Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83937 |
| ensemblid | ENSG00000107551.21 |
| hgncid | 20793 |
| symbol | RASSF4 |
| name | Ras association domain family member 4 |
| refseq_nuc | NM_032023.4 |
| refseq_prot | NP_114412.2 |
| ensembl_nuc | ENST00000340258.10 |
| ensembl_prot | ENSP00000339692.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 44959802 |
| end | 44995891 |
| strand | + |
| ver | v1.2 |
| region | chr10:44959802-44995891 |
| region5000 | chr10:44954802-45000891 |
| regionname0 | RASSF4_chr10_44959802_44995891 |
| regionname5000 | RASSF4_chr10_44954802_45000891 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 321 | 264 | 52 | 46 | 126 | 10 | 28 | 89 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(316): Show |
chr10 | 44954802 | 45000891 |
| a0002 | 0/0 | 321 | 109 | 28 | 12 | 60 | 0 | 9 | 49 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(316): Show |
chr10 | 44954802 | 45000891 |
| a0003 | 0/0 | 321 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(316): Show |
chr10 | 44954802 | 45000891 |
| a0004 | 0/0 | 321 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(316): Show |
chr10 | 44954802 | 45000891 |
| a0005 | 0/0 | 321 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(316): Show |
chr10 | 44954802 | 45000891 |
| a0006 | 0/0 | 321 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(316): Show |
chr10 | 44954802 | 45000891 |
| a0007 | 0/0 | 321 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(316): Show |
chr10 | 44954802 | 45000891 |
| a0008 | 0/0 | 321 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(316): Show |
chr10 | 44954802 | 45000891 |
| a0009 | 0/0 | 321 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(316): Show |
chr10 | 44954802 | 45000891 |
| a0010 | 0/0 | 321 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(316): Show |
chr10 | 44954802 | 45000891 |
| a0011 | 0/0 | 321 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(316): Show |
chr10 | 44954802 | 45000891 |
| a0012 | 0/0 | 321 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(316): Show |
chr10 | 44954802 | 45000891 |
| a0013 | 0/0 | 321 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(316): Show |
chr10 | 44954802 | 45000891 |
| a0014 | 0/0 | 169 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | MKEDC others(164): Show |
chr10 | 44954802 | 45000891 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 963 | 263 | 52 | 46 | 125 | 10 | 28 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0001c0016 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0002c0002 | 0/0 | 963 | 108 | 27 | 12 | 60 | 0 | 9 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0002c0012 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0003c0003 | 0/0 | 963 | 5 | 3 | 2 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0004c0004 | 0/0 | 963 | 4 | 3 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0005c0005 | 0/0 | 963 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0006c0006 | 0/0 | 963 | 2 | 1 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0007c0007 | 0/0 | 963 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0008c0008 | 0/0 | 963 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0009c0015 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0010c0011 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0011c0010 | 0/0 | 963 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0012c0013 | 0/0 | 963 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0013c0014 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 | ||
| a0014c0009 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | ATGAA others(958): Show |
chr10 | 44954802 | 45000891 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3631 | 167 | 26 | 32 | 73 | 9 | 26 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0002 | 0/0 | 3632 | 41 | 0 | 9 | 32 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3627): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0003 | 0/0 | 3631 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0004 | 0/0 | 3632 | 6 | 0 | 1 | 5 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3627): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0005 | 0/0 | 3633 | 8 | 3 | 0 | 2 | 1 | 2 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3628): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0006 | 0/0 | 3631 | 5 | 5 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0007 | 0/0 | 3631 | 5 | 0 | 0 | 5 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0008 | 0/0 | 3631 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0009 | 0/0 | 3631 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0010 | 0/0 | 3633 | 2 | 0 | 1 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3628): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0012 | 0/0 | 3631 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0013 | 1/0 | 3631 | 2 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0015 | 0/0 | 3632 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3627): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0019 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0021 | 0/0 | 3632 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3627): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0022 | 0/0 | 3646 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3641): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0023 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0024 | 0/0 | 3631 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0025 | 0/0 | 3631 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0026 | 0/0 | 3631 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0029 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0033 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0034 | 0/0 | 3631 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0036 | 0/0 | 3632 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3627): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0037 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0001t0039 | 0/0 | 3631 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0001c0016t0001 | 0/0 | 3631 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0002c0002t0001 | 0/0 | 3631 | 63 | 17 | 11 | 26 | 0 | 9 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0002c0002t0002 | 0/0 | 3632 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3627): Show |
chr10 | 44954802 | 45000891 |
| a0002c0002t0003 | 0/0 | 3631 | 22 | 0 | 0 | 22 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0002c0002t0004 | 0/0 | 3632 | 9 | 2 | 1 | 6 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3627): Show |
chr10 | 44954802 | 45000891 |
| a0002c0002t0005 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3628): Show |
chr10 | 44954802 | 45000891 |
| a0002c0002t0011 | 0/0 | 3631 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0002c0002t0014 | 0/0 | 3631 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0002c0002t0018 | 0/0 | 3632 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3627): Show |
chr10 | 44954802 | 45000891 |
| a0002c0002t0028 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0002c0002t0030 | 0/0 | 3632 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3627): Show |
chr10 | 44954802 | 45000891 |
| a0002c0002t0031 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3628): Show |
chr10 | 44954802 | 45000891 |
| a0002c0002t0032 | 0/0 | 3632 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3627): Show |
chr10 | 44954802 | 45000891 |
| a0002c0012t0038 | 0/0 | 3632 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3627): Show |
chr10 | 44954802 | 45000891 |
| a0003c0003t0010 | 0/0 | 3633 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3628): Show |
chr10 | 44954802 | 45000891 |
| a0003c0003t0016 | 0/0 | 3633 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3628): Show |
chr10 | 44954802 | 45000891 |
| a0003c0003t0035 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0004c0004t0001 | 0/0 | 3631 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0004c0004t0020 | 0/0 | 3631 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0005c0005t0001 | 0/0 | 3631 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0006c0006t0002 | 0/0 | 3632 | 2 | 1 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3627): Show |
chr10 | 44954802 | 45000891 |
| a0007c0007t0001 | 0/0 | 3631 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0008c0008t0001 | 0/0 | 3631 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0009c0015t0017 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0010c0011t0027 | 0/0 | 3631 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0011c0010t0001 | 0/0 | 3631 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0012c0013t0001 | 0/0 | 3631 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0013c0014t0003 | 0/0 | 3631 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| a0014c0009t0012 | 0/0 | 3631 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | GCAGC others(3626): Show |
chr10 | 44954802 | 45000891 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 0 | 8 | 1 | 2 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 2 | 4 | 2 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0231 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0003 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0004g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0005g0004 | 0/0 | 4 | 1 | 0 | 1 | 1 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0005g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0007g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0009g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0009g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0010g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0010g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0013g0010 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0013g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0015g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0015g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0019g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0021g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0022g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0023g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0024g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0025g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0026g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0029g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0033g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0034g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0036g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0037g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0001t0039g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0001c0016t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0004g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0004g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0011g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0014g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0014g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0018g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0028g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0030g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0031g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0002t0032g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0002c0012t0038g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0003c0003t0010g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0003c0003t0010g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0003c0003t0016g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0003c0003t0016g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0003c0003t0035g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0004c0004t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0004c0004t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0004c0004t0020g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0005c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0005c0005t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0005c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0006c0006t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0006c0006t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0007c0007t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0007c0007t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0008c0008t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0009c0015t0017g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0010c0011t0027g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0011c0010t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0012c0013t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0013c0014t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| a0014c0009t0012g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0004 | EUR | GBR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00408 | hp2 | a0001 | c0001 | t0025 | g0140 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0009 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00544 | hp1 | a0001 | c0001 | t0039 | g0052 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00597 | hp1 | a0002 | c0002 | t0003 | g0026 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0159 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01069 | hp2 | a0006 | c0006 | t0002 | g0056 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01175 | hp1 | a0002 | c0002 | t0004 | g0218 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01192 | hp2 | a0003 | c0003 | t0010 | g0108 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01243 | hp1 | a0003 | c0003 | t0010 | g0109 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01256 | hp2 | a0001 | c0001 | t0034 | g0105 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01433 | hp1 | a0001 | c0001 | t0013 | g0071 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01496 | hp2 | a0001 | c0001 | t0010 | g0003 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01884 | hp1 | a0004 | c0004 | t0001 | g0223 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0047 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0141 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0121 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02056 | hp1 | a0001 | c0001 | t0021 | g0089 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02056 | hp2 | a0002 | c0002 | t0003 | g0255 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02132 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02145 | hp1 | a0003 | c0003 | t0016 | g0065 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02148 | hp1 | a0001 | c0001 | t0024 | g0044 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CDX | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | CDX | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02165 | hp2 | a0002 | c0002 | t0003 | g0035 | EAS | CDX | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02257 | hp1 | a0002 | c0002 | t0004 | g0173 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0176 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0120 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0162 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0188 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02602 | hp2 | a0008 | c0008 | t0001 | g0076 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02615 | hp1 | a0001 | c0001 | t0029 | g0166 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0135 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0100 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02647 | hp1 | a0004 | c0004 | t0001 | g0051 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0215 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0225 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0072 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02723 | hp2 | a0009 | c0015 | t0017 | g0067 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0110 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0195 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02809 | hp1 | a0002 | c0002 | t0014 | g0178 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0043 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02818 | hp2 | a0001 | c0001 | t0015 | g0190 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02895 | hp1 | a0007 | c0007 | t0001 | g0132 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02896 | hp2 | a0003 | c0003 | t0016 | g0117 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02922 | hp1 | a0002 | c0002 | t0004 | g0103 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02965 | hp2 | a0004 | c0004 | t0001 | g0051 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02976 | hp2 | a0001 | c0001 | t0019 | g0043 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0144 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0219 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | MSL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03098 | hp2 | a0002 | c0002 | t0005 | g0059 | AFR | MSL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0134 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0133 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03195 | hp1 | a0010 | c0011 | t0027 | g0057 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0066 | AFR | MSL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03453 | hp1 | a0007 | c0007 | t0001 | g0222 | AFR | MSL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03453 | hp2 | a0002 | c0002 | t0030 | g0208 | AFR | MSL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03486 | hp1 | a0001 | c0001 | t0023 | g0047 | AFR | MSL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03486 | hp2 | a0002 | c0012 | t0038 | g0068 | AFR | MSL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03516 | hp1 | a0005 | c0005 | t0001 | g0129 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03516 | hp2 | a0002 | c0002 | t0011 | g0019 | AFR | ESN | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03540 | hp2 | a0005 | c0005 | t0001 | g0131 | AFR | GWD | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03579 | hp1 | a0002 | c0002 | t0028 | g0136 | AFR | MSL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0025 | AFR | MSL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0179 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03710 | hp1 | a0011 | c0010 | t0001 | g0091 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | BEB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03834 | hp2 | a0012 | c0013 | t0001 | g0152 | SAS | BEB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0214 | SAS | BEB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0163 | SAS | BEB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0169 | SAS | STU | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18522 | hp2 | a0002 | c0002 | t0014 | g0220 | AFR | YRI | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18747 | hp1 | a0002 | c0002 | t0004 | g0216 | EAS | CHB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | CHB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0128 | AFR | YRI | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18939 | hp2 | a0013 | c0014 | t0003 | g0175 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18943 | hp1 | a0002 | c0002 | t0003 | g0236 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18944 | hp1 | a0001 | c0001 | t0012 | g0005 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18945 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18948 | hp1 | a0002 | c0002 | t0003 | g0009 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18951 | hp2 | a0002 | c0002 | t0003 | g0009 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18961 | hp1 | a0001 | c0016 | t0001 | g0006 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18962 | hp2 | a0002 | c0002 | t0004 | g0049 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18965 | hp1 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18966 | hp2 | a0002 | c0002 | t0003 | g0256 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18967 | hp1 | a0002 | c0002 | t0003 | g0249 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18974 | hp1 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18974 | hp2 | a0001 | c0001 | t0022 | g0001 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18975 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18978 | hp1 | a0002 | c0002 | t0003 | g0096 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18978 | hp2 | a0002 | c0002 | t0003 | g0094 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18988 | hp2 | a0002 | c0002 | t0004 | g0053 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18991 | hp1 | a0002 | c0002 | t0003 | g0234 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18999 | hp1 | a0002 | c0002 | t0018 | g0026 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19009 | hp2 | a0002 | c0002 | t0004 | g0209 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | LWK | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19030 | hp2 | a0001 | c0001 | t0037 | g0063 | AFR | LWK | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19055 | hp1 | a0014 | c0009 | t0012 | g0232 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19057 | hp1 | a0002 | c0002 | t0003 | g0009 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19058 | hp1 | a0001 | c0001 | t0026 | g0212 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19060 | hp1 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19063 | hp1 | a0002 | c0002 | t0003 | g0235 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19066 | hp1 | a0002 | c0002 | t0004 | g0053 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19070 | hp1 | a0002 | c0002 | t0004 | g0049 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19072 | hp1 | a0001 | c0001 | t0036 | g0202 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19079 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19080 | hp2 | a0002 | c0002 | t0003 | g0035 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19083 | hp2 | a0002 | c0002 | t0003 | g0153 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19084 | hp1 | a0002 | c0002 | t0032 | g0145 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19085 | hp1 | a0002 | c0002 | t0031 | g0097 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19086 | hp1 | a0002 | c0002 | t0003 | g0154 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19088 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19090 | hp2 | a0001 | c0001 | t0010 | g0039 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19091 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19240 | hp1 | a0002 | c0002 | t0011 | g0019 | AFR | YRI | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0127 | AFR | YRI | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ASW | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ASW | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01123 | hp1 | a0004 | c0004 | t0020 | g0102 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02109 | hp1 | a0006 | c0006 | t0002 | g0064 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02109 | hp2 | a0005 | c0005 | t0001 | g0130 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | ACB | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG03471 | hp2 | a0003 | c0003 | t0035 | g0259 | AFR | MSL | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0025 | AFR | USA | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| HG06807 | hp2 | a0002 | c0002 | t0011 | g0019 | AFR | USA | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| NA21309 | hp2 | a0001 | c0001 | t0033 | g0211 | AFR | LWK | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0231 | REF | REF | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0013 | g0010 | REF | REF | RASSF4_chr10_44954802_45000891 | RASSF4 | chr10 | 44954802 | 45000891 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:44970230 | C | T | 2 | a0005 a0007 |
5 | HG02109.hp2 HG02895.hp1 HG03453.hp1 others(2): Show |
missense_variant | MODERATE | c.28C>T | p.His10Tyr | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/11 | 131/3631 | 28/966 | 10/321 | chr10 | 44970230 | |||
| chr10:44982644 | A | G | 8 | a0002 a0003 a0005 others(5): Show |
123 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(120): Show |
missense_variant | MODERATE | c.262A>G | p.Arg88Gly | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/11 | 365/3631 | 262/966 | 88/321 | chr10 | 44982644 | |||
| chr10:44982648 | G | A | 1 | a0008 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.266G>A | p.Arg89Gln | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/11 | 369/3631 | 266/966 | 89/321 | chr10 | 44982648 | |||
| chr10:44984028 | G | T | 2 | a0003 a0006 |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
missense_variant | MODERATE | c.288G>T | p.Glu96Asp | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 5/11 | 391/3631 | 288/966 | 96/321 | chr10 | 44984028 | |||
| chr10:44984888 | G | C | 1 | a0010 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.449G>C | p.Arg150Thr | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 552/3631 | 449/966 | 150/321 | chr10 | 44984888 | |||
| chr10:44984902 | G | A | 1 | a0003 | 5 | HG01192.hp2 HG01243.hp1 HG02145.hp1 others(2): Show |
missense_variant | MODERATE | c.463G>A | p.Ala155Thr | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 566/3631 | 463/966 | 155/321 | chr10 | 44984902 | |||
| chr10:44984921 | G | A | 1 | a0004 | 4 | HG01123.hp1 HG01884.hp1 HG02647.hp1 others(1): Show |
missense_variant | MODERATE | c.482G>A | p.Arg161His | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 585/3631 | 482/966 | 161/321 | chr10 | 44984921 | |||
| chr10:44984930 | G | A | 1 | a0006 | 2 | HG01069.hp2 HG02109.hp1 |
missense_variant | MODERATE | c.491G>A | p.Arg164Gln | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 594/3631 | 491/966 | 164/321 | chr10 | 44984930 | |||
| chr10:44984944 | A | T | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.505A>T | p.Ile169Phe | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 608/3631 | 505/966 | 169/321 | chr10 | 44984944 | |||
| chr10:44984947 | A | T | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.508A>T | p.Asn170Tyr | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 611/3631 | 508/966 | 170/321 | chr10 | 44984947 | |||
| chr10:44984949 | C | G | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.510C>G | p.Asn170Lys | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 613/3631 | 510/966 | 170/321 | chr10 | 44984949 | |||
| chr10:44984953 | C | G | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.514C>G | p.His172Asp | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 617/3631 | 514/966 | 172/321 | chr10 | 44984953 | |||
| chr10:44984954 | A | C | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.515A>C | p.His172Pro | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 618/3631 | 515/966 | 172/321 | chr10 | 44984954 | |||
| chr10:44984956 | T | C | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.517T>C | p.Phe173Leu | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 620/3631 | 517/966 | 173/321 | chr10 | 44984956 | |||
| chr10:44984957 | T | A | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.518T>A | p.Phe173Tyr | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 621/3631 | 518/966 | 173/321 | chr10 | 44984957 | |||
| chr10:44984958 | C | G | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.519C>G | p.Phe173Leu | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 622/3631 | 519/966 | 173/321 | chr10 | 44984958 | |||
| chr10:44984959 | T | G | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.520T>G | p.Tyr174Asp | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 623/3631 | 520/966 | 174/321 | chr10 | 44984959 | |||
| chr10:44984961 | C | G | 1 | a0014 | 1 | NA19055.hp1 | stop_gained | HIGH | c.522C>G | p.Tyr174* | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 625/3631 | 522/966 | 174/321 | chr10 | 44984961 | |||
| chr10:44984962 | A | G | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.523A>G | p.Asn175Asp | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 626/3631 | 523/966 | 175/321 | chr10 | 44984962 | |||
| chr10:44984963 | A | G | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.524A>G | p.Asn175Ser | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 627/3631 | 524/966 | 175/321 | chr10 | 44984963 | |||
| chr10:44984964 | T | G | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.525T>G | p.Asn175Lys | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 628/3631 | 525/966 | 175/321 | chr10 | 44984964 | |||
| chr10:44984965 | C | G | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.526C>G | p.His176Asp | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 629/3631 | 526/966 | 176/321 | chr10 | 44984965 | |||
| chr10:44984966 | A | T | 1 | a0014 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.527A>T | p.His176Leu | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 630/3631 | 527/966 | 176/321 | chr10 | 44984966 | |||
| chr10:44989705 | C | G | 1 | a0009 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.669C>G | p.Ile223Met | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/11 | 772/3631 | 669/966 | 223/321 | chr10 | 44989705 | |||
| chr10:44991035 | T | C | 1 | a0009 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.773T>C | p.Met258Thr | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/11 | 876/3631 | 773/966 | 258/321 | chr10 | 44991035 | |||
| chr10:44991908 | G | T | 1 | a0013 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.811G>T | p.Ala271Ser | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/11 | 914/3631 | 811/966 | 271/321 | chr10 | 44991908 | |||
| chr10:44991933 | C | T | 1 | a0012 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.836C>T | p.Pro279Leu | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/11 | 939/3631 | 836/966 | 279/321 | chr10 | 44991933 | |||
| chr10:44993283 | G | A | 1 | a0011 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.920G>A | p.Arg307His | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 1023/3631 | 920/966 | 307/321 | chr10 | 44993283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:44971839 | A | G | 1 | a0001c0016 | 1 | NA18961.hp1 | synonymous_variant | LOW | c.129A>G | p.Arg43Arg | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/11 | 232/3631 | 129/966 | 43/321 | chr10 | 44971839 | |||
| chr10:44984943 | T | C | 1 | a0014c0009 | 1 | NA19055.hp1 | synonymous_variant | LOW | c.504T>C | p.Ser168Ser | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 607/3631 | 504/966 | 168/321 | chr10 | 44984943 | |||
| chr10:44984952 | C | G | 1 | a0014c0009 | 1 | NA19055.hp1 | synonymous_variant | LOW | c.513C>G | p.Gly171Gly | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/11 | 616/3631 | 513/966 | 171/321 | chr10 | 44984952 | |||
| chr10:44991934 | G | A | 1 | a0009c0015 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.837G>A | p.Pro279Pro | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/11 | 940/3631 | 837/966 | 279/321 | chr10 | 44991934 | |||
| chr10:44993290 | G | A | 1 | a0002c0012 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.927G>A | p.Thr309Thr | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 1030/3631 | 927/966 | 309/321 | chr10 | 44993290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:44993400 | C | T | 1 | a0001c0001t0039 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*71C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 71 | chr10 | 44993400 | ||||||
| chr10:44993434 | C | T | 2 | a0001c0001t0037 a0002c0012t0038 |
2 | HG03486.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*105C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 105 | chr10 | 44993434 | ||||||
| chr10:44993495 | C | G | 8 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0036 others(5): Show |
54 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*166C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 166 | chr10 | 44993495 | ||||||
| chr10:44993738 | T | C | 1 | a0009c0015t0017 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*409T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 409 | chr10 | 44993738 | ||||||
| chr10:44993741 | C | T | 1 | a0001c0001t0034 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*412C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 412 | chr10 | 44993741 | ||||||
| chr10:44993776 | G | A | 4 | a0001c0001t0003 a0002c0002t0003 a0002c0002t0018 others(1): Show |
27 | HG00423.hp1 HG00597.hp1 HG02056.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*447G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 447 | chr10 | 44993776 | ||||||
| chr10:44993835 | C | A | 1 | a0001c0001t0006 | 5 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*506C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 506 | chr10 | 44993835 | ||||||
| chr10:44993836 | G | A | 1 | a0001c0001t0019 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*507G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 507 | chr10 | 44993836 | ||||||
| chr10:44993880 | A | G | 2 | a0001c0001t0006 a0001c0001t0033 |
6 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*551A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 551 | chr10 | 44993880 | ||||||
| chr10:44993968 | T | C | 1 | a0004c0004t0020 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*639T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 639 | chr10 | 44993968 | ||||||
| chr10:44994009 | C | T | 1 | a0002c0002t0032 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 680 | chr10 | 44994009 | ||||||
| chr10:44994071 | G | C | 4 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0021 others(1): Show |
8 | HG02056.hp1 HG02132.hp2 NA18944.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*742G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 742 | chr10 | 44994071 | ||||||
| chr10:44994256 | G | C | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*927G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 927 | chr10 | 44994256 | ||||||
| chr10:44994263 | C | A | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*934C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 934 | chr10 | 44994263 | ||||||
| chr10:44994268 | T | C | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*939T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 939 | chr10 | 44994268 | ||||||
| chr10:44994270 | C | T | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*941C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 941 | chr10 | 44994270 | ||||||
| chr10:44994274 | A | T | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*945A>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 945 | chr10 | 44994274 | ||||||
| chr10:44994276 | A | T | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*947A>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 947 | chr10 | 44994276 | ||||||
| chr10:44994277 | A | C | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*948A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 948 | chr10 | 44994277 | ||||||
| chr10:44994278 | T | C | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*949T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 949 | chr10 | 44994278 | ||||||
| chr10:44994281 | G | A | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*952G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 952 | chr10 | 44994281 | ||||||
| chr10:44994283 | G | C | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*954G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 954 | chr10 | 44994283 | ||||||
| chr10:44994284 | T | A | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*955T>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 955 | chr10 | 44994284 | ||||||
| chr10:44994287 | G | C | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*958G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 958 | chr10 | 44994287 | ||||||
| chr10:44994289 | G | T | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*960G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 960 | chr10 | 44994289 | ||||||
| chr10:44994290 | A | C | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*961A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 961 | chr10 | 44994290 | ||||||
| chr10:44994293 | G | T | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*964G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 964 | chr10 | 44994293 | ||||||
| chr10:44994294 | A | C | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*965A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 965 | chr10 | 44994294 | ||||||
| chr10:44994295 | T | A | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*966T>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 966 | chr10 | 44994295 | ||||||
| chr10:44994298 | A | G | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*969A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 969 | chr10 | 44994298 | ||||||
| chr10:44994302 | T | G | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*973T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 973 | chr10 | 44994302 | ||||||
| chr10:44994304 | T | A | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*975T>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 975 | chr10 | 44994304 | ||||||
| chr10:44994305 | C | T | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*976C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 976 | chr10 | 44994305 | ||||||
| chr10:44994306 | A | T | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*977A>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 977 | chr10 | 44994306 | ||||||
| chr10:44994308 | G | A | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*979G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 979 | chr10 | 44994308 | ||||||
| chr10:44994311 | T | G | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*982T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 982 | chr10 | 44994311 | ||||||
| chr10:44994312 | G | T | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*983G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 983 | chr10 | 44994312 | ||||||
| chr10:44994313 | A | C | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*984A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 984 | chr10 | 44994313 | ||||||
| chr10:44994317 | A | T | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*988A>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 988 | chr10 | 44994317 | ||||||
| chr10:44994323 | C | T | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*994C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 994 | chr10 | 44994323 | ||||||
| chr10:44994325 | T | A | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*996T>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 996 | chr10 | 44994325 | ||||||
| chr10:44994326 | T | TCCCACCC others(8): Show |
1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*997_*998insCCCACC others(9): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 998 | chr10 | 44994326 | ||||||
| chr10:44994327 | T | A | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*998T>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 998 | chr10 | 44994327 | ||||||
| chr10:44994329 | C | A | 1 | a0001c0001t0022 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1000C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 1000 | chr10 | 44994329 | ||||||
| chr10:44994330 | G | A | 2 | a0001c0001t0023 a0001c0001t0037 |
2 | HG03486.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1001G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 1001 | chr10 | 44994330 | ||||||
| chr10:44994730 | C | CT | 12 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0015 others(9): Show |
69 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1417dupT | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 1418 | INFO_REALIGN_3_PRIME | chr10 | 44994730 | |||||
| chr10:44994730 | C | CTT | 6 | a0001c0001t0005 a0001c0001t0010 a0002c0002t0005 others(3): Show |
16 | HG00099.hp1 HG01192.hp2 HG01243.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1416_*1417dupTT | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 1418 | INFO_REALIGN_3_PRIME | chr10 | 44994730 | |||||
| chr10:44994841 | G | A | 1 | a0001c0001t0024 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1512G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 1512 | chr10 | 44994841 | ||||||
| chr10:44995031 | A | G | 1 | a0001c0001t0029 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1702A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 1702 | chr10 | 44995031 | ||||||
| chr10:44995087 | C | A | 1 | a0001c0001t0025 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1758C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 1758 | chr10 | 44995087 | ||||||
| chr10:44995282 | C | T | 1 | a0001c0001t0036 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1953C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 1953 | chr10 | 44995282 | ||||||
| chr10:44995345 | G | A | 1 | a0001c0001t0026 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2016G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 2016 | chr10 | 44995345 | ||||||
| chr10:44995374 | T | C | 4 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0023 others(1): Show |
10 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2045T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 2045 | chr10 | 44995374 | ||||||
| chr10:44995382 | C | T | 1 | a0001c0001t0009 | 4 | HG02647.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2053C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 2053 | chr10 | 44995382 | ||||||
| chr10:44995484 | G | C | 1 | a0002c0002t0011 | 3 | HG03516.hp2 HG06807.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2155G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 2155 | chr10 | 44995484 | ||||||
| chr10:44995511 | A | G | 1 | a0002c0002t0014 | 2 | HG02809.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2182A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 2182 | chr10 | 44995511 | ||||||
| chr10:44995530 | C | T | 4 | a0002c0002t0011 a0002c0002t0028 a0002c0002t0030 others(1): Show |
6 | HG03453.hp2 HG03486.hp2 HG03516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2201C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 2201 | chr10 | 44995530 | ||||||
| chr10:44995577 | C | T | 3 | a0002c0002t0028 a0002c0002t0030 a0002c0012t0038 |
3 | HG03453.hp2 HG03486.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2248C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 2248 | chr10 | 44995577 | ||||||
| chr10:44995594 | A | G | 1 | a0002c0002t0031 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2265A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 2265 | chr10 | 44995594 | ||||||
| chr10:44995724 | T | C | 1 | a0010c0011t0027 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2395T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 2395 | chr10 | 44995724 | ||||||
| chr10:44995732 | A | G | 2 | a0001c0001t0007 a0001c0001t0021 |
6 | HG02056.hp1 HG02132.hp2 NA18945.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2403A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 2403 | chr10 | 44995732 | ||||||
| chr10:44995764 | C | T | 1 | a0003c0003t0016 | 2 | HG02145.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2435C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 2435 | chr10 | 44995764 | ||||||
| chr10:44995810 | A | C | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(51): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
3_prime_UTR_variant | MODIFIER | c.*2481A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 2481 | chr10 | 44995810 | ||||||
| chr10:44995871 | C | T | 1 | a0001c0001t0015 | 2 | HG02451.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2542C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 11/11 | 2542 | chr10 | 44995871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:44959882 | G | A | 3 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0006c0006t0002g0056 |
3 | HG01069.hp2 HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-39+16G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44959882 | |||||||
| chr10:44960001 | G | C | 8 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0058 others(5): Show |
10 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+135G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44960001 | |||||||
| chr10:44960005 | G | A | 2 | a0001c0001t0037g0063 a0006c0006t0002g0064 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-39+139G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44960005 | |||||||
| chr10:44960095 | C | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(48): Show |
79 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-39+229C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44960095 | |||||||
| chr10:44960257 | G | T | 2 | a0004c0004t0001g0051 a0004c0004t0001g0223 |
3 | HG01884.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-39+391G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44960257 | |||||||
| chr10:44960274 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
5 | HG01167.hp2 HG01891.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-39+408A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44960274 | |||||||
| chr10:44960344 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-39+478C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44960344 | |||||||
| chr10:44960375 | C | G | 2 | a0002c0002t0001g0050 a0002c0002t0014g0220 |
3 | HG02559.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-39+509C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44960375 | |||||||
| chr10:44960701 | T | C | 1 | a0010c0011t0027g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-39+835T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44960701 | |||||||
| chr10:44960895 | A | AT | 147 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(144): Show |
196 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.-39+1038dupT | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | 44960895 | ||||||
| chr10:44961114 | A | G | 6 | a0002c0002t0001g0114 a0002c0002t0001g0115 a0002c0002t0001g0116 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39+1248A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44961114 | |||||||
| chr10:44961415 | C | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(144): Show |
220 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-39+1549C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44961415 | |||||||
| chr10:44961559 | T | C | 6 | a0002c0002t0001g0114 a0002c0002t0001g0115 a0002c0002t0001g0116 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39+1693T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44961559 | |||||||
| chr10:44961572 | G | A | 1 | a0001c0001t0002g0142 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-39+1706G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44961572 | |||||||
| chr10:44961613 | T | C | 26 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0119 others(23): Show |
35 | HG00738.hp1 HG01074.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.-39+1747T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44961613 | |||||||
| chr10:44961687 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0101 a0002c0002t0011g0019 others(1): Show |
8 | HG01123.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39+1821C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44961687 | |||||||
| chr10:44961714 | T | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0052 a0001c0001t0001g0224 others(1): Show |
6 | HG00544.hp1 NA18971.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39+1848T>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44961714 | |||||||
| chr10:44961791 | C | G | 5 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0002c0002t0001g0100 others(2): Show |
5 | HG01069.hp2 HG02004.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-39+1925C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44961791 | |||||||
| chr10:44962021 | C | G | 1 | a0001c0001t0001g0250 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-39+2155C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962021 | |||||||
| chr10:44962021 | C | T | 9 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(6): Show |
12 | HG00408.hp2 HG00597.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.-39+2155C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962021 | |||||||
| chr10:44962023 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-39+2157G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962023 | |||||||
| chr10:44962025 | A | C | 1 | a0001c0001t0001g0250 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-39+2159A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962025 | |||||||
| chr10:44962106 | C | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0092 others(10): Show |
21 | HG00621.hp2 HG02165.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.-39+2240C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962106 | |||||||
| chr10:44962164 | C | T | 3 | a0002c0002t0001g0116 a0002c0002t0001g0118 a0003c0003t0016g0117 |
3 | HG00741.hp1 HG01192.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-39+2298C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962164 | |||||||
| chr10:44962168 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-39+2302G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962168 | |||||||
| chr10:44962274 | G | T | 1 | a0002c0002t0004g0218 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-39+2408G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962274 | |||||||
| chr10:44962347 | G | A | 1 | a0002c0002t0001g0116 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-39+2481G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962347 | |||||||
| chr10:44962577 | G | A | 20 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0119 others(17): Show |
24 | HG00738.hp1 HG01074.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.-39+2711G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962577 | |||||||
| chr10:44962677 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(54): Show |
87 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-39+2811C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962677 | |||||||
| chr10:44962678 | G | A | 24 | a0001c0001t0001g0037 a0001c0001t0001g0146 a0001c0001t0001g0147 others(21): Show |
30 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.-39+2812G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962678 | |||||||
| chr10:44962742 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0092 |
5 | NA18949.hp1 NA19004.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.-39+2876G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962742 | |||||||
| chr10:44962822 | G | C | 1 | a0001c0001t0001g0226 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-39+2956G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962822 | |||||||
| chr10:44962822 | G | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(31): Show |
57 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.-39+2956G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962822 | |||||||
| chr10:44962896 | G | T | 1 | a0001c0001t0001g0248 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-39+3030G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962896 | |||||||
| chr10:44962907 | T | C | 1 | a0002c0002t0001g0160 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-39+3041T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44962907 | |||||||
| chr10:44963037 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(55): Show |
88 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.-39+3171C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963037 | |||||||
| chr10:44963085 | G | A | 10 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0061 others(7): Show |
14 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39+3219G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963085 | |||||||
| chr10:44963100 | G | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(25): Show |
46 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.-39+3234G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963100 | |||||||
| chr10:44963133 | C | T | 1 | a0002c0002t0001g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-39+3267C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963133 | |||||||
| chr10:44963218 | T | A | 23 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0031 others(20): Show |
35 | HG00621.hp2 HG01167.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.-39+3352T>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963218 | |||||||
| chr10:44963236 | T | G | 1 | a0001c0001t0025g0140 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-39+3370T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963236 | |||||||
| chr10:44963247 | G | A | 20 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0119 others(17): Show |
24 | HG00738.hp1 HG01074.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.-39+3381G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963247 | |||||||
| chr10:44963284 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0101 a0002c0002t0011g0019 others(1): Show |
8 | HG01123.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39+3418G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963284 | |||||||
| chr10:44963436 | G | A | 1 | a0002c0002t0011g0019 | 3 | HG03516.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-39+3570G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963436 | |||||||
| chr10:44963469 | A | G | 1 | a0002c0002t0028g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-39+3603A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963469 | |||||||
| chr10:44963496 | T | G | 7 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0002c0002t0001g0100 others(4): Show |
7 | HG01069.hp2 HG02004.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-39+3630T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963496 | |||||||
| chr10:44963601 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-39+3735G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963601 | |||||||
| chr10:44963623 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-39+3757T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963623 | |||||||
| chr10:44963654 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(48): Show |
81 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.-39+3788C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963654 | |||||||
| chr10:44963999 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
140 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.-39+4133T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44963999 | |||||||
| chr10:44964185 | T | A | 37 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(34): Show |
58 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.-39+4319T>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44964185 | |||||||
| chr10:44964397 | A | T | 4 | a0005c0005t0001g0129 a0005c0005t0001g0130 a0005c0005t0001g0131 others(1): Show |
4 | HG02109.hp2 HG02895.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+4531A>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44964397 | |||||||
| chr10:44964437 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
225 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-39+4571A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44964437 | |||||||
| chr10:44964474 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(80): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-39+4608G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44964474 | |||||||
| chr10:44964654 | A | G | 5 | a0002c0002t0001g0011 a0002c0002t0001g0022 a0002c0002t0001g0133 others(2): Show |
10 | HG01243.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+4788A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44964654 | |||||||
| chr10:44964867 | G | GA | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(138): Show |
214 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.-39+5002dupA | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | 44964867 | ||||||
| chr10:44964968 | G | A | 1 | a0002c0002t0001g0163 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-39+5102G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44964968 | |||||||
| chr10:44964986 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
6 | NA18955.hp1 NA18960.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39+5120G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44964986 | |||||||
| chr10:44965371 | G | A | 1 | a0010c0011t0027g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-38-4794G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44965371 | |||||||
| chr10:44965426 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-38-4739A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44965426 | |||||||
| chr10:44965478 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-38-4687C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44965478 | |||||||
| chr10:44965535 | C | T | 1 | a0002c0002t0028g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-38-4630C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44965535 | |||||||
| chr10:44965613 | G | T | 3 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0006c0006t0002g0056 |
3 | HG01069.hp2 HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-38-4552G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44965613 | |||||||
| chr10:44965623 | C | A | 2 | a0002c0002t0004g0103 a0006c0006t0002g0064 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-38-4542C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44965623 | |||||||
| chr10:44965666 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(124): Show |
198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.-38-4499T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44965666 | |||||||
| chr10:44965708 | C | T | 2 | a0002c0002t0001g0214 a0002c0002t0001g0215 |
2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-38-4457C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44965708 | |||||||
| chr10:44965709 | G | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0092 others(10): Show |
21 | HG00621.hp2 HG02165.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.-38-4456G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44965709 | |||||||
| chr10:44965745 | C | T | 1 | a0002c0002t0005g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38-4420C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44965745 | |||||||
| chr10:44965815 | C | A | 6 | a0002c0002t0001g0066 a0002c0002t0001g0114 a0002c0002t0001g0115 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38-4350C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44965815 | |||||||
| chr10:44965894 | G | A | 1 | a0001c0001t0029g0166 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-38-4271G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44965894 | |||||||
| chr10:44965966 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-38-4199G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44965966 | |||||||
| chr10:44966310 | T | G | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-38-3855T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44966310 | |||||||
| chr10:44966355 | T | C | 2 | a0002c0002t0001g0116 a0002c0002t0001g0118 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-38-3810T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44966355 | |||||||
| chr10:44966619 | G | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0224 |
4 | NA18971.hp2 NA18981.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38-3546G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44966619 | |||||||
| chr10:44966673 | T | C | 2 | a0002c0002t0001g0050 a0002c0002t0014g0220 |
3 | HG02559.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-38-3492T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44966673 | |||||||
| chr10:44966771 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
173 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-38-3394C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44966771 | |||||||
| chr10:44966812 | G | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0031 others(14): Show |
22 | HG01123.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-38-3353G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44966812 | |||||||
| chr10:44967148 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-38-3017G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967148 | |||||||
| chr10:44967175 | A | G | 1 | a0002c0002t0001g0213 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-38-2990A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967175 | |||||||
| chr10:44967191 | A | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG01261.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-38-2974A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967191 | |||||||
| chr10:44967229 | A | C | 1 | a0001c0001t0001g0247 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-38-2936A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967229 | |||||||
| chr10:44967243 | C | T | 1 | a0001c0001t0026g0212 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-38-2922C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967243 | |||||||
| chr10:44967328 | C | G | 1 | a0001c0001t0033g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-38-2837C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967328 | |||||||
| chr10:44967363 | A | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0101 others(4): Show |
11 | HG01123.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38-2802A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967363 | |||||||
| chr10:44967441 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0101 others(4): Show |
11 | HG01123.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38-2724C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967441 | |||||||
| chr10:44967448 | G | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
5 | HG01167.hp2 HG01891.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38-2717G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967448 | |||||||
| chr10:44967460 | A | G | 31 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0101 others(28): Show |
42 | HG00741.hp1 HG01069.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-38-2705A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967460 | |||||||
| chr10:44967617 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0230 a0001c0001t0001g0246 others(1): Show |
7 | HG00323.hp1 HG00741.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38-2548C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967617 | |||||||
| chr10:44967772 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-38-2393C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967772 | |||||||
| chr10:44967942 | G | A | 3 | a0001c0001t0005g0033 a0001c0001t0008g0072 a0001c0001t0037g0063 |
4 | HG02559.hp2 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38-2223G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967942 | |||||||
| chr10:44967971 | G | A | 1 | a0002c0002t0001g0167 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-38-2194G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44967971 | |||||||
| chr10:44968381 | C | T | 1 | a0002c0002t0001g0163 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-38-1784C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44968381 | |||||||
| chr10:44968400 | T | C | 6 | a0002c0002t0001g0011 a0002c0002t0001g0022 a0002c0002t0001g0133 others(3): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38-1765T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44968400 | |||||||
| chr10:44968423 | A | G | 2 | a0001c0001t0008g0127 a0001c0001t0008g0128 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-38-1742A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44968423 | |||||||
| chr10:44968586 | C | T | 1 | a0002c0002t0003g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-38-1579C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44968586 | |||||||
| chr10:44968587 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): Show |
205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.-38-1578A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44968587 | |||||||
| chr10:44968625 | G | C | 16 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0092 others(13): Show |
24 | HG00621.hp2 HG01069.hp2 HG02165.hp2 others(21): Show |
intron_variant | MODIFIER | c.-38-1540G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44968625 | |||||||
| chr10:44968651 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG00642.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-38-1514C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44968651 | |||||||
| chr10:44968652 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): Show |
184 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.-38-1513A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44968652 | |||||||
| chr10:44968713 | C | T | 1 | a0002c0002t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-38-1452C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44968713 | |||||||
| chr10:44968790 | G | A | 11 | a0002c0002t0001g0066 a0002c0002t0001g0100 a0002c0002t0001g0114 others(8): Show |
11 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38-1375G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44968790 | |||||||
| chr10:44968839 | G | A | 1 | a0002c0002t0004g0218 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-38-1326G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44968839 | |||||||
| chr10:44968897 | C | T | 2 | a0005c0005t0001g0131 a0007c0007t0001g0132 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-38-1268C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44968897 | |||||||
| chr10:44969000 | A | ATG | 7 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0101 others(4): Show |
11 | HG01123.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38-1150_-38-1149d others(4): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | 44969000 | ||||||
| chr10:44969062 | G | C | 1 | a0001c0001t0001g0226 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-38-1103G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969062 | |||||||
| chr10:44969070 | GTA | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0126 a0001c0001t0008g0127 others(2): Show |
8 | HG01167.hp1 HG01169.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-1093_-38-1092d others(4): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | 44969070 | ||||||
| chr10:44969086 | G | A | 1 | a0002c0002t0032g0145 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-38-1079G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969086 | |||||||
| chr10:44969104 | G | GTT | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(81): Show |
131 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.-38-1057_-38-1056d others(4): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | 44969104 | ||||||
| chr10:44969104 | G | GTTTT | 5 | a0002c0002t0001g0016 a0002c0002t0001g0254 a0002c0002t0003g0255 others(2): Show |
8 | HG02056.hp2 NA18747.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.-38-1059_-38-1056d others(6): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | 44969104 | ||||||
| chr10:44969108 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-38-1057T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969108 | |||||||
| chr10:44969108 | T | TTG | 6 | a0002c0002t0001g0162 a0005c0005t0001g0129 a0005c0005t0001g0130 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38-1037_-38-1036d others(4): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | 44969108 | ||||||
| chr10:44969108 | TTG | T | 12 | a0001c0001t0001g0031 a0001c0001t0001g0126 a0001c0001t0008g0127 others(9): Show |
15 | HG00741.hp1 HG01109.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38-1037_-38-1036d others(4): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | 44969108 | ||||||
| chr10:44969108 | TTGTG | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0092 others(9): Show |
20 | HG00621.hp2 HG02165.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-38-1039_-38-1036d others(6): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | 44969108 | ||||||
| chr10:44969110 | G | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(83): Show |
131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.-38-1055G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969110 | |||||||
| chr10:44969112 | G | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0034 others(5): Show |
10 | HG00735.hp2 HG03017.hp1 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38-1053G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969112 | |||||||
| chr10:44969206 | A | T | 2 | a0001c0001t0002g0156 a0001c0001t0002g0260 |
2 | NA18747.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-38-959A>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969206 | |||||||
| chr10:44969280 | G | A | 10 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0062 others(7): Show |
16 | HG01167.hp2 HG01243.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-38-885G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969280 | |||||||
| chr10:44969329 | CTGTGTGT others(17): Show |
C | 2 | a0002c0002t0004g0049 a0002c0002t0004g0209 |
3 | NA18962.hp2 NA19009.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-38-824_-38-801del others(24): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | 44969329 | ||||||
| chr10:44969350 | A | G | 6 | a0002c0002t0001g0050 a0002c0002t0014g0220 a0002c0012t0038g0068 others(3): Show |
8 | HG01884.hp1 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-38-815A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969350 | |||||||
| chr10:44969498 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-38-667A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969498 | |||||||
| chr10:44969515 | G | A | 2 | a0001c0001t0002g0170 a0001c0001t0002g0171 |
2 | NA18951.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-38-650G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969515 | |||||||
| chr10:44969628 | TACTC | T | 1 | a0001c0001t0001g0013 | 4 | HG00099.hp2 HG01515.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-534_-38-531del others(4): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | 44969628 | ||||||
| chr10:44969648 | T | C | 6 | a0002c0002t0001g0066 a0002c0002t0001g0114 a0002c0002t0001g0115 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38-517T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969648 | |||||||
| chr10:44969727 | T | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0092 others(9): Show |
20 | HG00621.hp2 HG02165.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-38-438T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969727 | |||||||
| chr10:44969766 | G | A | 1 | a0001c0001t0029g0166 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-38-399G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969766 | |||||||
| chr10:44969783 | G | C | 2 | a0002c0002t0004g0103 a0006c0006t0002g0064 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-38-382G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969783 | |||||||
| chr10:44969817 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-38-348C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969817 | |||||||
| chr10:44969868 | G | A | 5 | a0005c0005t0001g0129 a0005c0005t0001g0130 a0005c0005t0001g0131 others(2): Show |
5 | HG02109.hp2 HG02895.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38-297G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44969868 | |||||||
| chr10:44969912 | GGA | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
5 | HG01167.hp2 HG01891.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38-249_-38-248del others(2): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr10 | 44969912 | ||||||
| chr10:44970055 | G | A | 2 | a0002c0002t0004g0103 a0006c0006t0002g0064 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-38-110G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44970055 | |||||||
| chr10:44970087 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01256.hp2 HG01993.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38-78G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 1/10 | chr10 | 44970087 | |||||||
| chr10:44970289 | C | T | 5 | a0005c0005t0001g0129 a0005c0005t0001g0130 a0005c0005t0001g0131 others(2): Show |
5 | HG02109.hp2 HG02895.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.62+25C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44970289 | |||||||
| chr10:44970290 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0146 |
3 | HG00558.hp2 NA18612.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.62+26G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44970290 | |||||||
| chr10:44970309 | C | T | 15 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0101 others(12): Show |
24 | HG01123.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.62+45C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44970309 | |||||||
| chr10:44970379 | G | A | 7 | a0002c0002t0001g0011 a0002c0002t0001g0022 a0002c0002t0001g0133 others(4): Show |
12 | HG01243.hp2 HG02486.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+115G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44970379 | |||||||
| chr10:44970753 | A | G | 1 | a0001c0001t0033g0211 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.62+489A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44970753 | |||||||
| chr10:44970771 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0092 others(8): Show |
19 | HG02165.hp2 HG02280.hp1 NA18942.hp1 others(16): Show |
intron_variant | MODIFIER | c.62+507G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44970771 | |||||||
| chr10:44970805 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.62+541C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44970805 | |||||||
| chr10:44970916 | G | T | 6 | a0002c0002t0001g0011 a0002c0002t0001g0022 a0002c0002t0001g0133 others(3): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.62+652G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44970916 | |||||||
| chr10:44970990 | T | C | 2 | a0002c0002t0001g0116 a0002c0002t0001g0118 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.62+726T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44970990 | |||||||
| chr10:44971137 | A | C | 1 | a0001c0001t0001g0243 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.63-636A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44971137 | |||||||
| chr10:44971147 | G | C | 1 | a0002c0002t0001g0137 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.63-626G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44971147 | |||||||
| chr10:44971215 | C | G | 1 | a0001c0001t0001g0242 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.63-558C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44971215 | |||||||
| chr10:44971278 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(143): Show |
217 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.63-495G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44971278 | |||||||
| chr10:44971511 | A | G | 1 | a0001c0001t0003g0206 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.63-262A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44971511 | |||||||
| chr10:44971521 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.63-252C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44971521 | |||||||
| chr10:44971580 | C | T | 6 | a0002c0002t0001g0066 a0002c0002t0001g0114 a0002c0002t0001g0115 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.63-193C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44971580 | |||||||
| chr10:44971651 | C | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0058 a0001c0001t0001g0139 others(33): Show |
54 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.63-122C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44971651 | |||||||
| chr10:44971698 | G | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
5 | HG01167.hp2 HG01891.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.63-75G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44971698 | |||||||
| chr10:44971756 | T | C | 20 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0020 others(17): Show |
30 | HG00597.hp2 HG00621.hp2 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.63-17T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 2/10 | chr10 | 44971756 | |||||||
| chr10:44971863 | C | T | 1 | a0002c0002t0030g0208 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.138+15C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44971863 | |||||||
| chr10:44971888 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0126 |
3 | HG01167.hp1 HG01169.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.138+40C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44971888 | |||||||
| chr10:44971938 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0062 others(3): Show |
7 | HG01167.hp2 HG01891.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.138+90T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44971938 | |||||||
| chr10:44971999 | T | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.138+151T>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44971999 | |||||||
| chr10:44971999 | T | G | 2 | a0002c0002t0001g0050 a0002c0002t0014g0220 |
3 | HG02559.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.138+151T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44971999 | |||||||
| chr10:44972078 | A | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0101 others(9): Show |
16 | HG01069.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.138+230A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44972078 | |||||||
| chr10:44972255 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(91): Show |
141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.138+407G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44972255 | |||||||
| chr10:44972270 | C | T | 1 | a0002c0002t0001g0162 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.138+422C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44972270 | |||||||
| chr10:44972500 | T | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.138+652T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44972500 | |||||||
| chr10:44972670 | A | T | 2 | a0002c0002t0001g0022 a0002c0002t0001g0135 |
4 | HG02486.hp1 HG02615.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+822A>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44972670 | |||||||
| chr10:44972741 | A | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.138+893A>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44972741 | |||||||
| chr10:44972749 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(142): Show |
207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.138+901G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44972749 | |||||||
| chr10:44972796 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.138+948G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44972796 | |||||||
| chr10:44972887 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.138+1039T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44972887 | |||||||
| chr10:44973131 | G | A | 1 | a0001c0001t0013g0071 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.138+1283G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44973131 | |||||||
| chr10:44973440 | G | A | 2 | a0002c0002t0028g0136 a0002c0002t0030g0208 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.138+1592G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44973440 | |||||||
| chr10:44973566 | C | T | 2 | a0002c0002t0001g0116 a0002c0002t0001g0118 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.138+1718C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44973566 | |||||||
| chr10:44973694 | G | A | 7 | a0002c0002t0003g0035 a0002c0002t0003g0096 a0002c0002t0003g0234 others(4): Show |
8 | HG02165.hp2 NA18939.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+1846G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44973694 | |||||||
| chr10:44973773 | C | T | 1 | a0001c0001t0008g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+1925C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44973773 | |||||||
| chr10:44973813 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.138+1965G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44973813 | |||||||
| chr10:44973882 | T | TAGAAAGT others(323): Show |
1 | a0001c0001t0001g0101 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.138+2050_138+2051i others(332): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr10 | 44973882 | ||||||
| chr10:44974004 | C | A | 1 | a0001c0001t0002g0142 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.138+2156C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44974004 | |||||||
| chr10:44974008 | GTACC | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
319 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.138+2161_138+2164d others(6): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44974008 | |||||||
| chr10:44974019 | G | T | 1 | a0001c0001t0006g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.138+2171G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44974019 | |||||||
| chr10:44974066 | A | G | 1 | a0002c0002t0001g0187 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.138+2218A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44974066 | |||||||
| chr10:44974081 | G | C | 1 | a0002c0002t0011g0019 | 3 | HG03516.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.138+2233G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44974081 | |||||||
| chr10:44974271 | C | G | 7 | a0002c0002t0003g0035 a0002c0002t0003g0096 a0002c0002t0003g0234 others(4): Show |
8 | HG02165.hp2 NA18939.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+2423C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44974271 | |||||||
| chr10:44974275 | A | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
11 | HG01123.hp1 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+2427A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44974275 | |||||||
| chr10:44974427 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
281 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.138+2579T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44974427 | |||||||
| chr10:44974466 | G | A | 1 | a0002c0002t0011g0019 | 3 | HG03516.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.138+2618G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44974466 | |||||||
| chr10:44974565 | C | G | 1 | a0007c0007t0001g0132 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.138+2717C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44974565 | |||||||
| chr10:44974580 | G | C | 5 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(2): Show |
5 | HG01192.hp2 HG01243.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+2732G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44974580 | |||||||
| chr10:44974622 | A | AC | 10 | a0001c0001t0008g0072 a0001c0001t0008g0127 a0001c0001t0008g0128 others(7): Show |
11 | HG02165.hp2 HG02717.hp1 NA18906.hp2 others(8): Show |
intron_variant | MODIFIER | c.138+2781dupC | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr10 | 44974622 | ||||||
| chr10:44974622 | A | ACC | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
262 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.138+2780_138+2781d others(4): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr10 | 44974622 | ||||||
| chr10:44974622 | A | ACCC | 14 | a0001c0001t0001g0073 a0001c0001t0001g0084 a0001c0001t0001g0088 others(11): Show |
16 | HG01261.hp1 HG01346.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.138+2779_138+2781d others(5): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr10 | 44974622 | ||||||
| chr10:44974740 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
282 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.138+2892T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44974740 | |||||||
| chr10:44974776 | C | G | 1 | a0001c0001t0002g0205 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.138+2928C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44974776 | |||||||
| chr10:44975182 | T | C | 4 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(1): Show |
4 | HG00408.hp2 HG00597.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+3334T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44975182 | |||||||
| chr10:44975290 | C | A | 7 | a0002c0002t0003g0035 a0002c0002t0003g0096 a0002c0002t0003g0234 others(4): Show |
8 | HG02165.hp2 NA18939.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+3442C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44975290 | |||||||
| chr10:44975336 | ATC | A | 5 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(2): Show |
5 | HG01192.hp2 HG01243.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+3490_138+3491d others(4): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr10 | 44975336 | ||||||
| chr10:44975376 | C | G | 5 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(2): Show |
5 | HG01192.hp2 HG01243.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+3528C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44975376 | |||||||
| chr10:44975408 | C | G | 1 | a0002c0002t0001g0113 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.138+3560C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44975408 | |||||||
| chr10:44975527 | C | T | 9 | a0002c0002t0001g0011 a0002c0002t0001g0022 a0002c0002t0001g0133 others(6): Show |
14 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+3679C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44975527 | |||||||
| chr10:44975552 | A | AC | 5 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
8 | HG01167.hp2 HG01891.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+3706dupC | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr10 | 44975552 | ||||||
| chr10:44975592 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0233 |
2 | HG00280.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.138+3744C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44975592 | |||||||
| chr10:44975611 | A | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
281 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.138+3763A>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44975611 | |||||||
| chr10:44975624 | G | A | 1 | a0002c0002t0032g0145 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.138+3776G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44975624 | |||||||
| chr10:44975692 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
8 | HG01167.hp2 HG01891.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+3844T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44975692 | |||||||
| chr10:44975774 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(90): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.138+3926G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44975774 | |||||||
| chr10:44975830 | C | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(90): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.138+3982C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44975830 | |||||||
| chr10:44975974 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
164 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.138+4126C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44975974 | |||||||
| chr10:44975998 | TG | T | 3 | a0002c0002t0001g0066 a0002c0002t0001g0115 a0002c0002t0001g0219 |
3 | HG02886.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.138+4153delG | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr10 | 44975998 | ||||||
| chr10:44976035 | TGGCTAAA others(9): Show |
T | 3 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0002c0002t0014g0178 |
3 | HG02630.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.138+4204_138+4219d others(18): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr10 | 44976035 | ||||||
| chr10:44976072 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.138+4224G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44976072 | |||||||
| chr10:44976149 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG00735.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.138+4301T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44976149 | |||||||
| chr10:44976363 | T | C | 20 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0101 others(17): Show |
26 | HG01123.hp1 HG01884.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.138+4515T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44976363 | |||||||
| chr10:44976424 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
8 | HG01167.hp2 HG01891.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+4576C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44976424 | |||||||
| chr10:44976464 | C | G | 1 | a0002c0002t0003g0236 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.138+4616C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44976464 | |||||||
| chr10:44976590 | T | C | 4 | a0002c0012t0038g0068 a0004c0004t0001g0051 a0004c0004t0001g0223 others(1): Show |
5 | HG01123.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+4742T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44976590 | |||||||
| chr10:44976597 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
306 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.138+4749A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44976597 | |||||||
| chr10:44976740 | G | A | 5 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(2): Show |
5 | HG01192.hp2 HG01243.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+4892G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44976740 | |||||||
| chr10:44976972 | G | A | 1 | a0002c0002t0002g0090 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.138+5124G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44976972 | |||||||
| chr10:44976978 | C | A | 2 | a0001c0001t0006g0120 a0001c0001t0006g0121 |
2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.138+5130C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44976978 | |||||||
| chr10:44976980 | C | T | 5 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(2): Show |
5 | HG01192.hp2 HG01243.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+5132C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44976980 | |||||||
| chr10:44977050 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.138+5202C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44977050 | |||||||
| chr10:44977194 | T | G | 1 | a0002c0002t0004g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.139-5327T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44977194 | |||||||
| chr10:44977337 | C | T | 5 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(2): Show |
5 | HG01192.hp2 HG01243.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-5184C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44977337 | |||||||
| chr10:44977450 | C | CG | 28 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(25): Show |
28 | HG00621.hp1 HG00642.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.139-5066dupG | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr10 | 44977450 | ||||||
| chr10:44977451 | G | A | 3 | a0002c0002t0003g0234 a0002c0002t0003g0235 a0002c0002t0003g0236 |
3 | NA18943.hp1 NA18991.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.139-5070G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44977451 | |||||||
| chr10:44977595 | C | G | 1 | a0001c0001t0001g0138 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.139-4926C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44977595 | |||||||
| chr10:44977730 | T | C | 3 | a0004c0004t0001g0051 a0004c0004t0001g0223 a0004c0004t0020g0102 |
4 | HG01123.hp1 HG01884.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-4791T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44977730 | |||||||
| chr10:44977843 | G | T | 1 | a0002c0002t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.139-4678G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44977843 | |||||||
| chr10:44977869 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(48): Show |
77 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.139-4652C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44977869 | |||||||
| chr10:44977939 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.139-4582G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44977939 | |||||||
| chr10:44977984 | C | T | 1 | a0002c0012t0038g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.139-4537C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44977984 | |||||||
| chr10:44978096 | C | T | 1 | a0001c0001t0013g0071 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.139-4425C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978096 | |||||||
| chr10:44978104 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.139-4417C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978104 | |||||||
| chr10:44978198 | C | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(112): Show |
169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.139-4323C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978198 | |||||||
| chr10:44978227 | G | A | 1 | a0002c0002t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.139-4294G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978227 | |||||||
| chr10:44978364 | C | A | 1 | a0003c0003t0010g0108 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.139-4157C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978364 | |||||||
| chr10:44978390 | C | T | 3 | a0004c0004t0001g0051 a0004c0004t0001g0223 a0004c0004t0020g0102 |
4 | HG01123.hp1 HG01884.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-4131C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978390 | |||||||
| chr10:44978435 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0073 others(5): Show |
10 | HG01261.hp1 HG01346.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-4086G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978435 | |||||||
| chr10:44978501 | C | G | 7 | a0002c0002t0003g0035 a0002c0002t0003g0096 a0002c0002t0003g0234 others(4): Show |
8 | HG02165.hp2 NA18939.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-4020C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978501 | |||||||
| chr10:44978528 | G | A | 6 | a0001c0001t0006g0043 a0001c0001t0006g0120 a0001c0001t0006g0121 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-3993G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978528 | |||||||
| chr10:44978599 | G | A | 2 | a0002c0002t0001g0133 a0002c0002t0001g0134 |
2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.139-3922G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978599 | |||||||
| chr10:44978631 | G | C | 1 | a0002c0002t0001g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.139-3890G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978631 | |||||||
| chr10:44978705 | C | T | 1 | a0009c0015t0017g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139-3816C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978705 | |||||||
| chr10:44978706 | G | A | 6 | a0001c0001t0006g0043 a0001c0001t0006g0120 a0001c0001t0006g0121 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-3815G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978706 | |||||||
| chr10:44978722 | G | A | 1 | a0002c0002t0004g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.139-3799G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978722 | |||||||
| chr10:44978775 | C | T | 1 | a0004c0004t0001g0223 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.139-3746C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978775 | |||||||
| chr10:44978792 | C | A | 15 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0031 others(12): Show |
21 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.139-3729C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978792 | |||||||
| chr10:44978833 | C | T | 3 | a0001c0001t0002g0040 a0001c0001t0002g0048 a0001c0001t0002g0204 |
5 | HG00558.hp1 HG02040.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-3688C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978833 | |||||||
| chr10:44978845 | C | A | 1 | a0001c0001t0003g0206 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.139-3676C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978845 | |||||||
| chr10:44978869 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.139-3652C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978869 | |||||||
| chr10:44978892 | G | C | 12 | a0002c0002t0001g0050 a0002c0002t0003g0035 a0002c0002t0003g0096 others(9): Show |
14 | HG02056.hp2 HG02165.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-3629G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978892 | |||||||
| chr10:44978995 | A | C | 16 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0027 others(13): Show |
25 | HG00621.hp2 HG02071.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.139-3526A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44978995 | |||||||
| chr10:44979150 | T | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0061 others(2): Show |
7 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-3371T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44979150 | |||||||
| chr10:44979270 | C | T | 3 | a0002c0002t0001g0050 a0002c0002t0014g0178 a0002c0002t0014g0220 |
4 | HG02559.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-3251C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44979270 | |||||||
| chr10:44979285 | G | A | 1 | a0002c0002t0001g0186 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.139-3236G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44979285 | |||||||
| chr10:44979289 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.139-3232T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44979289 | |||||||
| chr10:44979393 | A | C | 1 | a0001c0001t0001g0228 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.139-3128A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44979393 | |||||||
| chr10:44979551 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.139-2970C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44979551 | |||||||
| chr10:44979571 | G | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0101 others(4): Show |
11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.139-2950G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44979571 | |||||||
| chr10:44979664 | C | G | 1 | a0008c0008t0001g0076 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.139-2857C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44979664 | |||||||
| chr10:44979683 | C | T | 1 | a0012c0013t0001g0152 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.139-2838C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44979683 | |||||||
| chr10:44979703 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.139-2818A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44979703 | |||||||
| chr10:44979704 | C | T | 1 | a0009c0015t0017g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139-2817C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44979704 | |||||||
| chr10:44979705 | AGCAAGGG others(4): Show |
A | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-2812_139-2802d others(13): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr10 | 44979705 | ||||||
| chr10:44979842 | A | G | 1 | a0002c0002t0005g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.139-2679A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44979842 | |||||||
| chr10:44979845 | G | A | 1 | a0002c0002t0005g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.139-2676G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44979845 | |||||||
| chr10:44980132 | C | T | 6 | a0002c0002t0001g0066 a0002c0002t0001g0114 a0002c0002t0001g0115 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-2389C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44980132 | |||||||
| chr10:44980332 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0158 |
2 | HG00738.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.139-2189T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44980332 | |||||||
| chr10:44980355 | T | A | 6 | a0002c0002t0001g0066 a0002c0002t0001g0114 a0002c0002t0001g0115 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-2166T>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44980355 | |||||||
| chr10:44980469 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
263 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.139-2052C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44980469 | |||||||
| chr10:44980518 | A | C | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-2003A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44980518 | |||||||
| chr10:44980527 | C | T | 3 | a0002c0002t0001g0050 a0002c0002t0014g0178 a0002c0002t0014g0220 |
4 | HG02559.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-1994C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44980527 | |||||||
| chr10:44980589 | G | A | 7 | a0002c0002t0001g0066 a0002c0002t0001g0114 a0002c0002t0001g0115 others(4): Show |
7 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-1932G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44980589 | |||||||
| chr10:44980680 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
214 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.139-1841C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44980680 | |||||||
| chr10:44980688 | C | T | 1 | a0010c0011t0027g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.139-1833C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44980688 | |||||||
| chr10:44980764 | T | C | 9 | a0002c0002t0003g0035 a0002c0002t0003g0096 a0002c0002t0003g0234 others(6): Show |
10 | HG02056.hp2 HG02165.hp2 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.139-1757T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44980764 | |||||||
| chr10:44980772 | C | A | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-1749C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44980772 | |||||||
| chr10:44980847 | T | G | 12 | a0002c0002t0001g0050 a0002c0002t0003g0035 a0002c0002t0003g0096 others(9): Show |
14 | HG02056.hp2 HG02165.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-1674T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44980847 | |||||||
| chr10:44980991 | G | A | 1 | a0001c0001t0008g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.139-1530G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44980991 | |||||||
| chr10:44981277 | A | G | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-1244A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44981277 | |||||||
| chr10:44981389 | T | C | 3 | a0001c0001t0002g0014 a0001c0001t0002g0039 a0001c0001t0010g0039 |
6 | NA18946.hp2 NA18962.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-1132T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44981389 | |||||||
| chr10:44981569 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.139-952A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44981569 | |||||||
| chr10:44981632 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
342 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.139-889T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44981632 | |||||||
| chr10:44981651 | T | G | 1 | a0001c0001t0009g0046 | 2 | HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.139-870T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44981651 | |||||||
| chr10:44981692 | G | A | 7 | a0002c0002t0001g0060 a0002c0002t0001g0066 a0002c0002t0001g0114 others(4): Show |
7 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-829G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44981692 | |||||||
| chr10:44981722 | T | C | 1 | a0002c0002t0001g0181 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.139-799T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44981722 | |||||||
| chr10:44982027 | C | T | 1 | a0002c0002t0001g0016 | 4 | NA18946.hp1 NA18969.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-494C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982027 | |||||||
| chr10:44982034 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.139-487A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982034 | |||||||
| chr10:44982078 | C | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
341 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(338): Show |
intron_variant | MODIFIER | c.139-443C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982078 | |||||||
| chr10:44982084 | G | A | 1 | a0002c0012t0038g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.139-437G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982084 | |||||||
| chr10:44982102 | C | T | 1 | a0002c0002t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.139-419C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982102 | |||||||
| chr10:44982122 | C | A | 1 | a0001c0001t0001g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.139-399C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982122 | |||||||
| chr10:44982128 | G | A | 3 | a0002c0002t0001g0016 a0002c0002t0001g0198 a0002c0002t0001g0254 |
6 | HG02129.hp2 NA18946.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-393G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982128 | |||||||
| chr10:44982200 | G | A | 1 | a0002c0002t0003g0234 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.139-321G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982200 | |||||||
| chr10:44982217 | T | C | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-304T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982217 | |||||||
| chr10:44982242 | C | A | 3 | a0002c0002t0028g0136 a0002c0002t0030g0208 a0009c0015t0017g0067 |
3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.139-279C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982242 | |||||||
| chr10:44982242 | C | T | 1 | a0002c0002t0005g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.139-279C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982242 | |||||||
| chr10:44982277 | C | T | 1 | a0002c0002t0003g0154 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.139-244C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982277 | |||||||
| chr10:44982311 | G | T | 11 | a0002c0002t0001g0060 a0002c0002t0001g0066 a0002c0002t0001g0114 others(8): Show |
11 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-210G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982311 | |||||||
| chr10:44982313 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.139-208A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982313 | |||||||
| chr10:44982427 | C | T | 1 | a0001c0001t0003g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.139-94C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982427 | |||||||
| chr10:44982447 | C | T | 10 | a0002c0002t0003g0009 a0002c0002t0003g0035 a0002c0002t0003g0096 others(7): Show |
14 | HG00423.hp1 HG02056.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.139-74C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982447 | |||||||
| chr10:44982487 | T | G | 3 | a0002c0002t0002g0090 a0002c0002t0002g0099 a0002c0002t0002g0182 |
3 | NA18939.hp1 NA18964.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.139-34T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 3/10 | chr10 | 44982487 | |||||||
| chr10:44982850 | C | T | 1 | a0002c0002t0001g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.281+187C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44982850 | |||||||
| chr10:44982881 | T | C | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.281+218T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44982881 | |||||||
| chr10:44983195 | C | T | 1 | a0003c0003t0010g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.281+532C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983195 | |||||||
| chr10:44983196 | G | A | 1 | a0002c0002t0003g0235 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.281+533G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983196 | |||||||
| chr10:44983205 | A | G | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.281+542A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983205 | |||||||
| chr10:44983233 | T | G | 63 | a0002c0002t0001g0011 a0002c0002t0001g0016 a0002c0002t0001g0022 others(60): Show |
87 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.281+570T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983233 | |||||||
| chr10:44983382 | G | C | 1 | a0005c0005t0001g0131 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.282-640G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983382 | |||||||
| chr10:44983428 | T | C | 13 | a0001c0001t0003g0206 a0002c0002t0003g0009 a0002c0002t0003g0035 others(10): Show |
17 | HG00423.hp1 HG02056.hp2 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.282-594T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983428 | |||||||
| chr10:44983469 | C | T | 1 | a0009c0015t0017g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.282-553C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983469 | |||||||
| chr10:44983560 | T | C | 11 | a0001c0001t0003g0206 a0002c0002t0003g0009 a0002c0002t0003g0035 others(8): Show |
15 | HG00423.hp1 HG02056.hp2 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.282-462T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983560 | |||||||
| chr10:44983598 | A | G | 16 | a0001c0001t0003g0206 a0002c0002t0003g0009 a0002c0002t0003g0035 others(13): Show |
20 | HG00423.hp1 HG02056.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.282-424A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983598 | |||||||
| chr10:44983604 | C | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
143 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.282-418C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983604 | |||||||
| chr10:44983665 | C | T | 2 | a0002c0002t0014g0178 a0002c0002t0014g0220 |
2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.282-357C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983665 | |||||||
| chr10:44983677 | C | T | 11 | a0001c0001t0003g0206 a0002c0002t0003g0009 a0002c0002t0003g0035 others(8): Show |
15 | HG00423.hp1 HG02056.hp2 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.282-345C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983677 | |||||||
| chr10:44983817 | C | T | 1 | a0001c0001t0037g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282-205C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983817 | |||||||
| chr10:44983923 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.282-99G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983923 | |||||||
| chr10:44983986 | G | A | 91 | a0001c0001t0003g0206 a0002c0002t0001g0011 a0002c0002t0001g0016 others(88): Show |
119 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.282-36G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 4/10 | chr10 | 44983986 | |||||||
| chr10:44984154 | C | T | 7 | a0002c0002t0001g0060 a0002c0002t0001g0066 a0002c0002t0001g0114 others(4): Show |
7 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.373+41C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 5/10 | chr10 | 44984154 | |||||||
| chr10:44984204 | G | T | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.373+91G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 5/10 | chr10 | 44984204 | |||||||
| chr10:44984266 | G | A | 63 | a0002c0002t0001g0011 a0002c0002t0001g0016 a0002c0002t0001g0022 others(60): Show |
87 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.373+153G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 5/10 | chr10 | 44984266 | |||||||
| chr10:44984361 | G | A | 61 | a0002c0002t0001g0011 a0002c0002t0001g0016 a0002c0002t0001g0022 others(58): Show |
85 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.373+248G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 5/10 | chr10 | 44984361 | |||||||
| chr10:44984407 | C | T | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.373+294C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 5/10 | chr10 | 44984407 | |||||||
| chr10:44984424 | A | G | 94 | a0001c0001t0003g0206 a0002c0002t0001g0011 a0002c0002t0001g0016 others(91): Show |
122 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.373+311A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 5/10 | chr10 | 44984424 | |||||||
| chr10:44984573 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.374-240A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 5/10 | chr10 | 44984573 | |||||||
| chr10:44984782 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.374-31C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 5/10 | chr10 | 44984782 | |||||||
| chr10:44985115 | C | G | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.531+145C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44985115 | |||||||
| chr10:44985223 | G | A | 1 | a0002c0002t0001g0045 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.531+253G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44985223 | |||||||
| chr10:44985246 | C | T | 1 | a0010c0011t0027g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.531+276C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44985246 | |||||||
| chr10:44985310 | C | CT | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.531+340_531+341ins others(1): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44985310 | |||||||
| chr10:44985323 | G | A | 1 | a0001c0001t0005g0172 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.531+353G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44985323 | |||||||
| chr10:44985364 | G | A | 3 | a0002c0002t0028g0136 a0002c0002t0030g0208 a0009c0015t0017g0067 |
3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.531+394G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44985364 | |||||||
| chr10:44985381 | C | T | 2 | a0001c0001t0003g0054 a0001c0001t0003g0055 |
2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.531+411C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44985381 | |||||||
| chr10:44985556 | C | T | 2 | a0002c0002t0001g0214 a0002c0002t0001g0215 |
2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.531+586C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44985556 | |||||||
| chr10:44985673 | G | C | 21 | a0001c0001t0003g0206 a0002c0002t0001g0060 a0002c0002t0001g0066 others(18): Show |
25 | HG00423.hp1 HG00741.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.531+703G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44985673 | |||||||
| chr10:44985741 | C | G | 1 | a0001c0001t0001g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.531+771C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44985741 | |||||||
| chr10:44985838 | C | T | 1 | a0002c0002t0001g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.531+868C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44985838 | |||||||
| chr10:44985942 | G | A | 3 | a0001c0001t0006g0025 a0001c0001t0009g0025 a0001c0001t0009g0046 |
5 | HG02647.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.531+972G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44985942 | |||||||
| chr10:44986004 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(183): Show |
260 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.531+1034G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44986004 | |||||||
| chr10:44986014 | G | C | 1 | a0002c0002t0001g0214 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.531+1044G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44986014 | |||||||
| chr10:44986044 | G | C | 6 | a0001c0001t0006g0043 a0001c0001t0006g0120 a0001c0001t0006g0121 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.531+1074G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44986044 | |||||||
| chr10:44986121 | A | G | 3 | a0002c0002t0028g0136 a0002c0002t0030g0208 a0009c0015t0017g0067 |
3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.531+1151A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44986121 | |||||||
| chr10:44986182 | A | G | 1 | a0002c0002t0004g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.531+1212A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44986182 | |||||||
| chr10:44986185 | A | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0101 others(5): Show |
12 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.531+1215A>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44986185 | |||||||
| chr10:44986255 | C | T | 1 | a0002c0002t0001g0241 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.531+1285C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44986255 | |||||||
| chr10:44986265 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.531+1295C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44986265 | |||||||
| chr10:44986574 | C | A | 1 | a0002c0012t0038g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.531+1604C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44986574 | |||||||
| chr10:44986714 | G | C | 31 | a0001c0001t0003g0206 a0002c0002t0001g0060 a0002c0002t0001g0066 others(28): Show |
35 | HG00423.hp1 HG00741.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.531+1744G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44986714 | |||||||
| chr10:44986975 | T | C | 5 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(2): Show |
5 | HG01192.hp2 HG01243.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.531+2005T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44986975 | |||||||
| chr10:44987076 | C | G | 1 | a0001c0001t0036g0202 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.531+2106C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987076 | |||||||
| chr10:44987161 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.532-2113G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987161 | |||||||
| chr10:44987167 | C | T | 3 | a0002c0002t0028g0136 a0002c0002t0030g0208 a0009c0015t0017g0067 |
3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.532-2107C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987167 | |||||||
| chr10:44987252 | C | G | 1 | a0002c0002t0004g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.532-2022C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987252 | |||||||
| chr10:44987253 | G | C | 31 | a0001c0001t0003g0206 a0002c0002t0001g0060 a0002c0002t0001g0066 others(28): Show |
35 | HG00423.hp1 HG00741.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.532-2021G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987253 | |||||||
| chr10:44987344 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0217 |
3 | HG02083.hp1 NA18965.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.532-1930G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987344 | |||||||
| chr10:44987406 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.532-1868A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987406 | |||||||
| chr10:44987421 | A | G | 21 | a0001c0001t0003g0206 a0002c0002t0001g0060 a0002c0002t0001g0066 others(18): Show |
25 | HG00423.hp1 HG00741.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.532-1853A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987421 | |||||||
| chr10:44987427 | C | A | 2 | a0006c0006t0002g0056 a0006c0006t0002g0064 |
2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.532-1847C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987427 | |||||||
| chr10:44987530 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.532-1744G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987530 | |||||||
| chr10:44987595 | T | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(142): Show |
202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.532-1679T>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987595 | |||||||
| chr10:44987596 | T | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(142): Show |
202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.532-1678T>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987596 | |||||||
| chr10:44987614 | C | A | 1 | a0002c0002t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.532-1660C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987614 | |||||||
| chr10:44987626 | C | CT | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(84): Show |
127 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.532-1632dupT | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr10 | 44987626 | ||||||
| chr10:44987626 | C | CTT | 37 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0061 others(34): Show |
48 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.532-1633_532-1632d others(4): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr10 | 44987626 | ||||||
| chr10:44987626 | CT | C | 6 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0006c0006t0002g0056 others(3): Show |
6 | HG01069.hp2 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.532-1632delT | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr10 | 44987626 | ||||||
| chr10:44987626 | CTT | C | 16 | a0001c0001t0003g0206 a0002c0002t0003g0009 a0002c0002t0003g0035 others(13): Show |
20 | HG00423.hp1 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.532-1633_532-1632d others(4): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr10 | 44987626 | ||||||
| chr10:44987646 | G | A | 3 | a0002c0002t0003g0035 a0002c0002t0003g0096 a0013c0014t0003g0175 |
4 | HG02165.hp2 NA18939.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.532-1628G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987646 | |||||||
| chr10:44987980 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.532-1294T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44987980 | |||||||
| chr10:44988043 | A | G | 1 | a0002c0002t0004g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.532-1231A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44988043 | |||||||
| chr10:44988254 | A | G | 1 | a0003c0003t0035g0259 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.532-1020A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44988254 | |||||||
| chr10:44988294 | A | T | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.532-980A>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44988294 | |||||||
| chr10:44988530 | C | G | 7 | a0002c0002t0001g0060 a0002c0002t0001g0066 a0002c0002t0001g0114 others(4): Show |
7 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.532-744C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44988530 | |||||||
| chr10:44988648 | G | A | 1 | a0002c0002t0001g0045 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.532-626G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44988648 | |||||||
| chr10:44988670 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.532-604C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44988670 | |||||||
| chr10:44988697 | G | T | 7 | a0002c0002t0001g0060 a0002c0002t0001g0066 a0002c0002t0001g0114 others(4): Show |
7 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.532-577G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44988697 | |||||||
| chr10:44988702 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.532-572G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44988702 | |||||||
| chr10:44988852 | T | C | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.532-422T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44988852 | |||||||
| chr10:44988860 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
201 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.532-414T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44988860 | |||||||
| chr10:44989146 | C | T | 3 | a0002c0002t0028g0136 a0002c0002t0030g0208 a0009c0015t0017g0067 |
3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.532-128C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44989146 | |||||||
| chr10:44989216 | A | G | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.532-58A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 6/10 | chr10 | 44989216 | |||||||
| chr10:44989403 | C | T | 1 | a0005c0005t0001g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.633+28C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 7/10 | chr10 | 44989403 | |||||||
| chr10:44989459 | C | A | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.633+84C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 7/10 | chr10 | 44989459 | |||||||
| chr10:44989460 | G | A | 3 | a0002c0002t0028g0136 a0002c0002t0030g0208 a0009c0015t0017g0067 |
3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.633+85G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 7/10 | chr10 | 44989460 | |||||||
| chr10:44989542 | T | G | 6 | a0001c0001t0006g0043 a0001c0001t0006g0120 a0001c0001t0006g0121 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.634-128T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 7/10 | chr10 | 44989542 | |||||||
| chr10:44989565 | A | G | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.634-105A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 7/10 | chr10 | 44989565 | |||||||
| chr10:44989736 | C | G | 1 | a0003c0003t0016g0117 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.685+15C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44989736 | |||||||
| chr10:44989766 | T | C | 2 | a0001c0001t0003g0054 a0001c0001t0003g0055 |
2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.685+45T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44989766 | |||||||
| chr10:44989814 | T | C | 19 | a0002c0002t0001g0060 a0002c0002t0001g0066 a0002c0002t0001g0114 others(16): Show |
19 | HG00741.hp1 HG01069.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.685+93T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44989814 | |||||||
| chr10:44989875 | A | G | 1 | a0001c0001t0006g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.685+154A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44989875 | |||||||
| chr10:44990057 | C | T | 1 | a0007c0007t0001g0222 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.685+336C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990057 | |||||||
| chr10:44990119 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.685+398A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990119 | |||||||
| chr10:44990162 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.685+441G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990162 | |||||||
| chr10:44990207 | A | T | 1 | a0001c0001t0003g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.685+486A>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990207 | |||||||
| chr10:44990272 | G | T | 3 | a0002c0002t0028g0136 a0002c0002t0030g0208 a0009c0015t0017g0067 |
3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.685+551G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990272 | |||||||
| chr10:44990455 | AGAG | A | 9 | a0002c0002t0001g0011 a0002c0002t0001g0022 a0002c0002t0001g0050 others(6): Show |
15 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.686-489_686-487del others(3): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr10 | 44990455 | ||||||
| chr10:44990467 | C | T | 7 | a0003c0003t0010g0108 a0003c0003t0010g0109 a0003c0003t0016g0065 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.686-481C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990467 | |||||||
| chr10:44990486 | G | A | 21 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0101 others(18): Show |
29 | HG00423.hp1 HG01884.hp2 HG02056.hp2 others(26): Show |
intron_variant | MODIFIER | c.686-462G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990486 | |||||||
| chr10:44990504 | C | T | 18 | a0002c0002t0001g0023 a0002c0002t0001g0038 a0002c0002t0001g0110 others(15): Show |
25 | HG00597.hp1 HG00639.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.686-444C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990504 | |||||||
| chr10:44990544 | G | C | 9 | a0002c0002t0001g0060 a0002c0002t0001g0066 a0002c0002t0001g0114 others(6): Show |
9 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.686-404G>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990544 | |||||||
| chr10:44990651 | C | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG00735.hp1 HG02698.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.686-297C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990651 | |||||||
| chr10:44990729 | C | T | 2 | a0002c0002t0028g0136 a0002c0002t0030g0208 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.686-219C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990729 | |||||||
| chr10:44990816 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.686-132C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990816 | |||||||
| chr10:44990863 | G | A | 3 | a0001c0001t0006g0025 a0001c0001t0009g0025 a0001c0001t0009g0046 |
5 | HG02647.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.686-85G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990863 | |||||||
| chr10:44990917 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.686-31C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990917 | |||||||
| chr10:44990918 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0184 a0001c0001t0001g0185 |
7 | HG01106.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.686-30G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 8/10 | chr10 | 44990918 | |||||||
| chr10:44991127 | G | A | 28 | a0002c0002t0001g0016 a0002c0002t0001g0024 a0002c0002t0001g0041 others(25): Show |
37 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.807+58G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/10 | chr10 | 44991127 | |||||||
| chr10:44991251 | G | A | 1 | a0001c0001t0002g0196 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.807+182G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/10 | chr10 | 44991251 | |||||||
| chr10:44991360 | T | G | 2 | a0002c0002t0001g0162 a0010c0011t0027g0057 |
2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.807+291T>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/10 | chr10 | 44991360 | |||||||
| chr10:44991372 | A | G | 1 | a0002c0002t0001g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.807+303A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/10 | chr10 | 44991372 | |||||||
| chr10:44991397 | C | G | 1 | a0002c0012t0038g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.807+328C>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/10 | chr10 | 44991397 | |||||||
| chr10:44991432 | A | C | 2 | a0002c0002t0001g0162 a0010c0011t0027g0057 |
2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.807+363A>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/10 | chr10 | 44991432 | |||||||
| chr10:44991537 | C | T | 1 | a0009c0015t0017g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.808-368C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/10 | chr10 | 44991537 | |||||||
| chr10:44991549 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.808-356G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/10 | chr10 | 44991549 | |||||||
| chr10:44991593 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.808-312T>C | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/10 | chr10 | 44991593 | |||||||
| chr10:44991615 | C | A | 3 | a0001c0001t0006g0120 a0001c0001t0006g0121 a0001c0001t0006g0176 |
3 | HG02055.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.808-290C>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/10 | chr10 | 44991615 | |||||||
| chr10:44991631 | C | T | 2 | a0001c0001t0003g0054 a0001c0001t0003g0055 |
2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.808-274C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/10 | chr10 | 44991631 | |||||||
| chr10:44991765 | G | A | 1 | a0002c0002t0004g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.808-140G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/10 | chr10 | 44991765 | |||||||
| chr10:44991867 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0024g0044 |
2 | HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.808-38G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 9/10 | chr10 | 44991867 | |||||||
| chr10:44992009 | A | G | 1 | a0001c0001t0002g0197 | 1 | NA18980.hp1 | splice_region_variant&intron_variant | LOW | c.905+7A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44992009 | |||||||
| chr10:44992120 | G | A | 1 | a0002c0002t0001g0214 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.905+118G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44992120 | |||||||
| chr10:44992171 | C | T | 1 | a0001c0001t0008g0072 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.905+169C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44992171 | |||||||
| chr10:44992258 | CGCAGGCA others(6): Show |
C | 1 | a0007c0007t0001g0222 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.905+261_905+273del others(13): Show |
RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr10 | 44992258 | ||||||
| chr10:44992259 | G | A | 1 | a0009c0015t0017g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.905+257G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44992259 | |||||||
| chr10:44992281 | C | T | 7 | a0002c0002t0001g0060 a0002c0002t0001g0066 a0002c0002t0001g0114 others(4): Show |
7 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.905+279C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44992281 | |||||||
| chr10:44992463 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.905+461G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44992463 | |||||||
| chr10:44992464 | A | G | 2 | a0002c0002t0014g0178 a0002c0002t0014g0220 |
2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.905+462A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44992464 | |||||||
| chr10:44992607 | T | A | 1 | a0009c0015t0017g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.905+605T>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44992607 | |||||||
| chr10:44992624 | G | T | 2 | a0002c0002t0011g0019 a0010c0011t0027g0057 |
4 | HG03195.hp1 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+622G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44992624 | |||||||
| chr10:44992637 | C | T | 8 | a0001c0001t0002g0014 a0001c0001t0002g0039 a0001c0001t0002g0042 others(5): Show |
12 | HG01257.hp1 HG01346.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.906-632C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44992637 | |||||||
| chr10:44992742 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0258 |
2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.906-527G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44992742 | |||||||
| chr10:44992833 | G | T | 1 | a0009c0015t0017g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.906-436G>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44992833 | |||||||
| chr10:44992854 | A | G | 22 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0003g0206 others(19): Show |
32 | HG00423.hp1 HG00597.hp1 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.906-415A>G | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44992854 | |||||||
| chr10:44993086 | C | T | 1 | a0011c0010t0001g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.906-183C>T | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44993086 | |||||||
| chr10:44993192 | G | A | 2 | a0002c0002t0014g0178 a0002c0002t0014g0220 |
2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.906-77G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44993192 | |||||||
| chr10:44993254 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0189 |
2 | NA18973.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.906-15G>A | RASSF4 | ENSG00000107551.21 | transcript | ENST00000340258.10 | protein_coding | 10/10 | chr10 | 44993254 |