | 3 | a0002c0002t0005g0287a0002c0002t0011g0074a0002c0002t0011g0075 | 3 | HG02970.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.432-6825A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83032746 | ||||||
| chr9:83032753
|
G | A | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.432-6832C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83032753 | ||||||
| chr9:83032828
|
C | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-6907G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83032828 | ||||||
| chr9:83033097
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.432-7176A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83033097 | ||||||
| chr9:83033192
|
T | A | 1 | a0002c0002t0002g0060 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.432-7271A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83033192 | ||||||
| chr9:83033392
|
C | T | 16 | a0002c0002t0001g0054a0002c0002t0001g0061a0002c0002t0001g0062others(13): Show | 16 | HG00558.hp1 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.432-7471G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83033392 | ||||||
| chr9:83033490
|
G | A | 1 | a0002c0002t0002g0034 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.432-7569C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83033490 | ||||||
| chr9:83033567
|
G | A | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.432-7646C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83033567 | ||||||
| chr9:83033756
|
G | T | 1 | a0002c0002t0023g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.432-7835C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83033756 | ||||||
| chr9:83033899
|
G | A | 6 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 6 | HG00280.hp1 HG01123.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-7978C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83033899 | ||||||
| chr9:83034204
|
G | C | 1 | a0001c0001t0001g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.432-8283C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83034204 | ||||||
| chr9:83034506
|
C | T | 1 | a0001c0001t0002g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.432-8585G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83034506 | ||||||
| chr9:83034636
|
G | A | 231 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(228): Show | 233 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.432-8715C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83034636 | ||||||
| chr9:83034666
|
C | A | 22 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(19): Show | 22 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.432-8745G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83034666 | ||||||
| chr9:83034842
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.432-8921C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83034842 | ||||||
| chr9:83034967
|
A | G | 4 | a0001c0001t0001g0312a0001c0001t0014g0008a0001c0001t0014g0157others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-9046T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83034967 | ||||||
| chr9:83035065
|
T | C | 1 | a0001c0001t0001g0301 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.432-9144A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035065 | ||||||
| chr9:83035069
|
C | T | 30 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0047others(27): Show | 30 | HG00438.hp2 HG02071.hp2 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.432-9148G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035069 | ||||||
| chr9:83035092
|
T | C | 7 | a0002c0002t0002g0052a0002c0002t0008g0155a0002c0002t0008g0212others(4): Show | 7 | HG02055.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.432-9171A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035092 | ||||||
| chr9:83035144
|
C | T | 15 | a0001c0001t0003g0144a0001c0001t0003g0207a0001c0001t0003g0214others(12): Show | 16 | HG00140.hp2 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.432-9223G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035144 | ||||||
| chr9:83035156
|
T | C | 1 | a0002c0002t0020g0003 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.432-9235A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035156 | ||||||
| chr9:83035166
|
G | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-9245C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035166 | ||||||
| chr9:83035300
|
T | C | 1 | a0001c0001t0003g0291 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.432-9379A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035300 | ||||||
| chr9:83035383
|
A | G | 2 | a0003c0003t0006g0217a0003c0003t0034g0135 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.432-9462T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035383 | ||||||
| chr9:83035428
|
G | C | 1 | a0009c0012t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.432-9507C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035428 | ||||||
| chr9:83035553
|
G | A | 1 | a0001c0001t0016g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.432-9632C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035553 | ||||||
| chr9:83035559
|
G | T | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.432-9638C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035559 | ||||||
| chr9:83035611
|
A | G | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.432-9690T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035611 | ||||||
| chr9:83035744
|
CA | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-9824delT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035744 | ||||||
| chr9:83035860
|
G | A | 1 | a0002c0002t0009g0163 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.432-9939C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83035860 | ||||||
| chr9:83036001
|
C | T | 218 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0123others(215): Show | 220 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.432-10080G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036001 | ||||||
| chr9:83036171
|
G | C | 1 | a0002c0004t0010g0280 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.432-10250C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036171 | ||||||
| chr9:83036263
|
T | C | 6 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0002g0028others(3): Show | 6 | NA18612.hp2 NA18975.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-10342A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036263 | ||||||
| chr9:83036279
|
T | C | 2 | a0001c0001t0006g0209a0002c0002t0002g0120 | 2 | HG01175.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.432-10358A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036279 | ||||||
| chr9:83036295
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | NA18953.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.432-10374G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036295 | ||||||
| chr9:83036366
|
G | T | 1 | a0001c0001t0001g0183 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.432-10445C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036366 | ||||||
| chr9:83036388
|
T | C | 4 | a0001c0001t0035g0327a0002c0011t0010g0041a0006c0007t0010g0323others(1): Show | 4 | HG02257.hp1 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.432-10467A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036388 | ||||||
| chr9:83036498
|
G | T | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.432-10577C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036498 | ||||||
| chr9:83036558
|
C | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-10637G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036558 | ||||||
| chr9:83036563
|
C | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-10642G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036563 | ||||||
| chr9:83036679
|
G | A | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.432-10758C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036679 | ||||||
| chr9:83036810
|
A | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-10889T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036810 | ||||||
| chr9:83036855
|
T | C | 1 | a0002c0002t0002g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.432-10934A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036855 | ||||||
| chr9:83036903
|
T | A | 1 | a0002c0002t0002g0138 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.432-10982A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036903 | ||||||
| chr9:83036904
|
A | T | 34 | a0001c0001t0003g0144a0001c0001t0003g0207a0001c0001t0003g0214others(31): Show | 35 | HG00140.hp2 HG01123.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.432-10983T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036904 | ||||||
| chr9:83036977
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.432-11056T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036977 | ||||||
| chr9:83036982
|
G | A | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.432-11061C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83036982 | ||||||
| chr9:83037247
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG01346.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.432-11326A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037247 | ||||||
| chr9:83037254
|
A | G | 22 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(19): Show | 22 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.432-11333T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037254 | ||||||
| chr9:83037295
|
A | G | 22 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(19): Show | 22 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.432-11374T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037295 | ||||||
| chr9:83037311
|
C | CA | 22 | a0001c0001t0001g0219a0001c0001t0015g0037a0001c0001t0015g0038others(19): Show | 22 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.432-11391dupT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037311 | ||||||
| chr9:83037425
|
C | CTTA | 22 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(19): Show | 22 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.432-11507_432-1150 others(7): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037425 | ||||||
| chr9:83037437
|
G | A | 4 | a0001c0001t0001g0312a0001c0001t0014g0008a0001c0001t0014g0157others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-11516C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037437 | ||||||
| chr9:83037470
|
A | G | 1 | a0005c0006t0037g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.432-11549T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037470 | ||||||
| chr9:83037474
|
A | G | 22 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(19): Show | 22 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.432-11553T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037474 | ||||||
| chr9:83037744
|
A | AT | 49 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0051others(46): Show | 49 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.432-11824dupA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037744 | ||||||
| chr9:83037744
|
A | ATT | 130 | a0001c0001t0001g0002a0001c0001t0001g0123a0001c0001t0001g0139others(127): Show | 132 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.432-11825_432-1182 others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037744 | ||||||
| chr9:83037744
|
AT | A | 39 | a0002c0002t0001g0011a0002c0002t0001g0097a0002c0002t0002g0065others(36): Show | 39 | HG01123.hp1 HG01175.hp2 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.432-11824delA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037744 | ||||||
| chr9:83037744
|
ATT | A | 8 | a0003c0003t0006g0210a0003c0003t0006g0215a0003c0003t0006g0216others(5): Show | 8 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.432-11825_432-1182 others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037744 | ||||||
| chr9:83037749
|
T | C | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.432-11828A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037749 | ||||||
| chr9:83037770
|
A | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-11849T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037770 | ||||||
| chr9:83037844
|
C | A | 1 | a0001c0001t0001g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.432-11923G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83037844 | ||||||
| chr9:83038123
|
A | T | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.432-12202T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038123 | ||||||
| chr9:83038305
|
C | T | 1 | a0002c0002t0005g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.432-12384G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038305 | ||||||
| chr9:83038306
|
G | A | 1 | a0002c0004t0012g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.432-12385C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038306 | ||||||
| chr9:83038418
|
T | G | 1 | a0002c0002t0002g0098 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.432-12497A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038418 | ||||||
| chr9:83038447
|
T | G | 1 | a0002c0002t0005g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.432-12526A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038447 | ||||||
| chr9:83038463
|
A | G | 17 | a0001c0001t0006g0209a0002c0002t0001g0011a0002c0002t0004g0009others(14): Show | 17 | HG03017.hp2 HG03195.hp2 HG03942.hp1 others(14): Show |
intron_variant | MODIFIER | c.432-12542T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038463 | ||||||
| chr9:83038474
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.432-12553A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038474 | ||||||
| chr9:83038483
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.432-12562A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038483 | ||||||
| chr9:83038491
|
A | G | 1 | a0006c0007t0010g0323 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.432-12570T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038491 | ||||||
| chr9:83038492
|
C | T | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.432-12571G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038492 | ||||||
| chr9:83038505
|
C | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-12584G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038505 | ||||||
| chr9:83038637
|
G | GAA | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-12718_432-1271 others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038637 | ||||||
| chr9:83038693
|
T | C | 1 | a0002c0004t0012g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.432-12772A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038693 | ||||||
| chr9:83038718
|
C | T | 22 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(19): Show | 22 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.432-12797G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038718 | ||||||
| chr9:83038868
|
T | C | 1 | a0002c0002t0001g0137 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.432-12947A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83038868 | ||||||
| chr9:83039138
|
T | C | 1 | a0009c0012t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.432-13217A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83039138 | ||||||
| chr9:83039197
|
G | C | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.432-13276C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83039197 | ||||||
| chr9:83039204
|
G | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-13283C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83039204 | ||||||
| chr9:83039624
|
G | A | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-13703C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83039624 | ||||||
| chr9:83039662
|
T | C | 1 | a0002c0002t0002g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.432-13741A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83039662 | ||||||
| chr9:83039696
|
A | G | 20 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(17): Show | 20 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.432-13775T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83039696 | ||||||
| chr9:83039811
|
A | G | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180 | 3 | HG01243.hp2 HG03239.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.432-13890T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83039811 | ||||||
| chr9:83039978
|
C | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-14057G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83039978 | ||||||
| chr9:83039980
|
G | T | 1 | a0002c0002t0002g0044 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.432-14059C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83039980 | ||||||
| chr9:83040022
|
G | A | 17 | a0001c0001t0006g0209a0002c0002t0001g0011a0002c0002t0004g0009others(14): Show | 17 | HG03017.hp2 HG03195.hp2 HG03942.hp1 others(14): Show |
intron_variant | MODIFIER | c.432-14101C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040022 | ||||||
| chr9:83040060
|
C | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-14139G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040060 | ||||||
| chr9:83040065
|
C | T | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-14144G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040065 | ||||||
| chr9:83040101
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-14180A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040101 | ||||||
| chr9:83040121
|
G | A | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.432-14200C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040121 | ||||||
| chr9:83040308
|
T | C | 4 | a0001c0001t0001g0312a0001c0001t0014g0008a0001c0001t0014g0157others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-14387A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040308 | ||||||
| chr9:83040363
|
T | C | 1 | a0002c0002t0023g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.432-14442A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040363 | ||||||
| chr9:83040423
|
T | G | 1 | a0001c0001t0001g0191 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.432-14502A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040423 | ||||||
| chr9:83040447
|
C | T | 22 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(19): Show | 22 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.432-14526G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040447 | ||||||
| chr9:83040463
|
A | G | 2 | a0002c0002t0002g0108a0002c0002t0002g0110 | 2 | HG02735.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.432-14542T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040463 | ||||||
| chr9:83040512
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.432-14591T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040512 | ||||||
| chr9:83040661
|
A | G | 4 | a0001c0001t0001g0312a0001c0001t0014g0008a0001c0001t0014g0157others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-14740T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040661 | ||||||
| chr9:83040758
|
G | A | 22 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(19): Show | 22 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.432-14837C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040758 | ||||||
| chr9:83040955
|
G | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-15034C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040955 | ||||||
| chr9:83040973
|
G | T | 1 | a0001c0001t0018g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.432-15052C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83040973 | ||||||
| chr9:83041204
|
T | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-15283A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83041204 | ||||||
| chr9:83041394
|
A | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-15473T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83041394 | ||||||
| chr9:83041438
|
C | G | 22 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(19): Show | 22 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.432-15517G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83041438 | ||||||
| chr9:83041487
|
G | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-15566C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83041487 | ||||||
| chr9:83041568
|
G | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-15647C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83041568 | ||||||
| chr9:83041575
|
G | C | 6 | a0003c0003t0006g0210a0003c0003t0006g0215a0003c0003t0006g0216others(3): Show | 6 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.432-15654C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83041575 | ||||||
| chr9:83041594
|
G | A | 3 | a0002c0002t0002g0066a0002c0002t0002g0070a0002c0002t0002g0100 | 3 | HG01255.hp1 HG01346.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.432-15673C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83041594 | ||||||
| chr9:83041641
|
C | T | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-15720G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83041641 | ||||||
| chr9:83041736
|
G | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-15815C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83041736 | ||||||
| chr9:83041812
|
G | C | 1 | a0002c0002t0002g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.432-15891C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83041812 | ||||||
| chr9:83041844
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-15923A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83041844 | ||||||
| chr9:83041939
|
C | T | 1 | a0002c0002t0005g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.432-16018G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83041939 | ||||||
| chr9:83042175
|
T | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-16254A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83042175 | ||||||
| chr9:83042200
|
T | C | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.432-16279A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83042200 | ||||||
| chr9:83042370
|
G | A | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.432-16449C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83042370 | ||||||
| chr9:83042402
|
A | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-16481T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83042402 | ||||||
| chr9:83042470
|
C | G | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-16549G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83042470 | ||||||
| chr9:83042571
|
G | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-16650C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83042571 | ||||||
| chr9:83042699
|
TCTGA | T | 19 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(16): Show | 19 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.432-16782_432-1677 others(8): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83042699 | ||||||
| chr9:83042737
|
G | GA | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-16817dupT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83042737 | ||||||
| chr9:83042771
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.432-16850A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83042771 | ||||||
| chr9:83042851
|
A | C | 1 | a0001c0001t0001g0318 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.432-16930T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83042851 | ||||||
| chr9:83042921
|
C | T | 16 | a0002c0002t0001g0011a0002c0002t0004g0009a0002c0002t0004g0012others(13): Show | 16 | HG03017.hp2 HG03942.hp1 NA18939.hp2 others(13): Show |
intron_variant | MODIFIER | c.432-17000G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83042921 | ||||||
| chr9:83043051
|
C | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | NA18951.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.432-17130G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83043051 | ||||||
| chr9:83043122
|
A | T | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-17201T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83043122 | ||||||
| chr9:83043221
|
C | T | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.432-17300G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83043221 | ||||||
| chr9:83043222
|
G | A | 1 | a0002c0002t0002g0043 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.432-17301C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83043222 | ||||||
| chr9:83043397
|
T | TG | 47 | a0001c0001t0001g0230a0001c0001t0002g0302a0001c0001t0002g0303others(44): Show | 48 | HG00140.hp2 HG00673.hp1 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.432-17477dupC | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83043397 | ||||||
| chr9:83043397
|
T | TGG | 25 | a0001c0001t0006g0209a0001c0001t0016g0211a0002c0002t0001g0011others(22): Show | 25 | HG00735.hp2 HG02257.hp1 HG02886.hp1 others(22): Show |
intron_variant | MODIFIER | c.432-17478_432-1747 others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83043397 | ||||||
| chr9:83043398
|
G | GA | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.432-17478_432-1747 others(5): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83043398 | ||||||
| chr9:83043399
|
G | GT | 129 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(126): Show | 130 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.432-17479_432-1747 others(5): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83043399 | ||||||
| chr9:83043400
|
G | C | 3 | a0001c0001t0005g0036a0005c0006t0036g0331a0005c0006t0037g0330 | 3 | HG01884.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.432-17479C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83043400 | ||||||
| chr9:83043509
|
G | A | 1 | a0009c0012t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.432-17588C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83043509 | ||||||
| chr9:83043512
|
C | T | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.432-17591G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83043512 | ||||||
| chr9:83043513
|
T | C | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.432-17592A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83043513 | ||||||
| chr9:83043594
|
C | T | 1 | a0002c0002t0008g0194 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.432-17673G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83043594 | ||||||
| chr9:83044203
|
C | T | 22 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(19): Show | 22 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.431+18234G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044203 | ||||||
| chr9:83044260
|
A | G | 2 | a0002c0002t0009g0193a0002c0002t0009g0200 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.431+18177T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044260 | ||||||
| chr9:83044402
|
T | C | 2 | a0002c0002t0002g0056a0002c0002t0002g0057 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.431+18035A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044402 | ||||||
| chr9:83044411
|
G | A | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.431+18026C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044411 | ||||||
| chr9:83044507
|
AT | A | 3 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0033g0040 | 3 | HG02615.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+17929delA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044507 | ||||||
| chr9:83044508
|
TA | T | 22 | a0001c0001t0002g0322a0001c0001t0006g0209a0002c0002t0001g0011others(19): Show | 22 | HG02135.hp1 HG02723.hp1 HG03017.hp2 others(19): Show |
intron_variant | MODIFIER | c.431+17928delT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044508 | ||||||
| chr9:83044509
|
A | C | 3 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0033g0040 | 3 | HG02615.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+17928T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044509 | ||||||
| chr9:83044517
|
A | T | 23 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(20): Show | 23 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.431+17920T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044517 | ||||||
| chr9:83044523
|
T | C | 23 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(20): Show | 23 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.431+17914A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044523 | ||||||
| chr9:83044660
|
A | C | 1 | a0001c0001t0018g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.431+17777T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044660 | ||||||
| chr9:83044673
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.431+17764C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044673 | ||||||
| chr9:83044732
|
A | C | 18 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(15): Show | 18 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.431+17705T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044732 | ||||||
| chr9:83044762
|
G | A | 236 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(233): Show | 238 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.431+17675C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044762 | ||||||
| chr9:83044809
|
A | G | 3 | a0002c0002t0002g0030a0002c0002t0011g0074a0002c0002t0011g0075 | 3 | HG02970.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.431+17628T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044809 | ||||||
| chr9:83044989
|
A | G | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+17448T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83044989 | ||||||
| chr9:83045225
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.431+17212G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83045225 | ||||||
| chr9:83045246
|
A | T | 1 | a0002c0002t0004g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.431+17191T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83045246 | ||||||
| chr9:83045354
|
C | T | 3 | a0001c0001t0003g0207a0002c0002t0003g0001a0002c0004t0012g0208 | 4 | HG01243.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+17083G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83045354 | ||||||
| chr9:83045367
|
T | C | 1 | a0001c0001t0017g0311 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.431+17070A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83045367 | ||||||
| chr9:83045432
|
C | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0284 | 2 | NA18942.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.431+17005G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83045432 | ||||||
| chr9:83045504
|
T | C | 2 | a0001c0001t0003g0291a0001c0001t0003g0308 | 2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.431+16933A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83045504 | ||||||
| chr9:83045759
|
A | C | 7 | a0002c0002t0007g0192a0002c0002t0007g0195a0002c0002t0007g0197others(4): Show | 7 | HG01123.hp1 HG01255.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+16678T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83045759 | ||||||
| chr9:83045845
|
A | G | 23 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(20): Show | 23 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.431+16592T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83045845 | ||||||
| chr9:83046025
|
G | GA | 21 | a0001c0001t0001g0150a0001c0001t0001g0189a0001c0001t0001g0262others(18): Show | 22 | HG00673.hp2 HG00735.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.431+16411dupT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046025 | ||||||
| chr9:83046039
|
AC | A | 14 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.431+16397delG | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046039 | ||||||
| chr9:83046040
|
C | A | 3 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0013g0198 | 3 | HG01123.hp1 HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+16397G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046040 | ||||||
| chr9:83046073
|
C | T | 23 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(20): Show | 23 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.431+16364G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046073 | ||||||
| chr9:83046119
|
T | C | 2 | a0002c0002t0007g0073a0002c0002t0026g0055 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.431+16318A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046119 | ||||||
| chr9:83046248
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.431+16189G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046248 | ||||||
| chr9:83046262
|
T | C | 1 | a0002c0004t0012g0281 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431+16175A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046262 | ||||||
| chr9:83046279
|
G | T | 1 | a0002c0002t0002g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.431+16158C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046279 | ||||||
| chr9:83046443
|
C | T | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | NA18951.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.431+15994G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046443 | ||||||
| chr9:83046529
|
G | A | 1 | a0002c0011t0010g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431+15908C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046529 | ||||||
| chr9:83046717
|
T | C | 7 | a0002c0002t0007g0192a0002c0002t0007g0195a0002c0002t0007g0197others(4): Show | 7 | HG01123.hp1 HG01255.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+15720A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046717 | ||||||
| chr9:83046737
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.431+15700G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046737 | ||||||
| chr9:83046967
|
CAA | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0123a0001c0001t0001g0139others(156): Show | 160 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.431+15468_431+1546 others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046967 | ||||||
| chr9:83046984
|
T | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0123a0001c0001t0001g0139others(149): Show | 153 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.431+15453A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83046984 | ||||||
| chr9:83047038
|
G | A | 20 | a0001c0001t0002g0028a0002c0002t0001g0011a0002c0002t0002g0010others(17): Show | 20 | HG02135.hp1 HG03017.hp2 HG03942.hp1 others(17): Show |
intron_variant | MODIFIER | c.431+15399C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83047038 | ||||||
| chr9:83047103
|
A | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0213a0001c0001t0001g0242others(8): Show | 12 | HG00544.hp2 HG01106.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.431+15334T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83047103 | ||||||
| chr9:83047117
|
T | A | 1 | a0002c0002t0002g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.431+15320A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83047117 | ||||||
| chr9:83047332
|
G | A | 3 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0033g0040 | 3 | HG02615.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+15105C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83047332 | ||||||
| chr9:83047465
|
A | G | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.431+14972T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83047465 | ||||||
| chr9:83047634
|
G | T | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.431+14803C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83047634 | ||||||
| chr9:83047731
|
A | T | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.431+14706T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83047731 | ||||||
| chr9:83047781
|
G | A | 2 | a0002c0002t0003g0202a0002c0002t0005g0201 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.431+14656C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83047781 | ||||||
| chr9:83047878
|
T | C | 3 | a0001c0001t0002g0322a0001c0001t0018g0006a0001c0001t0018g0007 | 3 | HG02723.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.431+14559A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83047878 | ||||||
| chr9:83047937
|
G | T | 1 | a0001c0001t0022g0320 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.431+14500C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83047937 | ||||||
| chr9:83047995
|
C | T | 1 | a0010c0013t0001g0326 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.431+14442G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83047995 | ||||||
| chr9:83048092
|
T | C | 1 | a0002c0002t0002g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.431+14345A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83048092 | ||||||
| chr9:83048220
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.431+14217C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83048220 | ||||||
| chr9:83048443
|
G | C | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+13994C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83048443 | ||||||
| chr9:83048444
|
G | A | 23 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(20): Show | 23 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.431+13993C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83048444 | ||||||
| chr9:83048445
|
G | T | 1 | a0001c0001t0001g0241 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.431+13992C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83048445 | ||||||
| chr9:83048470
|
T | C | 2 | a0001c0001t0001g0219a0001c0001t0001g0282 | 2 | HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.431+13967A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83048470 | ||||||
| chr9:83048566
|
A | AAATG | 5 | a0001c0001t0001g0294a0004c0005t0019g0328a0004c0005t0019g0329others(2): Show | 5 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.431+13867_431+1387 others(8): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83048566 | ||||||
| chr9:83048566
|
AAATG | A | 7 | a0002c0002t0002g0052a0002c0002t0008g0155a0002c0002t0008g0212others(4): Show | 7 | HG02055.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+13867_431+1387 others(8): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83048566 | ||||||
| chr9:83048759
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0123a0001c0001t0001g0139others(146): Show | 150 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.431+13678C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83048759 | ||||||
| chr9:83048957
|
G | T | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+13480C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83048957 | ||||||
| chr9:83049099
|
G | C | 1 | a0002c0002t0005g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.431+13338C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049099 | ||||||
| chr9:83049102
|
T | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+13335A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049102 | ||||||
| chr9:83049116
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.431+13321A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049116 | ||||||
| chr9:83049124
|
CA | C | 21 | a0001c0001t0003g0288a0001c0001t0014g0008a0001c0001t0014g0157others(18): Show | 21 | HG01123.hp1 HG01255.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.431+13312delT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049124 | ||||||
| chr9:83049186
|
T | C | 23 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(20): Show | 23 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.431+13251A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049186 | ||||||
| chr9:83049237
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | NA18953.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.431+13200G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049237 | ||||||
| chr9:83049262
|
T | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+13175A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049262 | ||||||
| chr9:83049271
|
A | G | 1 | a0002c0002t0013g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.431+13166T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049271 | ||||||
| chr9:83049281
|
T | C | 4 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0025others(1): Show | 4 | NA18972.hp2 NA18979.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+13156A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049281 | ||||||
| chr9:83049404
|
A | T | 6 | a0003c0003t0006g0210a0003c0003t0006g0215a0003c0003t0006g0216others(3): Show | 6 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+13033T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049404 | ||||||
| chr9:83049477
|
C | T | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+12960G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049477 | ||||||
| chr9:83049499
|
G | A | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.431+12938C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049499 | ||||||
| chr9:83049519
|
TTCTGCCT others(6066): Show |
T | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+6845_431+12917 others(3): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049519 | ||||||
| chr9:83049528
|
C | T | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.431+12909G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049528 | ||||||
| chr9:83049529
|
C | CT | 12 | a0001c0001t0001g0187a0001c0001t0002g0177a0001c0001t0014g0008others(9): Show | 12 | HG00639.hp1 HG01081.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.431+12907dupA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049529 | ||||||
| chr9:83049529
|
C | CTT | 47 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0047others(44): Show | 47 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.431+12906_431+1290 others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049529 | ||||||
| chr9:83049529
|
C | CTTT | 105 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0143others(102): Show | 106 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.431+12905_431+1290 others(7): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049529 | ||||||
| chr9:83049529
|
C | CTTTT | 16 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(13): Show | 17 | HG00280.hp1 HG01169.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.431+12904_431+1290 others(8): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049529 | ||||||
| chr9:83049529
|
C | CTTTTT | 16 | a0001c0001t0001g0184a0001c0001t0002g0028a0001c0001t0012g0046others(13): Show | 16 | HG01175.hp1 HG02135.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.431+12903_431+1290 others(9): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049529 | ||||||
| chr9:83049529
|
C | T | 15 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(12): Show | 15 | HG00597.hp2 HG00609.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.431+12908G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049529 | ||||||
| chr9:83049529
|
CT | C | 22 | a0001c0001t0002g0322a0001c0001t0018g0006a0002c0002t0001g0054others(19): Show | 22 | HG00558.hp1 HG01071.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.431+12907delA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049529 | ||||||
| chr9:83049552
|
T | A | 1 | a0002c0002t0002g0138 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.431+12885A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049552 | ||||||
| chr9:83049629
|
C | T | 5 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0183others(2): Show | 5 | HG00544.hp1 HG03195.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.431+12808G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049629 | ||||||
| chr9:83049637
|
G | C | 43 | a0001c0001t0002g0028a0001c0001t0006g0209a0001c0001t0014g0008others(40): Show | 43 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.431+12800C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049637 | ||||||
| chr9:83049704
|
A | C | 1 | a0001c0001t0003g0267 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.431+12733T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049704 | ||||||
| chr9:83049708
|
C | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(170): Show | 174 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.431+12729G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049708 | ||||||
| chr9:83049712
|
C | T | 3 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0033g0040 | 3 | HG02615.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+12725G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049712 | ||||||
| chr9:83049780
|
G | C | 3 | a0002c0002t0001g0054a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG00558.hp1 NA19011.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.431+12657C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049780 | ||||||
| chr9:83049798
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG01346.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.431+12639A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049798 | ||||||
| chr9:83049804
|
T | C | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.431+12633A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049804 | ||||||
| chr9:83049810
|
C | T | 7 | a0002c0002t0002g0052a0002c0002t0008g0155a0002c0002t0008g0212others(4): Show | 7 | HG02055.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+12627G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049810 | ||||||
| chr9:83049867
|
G | A | 3 | a0002c0002t0002g0030a0002c0002t0011g0074a0002c0002t0011g0075 | 3 | HG02970.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.431+12570C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049867 | ||||||
| chr9:83049867
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.431+12570C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049867 | ||||||
| chr9:83049941
|
T | C | 1 | a0001c0001t0001g0301 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.431+12496A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83049941 | ||||||
| chr9:83050003
|
C | T | 4 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0015g0037others(1): Show | 4 | HG01167.hp2 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+12434G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050003 | ||||||
| chr9:83050025
|
A | G | 1 | a0002c0002t0002g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.431+12412T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050025 | ||||||
| chr9:83050111
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.431+12326G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050111 | ||||||
| chr9:83050226
|
T | C | 11 | a0001c0001t0003g0144a0001c0001t0003g0214a0001c0001t0003g0231others(8): Show | 11 | HG00140.hp2 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.431+12211A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050226 | ||||||
| chr9:83050308
|
C | T | 21 | a0001c0001t0002g0028a0001c0001t0006g0209a0002c0002t0001g0011others(18): Show | 21 | HG02135.hp1 HG03017.hp2 HG03195.hp2 others(18): Show |
intron_variant | MODIFIER | c.431+12129G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050308 | ||||||
| chr9:83050323
|
G | C | 3 | a0001c0001t0002g0322a0001c0001t0018g0006a0001c0001t0018g0007 | 3 | HG02723.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.431+12114C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050323 | ||||||
| chr9:83050369
|
T | G | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.431+12068A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050369 | ||||||
| chr9:83050536
|
CTT | C | 3 | a0006c0007t0010g0323a0006c0007t0010g0324a0009c0012t0001g0325 | 3 | HG02572.hp1 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.431+11899_431+1190 others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050536 | ||||||
| chr9:83050539
|
G | T | 1 | a0001c0001t0002g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.431+11898C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050539 | ||||||
| chr9:83050558
|
T | C | 1 | a0002c0002t0001g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.431+11879A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050558 | ||||||
| chr9:83050569
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.431+11868C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050569 | ||||||
| chr9:83050619
|
C | T | 3 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0033g0040 | 3 | HG02615.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+11818G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050619 | ||||||
| chr9:83050670
|
T | G | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.431+11767A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050670 | ||||||
| chr9:83050807
|
C | T | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.431+11630G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050807 | ||||||
| chr9:83050858
|
T | C | 1 | a0001c0001t0030g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.431+11579A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050858 | ||||||
| chr9:83050860
|
C | T | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+11577G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050860 | ||||||
| chr9:83050864
|
A | G | 4 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0011g0077others(1): Show | 4 | HG01167.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+11573T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050864 | ||||||
| chr9:83050864
|
A | T | 1 | a0002c0002t0026g0055 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.431+11573T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050864 | ||||||
| chr9:83050867
|
A | C | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+11570T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050867 | ||||||
| chr9:83050915
|
T | C | 1 | a0002c0002t0002g0060 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.431+11522A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050915 | ||||||
| chr9:83050917
|
C | A | 6 | a0003c0003t0006g0210a0003c0003t0006g0215a0003c0003t0006g0216others(3): Show | 6 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+11520G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050917 | ||||||
| chr9:83050949
|
C | T | 23 | a0001c0001t0001g0239a0001c0001t0014g0008a0001c0001t0014g0157others(20): Show | 23 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.431+11488G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050949 | ||||||
| chr9:83050958
|
G | C | 1 | a0001c0001t0001g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.431+11479C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050958 | ||||||
| chr9:83050965
|
G | A | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.431+11472C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83050965 | ||||||
| chr9:83051047
|
A | G | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.431+11390T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051047 | ||||||
| chr9:83051111
|
T | C | 3 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0011t0010g0041 | 3 | HG01167.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.431+11326A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051111 | ||||||
| chr9:83051151
|
G | A | 6 | a0001c0001t0001g0312a0001c0001t0002g0302a0001c0001t0002g0303others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+11286C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051151 | ||||||
| chr9:83051159
|
T | C | 1 | a0001c0001t0003g0293 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.431+11278A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051159 | ||||||
| chr9:83051200
|
G | T | 3 | a0001c0001t0001g0219a0001c0001t0001g0282a0001c0001t0022g0320 | 3 | HG02647.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.431+11237C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051200 | ||||||
| chr9:83051207
|
C | G | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+11230G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051207 | ||||||
| chr9:83051257
|
A | C | 6 | a0001c0001t0003g0207a0002c0002t0003g0001a0002c0004t0012g0208others(3): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+11180T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051257 | ||||||
| chr9:83051259
|
A | G | 1 | a0001c0001t0030g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.431+11178T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051259 | ||||||
| chr9:83051283
|
G | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0123a0001c0001t0001g0139others(156): Show | 160 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.431+11154C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051283 | ||||||
| chr9:83051313
|
T | A | 1 | a0002c0011t0010g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431+11124A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051313 | ||||||
| chr9:83051394
|
G | A | 1 | a0002c0002t0002g0060 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.431+11043C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051394 | ||||||
| chr9:83051451
|
A | G | 1 | a0002c0002t0008g0194 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.431+10986T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051451 | ||||||
| chr9:83051469
|
A | T | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+10968T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051469 | ||||||
| chr9:83051471
|
C | A | 3 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0033g0040 | 3 | HG02615.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+10966G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051471 | ||||||
| chr9:83051475
|
C | A | 20 | a0001c0001t0002g0028a0002c0002t0001g0011a0002c0002t0002g0010others(17): Show | 20 | HG02135.hp1 HG03017.hp2 HG03942.hp1 others(17): Show |
intron_variant | MODIFIER | c.431+10962G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051475 | ||||||
| chr9:83051485
|
G | A | 9 | a0001c0001t0003g0214a0001c0001t0003g0231a0001c0001t0003g0269others(6): Show | 9 | HG00140.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.431+10952C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051485 | ||||||
| chr9:83051520
|
T | C | 1 | a0001c0001t0002g0177 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.431+10917A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051520 | ||||||
| chr9:83051533
|
A | T | 6 | a0003c0003t0006g0210a0003c0003t0006g0215a0003c0003t0006g0216others(3): Show | 6 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+10904T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051533 | ||||||
| chr9:83051577
|
T | G | 4 | a0002c0002t0005g0122a0002c0002t0005g0124a0002c0002t0005g0133others(1): Show | 4 | HG02055.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+10860A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051577 | ||||||
| chr9:83051635
|
A | T | 1 | a0002c0002t0002g0110 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.431+10802T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051635 | ||||||
| chr9:83051695
|
C | G | 1 | a0002c0002t0005g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.431+10742G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051695 | ||||||
| chr9:83051712
|
C | T | 5 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(2): Show | 5 | NA18522.hp2 NA18953.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.431+10725G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051712 | ||||||
| chr9:83051713
|
G | A | 1 | a0002c0002t0007g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.431+10724C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051713 | ||||||
| chr9:83051751
|
G | T | 1 | a0001c0001t0001g0259 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.431+10686C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051751 | ||||||
| chr9:83051755
|
G | C | 17 | a0001c0001t0001g0258a0002c0002t0003g0202a0002c0002t0005g0201others(14): Show | 17 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.431+10682C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051755 | ||||||
| chr9:83051791
|
G | A | 3 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0011t0010g0041 | 3 | HG01167.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.431+10646C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051791 | ||||||
| chr9:83051858
|
G | A | 1 | a0002c0002t0002g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.431+10579C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051858 | ||||||
| chr9:83051872
|
C | A | 1 | a0002c0011t0010g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431+10565G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051872 | ||||||
| chr9:83051939
|
G | A | 4 | a0002c0002t0005g0287a0006c0007t0010g0323a0006c0007t0010g0324others(1): Show | 4 | HG02572.hp1 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+10498C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051939 | ||||||
| chr9:83051966
|
T | C | 20 | a0001c0001t0002g0028a0002c0002t0001g0011a0002c0002t0002g0010others(17): Show | 20 | HG02135.hp1 HG03017.hp2 HG03942.hp1 others(17): Show |
intron_variant | MODIFIER | c.431+10471A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83051966 | ||||||
| chr9:83052028
|
G | A | 3 | a0006c0007t0010g0323a0006c0007t0010g0324a0009c0012t0001g0325 | 3 | HG02572.hp1 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.431+10409C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052028 | ||||||
| chr9:83052030
|
C | T | 1 | a0001c0001t0003g0267 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.431+10407G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052030 | ||||||
| chr9:83052078
|
T | G | 3 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0033g0040 | 3 | HG02615.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+10359A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052078 | ||||||
| chr9:83052092
|
A | T | 43 | a0001c0001t0002g0028a0001c0001t0006g0209a0001c0001t0014g0008others(40): Show | 43 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.431+10345T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052092 | ||||||
| chr9:83052142
|
T | C | 1 | a0002c0002t0001g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.431+10295A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052142 | ||||||
| chr9:83052258
|
G | C | 14 | a0001c0001t0002g0322a0001c0001t0015g0037a0001c0001t0015g0038others(11): Show | 14 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.431+10179C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052258 | ||||||
| chr9:83052260
|
G | T | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+10177C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052260 | ||||||
| chr9:83052276
|
G | A | 3 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0011t0010g0041 | 3 | HG01167.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.431+10161C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052276 | ||||||
| chr9:83052295
|
G | A | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+10142C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052295 | ||||||
| chr9:83052307
|
T | G | 24 | a0001c0001t0001g0123a0001c0001t0001g0139a0001c0001t0001g0141others(21): Show | 24 | HG00597.hp2 HG00609.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.431+10130A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052307 | ||||||
| chr9:83052353
|
T | C | 2 | a0001c0001t0014g0008a0001c0001t0014g0157 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.431+10084A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052353 | ||||||
| chr9:83052458
|
C | T | 1 | a0002c0002t0002g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.431+9979G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052458 | ||||||
| chr9:83052496
|
T | C | 1 | a0002c0002t0002g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.431+9941A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052496 | ||||||
| chr9:83052508
|
T | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(170): Show | 174 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.431+9929A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052508 | ||||||
| chr9:83052601
|
G | T | 1 | a0001c0001t0031g0220 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.431+9836C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052601 | ||||||
| chr9:83052615
|
A | G | 1 | a0002c0002t0005g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.431+9822T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052615 | ||||||
| chr9:83052627
|
T | G | 5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 5 | HG01243.hp2 HG02486.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.431+9810A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052627 | ||||||
| chr9:83052754
|
C | T | 1 | a0002c0004t0001g0278 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.431+9683G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052754 | ||||||
| chr9:83052755
|
G | A | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.431+9682C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052755 | ||||||
| chr9:83052902
|
A | T | 3 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0011t0010g0041 | 3 | HG01167.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.431+9535T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052902 | ||||||
| chr9:83052903
|
A | G | 3 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0011t0010g0041 | 3 | HG01167.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.431+9534T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052903 | ||||||
| chr9:83052951
|
G | A | 2 | a0002c0002t0011g0074a0002c0002t0011g0075 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.431+9486C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052951 | ||||||
| chr9:83052975
|
A | G | 2 | a0001c0001t0002g0302a0001c0001t0002g0303 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.431+9462T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83052975 | ||||||
| chr9:83053061
|
T | C | 1 | a0001c0001t0014g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.431+9376A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053061 | ||||||
| chr9:83053071
|
A | C | 167 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(164): Show | 168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.431+9366T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053071 | ||||||
| chr9:83053226
|
C | T | 222 | a0001c0001t0001g0002a0001c0001t0001g0123a0001c0001t0001g0139others(219): Show | 224 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.431+9211G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053226 | ||||||
| chr9:83053265
|
C | T | 3 | a0001c0001t0001g0219a0001c0001t0001g0282a0001c0001t0022g0320 | 3 | HG02647.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.431+9172G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053265 | ||||||
| chr9:83053267
|
C | G | 3 | a0001c0001t0001g0219a0001c0001t0001g0282a0001c0001t0022g0320 | 3 | HG02647.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.431+9170G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053267 | ||||||
| chr9:83053301
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02071.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.431+9136C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053301 | ||||||
| chr9:83053311
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.431+9126A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053311 | ||||||
| chr9:83053312
|
A | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(228): Show | 233 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.431+9125T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053312 | ||||||
| chr9:83053433
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.431+9004A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053433 | ||||||
| chr9:83053473
|
A | C | 1 | a0002c0002t0002g0060 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.431+8964T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053473 | ||||||
| chr9:83053484
|
C | T | 43 | a0001c0001t0002g0028a0001c0001t0006g0209a0001c0001t0014g0008others(40): Show | 43 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.431+8953G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053484 | ||||||
| chr9:83053500
|
T | C | 43 | a0001c0001t0002g0028a0001c0001t0006g0209a0001c0001t0014g0008others(40): Show | 43 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.431+8937A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053500 | ||||||
| chr9:83053560
|
G | T | 6 | a0003c0003t0006g0210a0003c0003t0006g0215a0003c0003t0006g0216others(3): Show | 6 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+8877C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053560 | ||||||
| chr9:83053623
|
C | T | 1 | a0002c0011t0010g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431+8814G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053623 | ||||||
| chr9:83053640
|
C | T | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+8797G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053640 | ||||||
| chr9:83053673
|
C | T | 3 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0011t0010g0041 | 3 | HG01167.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.431+8764G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053673 | ||||||
| chr9:83053684
|
G | A | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.431+8753C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053684 | ||||||
| chr9:83053689
|
A | T | 19 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0002t0003g0202others(16): Show | 19 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.431+8748T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053689 | ||||||
| chr9:83053706
|
C | T | 1 | a0002c0002t0005g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.431+8731G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053706 | ||||||
| chr9:83053773
|
A | C | 1 | a0002c0002t0008g0194 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.431+8664T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053773 | ||||||
| chr9:83053792
|
C | T | 4 | a0001c0001t0001g0312a0001c0001t0006g0305a0001c0001t0017g0310others(1): Show | 4 | HG01891.hp1 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+8645G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053792 | ||||||
| chr9:83053820
|
A | G | 1 | a0002c0002t0001g0136 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.431+8617T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053820 | ||||||
| chr9:83053835
|
T | C | 3 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0033g0040 | 3 | HG02615.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+8602A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053835 | ||||||
| chr9:83053847
|
T | G | 2 | a0001c0001t0001g0165a0002c0011t0010g0041 | 2 | HG02257.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.431+8590A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053847 | ||||||
| chr9:83053881
|
C | A | 1 | a0002c0002t0002g0060 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.431+8556G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053881 | ||||||
| chr9:83053904
|
C | T | 1 | a0002c0002t0024g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.431+8533G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053904 | ||||||
| chr9:83053948
|
C | T | 1 | a0002c0010t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.431+8489G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053948 | ||||||
| chr9:83053976
|
C | T | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.431+8461G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053976 | ||||||
| chr9:83053994
|
A | T | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+8443T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053994 | ||||||
| chr9:83054040
|
G | A | 1 | a0002c0011t0010g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431+8397C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054040 | ||||||
| chr9:83054051
|
T | C | 21 | a0001c0001t0002g0028a0001c0001t0006g0209a0002c0002t0001g0011others(18): Show | 21 | HG02135.hp1 HG03017.hp2 HG03195.hp2 others(18): Show |
intron_variant | MODIFIER | c.431+8386A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054051 | ||||||
| chr9:83054084
|
G | A | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+8353C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054084 | ||||||
| chr9:83054105
|
G | A | 1 | a0001c0001t0033g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.431+8332C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054105 | ||||||
| chr9:83054131
|
G | T | 3 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0011t0010g0041 | 3 | HG01167.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.431+8306C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054131 | ||||||
| chr9:83054163
|
A | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | NA18978.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.431+8274T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054163 | ||||||
| chr9:83054187
|
A | T | 4 | a0002c0011t0010g0041a0006c0007t0010g0323a0006c0007t0010g0324others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+8250T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054187 | ||||||
| chr9:83054190
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.431+8247G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054190 | ||||||
| chr9:83054287
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.431+8150G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054287 | ||||||
| chr9:83054366
|
T | C | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+8071A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054366 | ||||||
| chr9:83054511
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.431+7926A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054511 | ||||||
| chr9:83054522
|
T | C | 1 | a0002c0002t0004g0015 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.431+7915A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054522 | ||||||
| chr9:83054558
|
T | C | 6 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0011t0010g0041others(3): Show | 6 | HG01167.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+7879A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054558 | ||||||
| chr9:83054722
|
C | T | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.431+7715G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054722 | ||||||
| chr9:83054781
|
C | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0123a0001c0001t0001g0139others(156): Show | 160 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.431+7656G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054781 | ||||||
| chr9:83054813
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.431+7624C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054813 | ||||||
| chr9:83054814
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.431+7623A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054814 | ||||||
| chr9:83054844
|
A | C | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+7593T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054844 | ||||||
| chr9:83054856
|
T | C | 1 | a0002c0002t0009g0204 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.431+7581A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054856 | ||||||
| chr9:83054871
|
A | G | 1 | a0002c0002t0002g0071 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.431+7566T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054871 | ||||||
| chr9:83054900
|
G | C | 1 | a0001c0001t0021g0004 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.431+7537C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054900 | ||||||
| chr9:83054915
|
T | G | 1 | a0001c0001t0021g0004 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.431+7522A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054915 | ||||||
| chr9:83054927
|
G | A | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.431+7510C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83054927 | ||||||
| chr9:83055041
|
G | T | 5 | a0002c0002t0005g0321a0002c0004t0001g0278a0002c0004t0010g0280others(2): Show | 5 | HG00735.hp2 HG01192.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.431+7396C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055041 | ||||||
| chr9:83055088
|
A | G | 6 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0011t0010g0041others(3): Show | 6 | HG01167.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+7349T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055088 | ||||||
| chr9:83055106
|
A | G | 1 | a0002c0002t0002g0109 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.431+7331T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055106 | ||||||
| chr9:83055126
|
G | A | 1 | a0002c0002t0002g0109 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.431+7311C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055126 | ||||||
| chr9:83055147
|
G | A | 6 | a0003c0003t0006g0210a0003c0003t0006g0215a0003c0003t0006g0216others(3): Show | 6 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+7290C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055147 | ||||||
| chr9:83055148
|
T | C | 7 | a0001c0001t0001g0312a0001c0001t0002g0302a0001c0001t0002g0303others(4): Show | 7 | HG01891.hp1 HG02622.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+7289A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055148 | ||||||
| chr9:83055361
|
C | T | 11 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(8): Show | 11 | HG00597.hp2 HG00609.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.431+7076G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055361 | ||||||
| chr9:83055399
|
C | G | 3 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0011t0010g0041 | 3 | HG01167.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.431+7038G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055399 | ||||||
| chr9:83055405
|
G | A | 23 | a0001c0001t0001g0230a0001c0001t0003g0144a0001c0001t0003g0214others(20): Show | 23 | HG00140.hp2 HG00673.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.431+7032C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055405 | ||||||
| chr9:83055406
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.431+7031G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055406 | ||||||
| chr9:83055431
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.431+7006A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055431 | ||||||
| chr9:83055433
|
C | T | 1 | a0001c0001t0016g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.431+7004G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055433 | ||||||
| chr9:83055458
|
G | C | 1 | a0001c0001t0001g0206 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.431+6979C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055458 | ||||||
| chr9:83055467
|
C | G | 1 | a0002c0002t0002g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.431+6970G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055467 | ||||||
| chr9:83055521
|
GGGAGCTG others(6): Show |
G | 1 | a0002c0002t0001g0061 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.431+6903_431+6915d others(15): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055521 | ||||||
| chr9:83055534
|
C | G | 1 | a0002c0002t0002g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.431+6903G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055534 | ||||||
| chr9:83055820
|
C | T | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+6617G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055820 | ||||||
| chr9:83055855
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.431+6582G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055855 | ||||||
| chr9:83055876
|
C | T | 1 | a0001c0001t0002g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.431+6561G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055876 | ||||||
| chr9:83055954
|
A | G | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.431+6483T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83055954 | ||||||
| chr9:83056014
|
G | A | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.431+6423C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83056014 | ||||||
| chr9:83056130
|
C | T | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.431+6307G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83056130 | ||||||
| chr9:83056183
|
G | A | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+6254C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83056183 | ||||||
| chr9:83056223
|
CTTGT | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+6210_431+6213d others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83056223 | ||||||
| chr9:83056241
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.431+6196A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83056241 | ||||||
| chr9:83056359
|
T | C | 16 | a0002c0002t0003g0202a0002c0002t0005g0201a0002c0002t0007g0192others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.431+6078A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83056359 | ||||||
| chr9:83056573
|
T | C | 1 | a0002c0002t0001g0136 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.431+5864A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83056573 | ||||||
| chr9:83056581
|
T | C | 6 | a0001c0001t0001g0145a0001c0001t0001g0160a0001c0001t0001g0161others(3): Show | 6 | HG00544.hp1 NA18939.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+5856A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83056581 | ||||||
| chr9:83056647
|
G | C | 21 | a0001c0001t0002g0028a0001c0001t0006g0209a0002c0002t0001g0011others(18): Show | 21 | HG02135.hp1 HG03017.hp2 HG03195.hp2 others(18): Show |
intron_variant | MODIFIER | c.431+5790C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83056647 | ||||||
| chr9:83056744
|
G | C | 2 | a0002c0002t0002g0042a0002c0002t0002g0044 | 2 | NA18969.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.431+5693C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83056744 | ||||||
| chr9:83056825
|
A | G | 21 | a0001c0001t0002g0028a0001c0001t0006g0209a0002c0002t0001g0011others(18): Show | 21 | HG02135.hp1 HG03017.hp2 HG03195.hp2 others(18): Show |
intron_variant | MODIFIER | c.431+5612T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83056825 | ||||||
| chr9:83057226
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.431+5211A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057226 | ||||||
| chr9:83057328
|
G | A | 8 | a0002c0002t0007g0192a0002c0002t0007g0195a0002c0002t0007g0197others(5): Show | 8 | HG01123.hp1 HG01255.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.431+5109C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057328 | ||||||
| chr9:83057480
|
G | A | 1 | a0001c0001t0033g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.431+4957C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057480 | ||||||
| chr9:83057603
|
T | G | 51 | a0001c0001t0002g0028a0001c0001t0006g0209a0001c0001t0014g0008others(48): Show | 51 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(48): Show |
intron_variant | MODIFIER | c.431+4834A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057603 | ||||||
| chr9:83057661
|
A | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+4776T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057661 | ||||||
| chr9:83057733
|
A | C | 1 | a0001c0001t0016g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.431+4704T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057733 | ||||||
| chr9:83057761
|
A | G | 1 | a0001c0001t0003g0231 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.431+4676T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057761 | ||||||
| chr9:83057791
|
A | G | 2 | a0004c0005t0019g0328a0004c0005t0019g0329 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.431+4646T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057791 | ||||||
| chr9:83057815
|
A | C | 4 | a0002c0002t0009g0162a0002c0002t0009g0163a0002c0002t0009g0204others(1): Show | 4 | HG01884.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+4622T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057815 | ||||||
| chr9:83057823
|
A | T | 6 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 6 | HG00280.hp1 HG01123.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+4614T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057823 | ||||||
| chr9:83057846
|
C | CAT | 14 | a0002c0002t0002g0030a0002c0002t0002g0031a0002c0002t0002g0053others(11): Show | 14 | HG00438.hp1 HG01256.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.431+4589_431+4590d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057846 | ||||||
| chr9:83057846
|
C | CATAT | 4 | a0002c0002t0002g0058a0002c0002t0002g0060a0002c0002t0002g0138others(1): Show | 4 | HG00621.hp2 HG01516.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+4587_431+4590d others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057846 | ||||||
| chr9:83057846
|
CAT | C | 7 | a0002c0002t0001g0137a0002c0002t0002g0042a0002c0002t0002g0111others(4): Show | 7 | HG01261.hp1 NA18942.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.431+4589_431+4590d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057846 | ||||||
| chr9:83057846
|
CATAT | C | 16 | a0001c0001t0001g0140a0001c0001t0001g0191a0001c0001t0001g0229others(13): Show | 16 | HG00621.hp1 HG00733.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.431+4587_431+4590d others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057846 | ||||||
| chr9:83057846
|
CATATAT | C | 179 | a0001c0001t0001g0002a0001c0001t0001g0123a0001c0001t0001g0139others(176): Show | 181 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.431+4585_431+4590d others(8): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057846 | ||||||
| chr9:83057846
|
CATATATA others(1): Show |
C | 16 | a0001c0001t0001g0146a0001c0001t0003g0293a0001c0001t0014g0008others(13): Show | 16 | HG00673.hp1 HG01167.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.431+4583_431+4590d others(10): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057846 | ||||||
| chr9:83057846
|
CATATATA others(3): Show |
C | 4 | a0002c0002t0009g0163a0002c0002t0009g0204a0002c0002t0024g0203others(1): Show | 4 | HG02717.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+4581_431+4590d others(12): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057846 | ||||||
| chr9:83057924
|
G | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0183others(1): Show | 4 | HG00544.hp1 NA18939.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+4513C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83057924 | ||||||
| chr9:83058077
|
G | T | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+4360C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058077 | ||||||
| chr9:83058100
|
A | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+4337T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058100 | ||||||
| chr9:83058161
|
TGTATTTA others(313): Show |
T | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+3956_431+4275d others(2): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058161 | ||||||
| chr9:83058169
|
T | C | 1 | a0002c0002t0013g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.431+4268A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058169 | ||||||
| chr9:83058171
|
T | C | 1 | a0002c0002t0004g0016 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.431+4266A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058171 | ||||||
| chr9:83058172
|
C | CT | 142 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0123others(139): Show | 143 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.431+4264dupA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058172 | ||||||
| chr9:83058172
|
C | CTT | 22 | a0001c0001t0001g0045a0001c0001t0001g0139a0001c0001t0001g0167others(19): Show | 22 | HG00280.hp1 HG01071.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.431+4263_431+4264d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058172 | ||||||
| chr9:83058172
|
CT | C | 7 | a0001c0001t0001g0051a0002c0002t0002g0058a0002c0002t0002g0117others(4): Show | 7 | HG00738.hp1 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.431+4264delA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058172 | ||||||
| chr9:83058172
|
CTTTTTTT others(3): Show |
C | 19 | a0001c0001t0002g0028a0002c0002t0001g0011a0002c0002t0002g0010others(16): Show | 19 | HG02135.hp1 HG03017.hp2 HG03942.hp1 others(16): Show |
intron_variant | MODIFIER | c.431+4255_431+4264d others(12): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058172 | ||||||
| chr9:83058172
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0006g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.431+4253_431+4264d others(14): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058172 | ||||||
| chr9:83058214
|
G | T | 3 | a0002c0002t0002g0056a0002c0002t0002g0057a0002c0002t0002g0058 | 3 | HG01256.hp2 HG01258.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.431+4223C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058214 | ||||||
| chr9:83058287
|
A | G | 3 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0033g0040 | 3 | HG02615.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+4150T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058287 | ||||||
| chr9:83058307
|
C | T | 3 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0033g0040 | 3 | HG02615.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+4130G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058307 | ||||||
| chr9:83058308
|
G | A | 1 | a0002c0002t0002g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.431+4129C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058308 | ||||||
| chr9:83058327
|
T | C | 9 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0015g0037others(6): Show | 9 | HG01167.hp2 HG02257.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.431+4110A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058327 | ||||||
| chr9:83058404
|
C | G | 47 | a0001c0001t0002g0028a0001c0001t0006g0209a0001c0001t0014g0008others(44): Show | 47 | HG01123.hp1 HG01167.hp2 HG01255.hp2 others(44): Show |
intron_variant | MODIFIER | c.431+4033G>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058404 | ||||||
| chr9:83058658
|
A | G | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+3779T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058658 | ||||||
| chr9:83058752
|
T | C | 1 | a0002c0002t0026g0055 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.431+3685A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058752 | ||||||
| chr9:83058912
|
G | A | 4 | a0002c0011t0010g0041a0006c0007t0010g0323a0006c0007t0010g0324others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+3525C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058912 | ||||||
| chr9:83058971
|
C | T | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+3466G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83058971 | ||||||
| chr9:83059114
|
TTTTCTAA others(9): Show |
T | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+3307_431+3322d others(18): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059114 | ||||||
| chr9:83059181
|
T | G | 1 | a0001c0001t0002g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.431+3256A>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059181 | ||||||
| chr9:83059190
|
A | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+3247T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059190 | ||||||
| chr9:83059218
|
G | C | 1 | a0002c0002t0002g0138 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.431+3219C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059218 | ||||||
| chr9:83059257
|
T | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+3180A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059257 | ||||||
| chr9:83059269
|
T | TAC | 49 | a0001c0001t0001g0123a0001c0001t0001g0129a0001c0001t0001g0130others(46): Show | 49 | HG00140.hp2 HG00558.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.431+3166_431+3167d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059269 | ||||||
| chr9:83059269
|
T | TACAC | 138 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0045others(135): Show | 139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.431+3164_431+3167d others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059269 | ||||||
| chr9:83059269
|
T | TACACAC | 23 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0189others(20): Show | 23 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.431+3162_431+3167d others(8): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059269 | ||||||
| chr9:83059269
|
T | TACACACA others(1): Show |
8 | a0001c0001t0001g0191a0001c0001t0003g0308a0001c0001t0014g0008others(5): Show | 8 | HG02615.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.431+3160_431+3167d others(10): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059269 | ||||||
| chr9:83059269
|
T | TACACACA others(3): Show |
2 | a0001c0001t0001g0312a0001c0001t0002g0322 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.431+3158_431+3167d others(12): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059269 | ||||||
| chr9:83059269
|
T | TACACACA others(5): Show |
2 | a0001c0001t0033g0040a0004c0005t0019g0329 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+3156_431+3167d others(14): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059269 | ||||||
| chr9:83059269
|
TAC | T | 15 | a0002c0002t0001g0054a0002c0002t0003g0202a0002c0002t0005g0201others(12): Show | 15 | HG01123.hp1 HG01255.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.431+3166_431+3167d others(4): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059269 | ||||||
| chr9:83059269
|
TACAC | T | 3 | a0002c0002t0002g0042a0002c0002t0002g0053a0002c0002t0009g0163 | 3 | HG02698.hp2 HG02717.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.431+3164_431+3167d others(6): Show |
RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059269 | ||||||
| chr9:83059332
|
G | T | 3 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0033g0040 | 3 | HG02615.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+3105C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059332 | ||||||
| chr9:83059355
|
A | G | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+3082T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059355 | ||||||
| chr9:83059362
|
GA | G | 44 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(41): Show | 44 | HG00280.hp1 HG01123.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.431+3074delT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059362 | ||||||
| chr9:83059431
|
T | C | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.431+3006A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059431 | ||||||
| chr9:83059478
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.431+2959A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059478 | ||||||
| chr9:83059690
|
T | C | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+2747A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059690 | ||||||
| chr9:83059691
|
G | A | 3 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0033g0040 | 3 | HG02615.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+2746C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059691 | ||||||
| chr9:83059790
|
A | G | 1 | a0002c0011t0010g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431+2647T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059790 | ||||||
| chr9:83059964
|
G | A | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+2473C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83059964 | ||||||
| chr9:83060033
|
A | G | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+2404T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83060033 | ||||||
| chr9:83060057
|
T | C | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+2380A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83060057 | ||||||
| chr9:83060095
|
C | T | 7 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0011t0010g0041others(4): Show | 7 | HG01167.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.431+2342G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83060095 | ||||||
| chr9:83060190
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG01346.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.431+2247A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83060190 | ||||||
| chr9:83060424
|
C | T | 7 | a0001c0001t0015g0037a0001c0001t0015g0038a0002c0011t0010g0041others(4): Show | 7 | HG01167.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.431+2013G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83060424 | ||||||
| chr9:83060556
|
T | C | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG00544.hp2 HG02056.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.431+1881A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83060556 | ||||||
| chr9:83060847
|
T | A | 2 | a0002c0002t0002g0035a0002c0002t0002g0156 | 2 | HG00642.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.431+1590A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83060847 | ||||||
| chr9:83060935
|
C | T | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.431+1502G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83060935 | ||||||
| chr9:83060992
|
C | A | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+1445G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83060992 | ||||||
| chr9:83061119
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.431+1318C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061119 | ||||||
| chr9:83061199
|
A | G | 1 | a0002c0002t0009g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.431+1238T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061199 | ||||||
| chr9:83061302
|
G | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG00544.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.431+1135C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061302 | ||||||
| chr9:83061401
|
A | C | 3 | a0002c0002t0002g0042a0002c0002t0002g0043a0002c0002t0002g0044 | 3 | NA18968.hp2 NA18969.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.431+1036T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061401 | ||||||
| chr9:83061631
|
G | A | 1 | a0001c0001t0005g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.431+806C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061631 | ||||||
| chr9:83061646
|
C | T | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+791G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061646 | ||||||
| chr9:83061654
|
C | A | 1 | a0001c0001t0022g0320 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.431+783G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061654 | ||||||
| chr9:83061737
|
C | T | 1 | a0001c0001t0018g0006 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.431+700G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061737 | ||||||
| chr9:83061755
|
C | T | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+682G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061755 | ||||||
| chr9:83061757
|
T | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | NA18953.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.431+680A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061757 | ||||||
| chr9:83061758
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | NA18953.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.431+679G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061758 | ||||||
| chr9:83061785
|
C | T | 2 | a0006c0007t0010g0323a0006c0007t0010g0324 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.431+652G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061785 | ||||||
| chr9:83061826
|
C | T | 1 | a0002c0011t0010g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431+611G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061826 | ||||||
| chr9:83061974
|
C | T | 4 | a0004c0005t0019g0328a0004c0005t0019g0329a0005c0006t0036g0331others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+463G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83061974 | ||||||
| chr9:83062010
|
A | G | 3 | a0001c0001t0014g0008a0001c0001t0014g0157a0001c0001t0033g0040 | 3 | HG02615.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.431+427T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062010 | ||||||
| chr9:83062043
|
G | A | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.431+394C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062043 | ||||||
| chr9:83062126
|
G | C | 1 | a0001c0001t0001g0039 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.431+311C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062126 | ||||||
| chr9:83062176
|
G | C | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | NA18951.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.431+261C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062176 | ||||||
| chr9:83062182
|
C | A | 1 | a0001c0001t0022g0320 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.431+255G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062182 | ||||||
| chr9:83062338
|
TA | T | 18 | a0002c0002t0001g0011a0002c0002t0002g0010a0002c0002t0002g0014others(15): Show | 18 | HG03017.hp2 HG03942.hp1 NA18939.hp2 others(15): Show |
intron_variant | MODIFIER | c.431+98delT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062338 | ||||||
| chr9:83062339
|
A | G | 6 | a0001c0001t0002g0028a0002c0002t0002g0027a0004c0005t0019g0328others(3): Show | 6 | HG02135.hp1 HG02258.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+98T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062339 | ||||||
| chr9:83062339
|
AG | A | 120 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(117): Show | 120 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.431+97delC | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062339 | ||||||
| chr9:83062339
|
AGG | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0158a0001c0001t0001g0159others(171): Show | 176 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.431+96_431+97delCC | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062339 | ||||||
| chr9:83062343
|
G | T | 1 | a0001c0001t0014g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.431+94C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062343 | ||||||
| chr9:83062347
|
G | C | 1 | a0002c0002t0005g0321 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.431+90C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062347 | ||||||
| chr9:83062376
|
A | T | 3 | a0001c0001t0002g0322a0001c0001t0018g0006a0001c0001t0018g0007 | 3 | HG02723.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.431+61T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062376 | ||||||
| chr9:83062381
|
G | A | 1 | a0001c0001t0002g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.431+56C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062381 | ||||||
| chr9:83062388
|
C | A | 2 | a0005c0006t0036g0331a0005c0006t0037g0330 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.431+49G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062388 |