Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MEADG others(735): Show |
chr9 | 82974590 | 83068142 |
| a0002 | 1/0 | 740 | 146 | 41 | 27 | 58 | 5 | 14 | 50 | RASEF_chr9_82974590_83068142 | RASEF | MEADG others(735): Show |
chr9 | 82974590 | 83068142 |
| a0003 | 0/0 | 740 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | MEADG others(735): Show |
chr9 | 82974590 | 83068142 |
| a0004 | 0/0 | 740 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | MEADG others(735): Show |
chr9 | 82974590 | 83068142 |
| a0005 | 0/0 | 740 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | MEADG others(735): Show |
chr9 | 82974590 | 83068142 |
| a0006 | 0/0 | 740 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | MEADG others(735): Show |
chr9 | 82974590 | 83068142 |
| a0007 | 0/0 | 740 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | MEADG others(735): Show |
chr9 | 82974590 | 83068142 |
| a0008 | 0/0 | 740 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | MEADE others(735): Show |
chr9 | 82974590 | 83068142 |
| a0009 | 0/0 | 740 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | MEADG others(735): Show |
chr9 | 82974590 | 83068142 |
| a0010 | 0/0 | 740 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | MEADG others(735): Show |
chr9 | 82974590 | 83068142 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2220 | 172 | 37 | 28 | 85 | 5 | 16 | RASEF_chr9_82974590_83068142 | RASEF | ATGGA others(2215): Show |
chr9 | 82974590 | 83068142 | ||
| a0002c0002 | 1/0 | 2220 | 139 | 36 | 26 | 58 | 5 | 13 | RASEF_chr9_82974590_83068142 | RASEF | ATGGA others(2215): Show |
chr9 | 82974590 | 83068142 | ||
| a0002c0004 | 0/0 | 2220 | 5 | 3 | 1 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | ATGGA others(2215): Show |
chr9 | 82974590 | 83068142 | ||
| a0002c0010 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | ATGGA others(2215): Show |
chr9 | 82974590 | 83068142 | ||
| a0002c0011 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | ATGGA others(2215): Show |
chr9 | 82974590 | 83068142 | ||
| a0003c0003 | 0/0 | 2220 | 6 | 6 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | ATGGA others(2215): Show |
chr9 | 82974590 | 83068142 | ||
| a0004c0006 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | ATGGA others(2215): Show |
chr9 | 82974590 | 83068142 | ||
| a0005c0007 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | ATGGA others(2215): Show |
chr9 | 82974590 | 83068142 | ||
| a0006c0005 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | ATGGA others(2215): Show |
chr9 | 82974590 | 83068142 | ||
| a0007c0013 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | ATGGA others(2215): Show |
chr9 | 82974590 | 83068142 | ||
| a0008c0008 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | ATGGA others(2215): Show |
chr9 | 82974590 | 83068142 | ||
| a0009c0012 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | ATGGA others(2215): Show |
chr9 | 82974590 | 83068142 | ||
| a0010c0009 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | ATGGA others(2215): Show |
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 | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0002 | 0/0 | 5585 | 10 | 5 | 0 | 5 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0003 | 0/0 | 5575 | 21 | 9 | 4 | 3 | 3 | 2 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5570): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0005 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0006 | 0/0 | 5580 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5575): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0012 | 0/0 | 5566 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5561): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0014 | 0/0 | 5579 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5574): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0015 | 0/0 | 5579 | 2 | 1 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5574): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0016 | 0/0 | 5569 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0017 | 0/0 | 5569 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0018 | 0/0 | 5569 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0021 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0022 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5574): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0030 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5575): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0031 | 0/0 | 5569 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0033 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0035 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0001c0001t0038 | 0/0 | 5575 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5570): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0001 | 0/0 | 5569 | 16 | 0 | 1 | 15 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0002 | 1/0 | 5585 | 70 | 5 | 20 | 29 | 5 | 10 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0003 | 0/0 | 5575 | 3 | 3 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5570): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0004 | 0/0 | 5569 | 14 | 0 | 0 | 11 | 0 | 3 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0005 | 0/0 | 5585 | 7 | 6 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0007 | 0/0 | 5575 | 5 | 4 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5570): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0008 | 0/0 | 5580 | 5 | 5 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5575): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0009 | 0/0 | 5586 | 5 | 5 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5581): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0010 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5574): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0011 | 0/0 | 5579 | 3 | 3 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5574): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0013 | 0/0 | 5585 | 2 | 1 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0020 | 0/0 | 5585 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0023 | 0/0 | 5586 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5581): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0024 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5575): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0025 | 0/0 | 5585 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0026 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0028 | 0/0 | 5585 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0029 | 0/0 | 5585 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0002c0002t0032 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0002c0004t0001 | 0/0 | 5569 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0002c0004t0010 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5574): Show |
chr9 | 82974590 | 83068142 |
| a0002c0004t0012 | 0/0 | 5566 | 2 | 1 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5561): Show |
chr9 | 82974590 | 83068142 |
| a0002c0004t0027 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5574): Show |
chr9 | 82974590 | 83068142 |
| a0002c0010t0002 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0002c0011t0010 | 0/0 | 5579 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5574): Show |
chr9 | 82974590 | 83068142 |
| a0003c0003t0006 | 0/0 | 5580 | 5 | 5 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5575): Show |
chr9 | 82974590 | 83068142 |
| a0003c0003t0034 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5575): Show |
chr9 | 82974590 | 83068142 |
| a0004c0006t0036 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0004c0006t0037 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0005c0007t0010 | 0/0 | 5579 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5574): Show |
chr9 | 82974590 | 83068142 |
| a0006c0005t0019 | 0/0 | 5569 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0007c0013t0001 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0008c0008t0002 | 0/0 | 5585 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5580): Show |
chr9 | 82974590 | 83068142 |
| a0009c0012t0001 | 0/0 | 5569 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5564): Show |
chr9 | 82974590 | 83068142 |
| a0010c0009t0007 | 0/0 | 5575 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | AGTCG others(5570): Show |
chr9 | 82974590 | 83068142 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0046 | 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 |
| 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 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0069 | 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 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| 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 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0292 | 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 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0001g0313 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0014g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0014g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0015g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0015g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0016g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0016g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0017g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0017g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0018g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0018g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0021g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0022g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0030g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0031g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0033g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0035g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0001c0001t0038g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 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 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 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 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0119 | 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 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0002c0002t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| a0002c0002t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0005g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0007g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0008g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0008g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0008g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0010g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0011g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0011g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0013g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0013g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0020g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0023g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0024g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0025g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0026g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0028g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0029g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0002t0032g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0004t0010g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0004t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0004t0012g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0004t0027g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0010t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0002c0011t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0003c0003t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0003c0003t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0003c0003t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0003c0003t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0003c0003t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0003c0003t0034g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0004c0006t0036g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0004c0006t0037g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0005c0007t0010g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0005c0007t0010g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0006c0005t0019g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0006c0005t0019g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0007c0013t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0008c0008t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0009c0012t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| a0010c0009t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0118 | EUR | GBR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0190 | EUR | GBR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0147 | EUR | FIN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00408 | hp2 | a0007 | c0013 | t0001 | g0319 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00609 | hp1 | a0001 | c0001 | t0021 | g0011 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00639 | hp1 | a0002 | c0002 | t0028 | g0116 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0303 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | CHS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0119 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00735 | hp2 | a0002 | c0004 | t0012 | g0269 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00738 | hp1 | a0002 | c0002 | t0025 | g0120 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0138 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0134 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0139 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01167 | hp2 | a0001 | c0001 | t0015 | g0308 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0155 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0257 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0135 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0145 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01192 | hp1 | a0002 | c0002 | t0005 | g0314 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0148 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01255 | hp2 | a0002 | c0002 | t0007 | g0002 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0158 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0101 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01358 | hp1 | a0001 | c0001 | t0031 | g0232 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01358 | hp2 | a0008 | c0008 | t0002 | g0012 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0136 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0205 | EUR | IBS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0095 | EUR | IBS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0259 | EUR | IBS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0304 | EUR | IBS | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01884 | hp1 | a0002 | c0002 | t0009 | g0044 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0306 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01891 | hp2 | a0002 | c0002 | t0005 | g0090 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0193 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0188 | 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 | g0107 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02055 | hp1 | a0002 | c0002 | t0008 | g0187 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02055 | hp2 | a0002 | c0002 | t0005 | g0178 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0166 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CDX | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | CDX | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02257 | hp1 | a0002 | c0011 | t0010 | g0036 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02257 | hp2 | a0002 | c0002 | t0008 | g0286 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02258 | hp1 | a0002 | c0002 | t0007 | g0002 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02258 | hp2 | a0004 | c0006 | t0037 | g0323 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0076 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0167 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0165 | AMR | PEL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02451 | hp1 | a0002 | c0002 | t0007 | g0154 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02572 | hp1 | a0009 | c0012 | t0001 | g0318 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02572 | hp2 | a0010 | c0009 | t0007 | g0086 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0117 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02615 | hp1 | a0001 | c0001 | t0014 | g0015 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02622 | hp1 | a0001 | c0001 | t0017 | g0298 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02622 | hp2 | a0002 | c0002 | t0008 | g0296 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02630 | hp1 | a0001 | c0001 | t0012 | g0062 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02630 | hp2 | a0003 | c0003 | t0006 | g0173 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0034 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0081 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02717 | hp1 | a0002 | c0002 | t0009 | g0045 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02717 | hp2 | a0003 | c0003 | t0006 | g0170 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02723 | hp2 | a0001 | c0001 | t0015 | g0307 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0102 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0182 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02809 | hp2 | a0003 | c0003 | t0034 | g0171 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02818 | hp1 | a0002 | c0002 | t0009 | g0093 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02818 | hp2 | a0002 | c0002 | t0011 | g0131 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02886 | hp1 | a0005 | c0007 | t0010 | g0317 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02886 | hp2 | a0001 | c0001 | t0030 | g0201 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02895 | hp1 | a0002 | c0002 | t0003 | g0006 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02895 | hp2 | a0002 | c0002 | t0008 | g0083 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02897 | hp1 | a0002 | c0002 | t0003 | g0006 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02922 | hp1 | a0003 | c0003 | t0006 | g0169 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02970 | hp1 | a0002 | c0002 | t0005 | g0180 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02970 | hp2 | a0002 | c0002 | t0011 | g0104 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02976 | hp1 | a0001 | c0001 | t0017 | g0297 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02976 | hp2 | a0001 | c0001 | t0018 | g0014 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03017 | hp1 | a0002 | c0004 | t0001 | g0263 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03017 | hp2 | a0002 | c0002 | t0004 | g0016 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03041 | hp1 | a0002 | c0002 | t0011 | g0103 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03098 | hp1 | a0002 | c0002 | t0007 | g0087 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03098 | hp2 | a0005 | c0007 | t0010 | g0316 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03130 | hp1 | a0006 | c0005 | t0019 | g0322 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03130 | hp2 | a0001 | c0001 | t0018 | g0013 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03139 | hp2 | a0002 | c0004 | t0027 | g0262 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03195 | hp1 | a0001 | c0001 | t0016 | g0186 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0185 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0255 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0097 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03225 | hp1 | a0002 | c0002 | t0026 | g0094 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03225 | hp2 | a0001 | c0001 | t0022 | g0312 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0149 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0137 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03516 | hp1 | a0002 | c0002 | t0003 | g0091 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03516 | hp2 | a0002 | c0002 | t0008 | g0285 | AFR | ESN | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03540 | hp1 | a0003 | c0003 | t0006 | g0172 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03540 | hp2 | a0001 | c0001 | t0033 | g0035 | AFR | GWD | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03579 | hp1 | a0003 | c0003 | t0006 | g0174 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0150 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0267 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0100 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0127 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0299 | SAS | STU | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0168 | SAS | STU | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0140 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03942 | hp1 | a0002 | c0002 | t0004 | g0019 | SAS | BEB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0126 | SAS | STU | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | STU | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0124 | SAS | STU | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18522 | hp1 | a0002 | c0004 | t0012 | g0161 | AFR | YRI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18522 | hp2 | a0002 | c0002 | t0024 | g0092 | AFR | YRI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CHB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18906 | hp1 | a0006 | c0005 | t0019 | g0321 | AFR | YRI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18906 | hp2 | a0002 | c0002 | t0009 | g0089 | AFR | YRI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18940 | hp1 | a0002 | c0002 | t0004 | g0029 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0156 | 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 | g0292 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18956 | hp1 | a0002 | c0002 | t0004 | g0024 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18972 | hp2 | a0002 | c0002 | t0004 | g0031 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18974 | hp1 | a0002 | c0002 | t0032 | g0025 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18975 | hp2 | a0002 | c0002 | t0020 | g0010 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18979 | hp1 | a0001 | c0001 | t0035 | g0320 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18979 | hp2 | a0002 | c0002 | t0004 | g0030 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18982 | hp1 | a0002 | c0002 | t0004 | g0020 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18998 | hp1 | a0002 | c0002 | t0004 | g0033 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19030 | hp1 | a0002 | c0002 | t0005 | g0272 | AFR | LWK | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0293 | AFR | LWK | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19043 | hp1 | a0002 | c0004 | t0010 | g0264 | AFR | LWK | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | LWK | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19057 | hp1 | a0002 | c0002 | t0004 | g0028 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19060 | hp1 | a0002 | c0002 | t0004 | g0021 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19066 | hp2 | a0002 | c0002 | t0029 | g0099 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19079 | hp2 | a0002 | c0002 | t0004 | g0032 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19087 | hp2 | a0002 | c0002 | t0004 | g0027 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19090 | hp2 | a0002 | c0002 | t0004 | g0026 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19240 | hp1 | a0002 | c0002 | t0007 | g0085 | AFR | YRI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | YRI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20129 | hp1 | a0002 | c0002 | t0023 | g0077 | AFR | ASW | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ASW | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0192 | EUR | TSI | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | GIH | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20905 | hp2 | a0002 | c0002 | t0004 | g0022 | SAS | GIH | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01123 | hp1 | a0002 | c0002 | t0013 | g0084 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02486 | hp1 | a0001 | c0001 | t0016 | g0049 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02486 | hp2 | a0001 | c0001 | t0038 | g0325 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02559 | hp1 | a0002 | c0002 | t0009 | g0088 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG02559 | hp2 | a0002 | c0002 | t0010 | g0287 | AFR | ACB | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03471 | hp1 | a0004 | c0006 | t0036 | g0324 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG03471 | hp2 | a0002 | c0002 | t0005 | g0164 | AFR | MSL | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG06807 | hp1 | a0002 | c0002 | t0013 | g0159 | AFR | USA | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | USA | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | USA | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA20300 | hp2 | a0002 | c0002 | t0005 | g0177 | AFR | USA | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | LWK | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| NA21309 | hp2 | a0002 | c0010 | t0002 | g0048 | AFR | LWK | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0313 | REF | REF | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0130 | REF | REF | RASEF_chr9_82974590_83068142 | RASEF | chr9 | 82974590 | 83068142 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:83000447 | 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 | a0010 | 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 | a0004 a0006 |
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 | a0001 a0007 a0009 |
173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): 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 | a0004 | 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 | a0005 a0009 |
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 | a0004 a0006 |
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 | a0007 | 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 | a0008 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:82998439 | 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 | a0002c0011 a0005c0007 |
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 | a0004c0006 a0006c0005 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:82979706 | A | T | 3 | a0001c0001t0017 a0001c0001t0022 a0002c0002t0011 |
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 | a0001c0001t0017 a0001c0001t0022 a0002c0002t0011 |
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 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0012 others(28): Show |
196 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(193): 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 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0012 others(27): Show |
195 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(192): 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 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0015 others(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 | a0004c0006t0036 | 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 | a0001c0001t0005 a0002c0002t0005 |
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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0012 others(17): Show |
178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): 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 | a0002c0002t0004 a0002c0002t0032 |
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 | a0006c0005t0019 | 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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(36): Show |
231 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(228): 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 | a0006c0005t0019 | 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 | a0002c0002t0009 a0002c0002t0024 |
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 | a0001c0001t0006 a0002c0002t0023 a0003c0003t0006 others(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 | a0001c0001t0012 a0002c0004t0012 |
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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0012 others(14): Show |
176 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(173): 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 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0018 others(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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0012 others(20): Show |
200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): 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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0012 others(19): Show |
199 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(196): 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 | a0001c0001t0006 a0002c0002t0008 a0002c0002t0023 others(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 | a0002c0002t0004 a0002c0002t0007 a0002c0002t0032 others(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 | a0004c0006t0036 a0004c0006t0037 a0006c0005t0019 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:82982805 | C | CAG | 4 | a0001c0001t0002g0056 a0001c0001t0002g0067 a0002c0002t0002g0005 others(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 | a0002c0002t0002g0101 a0002c0002t0002g0127 a0002c0002t0002g0135 others(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 | 178 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(175): Show |
182 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(179): 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 | 11 | a0001c0001t0003g0007 a0001c0001t0003g0190 a0001c0001t0003g0203 others(8): 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 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(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 | a0001c0001t0006g0185 a0001c0001t0006g0293 a0002c0002t0008g0083 others(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 | 172 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(169): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.2118-115C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82982897 | |||||||
| chr9:82982978 | G | A | 5 | a0002c0002t0007g0002 a0002c0002t0007g0085 a0002c0002t0007g0087 others(2): 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 | 48 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0073 others(45): 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 | 17 | a0001c0001t0003g0007 a0001c0001t0003g0251 a0001c0001t0003g0252 others(14): 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 | a0001c0001t0001g0037 a0001c0001t0003g0160 a0001c0001t0003g0255 others(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 | a0001c0001t0002g0284 a0001c0001t0002g0315 a0001c0001t0003g0260 others(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 | a0004c0006t0037g0323 | 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 | a0002c0002t0002g0023 | 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 | 77 | a0001c0001t0001g0046 a0001c0001t0001g0054 a0001c0001t0001g0055 others(74): 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 | 27 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0059 others(24): 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 | 58 | a0001c0001t0001g0009 a0001c0001t0001g0043 a0001c0001t0001g0050 others(55): Show |
59 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(56): 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 | a0001c0001t0001g0008 a0001c0001t0001g0206 a0001c0001t0001g0235 others(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 | a0007c0013t0001g0319 | 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 | a0001c0001t0012g0062 a0001c0001t0017g0297 a0001c0001t0017g0298 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0196 a0001c0001t0001g0248 others(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 | a0002c0002t0002g0076 | 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 | a0001c0001t0006g0185 a0001c0001t0006g0293 a0002c0002t0023g0077 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0239 a0001c0001t0001g0250 |
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 | a0001c0001t0002g0071 a0001c0001t0002g0078 |
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 | a0001c0001t0003g0203 | 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 | 22 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(19): 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 | a0001c0001t0014g0015 a0001c0001t0014g0034 |
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 | 172 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(169): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): 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 | a0002c0004t0012g0269 | 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 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
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 | a0009c0012t0001g0318 | 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 | a0001c0001t0001g0151 a0001c0001t0001g0195 a0001c0001t0001g0197 others(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 | 172 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(169): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.2118-2704C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82985486 | |||||||
| chr9:82985661 | C | T | 22 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(19): 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 | a0002c0002t0002g0121 a0002c0002t0002g0144 |
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 | 194 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(191): Show |
200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): 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 | a0001c0001t0001g0202 | 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 | a0002c0002t0009g0044 a0002c0002t0009g0045 a0002c0002t0009g0088 others(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 | 165 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(162): Show |
170 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(167): 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 | a0002c0010t0002g0048 | 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 | 194 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(191): Show |
200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): 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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0215 others(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 | 22 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(19): 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 | 162 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
167 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(164): 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 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(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 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(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 | 172 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(169): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): 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 | a0001c0001t0022g0312 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | 172 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(169): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0022g0312 | 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 | a0001c0001t0003g0254 | 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 | a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | 194 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(191): Show |
200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): 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 | a0001c0001t0033g0035 | 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 | a0001c0001t0003g0294 | 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 | 5 | a0002c0002t0007g0002 a0002c0002t0007g0085 a0002c0002t0007g0087 others(2): 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 | a0001c0001t0001g0249 | 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 | a0001c0001t0033g0035 | 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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0002c0002t0009g0088 a0002c0002t0009g0089 |
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 | 22 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(19): 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 | 194 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(191): Show |
200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.2117+1981A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82988410 | |||||||
| chr9:82988412 | A | C | 23 | a0001c0001t0003g0007 a0001c0001t0003g0160 a0001c0001t0003g0190 others(20): 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 | a0002c0002t0010g0287 a0002c0004t0010g0264 a0002c0011t0010g0036 others(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 | a0002c0002t0013g0084 a0004c0006t0037g0323 |
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 | 172 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(169): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): 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 | a0001c0001t0001g0231 | 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 | 165 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(162): Show |
170 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2117+1221A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989170 | |||||||
| chr9:82989222 | A | ATG | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
161 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(158): 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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(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 | 164 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
169 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.2117+1162G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989229 | |||||||
| chr9:82989244 | G | T | 22 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(19): 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 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0061 |
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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2117+674A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 16/16 | chr9 | 82989717 | |||||||
| chr9:82989791 | T | C | 1 | a0003c0003t0034g0171 | 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 | a0001c0001t0006g0185 | 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 | a0001c0001t0001g0300 a0001c0001t0014g0015 a0001c0001t0014g0034 others(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 | a0001c0001t0003g0203 | 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 | a0001c0001t0014g0015 a0001c0001t0014g0034 |
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 | 169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
174 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(171): 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 | a0001c0001t0014g0015 a0001c0001t0014g0034 |
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 | a0001c0001t0005g0306 | 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 | a0001c0001t0006g0185 | 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 | 25 | a0001c0001t0003g0007 a0001c0001t0003g0160 a0001c0001t0003g0190 others(22): 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 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(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 | a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | a0001c0001t0002g0315 a0001c0001t0005g0306 a0001c0001t0018g0013 others(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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | 230 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(227): Show |
236 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(233): 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 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(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 | a0001c0001t0006g0185 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0001c0001t0001g0229 | 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 | a0002c0004t0027g0262 | 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 | a0001c0001t0016g0049 a0002c0002t0002g0076 a0002c0002t0005g0272 others(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 | a0001c0001t0001g0268 | 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 | 2 | a0001c0001t0001g0009 a0001c0001t0001g0302 |
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 | a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | a0001c0001t0001g0289 a0002c0002t0005g0272 a0002c0004t0010g0264 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
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 | a0001c0001t0016g0186 | 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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0001c0001t0001g0310 | 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 | a0002c0002t0011g0104 | 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 | a0002c0002t0007g0154 | 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 | 188 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(185): Show |
192 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(189): 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 | a0002c0002t0002g0134 | 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 | a0001c0001t0017g0297 a0001c0001t0017g0298 |
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 | 169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
174 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1921-1134dupT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 14/16 | chr9 | 82994158 | |||||||
| chr9:82994225 | C | T | 2 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | 195 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(192): Show |
200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): 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 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0078 others(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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0001c0001t0006g0185 | 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 | a0002c0002t0005g0164 a0002c0002t0005g0178 a0002c0002t0005g0314 |
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 | a0002c0002t0002g0155 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0002c0002t0009g0044 a0002c0002t0009g0045 a0002c0002t0009g0088 others(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 | 23 | a0001c0001t0003g0007 a0001c0001t0003g0160 a0001c0001t0003g0190 others(20): 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 | a0001c0001t0001g0191 a0001c0001t0001g0271 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0001c0001t0014g0015 a0001c0001t0014g0034 |
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 | a0002c0002t0004g0019 | 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 | a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | a0002c0002t0005g0272 a0002c0004t0010g0264 a0002c0004t0012g0161 others(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 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0136 others(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 | a0002c0002t0002g0148 | 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 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(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 | a0001c0001t0001g0063 | 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 | a0002c0002t0002g0105 | 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 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
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 | a0001c0001t0006g0185 | 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 | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(167): Show |
175 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1806-387C>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82997513 | |||||||
| chr9:82997546 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(187): Show |
195 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1806-420T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82997546 | |||||||
| chr9:82997618 | T | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(187): Show |
195 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(192): 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 | a0001c0001t0003g0299 | 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 | a0002c0002t0002g0076 a0002c0002t0008g0187 a0002c0002t0008g0285 others(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 | 244 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(241): Show |
250 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.1805+409T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 13/16 | chr9 | 82997956 | |||||||
| chr9:82998128 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(186): Show |
194 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(191): 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 | a0001c0001t0001g0300 a0001c0001t0033g0035 |
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 | a0001c0001t0016g0186 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0004g0016 others(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 | a0001c0001t0001g0230 | 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 | a0002c0002t0001g0018 a0002c0002t0001g0108 a0002c0002t0001g0112 others(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 | a0001c0001t0001g0300 a0001c0001t0014g0015 a0001c0001t0014g0034 others(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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0004g0016 others(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 | a0002c0002t0002g0123 | 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 | a0002c0002t0005g0272 a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | 205 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(202): Show |
211 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(208): 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 | 189 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(186): Show |
194 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(191): 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 | 189 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(186): Show |
194 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(191): 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 | a0002c0002t0001g0082 a0002c0002t0001g0109 a0002c0002t0001g0110 others(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 | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(167): Show |
175 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(172): 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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0001c0001t0016g0186 | 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 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(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 | a0002c0002t0001g0108 a0002c0002t0001g0183 a0002c0002t0002g0119 others(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 | a0002c0002t0001g0110 a0002c0002t0001g0111 a0002c0002t0001g0115 others(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 | a0002c0002t0001g0082 a0002c0002t0001g0109 a0002c0002t0001g0114 |
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 | 22 | a0002c0002t0001g0128 a0002c0002t0002g0003 a0002c0002t0002g0017 others(19): 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0001g0122 others(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 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0143 others(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 | a0002c0002t0002g0124 a0002c0004t0001g0263 a0002c0004t0012g0161 others(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 | a0002c0002t0002g0097 a0002c0002t0002g0107 a0002c0002t0004g0016 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0204 a0001c0001t0001g0218 others(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 | 40 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0072 others(37): 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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0037 others(124): Show |
131 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(128): 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 | a0001c0001t0001g0051 a0001c0001t0001g0065 a0001c0001t0001g0207 others(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 | 5 | a0002c0002t0007g0002 a0002c0002t0007g0085 a0002c0002t0007g0087 others(2): 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 | a0004c0006t0037g0323 | 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 | a0005c0007t0010g0316 a0005c0007t0010g0317 |
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 | a0001c0001t0016g0186 | 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 | a0001c0001t0001g0216 a0001c0001t0001g0275 a0001c0001t0001g0288 others(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 | a0002c0002t0002g0158 | 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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0002c0002t0001g0122 a0002c0002t0001g0181 a0002c0002t0001g0184 |
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 | 173 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(170): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): 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 | a0002c0002t0005g0272 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0002c0002t0002g0127 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | 173 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(170): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): 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 | a0002c0010t0002g0048 | 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 | a0002c0002t0002g0076 a0002c0002t0003g0006 a0002c0002t0008g0187 others(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 | 223 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(220): Show |
229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): 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 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(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 | a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0002c0002t0002g0105 | 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 | a0002c0002t0002g0107 | 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 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(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 | a0001c0001t0005g0306 | 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 | a0002c0002t0002g0076 a0002c0002t0003g0006 a0002c0002t0008g0187 others(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 | 172 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(169): Show |
176 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(173): 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | 1 | a0001c0001t0001g0268 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1202+318G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 9/16 | chr9 | 83004180 | |||||||
| chr9:83004251 | T | A | 1 | a0001c0001t0001g0311 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0002c0002t0007g0087 | 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 |
167 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
171 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(168): 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 | 169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0002c0002t0005g0272 a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | a0002c0002t0007g0154 a0002c0002t0026g0094 |
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 | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(167): Show |
175 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(172): 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 | a0003c0003t0006g0169 a0003c0003t0006g0170 a0003c0003t0006g0172 others(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 | a0001c0001t0001g0235 | 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 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(167): Show |
175 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(172): 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 | a0001c0001t0001g0050 a0001c0001t0001g0213 a0001c0001t0001g0224 others(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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): 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 | a0002c0002t0002g0098 | 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 | a0001c0001t0001g0273 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0001c0001t0003g0190 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0003g0254 a0001c0001t0003g0256 |
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 | a0001c0001t0001g0238 a0001c0001t0001g0241 |
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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(217): Show |
226 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1028+365A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83007072 | |||||||
| chr9:83007088 | T | C | 173 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0037 others(170): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1028+349A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83007088 | |||||||
| chr9:83007093 | C | CA | 200 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(197): Show |
206 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1028+343dupT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 7/16 | chr9 | 83007093 | |||||||
| chr9:83007093 | C | CAA | 25 | a0001c0001t0001g0227 a0001c0001t0001g0265 a0001c0001t0001g0288 others(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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0001c0001t0001g0300 a0001c0001t0033g0035 |
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 | a0002c0004t0012g0269 | 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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | 173 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(170): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.960-366A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 6/16 | chr9 | 83007871 | |||||||
| chr9:83008173 | T | A | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | 82 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0042 others(79): Show |
84 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(81): 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 | a0002c0002t0011g0104 | 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 | 169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): 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 | a0001c0001t0001g0311 | 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 | a0003c0003t0006g0169 a0003c0003t0006g0170 a0003c0003t0006g0172 others(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 | a0001c0001t0005g0306 | 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 | 12 | a0001c0001t0001g0058 a0001c0001t0001g0200 a0001c0001t0001g0225 others(9): Show |
13 | HG01168.hp2 HG01169.hp1 HG01258.hp1 others(10): 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 | 37 | a0002c0002t0001g0108 a0002c0002t0001g0110 a0002c0002t0002g0005 others(34): 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 | a0002c0002t0002g0123 a0002c0002t0002g0167 a0002c0002t0009g0088 others(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 | a0001c0001t0015g0307 a0002c0002t0001g0181 a0002c0002t0001g0183 others(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 | a0002c0002t0001g0122 a0002c0002t0002g0142 a0002c0002t0002g0156 others(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 | a0001c0001t0015g0308 a0002c0002t0002g0132 a0002c0002t0002g0192 others(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 | a0002c0002t0002g0096 a0002c0002t0002g0140 a0002c0002t0004g0026 others(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 | a0001c0001t0001g0250 a0001c0001t0002g0315 a0001c0001t0003g0160 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0204 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0043 a0001c0001t0001g0057 others(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 |
33 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0059 others(30): 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 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0189 a0001c0001t0001g0202 others(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 | 25 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0054 others(22): 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 | 13 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0055 others(10): 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 | a0001c0001t0001g0051 a0001c0001t0001g0080 a0001c0001t0001g0151 others(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 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0136 others(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 | a0006c0005t0019g0321 | 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 | a0001c0001t0003g0294 a0001c0001t0006g0293 |
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 | a0001c0001t0001g0065 a0001c0001t0003g0258 a0002c0002t0002g0081 |
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 | 1 | a0002c0002t0002g0004 | 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 | a0001c0001t0001g0053 a0001c0001t0001g0207 a0001c0001t0001g0208 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0207 a0001c0001t0001g0208 others(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 | 11 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0054 others(8): 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 | 11 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0054 others(8): 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 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0080 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0080 a0001c0001t0001g0151 others(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 | a0001c0001t0003g0294 a0001c0001t0006g0293 |
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 | a0001c0001t0003g0294 a0001c0001t0006g0293 |
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 | a0001c0001t0001g0065 a0001c0001t0003g0258 |
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 | a0001c0001t0001g0065 a0001c0001t0003g0258 |
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 | a0001c0001t0001g0300 a0001c0001t0033g0035 |
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 | a0002c0002t0002g0121 a0002c0002t0002g0144 |
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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0002c0002t0002g0137 | 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 | a0002c0002t0002g0165 | 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 | a0006c0005t0019g0321 | 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 | a0001c0001t0006g0185 | 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 | 124 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(121): Show |
127 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(124): 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 | a0002c0002t0002g0153 | 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 | a0001c0001t0003g0203 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0002c0002t0002g0076 a0002c0002t0003g0006 a0002c0002t0008g0187 others(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 | a0002c0002t0005g0272 a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0001c0001t0014g0015 a0001c0001t0014g0034 |
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 | 2 | a0001c0001t0001g0009 a0001c0001t0001g0302 |
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 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(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 | 173 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(170): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0002c0002t0002g0096 | 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 | a0001c0001t0001g0289 | 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 | 169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.843+927C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011507 | |||||||
| chr9:83011550 | C | CA | 36 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0002c0002t0001g0108 others(33): 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 | a0001c0001t0001g0051 a0001c0001t0001g0300 a0001c0001t0016g0186 others(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 | 100 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0037 others(97): Show |
102 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(99): 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 | 47 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0043 others(44): 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 | a0001c0001t0001g0053 a0001c0001t0001g0189 a0001c0001t0001g0202 others(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 | a0002c0002t0002g0102 a0002c0002t0002g0156 a0002c0004t0001g0263 others(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 | a0002c0002t0005g0272 | 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 | 173 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(170): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.843+721delT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 5/16 | chr9 | 83011712 | |||||||
| chr9:83011726 | A | T | 1 | a0004c0006t0037g0323 | 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 | a0002c0002t0002g0121 | 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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0002c0002t0002g0155 | 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 | 169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.766-114T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 4/16 | chr9 | 83012625 | |||||||
| chr9:83012639 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(200): Show |
208 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(205): 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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0002c0004t0012g0269 | 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 | a0002c0002t0002g0133 a0002c0002t0002g0146 a0002c0002t0020g0010 |
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 | 7 | a0001c0001t0001g0189 a0001c0001t0001g0231 a0001c0001t0001g0233 others(4): Show |
7 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(4): 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 | a0002c0002t0008g0286 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0300 a0001c0001t0014g0015 a0001c0001t0014g0034 others(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 | a0001c0001t0022g0312 | 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 | 173 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(170): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): 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 | a0001c0001t0001g0220 | 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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0002c0002t0005g0272 a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0001c0001t0001g0305 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0001c0001t0001g0300 a0001c0001t0014g0015 a0001c0001t0014g0034 others(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 | a0001c0001t0016g0049 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0074 others(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 | a0001c0001t0017g0297 a0001c0001t0017g0298 |
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 | 165 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(162): Show |
169 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(166): 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 | a0001c0001t0001g0191 a0001c0001t0001g0271 a0001c0001t0022g0312 |
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 | a0001c0001t0001g0196 | 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 | a0002c0002t0002g0097 | 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 | a0002c0002t0001g0184 | 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 | a0002c0010t0002g0048 | 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 | a0002c0002t0013g0159 | 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 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
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 | 169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.670-572delC | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83016471 | |||||||
| chr9:83016626 | A | G | 1 | a0002c0010t0002g0048 | 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 | a0002c0002t0004g0016 a0002c0002t0004g0019 a0002c0002t0004g0020 others(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 | a0001c0001t0001g0227 | 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 | a0002c0002t0003g0006 a0002c0002t0008g0296 a0002c0002t0010g0287 |
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 | a0001c0001t0006g0185 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0276 a0001c0001t0001g0289 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0210 a0001c0001t0018g0013 |
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 | 166 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(163): Show |
170 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(167): 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 | a0002c0002t0002g0165 a0002c0002t0002g0166 a0002c0002t0002g0167 others(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 | 203 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(200): Show |
208 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.670-1469T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017369 | |||||||
| chr9:83017375 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
171 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.670-1475G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017375 | |||||||
| chr9:83017390 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(162): Show |
169 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(166): 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 | a0002c0004t0001g0263 a0002c0004t0010g0264 a0002c0004t0012g0161 others(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 | 203 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(200): Show |
208 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(205): 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 | a0002c0002t0002g0102 | 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 | 169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.670-1600dupT | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83017499 | |||||||
| chr9:83017706 | G | T | 58 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0002g0076 others(55): 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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0002c0002t0001g0108 a0003c0003t0006g0169 a0003c0003t0006g0170 others(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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | 30 | a0002c0002t0003g0091 a0002c0002t0004g0016 a0002c0002t0004g0019 others(27): 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 | a0002c0002t0025g0120 | 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 | a0001c0001t0002g0278 | 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 | a0002c0002t0002g0153 | 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 | 229 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(226): Show |
235 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(232): 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 | a0001c0001t0003g0252 | 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 | 36 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(33): 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 | a0002c0002t0002g0117 a0002c0002t0002g0118 a0002c0002t0002g0119 others(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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0001c0001t0001g0300 a0001c0001t0014g0015 a0001c0001t0014g0034 others(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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
167 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.670-2675A>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 3/16 | chr9 | 83018575 | |||||||
| chr9:83018594 | G | A | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0001g0300 a0001c0001t0014g0015 a0001c0001t0014g0034 others(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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
167 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(164): 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 | a0002c0002t0002g0005 | 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 | a0002c0002t0004g0016 a0002c0002t0004g0019 |
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 | a0002c0010t0002g0048 | 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 | 203 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(200): Show |
208 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(205): 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 | a0002c0002t0026g0094 | 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 | a0002c0002t0002g0102 | 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 | a0002c0002t0002g0133 a0002c0002t0002g0146 a0002c0002t0020g0010 |
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 | 46 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0202 others(43): 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 | a0001c0001t0006g0185 a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0001c0001t0006g0293 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0002g0076 | 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 | a0002c0002t0003g0091 a0002c0002t0005g0090 |
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 | 217 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(214): Show |
223 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(220): 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 | a0001c0001t0006g0293 | 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 | a0001c0001t0001g0246 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
167 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(164): 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 | a0002c0011t0010g0036 a0005c0007t0010g0316 a0005c0007t0010g0317 others(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 | a0002c0002t0002g0102 | 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 | a0002c0002t0009g0093 a0002c0002t0024g0092 |
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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(147): Show |
154 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(151): 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 | a0001c0001t0001g0075 a0001c0001t0001g0295 |
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 | a0001c0001t0001g0054 | 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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0002c0002t0002g0166 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0001c0001t0006g0185 | 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 | a0002c0002t0001g0110 a0002c0002t0001g0111 a0002c0002t0001g0115 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0001c0001t0006g0293 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0002c0002t0005g0272 a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | a0002c0011t0010g0036 a0005c0007t0010g0316 a0005c0007t0010g0317 |
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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0001g0109 | 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 | a0001c0001t0001g0220 | 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 | a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0002c0011t0010g0036 | 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 | a0002c0010t0002g0048 | 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 | a0001c0001t0006g0185 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0002g0097 | 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 | 185 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(182): Show |
191 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.579-238T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83022664 | |||||||
| chr9:83022803 | G | C | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0010t0002g0048 | 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 | a0002c0010t0002g0048 | 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 | a0001c0001t0003g0261 a0001c0001t0003g0280 |
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 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0136 others(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 | a0001c0001t0001g0300 a0001c0001t0033g0035 |
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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0002g0097 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 19 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0002g0303 others(16): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0006g0185 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0215 others(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 | 18 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(15): 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | 18 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(15): 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 | 186 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(183): Show |
192 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.578+1431T>C | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024344 | |||||||
| chr9:83024434 | T | A | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0004t0001g0263 a0002c0004t0010g0264 a0002c0004t0012g0161 others(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 | 185 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(182): Show |
191 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.578+1067C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024708 | |||||||
| chr9:83024762 | C | T | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0002g0076 a0002c0002t0008g0187 a0002c0002t0008g0285 others(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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 185 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(182): Show |
191 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.578+832A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 2/16 | chr9 | 83024943 | |||||||
| chr9:83024977 | T | G | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0014g0015 a0001c0001t0014g0034 |
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 | a0002c0004t0027g0262 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0202 a0001c0001t0001g0228 others(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 | 14 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(11): 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 | a0002c0002t0009g0045 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0006g0185 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0002g0081 a0002c0002t0002g0100 a0002c0002t0002g0137 others(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 | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0188 others(11): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0001g0224 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0001g0184 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0005g0272 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | 166 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(163): Show |
171 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.432-162C>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026083 | |||||||
| chr9:83026239 | A | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
167 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.432-318T>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026239 | |||||||
| chr9:83026266 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(202): Show |
211 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.432-345A>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83026266 | |||||||
| chr9:83026300 | G | A | 4 | a0001c0001t0003g0007 a0001c0001t0003g0251 a0001c0001t0003g0257 others(1): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0002g0076 a0002c0002t0008g0187 a0002c0002t0008g0285 others(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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0004t0001g0263 a0002c0004t0010g0264 a0002c0004t0012g0161 others(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 | a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0002c0002t0001g0109 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0002g0107 | 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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0002c0002t0005g0272 | 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 | a0001c0001t0001g0222 a0001c0001t0001g0270 a0001c0001t0002g0223 |
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 | 185 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(182): Show |
191 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(188): 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 | a0002c0002t0002g0192 | 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 | a0001c0001t0006g0185 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0002c0002t0002g0165 a0002c0002t0002g0166 a0002c0002t0002g0167 others(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 | 19 | a0001c0001t0001g0200 a0001c0001t0015g0307 a0001c0001t0015g0308 others(16): 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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(147): Show |
155 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.432-2767G>A | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83028688 | |||||||
| chr9:83028880 | T | C | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0221 | 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 | 5 | a0002c0002t0007g0002 a0002c0002t0007g0085 a0002c0002t0007g0087 others(2): 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 | a0001c0001t0006g0185 a0002c0002t0001g0018 a0002c0002t0004g0016 others(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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0001c0001t0001g0206 a0001c0001t0001g0247 a0001c0001t0002g0283 others(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 | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
212 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.432-3639delA | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83029559 | |||||||
| chr9:83029559 | ATT | A | 7 | a0001c0001t0001g0200 a0001c0001t0017g0297 a0001c0001t0017g0298 others(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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0002c0002t0002g0168 | 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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(147): Show |
155 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(152): 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 | a0001c0001t0016g0186 | 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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0002c0002t0002g0147 | 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 | a0001c0001t0018g0014 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0008g0296 a0002c0002t0010g0287 |
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 | a0002c0002t0007g0154 a0002c0002t0026g0094 |
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 | a0001c0001t0016g0186 | 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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): 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 | a0002c0002t0002g0141 | 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 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
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 | a0002c0002t0004g0022 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0001g0108 | 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 | a0001c0001t0001g0162 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0016g0186 | 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 | a0002c0002t0004g0030 a0002c0002t0004g0031 a0002c0002t0004g0032 others(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 | 221 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(218): Show |
227 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(224): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): 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 | a0002c0002t0002g0017 a0002c0002t0002g0023 a0002c0002t0002g0163 |
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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0215 others(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 | a0002c0011t0010g0036 a0005c0007t0010g0316 a0005c0007t0010g0317 |
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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): 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 | a0002c0002t0004g0027 a0002c0002t0004g0028 a0002c0002t0004g0029 |
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 | a0002c0002t0002g0168 | 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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0002c0002t0005g0272 a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | a0001c0001t0006g0185 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0001g0248 | 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 | a0002c0002t0002g0096 | 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 | 14 | a0002c0002t0001g0082 a0002c0002t0001g0108 a0002c0002t0001g0109 others(11): 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 | a0002c0002t0002g0142 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0002c0002t0023g0077 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0300 | 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 | a0001c0001t0002g0283 | 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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
232 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.432-8715C>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83034636 | |||||||
| chr9:83034666 | C | A | 21 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(18): 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0300 a0001c0001t0014g0015 a0001c0001t0014g0034 others(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 | a0001c0001t0001g0295 | 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 | 29 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(26): 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 | a0002c0002t0002g0076 a0002c0002t0008g0187 a0002c0002t0008g0285 others(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 | 14 | a0001c0001t0003g0007 a0001c0001t0003g0160 a0001c0001t0003g0190 others(11): 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 | a0002c0002t0020g0010 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0003g0267 | 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 | a0003c0003t0006g0172 a0003c0003t0034g0171 |
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 | a0009c0012t0001g0318 | 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 | a0001c0001t0016g0186 | 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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0009g0045 | 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 | 213 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): 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 | a0002c0004t0010g0264 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0002g0070 others(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 | a0001c0001t0006g0185 a0002c0002t0002g0145 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
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 | a0001c0001t0001g0075 | 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 | a0001c0001t0035g0320 a0002c0011t0010g0036 a0005c0007t0010g0316 others(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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0010t0002g0048 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0002g0149 | 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 | a0002c0002t0002g0192 | 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 | 32 | a0001c0001t0003g0007 a0001c0001t0003g0160 a0001c0001t0003g0190 others(29): 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 | a0001c0001t0001g0214 | 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 | a0002c0010t0002g0048 | 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 | a0001c0001t0001g0008 | 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 | 21 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(18): 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 | 21 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(18): 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 | 21 | a0001c0001t0001g0191 a0001c0001t0015g0307 a0001c0001t0015g0308 others(18): 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 | 21 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(18): 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 | a0001c0001t0001g0300 a0001c0001t0014g0015 a0001c0001t0014g0034 others(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 | a0004c0006t0037g0323 | 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 | 21 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(18): 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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0047 a0001c0001t0001g0050 others(44): 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 | 127 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0037 others(124): Show |
131 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(128): 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 | 38 | a0002c0002t0001g0018 a0002c0002t0001g0143 a0002c0002t0002g0101 others(35): 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 | a0003c0003t0006g0169 a0003c0003t0006g0170 a0003c0003t0006g0172 others(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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | |||||||
| chr9:83038123 | A | T | 2 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0002c0002t0005g0272 | 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 | a0002c0004t0012g0161 | 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 | a0002c0002t0002g0146 | 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 | a0002c0002t0005g0272 | 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 | a0001c0001t0006g0185 a0002c0002t0001g0018 a0002c0002t0004g0016 others(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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0075 | 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 | a0005c0007t0010g0316 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0004t0012g0161 | 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 | 21 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(18): 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 | a0002c0002t0001g0184 | 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 | a0009c0012t0001g0318 | 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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0002c0002t0002g0147 | 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 | 19 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(16): 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 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0074 |
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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0002g0041 | 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 | a0001c0001t0006g0185 a0002c0002t0001g0018 a0002c0002t0004g0016 others(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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0001g0300 a0001c0001t0014g0015 a0001c0001t0014g0034 others(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 | a0002c0002t0023g0077 | 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 | a0001c0001t0001g0080 | 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 | 21 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(18): 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 | a0002c0002t0002g0102 a0002c0002t0002g0105 |
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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0300 a0001c0001t0014g0015 a0001c0001t0014g0034 others(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 | 21 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(18): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0001c0001t0018g0014 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 21 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(18): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0003c0003t0006g0169 a0003c0003t0006g0170 a0003c0003t0006g0172 others(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 | a0002c0002t0002g0101 a0002c0002t0002g0148 a0002c0002t0002g0149 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0002g0150 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0002c0002t0005g0272 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 18 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(15): 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0310 | 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 | a0002c0002t0001g0018 a0002c0002t0004g0016 a0002c0002t0004g0019 others(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 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0002c0002t0002g0040 | 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 | 46 | a0001c0001t0001g0202 a0001c0001t0002g0283 a0001c0001t0002g0284 others(43): 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 | a0001c0001t0006g0185 a0001c0001t0016g0186 a0002c0002t0001g0018 others(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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 126 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(123): Show |
129 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(126): 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 | a0001c0001t0005g0306 a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0009c0012t0001g0318 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0002c0002t0008g0083 | 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 | 21 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(18): 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 | a0002c0002t0009g0088 a0002c0002t0009g0089 |
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 | 1 | a0002c0002t0002g0003 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0033g0035 |
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 | a0001c0001t0002g0315 a0001c0001t0006g0185 a0002c0002t0001g0018 others(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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0033g0035 |
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 | 22 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(19): 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 | 22 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(19): 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 | a0001c0001t0018g0014 | 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 | a0001c0001t0001g0265 | 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 | 17 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(14): 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 | 231 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(228): Show |
237 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(234): 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 | a0002c0002t0002g0097 a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0001g0063 | 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 | a0002c0002t0004g0016 | 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 | a0001c0001t0003g0160 a0002c0002t0003g0006 a0002c0004t0012g0161 |
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 | a0001c0001t0017g0298 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0266 |
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 | a0001c0001t0003g0267 a0001c0001t0003g0299 |
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 | 6 | a0002c0002t0007g0002 a0002c0002t0007g0085 a0002c0002t0007g0087 others(3): 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 | 22 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(19): 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 | 20 | a0001c0001t0001g0009 a0001c0001t0001g0079 a0001c0001t0001g0198 others(17): 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 | 13 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(10): 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0013g0084 |
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 | 22 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(19): 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 | a0002c0002t0007g0154 a0002c0002t0026g0094 |
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 | a0001c0001t0001g0212 | 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 | a0002c0004t0012g0269 | 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 | a0002c0002t0002g0102 | 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 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
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 | a0002c0011t0010g0036 | 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 | 6 | a0002c0002t0007g0002 a0002c0002t0007g0085 a0002c0002t0007g0087 others(3): 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 | a0001c0001t0001g0211 | 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 | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(152): Show |
159 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(156): 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 | 148 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(145): Show |
152 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(149): 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 | a0001c0001t0002g0278 a0002c0002t0001g0018 a0002c0002t0002g0017 others(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 | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0188 others(7): 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 | a0002c0002t0002g0182 | 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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0033g0035 |
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 | a0001c0001t0006g0185 | 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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0002c0002t0003g0091 a0002c0002t0005g0090 |
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 | a0001c0001t0002g0315 a0001c0001t0018g0013 a0001c0001t0018g0014 |
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 | a0001c0001t0022g0312 | 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 | a0007c0013t0001g0319 | 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 | a0002c0002t0002g0155 | 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | 22 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(19): 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0191 a0001c0001t0001g0271 |
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 | a0001c0001t0001g0288 a0004c0006t0036g0324 a0004c0006t0037g0323 others(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 | a0002c0002t0002g0076 a0002c0002t0008g0187 a0002c0002t0008g0285 others(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 | 145 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(142): Show |
149 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(146): 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0002c0002t0005g0272 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0001c0001t0001g0273 | 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 | 20 | a0001c0001t0003g0205 a0001c0001t0014g0015 a0001c0001t0014g0034 others(17): 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 | 22 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(19): 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0002c0002t0013g0159 | 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 | a0002c0002t0004g0030 a0002c0002t0004g0031 a0002c0002t0004g0032 others(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 | a0003c0003t0006g0169 a0003c0003t0006g0170 a0003c0003t0006g0172 others(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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0002c0010t0002g0048 | 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 | a0001c0001t0001g0073 a0001c0001t0002g0071 a0001c0001t0014g0015 others(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 | 46 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0046 others(43): 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 | 102 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0037 others(99): Show |
105 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(102): 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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0060 a0001c0001t0002g0278 a0001c0001t0012g0062 others(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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0002g0315 a0001c0001t0018g0013 a0002c0002t0001g0082 others(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 | a0002c0002t0002g0192 | 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 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0075 others(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 | 42 | a0001c0001t0002g0278 a0001c0001t0006g0185 a0001c0001t0014g0015 others(39): 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 | a0001c0001t0003g0256 | 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 | 169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): 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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0033g0035 |
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 | a0002c0002t0001g0082 a0002c0002t0001g0109 a0002c0002t0001g0114 |
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 | a0001c0001t0001g0008 | 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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0002c0002t0002g0076 a0002c0002t0008g0187 a0002c0002t0008g0285 others(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 | a0002c0002t0002g0097 a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0015g0307 others(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 | a0002c0002t0002g0102 | 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 | a0001c0001t0001g0214 | 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 | 10 | a0001c0001t0003g0007 a0001c0001t0003g0190 a0001c0001t0003g0203 others(7): 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 | a0001c0001t0002g0278 a0001c0001t0006g0185 a0002c0002t0001g0018 others(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 | a0001c0001t0002g0315 a0001c0001t0018g0013 a0001c0001t0018g0014 |
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 | a0002c0010t0002g0048 | 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 | a0005c0007t0010g0316 a0005c0007t0010g0317 a0009c0012t0001g0318 |
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 | a0001c0001t0002g0315 | 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 | a0002c0002t0001g0122 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0033g0035 |
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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0002c0010t0002g0048 | 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 | a0001c0001t0030g0201 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0011g0131 others(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 | a0002c0002t0026g0094 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0002c0002t0002g0096 | 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 | a0003c0003t0006g0169 a0003c0003t0006g0170 a0003c0003t0006g0172 others(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 | 22 | a0001c0001t0001g0247 a0001c0001t0014g0015 a0001c0001t0014g0034 others(19): 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 | a0001c0001t0001g0300 | 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 | a0001c0001t0006g0185 | 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 | a0001c0001t0006g0185 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0011t0010g0036 |
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 | a0001c0001t0001g0300 a0001c0001t0002g0283 a0001c0001t0002g0284 others(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 | a0001c0001t0003g0280 | 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 | a0001c0001t0001g0191 a0001c0001t0001g0271 a0001c0001t0022g0312 |
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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0003g0160 a0002c0002t0003g0006 a0002c0004t0012g0161 others(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 | a0001c0001t0030g0201 | 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 | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(152): Show |
159 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(156): 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 | a0002c0011t0010g0036 | 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 | a0002c0002t0002g0096 | 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 | a0002c0002t0008g0083 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0033g0035 |
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 | a0001c0001t0002g0278 a0002c0002t0001g0018 a0002c0002t0002g0017 others(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 | 8 | a0001c0001t0003g0007 a0001c0001t0003g0190 a0001c0001t0003g0203 others(5): 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 | a0001c0001t0002g0071 | 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 | a0003c0003t0006g0169 a0003c0003t0006g0170 a0003c0003t0006g0172 others(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 | a0002c0002t0005g0164 a0002c0002t0005g0177 a0002c0002t0005g0178 others(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 | a0002c0002t0002g0105 | 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 | a0002c0002t0005g0272 | 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 | 4 | a0002c0002t0002g0005 a0002c0002t0002g0156 a0002c0002t0002g0157 others(1): 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 | a0002c0002t0007g0154 | 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 | a0001c0001t0001g0228 | 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 | 16 | a0001c0001t0001g0266 a0002c0002t0003g0091 a0002c0002t0005g0090 others(13): 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0011t0010g0036 |
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 | a0002c0002t0002g0150 | 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 | a0002c0011t0010g0036 | 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 | a0002c0002t0005g0272 a0005c0007t0010g0316 a0005c0007t0010g0317 others(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 | a0001c0001t0002g0278 a0002c0002t0001g0018 a0002c0002t0002g0017 others(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 | a0005c0007t0010g0316 a0005c0007t0010g0317 a0009c0012t0001g0318 |
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 | a0001c0001t0003g0256 | 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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0033g0035 |
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 | 42 | a0001c0001t0002g0278 a0001c0001t0006g0185 a0001c0001t0014g0015 others(39): 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 | a0002c0002t0001g0122 | 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 | 13 | a0001c0001t0002g0315 a0001c0001t0015g0307 a0001c0001t0015g0308 others(10): 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0011t0010g0036 |
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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | 23 | a0001c0001t0001g0189 a0001c0001t0001g0215 a0001c0001t0001g0216 others(20): Show |
23 | HG00597.hp2 HG00609.hp2 HG00639.hp2 others(20): 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 | a0001c0001t0014g0015 a0001c0001t0014g0034 |
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 | a0002c0002t0002g0123 | 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 | a0002c0002t0002g0102 | 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 | 169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): 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 | a0001c0001t0031g0232 | 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 | a0002c0002t0005g0272 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0074 others(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 | a0002c0004t0001g0263 | 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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0011t0010g0036 |
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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0011t0010g0036 |
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 | a0002c0002t0011g0103 a0002c0002t0011g0104 |
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 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
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 | a0001c0001t0014g0015 | 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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
167 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.431+9366T>G | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83053071 | |||||||
| chr9:83053226 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(214): Show |
223 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(220): 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 | a0001c0001t0001g0191 a0001c0001t0001g0271 a0001c0001t0022g0312 |
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 | a0001c0001t0001g0191 a0001c0001t0001g0271 a0001c0001t0022g0312 |
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 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
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 | a0001c0001t0001g0224 | 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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
232 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(229): 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 | a0001c0001t0001g0220 | 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 | a0002c0002t0002g0096 | 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 | 42 | a0001c0001t0002g0278 a0001c0001t0006g0185 a0001c0001t0014g0015 others(39): 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 | 42 | a0001c0001t0002g0278 a0001c0001t0006g0185 a0001c0001t0014g0015 others(39): 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 | a0003c0003t0006g0169 a0003c0003t0006g0170 a0003c0003t0006g0172 others(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 | a0002c0011t0010g0036 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0011t0010g0036 |
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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | 18 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0002t0003g0091 others(15): 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 | a0002c0002t0005g0272 | 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 | a0002c0002t0008g0083 | 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 | a0001c0001t0001g0300 a0001c0001t0006g0293 a0001c0001t0017g0297 others(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 | a0002c0002t0001g0183 | 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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0033g0035 |
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 | a0001c0001t0001g0046 a0002c0011t0010g0036 |
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 | a0002c0002t0002g0096 | 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 | a0002c0002t0024g0092 | 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 | a0002c0010t0002g0048 | 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 | a0001c0001t0006g0185 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0002c0011t0010g0036 | 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 | a0001c0001t0002g0278 a0001c0001t0006g0185 a0002c0002t0001g0018 others(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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0033g0035 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0011t0010g0036 |
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 | a0001c0001t0001g0234 a0001c0001t0001g0244 |
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 | a0002c0011t0010g0036 a0005c0007t0010g0316 a0005c0007t0010g0317 others(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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0001g0197 | 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 | a0002c0002t0004g0019 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0011t0010g0036 others(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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(152): Show |
159 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(156): 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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0073 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0002c0002t0009g0093 | 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 | a0002c0002t0002g0117 | 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 | a0001c0001t0021g0011 | 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 | a0001c0001t0021g0011 | 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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0002c0002t0005g0314 a0002c0004t0001g0263 a0002c0004t0010g0264 others(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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0011t0010g0036 others(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 | a0002c0002t0002g0153 | 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 | a0002c0002t0002g0153 | 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 | a0003c0003t0006g0169 a0003c0003t0006g0170 a0003c0003t0006g0172 others(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 | a0001c0001t0001g0300 a0001c0001t0002g0283 a0001c0001t0002g0284 others(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 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0011t0010g0036 |
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 | 22 | a0001c0001t0001g0202 a0001c0001t0003g0007 a0001c0001t0003g0190 others(19): 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0002g0056 | 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 | a0001c0001t0016g0186 | 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 | a0001c0001t0001g0162 | 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 | a0002c0002t0002g0081 | 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 | a0002c0002t0001g0108 | 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 | a0002c0002t0002g0145 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0001c0001t0001g0204 | 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 | a0001c0001t0002g0315 | 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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | 15 | a0002c0002t0003g0091 a0002c0002t0005g0090 a0002c0002t0007g0002 others(12): 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 | a0002c0002t0001g0183 | 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 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0075 others(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 | a0001c0001t0002g0278 a0001c0001t0006g0185 a0002c0002t0001g0018 others(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 | a0002c0002t0002g0039 a0002c0002t0002g0041 |
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 | a0001c0001t0002g0278 a0001c0001t0006g0185 a0002c0002t0001g0018 others(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 | a0001c0001t0001g0277 | 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 | 7 | a0002c0002t0007g0002 a0002c0002t0007g0085 a0002c0002t0007g0087 others(4): 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 | a0001c0001t0033g0035 | 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 | 50 | a0001c0001t0002g0278 a0001c0001t0006g0185 a0001c0001t0014g0015 others(47): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0001c0001t0016g0186 | 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 | a0001c0001t0003g0203 | 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 | a0006c0005t0019g0321 a0006c0005t0019g0322 |
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 | a0002c0002t0009g0044 a0002c0002t0009g0045 a0002c0002t0009g0093 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(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 | 13 | a0002c0002t0002g0003 a0002c0002t0002g0081 a0002c0002t0002g0097 others(10): 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 | a0002c0002t0002g0095 a0002c0002t0002g0096 a0002c0002t0002g0192 others(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 | 6 | a0002c0002t0001g0184 a0002c0002t0002g0005 a0002c0002t0002g0039 others(3): 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 | a0001c0001t0001g0080 a0001c0001t0001g0199 a0001c0001t0001g0200 others(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 | 174 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
180 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(177): 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 | a0001c0001t0001g0279 a0001c0001t0003g0280 a0001c0001t0014g0015 others(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 | a0002c0002t0009g0045 a0002c0002t0009g0093 a0002c0002t0024g0092 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0075 others(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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0002c0002t0013g0159 | 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 | a0002c0002t0004g0022 | 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 | 141 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(138): 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 | 21 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0057 others(18): Show |
21 | HG00280.hp1 HG01071.hp1 HG01358.hp1 others(18): 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 | a0001c0001t0001g0050 a0002c0002t0002g0095 a0002c0002t0002g0127 others(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 | a0001c0001t0002g0278 a0002c0002t0001g0018 a0002c0002t0002g0017 others(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 | a0001c0001t0006g0185 | 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 | 2 | a0002c0002t0002g0003 a0002c0002t0002g0095 |
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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0033g0035 |
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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0033g0035 |
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 | a0002c0002t0002g0145 | 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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0015g0307 others(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 | 46 | a0001c0001t0002g0278 a0001c0001t0006g0185 a0001c0001t0014g0015 others(43): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0002c0002t0026g0094 | 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 | a0002c0011t0010g0036 a0005c0007t0010g0316 a0005c0007t0010g0317 others(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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0002g0315 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0002c0002t0002g0192 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0188 others(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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(132): Show |
138 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(135): 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 | 22 | a0001c0001t0001g0079 a0001c0001t0001g0281 a0001c0001t0001g0282 others(19): 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 | a0001c0001t0001g0080 a0001c0001t0003g0299 a0001c0001t0014g0015 others(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 | a0001c0001t0001g0300 a0001c0001t0002g0315 |
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 | a0001c0001t0033g0035 a0006c0005t0019g0322 |
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 | 14 | a0002c0002t0001g0082 a0002c0002t0003g0091 a0002c0002t0005g0090 others(11): 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 | a0002c0002t0002g0039 a0002c0002t0002g0081 a0002c0002t0009g0045 |
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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0033g0035 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | 43 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(40): 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0001c0001t0001g0301 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0033g0035 |
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 | a0002c0011t0010g0036 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0011t0010g0036 others(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 | a0001c0001t0001g0008 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 a0002c0011t0010g0036 others(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 | 2 | a0001c0001t0001g0009 a0001c0001t0001g0302 |
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 | a0002c0002t0002g0303 a0002c0002t0002g0304 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0001c0001t0001g0305 | 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 | a0002c0002t0009g0044 | 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 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
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 | a0002c0002t0002g0039 a0002c0002t0002g0040 a0002c0002t0002g0041 |
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 | a0001c0001t0005g0306 | 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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0022g0312 | 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 | a0001c0001t0018g0013 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
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 | a0005c0007t0010g0316 a0005c0007t0010g0317 |
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 | a0002c0011t0010g0036 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 a0006c0005t0019g0321 others(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 | a0001c0001t0014g0015 a0001c0001t0014g0034 a0001c0001t0033g0035 |
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 | a0001c0001t0015g0307 a0001c0001t0015g0308 |
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 | a0001c0001t0001g0309 | 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 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
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 | a0001c0001t0022g0312 | 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 | a0002c0002t0001g0018 a0002c0002t0002g0017 a0002c0002t0002g0023 others(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 | a0001c0001t0002g0278 a0002c0002t0002g0163 a0004c0006t0036g0324 others(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 | 117 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(114): 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 | 169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
175 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(172): 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 | a0001c0001t0014g0015 | 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 | a0002c0002t0005g0314 | 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 | a0001c0001t0002g0315 a0001c0001t0018g0013 a0001c0001t0018g0014 |
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 | a0001c0001t0002g0315 | 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 | a0004c0006t0036g0324 a0004c0006t0037g0323 |
2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.431+49G>T | RASEF | ENSG00000165105.10 | transcript | ENST00000376447.4 | protein_coding | 1/16 | chr9 | 83062388 |