Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 166824 |
| ensemblid | ENSG00000169435.14 |
| hgncid | 20796 |
| symbol | RASSF6 |
| name | Ras association domain family member 6 |
| refseq_nuc | NM_177532.5 |
| refseq_prot | NP_803876.1 |
| ensembl_nuc | ENST00000307439.10 |
| ensembl_prot | ENSP00000303877.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 73571550 |
| end | 73620436 |
| strand | - |
| ver | v1.2 |
| region | chr4:73571550-73620436 |
| region5000 | chr4:73566550-73625436 |
| regionname0 | RASSF6_chr4_73571550_73620436 |
| regionname5000 | RASSF6_chr4_73566550_73625436 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 337 | 227 | 50 | 29 | 115 | 10 | 22 | 85 | RASSF6_chr4_73566550_73625436 | RASSF6 | MTMMA others(332): Show |
chr4 | 73566550 | 73625436 |
| a0002 | 0/1 | 337 | 102 | 26 | 36 | 26 | 3 | 10 | 19 | RASSF6_chr4_73566550_73625436 | RASSF6 | MTMMA others(332): Show |
chr4 | 73566550 | 73625436 |
| a0003 | 0/0 | 337 | 3 | 1 | 1 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | MTMMA others(332): Show |
chr4 | 73566550 | 73625436 |
| a0004 | 0/0 | 337 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | MTMMA others(332): Show |
chr4 | 73566550 | 73625436 |
| a0005 | 0/0 | 337 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | MTMMA others(332): Show |
chr4 | 73566550 | 73625436 |
| a0006 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | MTMMA others(332): Show |
chr4 | 73566550 | 73625436 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1011 | 224 | 48 | 29 | 114 | 10 | 22 | RASSF6_chr4_73566550_73625436 | RASSF6 | ATGAC others(1006): Show |
chr4 | 73566550 | 73625436 | ||
| a0001c0007 | 0/0 | 1011 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | ATGAC others(1006): Show |
chr4 | 73566550 | 73625436 | ||
| a0001c0009 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | ATGAC others(1006): Show |
chr4 | 73566550 | 73625436 | ||
| a0002c0002 | 0/1 | 1011 | 99 | 25 | 36 | 26 | 3 | 8 | RASSF6_chr4_73566550_73625436 | RASSF6 | ATGAC others(1006): Show |
chr4 | 73566550 | 73625436 | ||
| a0002c0005 | 0/0 | 1011 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | ATGAC others(1006): Show |
chr4 | 73566550 | 73625436 | ||
| a0002c0008 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | ATGAC others(1006): Show |
chr4 | 73566550 | 73625436 | ||
| a0003c0004 | 0/0 | 1011 | 3 | 1 | 1 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | ATGAC others(1006): Show |
chr4 | 73566550 | 73625436 | ||
| a0004c0003 | 0/0 | 1011 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | ATGAC others(1006): Show |
chr4 | 73566550 | 73625436 | ||
| a0005c0006 | 0/0 | 1011 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | ATGAC others(1006): Show |
chr4 | 73566550 | 73625436 | ||
| a0006c0010 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | ATGAC others(1006): Show |
chr4 | 73566550 | 73625436 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5882 | 153 | 27 | 23 | 79 | 6 | 18 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0002 | 0/0 | 5882 | 7 | 5 | 0 | 0 | 1 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0003 | 0/0 | 5882 | 35 | 6 | 2 | 23 | 2 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0004 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0007 | 0/0 | 5882 | 3 | 1 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0008 | 0/0 | 5882 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0011 | 0/0 | 5882 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0012 | 0/0 | 5882 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0015 | 0/0 | 5885 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5880): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0016 | 0/0 | 5882 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0017 | 0/0 | 5882 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0018 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0019 | 0/0 | 5882 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0020 | 0/0 | 5882 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0021 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0024 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0025 | 0/0 | 5882 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0026 | 0/0 | 5882 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0028 | 0/0 | 5882 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0029 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0030 | 0/0 | 5882 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0031 | 0/0 | 5885 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5880): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0032 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0001t0033 | 1/0 | 5882 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0007t0014 | 0/0 | 5882 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0001c0009t0001 | 0/0 | 5882 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0002t0001 | 0/0 | 5882 | 2 | 0 | 1 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0002t0002 | 0/0 | 5882 | 56 | 0 | 29 | 22 | 3 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0002t0003 | 0/0 | 5882 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0002t0004 | 0/0 | 5882 | 18 | 15 | 3 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0002t0005 | 0/0 | 5882 | 10 | 2 | 0 | 3 | 0 | 5 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0002t0006 | 0/0 | 5882 | 5 | 5 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0002t0009 | 0/0 | 5882 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0002t0010 | 0/0 | 5882 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0002t0022 | 0/1 | 5882 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0002t0023 | 0/0 | 5882 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0002t0027 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0002t0034 | 0/0 | 5882 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0005t0009 | 0/0 | 5882 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0002c0008t0004 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0003c0004t0002 | 0/0 | 5882 | 3 | 1 | 1 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0004c0003t0005 | 0/0 | 5882 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0005c0006t0013 | 0/0 | 5882 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| a0006c0010t0001 | 0/0 | 5882 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | GAGTG others(5877): Show |
chr4 | 73566550 | 73625436 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0002 | 0/0 | 7 | 1 | 3 | 2 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 2 | 1 | 2 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0007g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0008g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0008g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0011g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0011g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0012g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0012g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0015g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0015g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0016g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0016g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0017g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0018g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0019g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0020g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0021g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0024g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0025g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0026g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0028g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0029g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0030g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0031g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0032g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0033g0248 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0007t0014g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0007t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0009t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0005 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0006 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0010 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0006g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0009g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0010g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0022g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0023g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0027g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0034g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0005t0009g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0005t0009g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0008t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0003c0004t0002g0012 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0004c0003t0005g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0005c0006t0013g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0005c0006t0013g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0006c0010t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0162 | EUR | GBR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00140 | hp2 | a0003 | c0004 | t0002 | g0012 | EUR | GBR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | FIN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0047 | EUR | FIN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00438 | hp2 | a0001 | c0001 | t0008 | g0228 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00621 | hp1 | a0001 | c0001 | t0030 | g0121 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00639 | hp2 | a0001 | c0001 | t0017 | g0161 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0097 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01069 | hp2 | a0002 | c0002 | t0034 | g0249 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01070 | hp1 | a0005 | c0006 | t0013 | g0068 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0023 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0023 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01081 | hp1 | a0005 | c0006 | t0013 | g0069 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0022 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01106 | hp2 | a0002 | c0002 | t0023 | g0091 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01109 | hp2 | a0002 | c0002 | t0004 | g0007 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0022 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01167 | hp2 | a0002 | c0002 | t0004 | g0058 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01243 | hp2 | a0002 | c0002 | t0004 | g0065 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0086 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0179 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0160 | EUR | IBS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0029 | EUR | IBS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0152 | EUR | IBS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0089 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01943 | hp2 | a0003 | c0004 | t0002 | g0012 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0098 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0093 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0083 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0020 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0090 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02004 | hp2 | a0001 | c0001 | t0019 | g0113 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02027 | hp1 | a0002 | c0002 | t0005 | g0024 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02056 | hp2 | a0002 | c0002 | t0005 | g0024 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02145 | hp1 | a0002 | c0002 | t0006 | g0056 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02148 | hp2 | a0002 | c0002 | t0009 | g0081 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | CDX | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CDX | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | CDX | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02258 | hp1 | a0002 | c0002 | t0004 | g0017 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0092 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02280 | hp2 | a0002 | c0002 | t0004 | g0007 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02615 | hp1 | a0002 | c0002 | t0004 | g0060 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02622 | hp1 | a0002 | c0002 | t0004 | g0007 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02622 | hp2 | a0002 | c0002 | t0005 | g0108 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02630 | hp2 | a0002 | c0002 | t0004 | g0050 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02647 | hp1 | a0001 | c0001 | t0024 | g0205 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02647 | hp2 | a0004 | c0003 | t0005 | g0013 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02723 | hp1 | a0001 | c0001 | t0018 | g0184 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0071 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02738 | hp1 | a0002 | c0002 | t0005 | g0109 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0100 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02895 | hp1 | a0001 | c0001 | t0015 | g0142 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02895 | hp2 | a0004 | c0003 | t0005 | g0013 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02896 | hp1 | a0002 | c0002 | t0004 | g0062 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02896 | hp2 | a0001 | c0001 | t0015 | g0140 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02897 | hp1 | a0002 | c0002 | t0004 | g0017 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02897 | hp2 | a0004 | c0003 | t0005 | g0013 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02922 | hp2 | a0002 | c0002 | t0004 | g0048 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02976 | hp1 | a0002 | c0002 | t0004 | g0007 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03041 | hp1 | a0002 | c0002 | t0010 | g0025 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03130 | hp2 | a0002 | c0002 | t0006 | g0052 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03139 | hp2 | a0002 | c0002 | t0004 | g0007 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03195 | hp2 | a0001 | c0001 | t0031 | g0141 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03453 | hp1 | a0002 | c0002 | t0004 | g0194 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03486 | hp1 | a0001 | c0001 | t0021 | g0185 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03486 | hp2 | a0002 | c0002 | t0006 | g0018 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03491 | hp1 | a0002 | c0005 | t0009 | g0073 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03492 | hp2 | a0002 | c0005 | t0009 | g0080 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03516 | hp1 | a0002 | c0002 | t0010 | g0025 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03516 | hp2 | a0002 | c0008 | t0004 | g0049 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03540 | hp1 | a0002 | c0002 | t0004 | g0063 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03540 | hp2 | a0002 | c0002 | t0006 | g0018 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03654 | hp2 | a0002 | c0002 | t0005 | g0106 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03688 | hp2 | a0002 | c0002 | t0005 | g0112 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03710 | hp1 | a0001 | c0001 | t0025 | g0242 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0155 | SAS | BEB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | BEB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04115 | hp2 | a0002 | c0002 | t0003 | g0070 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04199 | hp1 | a0002 | c0002 | t0005 | g0110 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04204 | hp2 | a0002 | c0002 | t0005 | g0111 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18522 | hp2 | a0001 | c0007 | t0014 | g0143 | AFR | YRI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18612 | hp1 | a0006 | c0010 | t0001 | g0127 | EAS | CHB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | CHB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18747 | hp1 | a0001 | c0001 | t0008 | g0221 | EAS | CHB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18906 | hp1 | a0001 | c0001 | t0029 | g0138 | AFR | YRI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18906 | hp2 | a0001 | c0007 | t0014 | g0144 | AFR | YRI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18942 | hp1 | a0002 | c0002 | t0005 | g0043 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18944 | hp2 | a0001 | c0001 | t0012 | g0169 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18954 | hp2 | a0001 | c0001 | t0008 | g0233 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18979 | hp2 | a0001 | c0001 | t0011 | g0168 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18983 | hp1 | a0001 | c0009 | t0001 | g0147 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19004 | hp2 | a0001 | c0001 | t0020 | g0123 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19030 | hp2 | a0002 | c0002 | t0004 | g0057 | AFR | LWK | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19043 | hp1 | a0002 | c0002 | t0027 | g0059 | AFR | LWK | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19060 | hp2 | a0001 | c0001 | t0012 | g0170 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19063 | hp1 | a0001 | c0001 | t0011 | g0220 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19078 | hp1 | a0001 | c0001 | t0016 | g0251 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19081 | hp2 | a0001 | c0001 | t0016 | g0250 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19091 | hp1 | a0001 | c0001 | t0026 | g0202 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19240 | hp2 | a0002 | c0002 | t0005 | g0107 | AFR | YRI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ASW | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20129 | hp2 | a0002 | c0002 | t0006 | g0051 | AFR | ASW | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0072 | EUR | TSI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | TSI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20805 | hp1 | a0001 | c0001 | t0028 | g0238 | EUR | TSI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0136 | SAS | GIH | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0029 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0019 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02486 | hp1 | a0002 | c0002 | t0004 | g0055 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03471 | hp2 | a0002 | c0002 | t0004 | g0061 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG06807 | hp1 | a0001 | c0001 | t0032 | g0247 | AFR | USA | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | USA | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | USA | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | USA | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA21309 | hp2 | a0003 | c0004 | t0002 | g0012 | AFR | LWK | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0022 | g0099 | REF | REF | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0033 | g0248 | REF | REF | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73576461 | A | C | 1 | a0004 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.887T>G | p.Leu296Arg | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 10/11 | 1070/5882 | 887/1014 | 296/337 | chr4 | 73576461 | |||
| chr4:73576632 | G | C | 1 | a0003 | 3 | HG00140.hp2 HG01943.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.821C>G | p.Ala274Gly | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 9/11 | 1004/5882 | 821/1014 | 274/337 | chr4 | 73576632 | |||
| chr4:73576707 | T | A | 1 | a0006 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.746A>T | p.Asp249Val | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 9/11 | 929/5882 | 746/1014 | 249/337 | chr4 | 73576707 | |||
| chr4:73582213 | T | C | 1 | a0005 | 2 | HG01070.hp1 HG01081.hp1 |
missense_variant | MODERATE | c.645A>G | p.Ile215Met | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 7/11 | 828/5882 | 645/1014 | 215/337 | chr4 | 73582213 | |||
| chr4:73585356 | A | G | 4 | a0002 a0003 a0004 others(1): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
missense_variant | MODERATE | c.391T>C | p.Ser131Pro | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/11 | 574/5882 | 391/1014 | 131/337 | chr4 | 73585356 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73576247 | C | T | 1 | a0001c0009 | 1 | NA18983.hp1 | synonymous_variant | LOW | c.1002G>A | p.Glu334Glu | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1185/5882 | 1002/1014 | 334/337 | chr4 | 73576247 | |||
| chr4:73576469 | T | C | 1 | a0001c0007 | 2 | NA18522.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.879A>G | p.Glu293Glu | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 10/11 | 1062/5882 | 879/1014 | 293/337 | chr4 | 73576469 | |||
| chr4:73585192 | G | A | 1 | a0002c0008 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.555C>T | p.Phe185Phe | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/11 | 738/5882 | 555/1014 | 185/337 | chr4 | 73585192 | |||
| chr4:73587868 | A | G | 1 | a0002c0005 | 2 | HG03491.hp1 HG03492.hp2 |
synonymous_variant | LOW | c.354T>C | p.Pro118Pro | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/11 | 537/5882 | 354/1014 | 118/337 | chr4 | 73587868 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73571914 | G | T | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(38): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
3_prime_UTR_variant | MODIFIER | c.*4321C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 4321 | chr4 | 73571914 | ||||||
| chr4:73571921 | A | G | 1 | a0001c0001t0012 | 2 | NA18944.hp2 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4314T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 4314 | chr4 | 73571921 | ||||||
| chr4:73572090 | C | T | 1 | a0001c0001t0025 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4145G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 4145 | chr4 | 73572090 | ||||||
| chr4:73572223 | A | G | 2 | a0001c0001t0018 a0001c0001t0019 |
2 | HG02004.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4012T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 4012 | chr4 | 73572223 | ||||||
| chr4:73572267 | C | T | 1 | a0002c0002t0023 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3968G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3968 | chr4 | 73572267 | ||||||
| chr4:73572281 | G | A | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(25): Show |
245 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*3954C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3954 | chr4 | 73572281 | ||||||
| chr4:73572556 | G | A | 6 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(3): Show |
43 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3679C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3679 | chr4 | 73572556 | ||||||
| chr4:73572861 | T | G | 7 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(4): Show |
45 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3374A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3374 | chr4 | 73572861 | ||||||
| chr4:73573001 | A | G | 2 | a0001c0001t0015 a0001c0001t0031 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3234T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3234 | chr4 | 73573001 | ||||||
| chr4:73573022 | G | A | 1 | a0001c0001t0008 | 3 | HG00438.hp2 NA18747.hp1 NA18954.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3213C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3213 | chr4 | 73573022 | ||||||
| chr4:73573113 | A | G | 1 | a0001c0001t0024 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3122T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3122 | chr4 | 73573113 | ||||||
| chr4:73573177 | G | T | 1 | a0001c0001t0011 | 2 | NA18979.hp2 NA19063.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3058C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3058 | chr4 | 73573177 | ||||||
| chr4:73573212 | C | T | 8 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0018 others(5): Show |
32 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3023G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3023 | chr4 | 73573212 | ||||||
| chr4:73573251 | C | T | 1 | a0002c0002t0027 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2984G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2984 | chr4 | 73573251 | ||||||
| chr4:73573271 | T | C | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(25): Show |
245 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*2964A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2964 | chr4 | 73573271 | ||||||
| chr4:73573671 | T | A | 1 | a0001c0001t0015 | 2 | HG02895.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2564A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2564 | chr4 | 73573671 | ||||||
| chr4:73573724 | G | GTATT | 2 | a0001c0001t0015 a0001c0001t0031 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2507_*2510dupAATA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2510 | chr4 | 73573724 | ||||||
| chr4:73573807 | G | A | 2 | a0002c0002t0009 a0002c0005t0009 |
3 | HG02148.hp2 HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2428C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2428 | chr4 | 73573807 | ||||||
| chr4:73573852 | T | C | 1 | a0005c0006t0013 | 2 | HG01070.hp1 HG01081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2383A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2383 | chr4 | 73573852 | ||||||
| chr4:73573940 | C | A | 1 | a0001c0001t0018 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2295G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2295 | chr4 | 73573940 | ||||||
| chr4:73573988 | G | C | 1 | a0001c0001t0026 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2247C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2247 | chr4 | 73573988 | ||||||
| chr4:73574236 | C | T | 1 | a0001c0001t0021 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1999G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1999 | chr4 | 73574236 | ||||||
| chr4:73574237 | G | A | 1 | a0002c0002t0027 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1998C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1998 | chr4 | 73574237 | ||||||
| chr4:73574535 | T | A | 1 | a0001c0001t0017 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1700A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1700 | chr4 | 73574535 | ||||||
| chr4:73574835 | G | A | 13 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(10): Show |
70 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1400C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1400 | chr4 | 73574835 | ||||||
| chr4:73575067 | T | C | 13 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(10): Show |
70 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1168A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1168 | chr4 | 73575067 | ||||||
| chr4:73575143 | C | T | 3 | a0001c0001t0004 a0002c0002t0004 a0002c0008t0004 |
20 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1092G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1092 | chr4 | 73575143 | ||||||
| chr4:73575180 | T | G | 1 | a0001c0001t0028 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1055A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1055 | chr4 | 73575180 | ||||||
| chr4:73575356 | A | G | 3 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0019 |
5 | HG01070.hp2 HG01071.hp2 HG02004.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*879T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 879 | chr4 | 73575356 | ||||||
| chr4:73575415 | C | T | 1 | a0001c0001t0020 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*820G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 820 | chr4 | 73575415 | ||||||
| chr4:73575473 | A | G | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(38): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
3_prime_UTR_variant | MODIFIER | c.*762T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 762 | chr4 | 73575473 | ||||||
| chr4:73575502 | T | C | 2 | a0001c0001t0015 a0001c0001t0031 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*733A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 733 | chr4 | 73575502 | ||||||
| chr4:73575536 | A | C | 6 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(3): Show |
43 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*699T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 699 | chr4 | 73575536 | ||||||
| chr4:73575586 | G | C | 1 | a0001c0001t0030 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 649 | chr4 | 73575586 | ||||||
| chr4:73575968 | T | C | 2 | a0001c0001t0015 a0001c0001t0031 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*267A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 267 | chr4 | 73575968 | ||||||
| chr4:73575989 | T | A | 1 | a0001c0001t0019 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 246 | chr4 | 73575989 | ||||||
| chr4:73576056 | A | G | 2 | a0001c0001t0015 a0001c0001t0031 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*179T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 179 | chr4 | 73576056 | ||||||
| chr4:73576069 | A | G | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(11): Show |
71 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*166T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 166 | chr4 | 73576069 | ||||||
| chr4:73576146 | G | A | 2 | a0001c0001t0015 a0001c0001t0031 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*89C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 89 | chr4 | 73576146 | ||||||
| chr4:73611812 | A | G | 3 | a0002c0002t0005 a0002c0002t0010 a0004c0003t0005 |
15 | HG02027.hp1 HG02056.hp2 HG02622.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-17T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/11 | 17 | chr4 | 73611812 | ||||||
| chr4:73620335 | C | A | 1 | a0002c0002t0034 | 1 | HG01069.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/11 | 8540 | chr4 | 73620335 | ||||||
| chr4:73620335 | C | G | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(37): Show |
334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
5_prime_UTR_variant | MODIFIER | c.-82G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/11 | 8540 | chr4 | 73620335 | ||||||
| chr4:73620422 | C | A | 1 | a0001c0001t0016 | 2 | NA19078.hp1 NA19081.hp2 |
5_prime_UTR_variant | MODIFIER | c.-169G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/11 | 8627 | chr4 | 73620422 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73576385 | T | C | 14 | a0002c0002t0002g0029 a0002c0002t0002g0162 a0002c0002t0002g0179 others(11): Show |
19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.938+25A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 10/10 | chr4 | 73576385 | |||||||
| chr4:73576511 | A | T | 1 | a0001c0001t0001g0036 | 2 | HG02135.hp1 NA19003.hp2 |
splice_region_variant&intron_variant | LOW | c.841-4T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 9/10 | chr4 | 73576511 | |||||||
| chr4:73576528 | A | G | 1 | a0002c0002t0004g0194 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.841-21T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 9/10 | chr4 | 73576528 | |||||||
| chr4:73576597 | G | A | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.840+16C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 9/10 | chr4 | 73576597 | |||||||
| chr4:73576839 | A | G | 1 | a0001c0001t0019g0113 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.722-108T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73576839 | |||||||
| chr4:73576896 | G | C | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-165C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73576896 | |||||||
| chr4:73576950 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.722-219C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73576950 | |||||||
| chr4:73576984 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.722-253G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73576984 | |||||||
| chr4:73577113 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.722-382A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577113 | |||||||
| chr4:73577296 | T | C | 15 | a0001c0001t0004g0183 a0002c0002t0004g0007 a0002c0002t0004g0017 others(12): Show |
20 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-565A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577296 | |||||||
| chr4:73577353 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.722-622G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577353 | |||||||
| chr4:73577523 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.722-792A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577523 | |||||||
| chr4:73577572 | A | G | 1 | a0002c0002t0005g0108 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.722-841T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577572 | |||||||
| chr4:73577574 | T | C | 4 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0227 others(1): Show |
4 | HG00408.hp2 HG02015.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-843A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577574 | |||||||
| chr4:73577586 | C | T | 2 | a0005c0006t0013g0068 a0005c0006t0013g0069 |
2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.722-855G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577586 | |||||||
| chr4:73577606 | T | C | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-875A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577606 | |||||||
| chr4:73577710 | C | T | 5 | a0001c0001t0003g0031 a0001c0001t0003g0146 a0001c0001t0003g0157 others(2): Show |
6 | HG00408.hp1 NA18974.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.722-979G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577710 | |||||||
| chr4:73577753 | C | T | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1022G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577753 | |||||||
| chr4:73577902 | T | G | 1 | a0001c0001t0001g0208 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.722-1171A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577902 | |||||||
| chr4:73577996 | T | C | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.722-1265A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577996 | |||||||
| chr4:73578020 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.722-1289C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578020 | |||||||
| chr4:73578024 | T | C | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1293A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578024 | |||||||
| chr4:73578029 | T | TTTTCTTT others(17): Show |
3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1299_722-1298i others(26): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578029 | |||||||
| chr4:73578029 | T | TTTTCTTT others(18): Show |
244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
331 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.722-1299_722-1298i others(27): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578029 | |||||||
| chr4:73578029 | T | TTTTCTTT others(19): Show |
1 | a0001c0001t0001g0124 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.722-1299_722-1298i others(28): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578029 | |||||||
| chr4:73578030 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.722-1299C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578030 | |||||||
| chr4:73578031 | A | AT | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1301_722-1300i others(3): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578031 | |||||||
| chr4:73578031 | A | C | 1 | a0001c0001t0001g0124 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.722-1300T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578031 | |||||||
| chr4:73578031 | A | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
331 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.722-1300T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578031 | |||||||
| chr4:73578048 | T | C | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1317A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578048 | |||||||
| chr4:73578071 | T | G | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1340A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578071 | |||||||
| chr4:73578160 | C | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
170 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.722-1429G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578160 | |||||||
| chr4:73578175 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0015g0140 a0001c0001t0015g0142 others(1): Show |
5 | HG01243.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.722-1444G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578175 | |||||||
| chr4:73578294 | G | A | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1563C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578294 | |||||||
| chr4:73578544 | G | C | 4 | a0001c0001t0002g0046 a0001c0001t0015g0140 a0001c0001t0015g0142 others(1): Show |
4 | HG02895.hp1 HG02896.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-1813C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578544 | |||||||
| chr4:73578638 | C | CT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
166 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.722-1908dupA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578638 | |||||||
| chr4:73578656 | C | T | 3 | a0001c0001t0008g0221 a0001c0001t0008g0228 a0001c0001t0008g0233 |
3 | HG00438.hp2 NA18747.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.722-1925G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578656 | |||||||
| chr4:73578694 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.722-1963G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578694 | |||||||
| chr4:73578721 | G | C | 1 | a0001c0001t0003g0155 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.722-1990C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578721 | |||||||
| chr4:73578724 | T | G | 1 | a0001c0001t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.722-1993A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578724 | |||||||
| chr4:73578729 | T | C | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1998A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578729 | |||||||
| chr4:73578757 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0122 |
2 | NA18947.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.722-2026G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578757 | |||||||
| chr4:73578835 | C | T | 1 | a0001c0001t0019g0113 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.722-2104G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578835 | |||||||
| chr4:73578908 | G | A | 14 | a0002c0002t0004g0007 a0002c0002t0004g0017 a0002c0002t0004g0048 others(11): Show |
19 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.722-2177C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578908 | |||||||
| chr4:73578917 | C | T | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-2186G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578917 | |||||||
| chr4:73579083 | C | T | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-2352G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579083 | |||||||
| chr4:73579142 | G | A | 37 | a0001c0001t0001g0014 a0001c0001t0003g0028 a0001c0001t0003g0030 others(34): Show |
42 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.722-2411C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579142 | |||||||
| chr4:73579146 | A | G | 1 | a0001c0001t0003g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.722-2415T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579146 | |||||||
| chr4:73579246 | T | C | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-2515A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579246 | |||||||
| chr4:73579250 | A | G | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-2519T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579250 | |||||||
| chr4:73579316 | A | G | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+2501T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579316 | |||||||
| chr4:73579376 | G | A | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+2441C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579376 | |||||||
| chr4:73579387 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.721+2430A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579387 | |||||||
| chr4:73579477 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.721+2340C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579477 | |||||||
| chr4:73579580 | T | C | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+2237A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579580 | |||||||
| chr4:73579581 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.721+2236C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579581 | |||||||
| chr4:73579626 | C | T | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+2191G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579626 | |||||||
| chr4:73579731 | C | A | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+2086G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579731 | |||||||
| chr4:73579735 | T | TA | 37 | a0001c0001t0001g0014 a0001c0001t0003g0028 a0001c0001t0003g0030 others(34): Show |
42 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.721+2081dupT | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579735 | |||||||
| chr4:73579979 | G | A | 6 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0209 others(3): Show |
7 | NA18947.hp2 NA18970.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.721+1838C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579979 | |||||||
| chr4:73580059 | T | G | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+1758A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580059 | |||||||
| chr4:73580101 | C | T | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+1716G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580101 | |||||||
| chr4:73580119 | G | A | 1 | a0001c0001t0018g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.721+1698C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580119 | |||||||
| chr4:73580135 | T | C | 1 | a0002c0002t0002g0095 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.721+1682A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580135 | |||||||
| chr4:73580143 | A | G | 1 | a0002c0002t0027g0059 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.721+1674T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580143 | |||||||
| chr4:73580218 | A | C | 4 | a0001c0001t0001g0151 a0001c0001t0015g0140 a0001c0001t0015g0142 others(1): Show |
4 | HG02895.hp1 HG02896.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.721+1599T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580218 | |||||||
| chr4:73580236 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.721+1581A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580236 | |||||||
| chr4:73580237 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.721+1580C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580237 | |||||||
| chr4:73580291 | C | G | 10 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(7): Show |
10 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.721+1526G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580291 | |||||||
| chr4:73580328 | A | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
213 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.721+1489T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580328 | |||||||
| chr4:73580454 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.721+1363A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580454 | |||||||
| chr4:73580518 | A | G | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+1299T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580518 | |||||||
| chr4:73580691 | A | G | 4 | a0001c0001t0007g0023 a0001c0001t0007g0100 a0001c0001t0018g0184 others(1): Show |
5 | HG01070.hp2 HG01071.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.721+1126T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580691 | |||||||
| chr4:73580716 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.721+1101C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580716 | |||||||
| chr4:73580775 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
218 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.721+1042A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580775 | |||||||
| chr4:73580781 | T | C | 1 | a0001c0001t0028g0238 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.721+1036A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580781 | |||||||
| chr4:73580791 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
213 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.721+1026T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580791 | |||||||
| chr4:73580806 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
213 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.721+1011G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580806 | |||||||
| chr4:73580879 | G | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
213 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.721+938C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580879 | |||||||
| chr4:73580901 | G | T | 1 | a0001c0001t0003g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.721+916C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580901 | |||||||
| chr4:73580908 | T | A | 1 | a0001c0001t0001g0195 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.721+909A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580908 | |||||||
| chr4:73580941 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
213 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.721+876G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580941 | |||||||
| chr4:73580970 | A | T | 1 | a0001c0001t0018g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.721+847T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580970 | |||||||
| chr4:73581071 | A | G | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+746T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581071 | |||||||
| chr4:73581079 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
220 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.721+738T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581079 | |||||||
| chr4:73581105 | G | GT | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
226 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.721+711dupA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581105 | |||||||
| chr4:73581166 | A | G | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.721+651T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581166 | |||||||
| chr4:73581178 | G | C | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+639C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581178 | |||||||
| chr4:73581274 | T | A | 1 | a0001c0001t0001g0193 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.721+543A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581274 | |||||||
| chr4:73581292 | T | A | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.721+525A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581292 | |||||||
| chr4:73581305 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.721+512C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581305 | |||||||
| chr4:73581334 | C | T | 5 | a0002c0002t0006g0018 a0002c0002t0006g0051 a0002c0002t0006g0052 others(2): Show |
6 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.721+483G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581334 | |||||||
| chr4:73581387 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
178 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.721+430G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581387 | |||||||
| chr4:73581392 | G | T | 7 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(4): Show |
7 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.721+425C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581392 | |||||||
| chr4:73581700 | C | G | 61 | a0001c0001t0001g0014 a0001c0001t0002g0044 a0001c0001t0002g0045 others(58): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.721+117G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581700 | |||||||
| chr4:73581722 | C | T | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+95G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581722 | |||||||
| chr4:73581735 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
246 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.721+82G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581735 | |||||||
| chr4:73581775 | G | A | 42 | a0001c0001t0001g0014 a0001c0001t0003g0028 a0001c0001t0003g0030 others(39): Show |
48 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.721+42C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581775 | |||||||
| chr4:73581793 | A | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
250 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.721+24T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581793 | |||||||
| chr4:73581982 | A | G | 1 | a0002c0002t0002g0090 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.670-114T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 7/10 | chr4 | 73581982 | |||||||
| chr4:73581997 | C | T | 5 | a0002c0002t0006g0018 a0002c0002t0006g0051 a0002c0002t0006g0052 others(2): Show |
6 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-129G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 7/10 | chr4 | 73581997 | |||||||
| chr4:73582083 | A | G | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.669+106T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 7/10 | chr4 | 73582083 | |||||||
| chr4:73582148 | TATATA | T | 7 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(4): Show |
7 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.669+36_669+40delTA others(3): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 7/10 | chr4 | 73582148 | |||||||
| chr4:73582361 | ATCT | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.568-74_568-72delAG others(1): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582361 | |||||||
| chr4:73582417 | TTTTG | T | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.568-131_568-128del others(4): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582417 | |||||||
| chr4:73582486 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
7 | HG00544.hp1 HG02015.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.568-196T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582486 | |||||||
| chr4:73582590 | T | C | 1 | a0001c0001t0003g0176 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.568-300A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582590 | |||||||
| chr4:73582599 | A | T | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.568-309T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582599 | |||||||
| chr4:73582623 | A | T | 1 | a0002c0002t0034g0249 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.568-333T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582623 | |||||||
| chr4:73582634 | G | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.568-344C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582634 | |||||||
| chr4:73582716 | T | G | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.568-426A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582716 | |||||||
| chr4:73582839 | A | AAC | 71 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(68): Show |
103 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.568-551_568-550dup others(2): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582839 | |||||||
| chr4:73582839 | A | AACAC | 5 | a0002c0002t0006g0018 a0002c0002t0006g0051 a0002c0002t0006g0052 others(2): Show |
6 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.568-553_568-550dup others(4): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582839 | |||||||
| chr4:73582843 | C | A | 1 | a0001c0001t0030g0121 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.568-553G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582843 | |||||||
| chr4:73582844 | G | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.568-554C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582844 | |||||||
| chr4:73582882 | T | G | 2 | a0001c0001t0002g0044 a0001c0001t0002g0047 |
2 | HG00323.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.568-592A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582882 | |||||||
| chr4:73582914 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.568-624C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582914 | |||||||
| chr4:73582921 | G | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.568-631C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582921 | |||||||
| chr4:73583008 | G | A | 14 | a0002c0002t0002g0029 a0002c0002t0002g0162 a0002c0002t0002g0179 others(11): Show |
19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.568-718C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583008 | |||||||
| chr4:73583064 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.568-774A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583064 | |||||||
| chr4:73583070 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.568-780C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583070 | |||||||
| chr4:73583303 | A | G | 2 | a0002c0002t0002g0021 a0002c0002t0002g0085 |
3 | NA18964.hp1 NA18981.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.568-1013T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583303 | |||||||
| chr4:73583358 | T | C | 5 | a0002c0002t0006g0018 a0002c0002t0006g0051 a0002c0002t0006g0052 others(2): Show |
6 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.568-1068A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583358 | |||||||
| chr4:73583415 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.568-1125T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583415 | |||||||
| chr4:73583436 | T | G | 3 | a0002c0002t0002g0029 a0002c0002t0002g0162 a0002c0002t0002g0179 |
4 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.568-1146A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583436 | |||||||
| chr4:73583548 | C | T | 1 | a0001c0001t0003g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.568-1258G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583548 | |||||||
| chr4:73583574 | T | C | 3 | a0001c0001t0003g0167 a0001c0001t0012g0169 a0001c0001t0012g0170 |
3 | HG02135.hp2 NA18944.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.568-1284A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583574 | |||||||
| chr4:73583753 | G | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+1427C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583753 | |||||||
| chr4:73583759 | G | GTTC | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+1418_567+1420d others(5): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583759 | |||||||
| chr4:73583915 | T | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0211 a0001c0001t0001g0212 others(4): Show |
8 | HG00438.hp2 HG00621.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.567+1265A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583915 | |||||||
| chr4:73583976 | C | T | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+1204G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583976 | |||||||
| chr4:73584005 | C | T | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+1175G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584005 | |||||||
| chr4:73584030 | C | T | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+1150G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584030 | |||||||
| chr4:73584107 | T | C | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+1073A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584107 | |||||||
| chr4:73584136 | T | C | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+1044A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584136 | |||||||
| chr4:73584172 | A | G | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+1008T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584172 | |||||||
| chr4:73584205 | C | T | 14 | a0002c0002t0002g0029 a0002c0002t0002g0162 a0002c0002t0002g0179 others(11): Show |
19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.567+975G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584205 | |||||||
| chr4:73584211 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.567+969G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584211 | |||||||
| chr4:73584215 | C | T | 1 | a0001c0001t0018g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.567+965G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584215 | |||||||
| chr4:73584334 | T | C | 2 | a0001c0001t0001g0223 a0001c0001t0001g0226 |
2 | HG00733.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.567+846A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584334 | |||||||
| chr4:73584350 | C | T | 36 | a0001c0001t0001g0014 a0001c0001t0003g0028 a0001c0001t0003g0030 others(33): Show |
41 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.567+830G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584350 | |||||||
| chr4:73584385 | T | C | 2 | a0002c0002t0006g0052 a0002c0002t0006g0056 |
2 | HG02145.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.567+795A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584385 | |||||||
| chr4:73584522 | A | G | 1 | a0002c0002t0002g0079 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.567+658T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584522 | |||||||
| chr4:73584591 | T | C | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+589A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584591 | |||||||
| chr4:73584644 | C | A | 1 | a0001c0001t0025g0242 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.567+536G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584644 | |||||||
| chr4:73584645 | G | A | 2 | a0002c0002t0005g0106 a0002c0002t0005g0110 |
2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.567+535C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584645 | |||||||
| chr4:73584647 | T | A | 4 | a0002c0002t0002g0006 a0002c0002t0002g0020 a0002c0002t0002g0079 others(1): Show |
10 | HG00733.hp2 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.567+533A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584647 | |||||||
| chr4:73584703 | T | C | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+477A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584703 | |||||||
| chr4:73584773 | T | G | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+407A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584773 | |||||||
| chr4:73584783 | A | G | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+397T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584783 | |||||||
| chr4:73584849 | G | A | 7 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(4): Show |
7 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.567+331C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584849 | |||||||
| chr4:73584860 | G | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+320C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584860 | |||||||
| chr4:73584937 | T | A | 1 | a0002c0002t0027g0059 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.567+243A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584937 | |||||||
| chr4:73584967 | A | T | 2 | a0002c0002t0006g0052 a0002c0002t0006g0056 |
2 | HG02145.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.567+213T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584967 | |||||||
| chr4:73585011 | A | G | 71 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(68): Show |
103 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.567+169T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73585011 | |||||||
| chr4:73585046 | G | T | 1 | a0002c0002t0002g0089 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.567+134C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73585046 | |||||||
| chr4:73585101 | T | G | 1 | a0001c0001t0001g0235 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.567+79A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73585101 | |||||||
| chr4:73585113 | G | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.567+67C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73585113 | |||||||
| chr4:73585375 | T | G | 36 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(33): Show |
52 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.383-11A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73585375 | |||||||
| chr4:73585406 | GTGTCCTA others(6): Show |
G | 1 | a0001c0001t0001g0206 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.383-55_383-43delGG others(11): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73585406 | |||||||
| chr4:73585542 | C | T | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.383-178G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73585542 | |||||||
| chr4:73585638 | TC | T | 7 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(4): Show |
7 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.383-275delG | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73585638 | |||||||
| chr4:73585829 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.383-465A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73585829 | |||||||
| chr4:73585979 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.383-615G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73585979 | |||||||
| chr4:73586017 | T | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.383-653A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586017 | |||||||
| chr4:73586200 | G | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.383-836C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586200 | |||||||
| chr4:73586405 | C | T | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.383-1041G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586405 | |||||||
| chr4:73586471 | T | C | 71 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(68): Show |
103 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.383-1107A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586471 | |||||||
| chr4:73586500 | C | T | 1 | a0001c0001t0019g0113 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.383-1136G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586500 | |||||||
| chr4:73586516 | A | C | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.383-1152T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586516 | |||||||
| chr4:73586520 | T | C | 57 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(54): Show |
84 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.383-1156A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586520 | |||||||
| chr4:73586528 | A | G | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.383-1164T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586528 | |||||||
| chr4:73586620 | A | T | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.382+1220T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586620 | |||||||
| chr4:73586635 | A | G | 1 | a0002c0002t0002g0072 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.382+1205T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586635 | |||||||
| chr4:73586640 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0021g0185 |
3 | HG02965.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.382+1200T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586640 | |||||||
| chr4:73586752 | C | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.382+1088G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586752 | |||||||
| chr4:73586785 | G | C | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.382+1055C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586785 | |||||||
| chr4:73586873 | C | T | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.382+967G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586873 | |||||||
| chr4:73586889 | G | A | 1 | a0002c0002t0004g0061 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.382+951C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586889 | |||||||
| chr4:73586911 | G | GAA | 67 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(64): Show |
94 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.382+927_382+928dup others(2): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586911 | |||||||
| chr4:73586911 | G | GAAA | 7 | a0002c0002t0002g0006 a0002c0002t0002g0020 a0002c0002t0002g0071 others(4): Show |
13 | HG00733.hp2 HG01257.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.382+926_382+928dup others(3): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586911 | |||||||
| chr4:73587116 | T | G | 1 | a0002c0002t0027g0059 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+724A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587116 | |||||||
| chr4:73587134 | G | A | 126 | a0001c0001t0001g0014 a0001c0001t0002g0044 a0001c0001t0002g0045 others(123): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.382+706C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587134 | |||||||
| chr4:73587137 | C | T | 1 | a0001c0001t0003g0155 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.382+703G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587137 | |||||||
| chr4:73587142 | T | G | 1 | a0001c0001t0003g0155 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.382+698A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587142 | |||||||
| chr4:73587144 | T | C | 1 | a0001c0001t0003g0155 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.382+696A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587144 | |||||||
| chr4:73587217 | C | T | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.382+623G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587217 | |||||||
| chr4:73587234 | A | G | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.382+606T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587234 | |||||||
| chr4:73587277 | G | T | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.382+563C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587277 | |||||||
| chr4:73587318 | C | T | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.382+522G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587318 | |||||||
| chr4:73587347 | T | C | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.382+493A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587347 | |||||||
| chr4:73587394 | T | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.382+446A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587394 | |||||||
| chr4:73587428 | C | T | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.382+412G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587428 | |||||||
| chr4:73587493 | G | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.382+347C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587493 | |||||||
| chr4:73587595 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
169 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.382+245C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587595 | |||||||
| chr4:73587687 | T | C | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.382+153A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587687 | |||||||
| chr4:73587730 | G | A | 5 | a0002c0002t0006g0018 a0002c0002t0006g0051 a0002c0002t0006g0052 others(2): Show |
6 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+110C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587730 | |||||||
| chr4:73587820 | A | C | 1 | a0001c0001t0002g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.382+20T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587820 | |||||||
| chr4:73587939 | G | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
splice_region_variant&intron_variant | LOW | c.288-5C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73587939 | |||||||
| chr4:73587974 | T | C | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.288-40A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73587974 | |||||||
| chr4:73588010 | A | G | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.288-76T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588010 | |||||||
| chr4:73588065 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
169 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.288-131T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588065 | |||||||
| chr4:73588110 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.288-176T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588110 | |||||||
| chr4:73588140 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
167 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.288-206A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588140 | |||||||
| chr4:73588160 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.288-226G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588160 | |||||||
| chr4:73588161 | G | A | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.288-227C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588161 | |||||||
| chr4:73588271 | A | G | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.288-337T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588271 | |||||||
| chr4:73588287 | C | T | 76 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(73): Show |
109 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.288-353G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588287 | |||||||
| chr4:73588379 | T | C | 1 | a0006c0010t0001g0127 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.288-445A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588379 | |||||||
| chr4:73588649 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
168 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.288-715T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588649 | |||||||
| chr4:73588675 | T | G | 37 | a0001c0001t0001g0014 a0001c0001t0003g0028 a0001c0001t0003g0030 others(34): Show |
42 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.288-741A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588675 | |||||||
| chr4:73588766 | T | A | 1 | a0001c0001t0001g0034 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.288-832A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588766 | |||||||
| chr4:73588783 | G | A | 5 | a0002c0002t0006g0018 a0002c0002t0006g0051 a0002c0002t0006g0052 others(2): Show |
6 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.288-849C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588783 | |||||||
| chr4:73588783 | G | GTCATCA | 48 | a0001c0001t0001g0119 a0001c0001t0001g0198 a0001c0001t0001g0213 others(45): Show |
61 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.288-855_288-850dup others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588783 | |||||||
| chr4:73588783 | G | GTCATCAT others(2): Show |
142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
208 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.288-858_288-850dup others(9): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588783 | |||||||
| chr4:73588783 | G | GTCATCAT others(5): Show |
17 | a0001c0001t0001g0026 a0001c0001t0001g0103 a0001c0001t0001g0114 others(14): Show |
19 | HG00741.hp2 HG01358.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-861_288-850dup others(12): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588783 | |||||||
| chr4:73588783 | G | GTCATCAT others(8): Show |
27 | a0001c0001t0001g0014 a0001c0001t0003g0028 a0001c0001t0003g0030 others(24): Show |
32 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.288-864_288-850dup others(15): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588783 | |||||||
| chr4:73588783 | G | GTCATCAT others(11): Show |
2 | a0001c0001t0003g0155 a0001c0001t0012g0170 |
2 | HG03831.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.288-867_288-850dup others(18): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588783 | |||||||
| chr4:73588913 | C | G | 1 | a0002c0002t0004g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.288-979G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588913 | |||||||
| chr4:73588996 | G | A | 14 | a0002c0002t0002g0029 a0002c0002t0002g0162 a0002c0002t0002g0179 others(11): Show |
19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-1062C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588996 | |||||||
| chr4:73589053 | G | A | 14 | a0002c0002t0002g0029 a0002c0002t0002g0162 a0002c0002t0002g0179 others(11): Show |
19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-1119C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589053 | |||||||
| chr4:73589144 | T | G | 56 | a0001c0001t0001g0014 a0001c0001t0003g0028 a0001c0001t0003g0030 others(53): Show |
67 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.288-1210A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589144 | |||||||
| chr4:73589420 | A | G | 1 | a0002c0002t0027g0059 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.288-1486T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589420 | |||||||
| chr4:73589500 | G | A | 6 | a0001c0001t0019g0113 a0002c0002t0006g0018 a0002c0002t0006g0051 others(3): Show |
7 | HG02004.hp2 HG02145.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-1566C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589500 | |||||||
| chr4:73589510 | G | A | 2 | a0002c0002t0002g0021 a0002c0002t0002g0085 |
3 | NA18964.hp1 NA18981.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.288-1576C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589510 | |||||||
| chr4:73589640 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.288-1706C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589640 | |||||||
| chr4:73589664 | A | G | 51 | a0001c0001t0001g0014 a0001c0001t0003g0028 a0001c0001t0003g0030 others(48): Show |
61 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.288-1730T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589664 | |||||||
| chr4:73589757 | C | A | 14 | a0002c0002t0002g0029 a0002c0002t0002g0162 a0002c0002t0002g0179 others(11): Show |
19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-1823G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589757 | |||||||
| chr4:73589821 | T | C | 14 | a0002c0002t0002g0029 a0002c0002t0002g0162 a0002c0002t0002g0179 others(11): Show |
19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-1887A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589821 | |||||||
| chr4:73589847 | A | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.288-1913T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589847 | |||||||
| chr4:73589909 | C | T | 14 | a0002c0002t0002g0029 a0002c0002t0002g0162 a0002c0002t0002g0179 others(11): Show |
19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-1975G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589909 | |||||||
| chr4:73589911 | G | A | 37 | a0001c0001t0001g0014 a0001c0001t0003g0028 a0001c0001t0003g0030 others(34): Show |
42 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.288-1977C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589911 | |||||||
| chr4:73589933 | C | T | 1 | a0001c0001t0031g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.288-1999G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589933 | |||||||
| chr4:73590003 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.288-2069G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590003 | |||||||
| chr4:73590037 | T | A | 14 | a0002c0002t0002g0029 a0002c0002t0002g0162 a0002c0002t0002g0179 others(11): Show |
19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-2103A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590037 | |||||||
| chr4:73590057 | A | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
166 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.288-2123T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590057 | |||||||
| chr4:73590123 | T | C | 1 | a0001c0001t0001g0236 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.288-2189A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590123 | |||||||
| chr4:73590152 | T | C | 1 | a0001c0001t0018g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.288-2218A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590152 | |||||||
| chr4:73590232 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.288-2298A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590232 | |||||||
| chr4:73590339 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.288-2405C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590339 | |||||||
| chr4:73590488 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.288-2554A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590488 | |||||||
| chr4:73590655 | T | C | 2 | a0002c0002t0004g0050 a0002c0002t0004g0060 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.288-2721A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590655 | |||||||
| chr4:73590998 | G | T | 1 | a0001c0001t0032g0247 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287+2453C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590998 | |||||||
| chr4:73591102 | C | T | 1 | a0001c0001t0032g0247 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287+2349G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591102 | |||||||
| chr4:73591126 | A | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
168 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.287+2325T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591126 | |||||||
| chr4:73591127 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287+2324C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591127 | |||||||
| chr4:73591143 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
7 | HG00544.hp1 HG02015.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.287+2308G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591143 | |||||||
| chr4:73591161 | A | G | 51 | a0001c0001t0001g0014 a0001c0001t0003g0028 a0001c0001t0003g0030 others(48): Show |
61 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.287+2290T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591161 | |||||||
| chr4:73591618 | AG | A | 4 | a0002c0002t0006g0018 a0002c0002t0006g0051 a0002c0002t0006g0052 others(1): Show |
5 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.287+1832delC | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591618 | |||||||
| chr4:73591723 | G | A | 1 | a0002c0002t0023g0091 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.287+1728C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591723 | |||||||
| chr4:73591779 | C | T | 2 | a0005c0006t0013g0068 a0005c0006t0013g0069 |
2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.287+1672G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591779 | |||||||
| chr4:73591854 | G | A | 1 | a0002c0002t0027g0059 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.287+1597C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591854 | |||||||
| chr4:73592313 | G | C | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.287+1138C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592313 | |||||||
| chr4:73592410 | C | T | 7 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(4): Show |
7 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.287+1041G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592410 | |||||||
| chr4:73592506 | T | G | 18 | a0001c0001t0007g0023 a0001c0001t0007g0100 a0001c0001t0019g0113 others(15): Show |
24 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.287+945A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592506 | |||||||
| chr4:73592730 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.287+721T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592730 | |||||||
| chr4:73592824 | T | C | 14 | a0002c0002t0002g0029 a0002c0002t0002g0162 a0002c0002t0002g0179 others(11): Show |
19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.287+627A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592824 | |||||||
| chr4:73592985 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.287+466T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592985 | |||||||
| chr4:73592992 | G | T | 14 | a0002c0002t0002g0029 a0002c0002t0002g0162 a0002c0002t0002g0179 others(11): Show |
19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.287+459C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592992 | |||||||
| chr4:73593019 | AT | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
265 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(262): Show |
intron_variant | MODIFIER | c.287+431delA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593019 | |||||||
| chr4:73593019 | ATT | A | 55 | a0001c0001t0001g0014 a0001c0001t0001g0130 a0001c0001t0001g0212 others(52): Show |
65 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.287+430_287+431del others(2): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593019 | |||||||
| chr4:73593080 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.287+371T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593080 | |||||||
| chr4:73593172 | C | T | 1 | a0002c0002t0006g0051 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.287+279G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593172 | |||||||
| chr4:73593270 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(50): Show |
77 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.287+181G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593270 | |||||||
| chr4:73593305 | C | A | 1 | a0001c0001t0018g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.287+146G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593305 | |||||||
| chr4:73593389 | C | T | 1 | a0002c0002t0004g0194 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.287+62G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593389 | |||||||
| chr4:73593945 | T | C | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.145-352A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73593945 | |||||||
| chr4:73594037 | A | T | 1 | a0001c0001t0018g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.145-444T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594037 | |||||||
| chr4:73594072 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.145-479C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594072 | |||||||
| chr4:73594185 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.145-592T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594185 | |||||||
| chr4:73594261 | A | T | 43 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(40): Show |
65 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.145-668T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594261 | |||||||
| chr4:73594302 | C | G | 4 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | NA18964.hp2 NA18971.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-709G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594302 | |||||||
| chr4:73594435 | C | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.145-842G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594435 | |||||||
| chr4:73594449 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.145-856T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594449 | |||||||
| chr4:73594571 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
206 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.145-978G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594571 | |||||||
| chr4:73595027 | A | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
206 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.145-1434T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595027 | |||||||
| chr4:73595060 | T | A | 1 | a0001c0001t0003g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.145-1467A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595060 | |||||||
| chr4:73595110 | G | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(50): Show |
77 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.145-1517C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595110 | |||||||
| chr4:73595207 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0224 a0001c0001t0024g0205 |
3 | HG02572.hp1 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.145-1614C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595207 | |||||||
| chr4:73595226 | G | A | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.145-1633C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595226 | |||||||
| chr4:73595236 | C | T | 1 | a0001c0001t0003g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.145-1643G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595236 | |||||||
| chr4:73595429 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.145-1836A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595429 | |||||||
| chr4:73595446 | G | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.145-1853C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595446 | |||||||
| chr4:73595456 | C | T | 1 | a0002c0002t0002g0067 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.145-1863G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595456 | |||||||
| chr4:73595462 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.145-1869C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595462 | |||||||
| chr4:73595468 | G | C | 2 | a0001c0007t0014g0143 a0001c0007t0014g0144 |
2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.145-1875C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595468 | |||||||
| chr4:73595590 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.145-1997A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595590 | |||||||
| chr4:73595707 | G | A | 11 | a0002c0002t0005g0024 a0002c0002t0005g0043 a0002c0002t0005g0106 others(8): Show |
15 | HG02027.hp1 HG02056.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.145-2114C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595707 | |||||||
| chr4:73595711 | ATATT | A | 68 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(65): Show |
96 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.145-2122_145-2119d others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595711 | |||||||
| chr4:73595729 | C | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.145-2136G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595729 | |||||||
| chr4:73595791 | A | T | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.145-2198T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595791 | |||||||
| chr4:73595818 | G | A | 2 | a0001c0001t0019g0113 a0001c0001t0029g0138 |
2 | HG02004.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.145-2225C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595818 | |||||||
| chr4:73595927 | G | A | 1 | a0001c0001t0025g0242 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.145-2334C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595927 | |||||||
| chr4:73595993 | A | C | 1 | a0001c0001t0003g0148 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.145-2400T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595993 | |||||||
| chr4:73596053 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.145-2460G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73596053 | |||||||
| chr4:73596210 | A | AGATGACA others(315): Show |
1 | a0001c0001t0001g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.144+2429_144+2430i others(324): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73596210 | |||||||
| chr4:73596298 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.144+2342A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73596298 | |||||||
| chr4:73596550 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
206 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.144+2090G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73596550 | |||||||
| chr4:73596694 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.144+1946C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73596694 | |||||||
| chr4:73596902 | G | A | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.144+1738C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73596902 | |||||||
| chr4:73597191 | C | T | 1 | a0001c0001t0003g0190 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.144+1449G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597191 | |||||||
| chr4:73597221 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.144+1419G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597221 | |||||||
| chr4:73597362 | T | G | 4 | a0001c0001t0001g0218 a0001c0001t0001g0224 a0001c0001t0018g0184 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+1278A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597362 | |||||||
| chr4:73597392 | T | C | 1 | a0002c0002t0005g0111 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.144+1248A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597392 | |||||||
| chr4:73597667 | C | A | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.144+973G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597667 | |||||||
| chr4:73597866 | T | C | 1 | a0001c0001t0003g0171 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.144+774A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597866 | |||||||
| chr4:73597880 | C | T | 19 | a0001c0001t0007g0023 a0001c0001t0007g0100 a0001c0001t0019g0113 others(16): Show |
25 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.144+760G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597880 | |||||||
| chr4:73597883 | T | A | 7 | a0001c0001t0003g0031 a0001c0001t0003g0146 a0001c0001t0003g0157 others(4): Show |
8 | HG00408.hp1 NA18974.hp1 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.144+757A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597883 | |||||||
| chr4:73598057 | AACC | A | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.144+580_144+582del others(3): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598057 | |||||||
| chr4:73598068 | C | T | 68 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(65): Show |
96 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.144+572G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598068 | |||||||
| chr4:73598405 | C | A | 5 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0053 others(2): Show |
5 | HG02258.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+235G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598405 | |||||||
| chr4:73598405 | C | T | 4 | a0001c0001t0001g0218 a0001c0001t0001g0224 a0001c0001t0018g0184 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+235G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598405 | |||||||
| chr4:73598423 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.144+217A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598423 | |||||||
| chr4:73598568 | T | TTG | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
299 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.144+70_144+71dupCA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598568 | |||||||
| chr4:73598568 | T | TTGTG | 14 | a0002c0002t0002g0029 a0002c0002t0002g0179 a0002c0002t0005g0024 others(11): Show |
19 | HG01123.hp1 HG01433.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.144+68_144+71dupCA others(2): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598568 | |||||||
| chr4:73598568 | T | TTGTGTG | 4 | a0001c0001t0007g0023 a0001c0001t0007g0100 a0001c0001t0019g0113 others(1): Show |
5 | HG01070.hp2 HG01071.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.144+66_144+71dupCA others(4): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598568 | |||||||
| chr4:73598585 | T | C | 5 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0053 others(2): Show |
5 | HG02258.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+55A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598585 | |||||||
| chr4:73598726 | TA | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.66-9delT | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73598726 | |||||||
| chr4:73598839 | T | C | 1 | a0002c0002t0002g0022 | 2 | HG01099.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.66-121A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73598839 | |||||||
| chr4:73599210 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.66-492C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73599210 | |||||||
| chr4:73599278 | C | T | 18 | a0002c0002t0004g0007 a0002c0002t0004g0017 a0002c0002t0004g0048 others(15): Show |
24 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.66-560G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73599278 | |||||||
| chr4:73599369 | C | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.66-651G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73599369 | |||||||
| chr4:73599754 | C | A | 1 | a0001c0001t0001g0039 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.66-1036G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73599754 | |||||||
| chr4:73599906 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.66-1188A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73599906 | |||||||
| chr4:73600106 | C | CTTCTCCC others(12): Show |
1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.66-1407_66-1389dup others(19): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600106 | |||||||
| chr4:73600160 | A | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.66-1442T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600160 | |||||||
| chr4:73600176 | C | T | 1 | a0001c0001t0003g0167 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.66-1458G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600176 | |||||||
| chr4:73600317 | C | T | 1 | a0001c0001t0018g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.66-1599G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600317 | |||||||
| chr4:73600415 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(124): Show |
165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.66-1697A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600415 | |||||||
| chr4:73600499 | G | A | 1 | a0001c0001t0001g0027 | 2 | NA19010.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.66-1781C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600499 | |||||||
| chr4:73600568 | C | G | 2 | a0001c0007t0014g0143 a0001c0007t0014g0144 |
2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.66-1850G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600568 | |||||||
| chr4:73600609 | T | C | 4 | a0002c0002t0001g0092 a0002c0002t0009g0081 a0002c0005t0009g0073 others(1): Show |
4 | HG02148.hp2 HG02273.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.66-1891A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600609 | |||||||
| chr4:73600692 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(124): Show |
165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.66-1974C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600692 | |||||||
| chr4:73600702 | A | T | 36 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(33): Show |
52 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.66-1984T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600702 | |||||||
| chr4:73600718 | C | G | 1 | a0002c0002t0005g0106 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.66-2000G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600718 | |||||||
| chr4:73600727 | T | TA | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.66-2010dupT | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600727 | |||||||
| chr4:73600803 | G | A | 1 | a0001c0001t0003g0156 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.66-2085C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600803 | |||||||
| chr4:73600863 | A | G | 2 | a0001c0007t0014g0143 a0001c0007t0014g0144 |
2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.66-2145T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600863 | |||||||
| chr4:73600918 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.66-2200C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600918 | |||||||
| chr4:73600925 | T | A | 1 | a0001c0001t0018g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.66-2207A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600925 | |||||||
| chr4:73600941 | C | T | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.66-2223G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600941 | |||||||
| chr4:73600999 | T | C | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.66-2281A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600999 | |||||||
| chr4:73601202 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.66-2484T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73601202 | |||||||
| chr4:73601548 | A | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0153 others(6): Show |
12 | HG01358.hp1 HG01496.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.66-2830T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73601548 | |||||||
| chr4:73601628 | T | C | 1 | a0001c0001t0003g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.66-2910A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73601628 | |||||||
| chr4:73601689 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.66-2971G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73601689 | |||||||
| chr4:73602101 | A | G | 1 | a0001c0001t0018g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.66-3383T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73602101 | |||||||
| chr4:73602204 | C | T | 11 | a0002c0002t0005g0024 a0002c0002t0005g0043 a0002c0002t0005g0106 others(8): Show |
15 | HG02027.hp1 HG02056.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.66-3486G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73602204 | |||||||
| chr4:73602569 | A | G | 1 | a0002c0002t0002g0076 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.66-3851T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73602569 | |||||||
| chr4:73602590 | C | CTAAG | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.66-3873_66-3872ins others(4): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73602590 | |||||||
| chr4:73602782 | C | T | 3 | a0001c0001t0003g0152 a0001c0001t0003g0160 a0001c0001t0017g0161 |
3 | HG00639.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.66-4064G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73602782 | |||||||
| chr4:73602811 | A | G | 4 | a0002c0002t0006g0018 a0002c0002t0006g0051 a0002c0002t0006g0052 others(1): Show |
5 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.66-4093T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73602811 | |||||||
| chr4:73603092 | G | GAAGA | 11 | a0002c0002t0005g0024 a0002c0002t0005g0043 a0002c0002t0005g0106 others(8): Show |
15 | HG02027.hp1 HG02056.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.66-4378_66-4375dup others(4): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73603092 | |||||||
| chr4:73603266 | G | A | 1 | a0001c0001t0003g0173 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.66-4548C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73603266 | |||||||
| chr4:73603584 | C | T | 2 | a0001c0001t0019g0113 a0001c0001t0029g0138 |
2 | HG02004.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.66-4866G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73603584 | |||||||
| chr4:73603870 | A | T | 1 | a0002c0002t0027g0059 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.66-5152T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73603870 | |||||||
| chr4:73603936 | T | C | 2 | a0001c0001t0003g0146 a0001c0001t0003g0182 |
2 | NA18983.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.66-5218A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73603936 | |||||||
| chr4:73604240 | C | A | 1 | a0001c0001t0003g0157 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.66-5522G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604240 | |||||||
| chr4:73604241 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.66-5523C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604241 | |||||||
| chr4:73604276 | C | T | 1 | a0002c0002t0002g0088 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.66-5558G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604276 | |||||||
| chr4:73604288 | C | T | 1 | a0001c0001t0018g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.66-5570G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604288 | |||||||
| chr4:73604461 | G | A | 4 | a0002c0002t0001g0092 a0002c0002t0009g0081 a0002c0005t0009g0073 others(1): Show |
4 | HG02148.hp2 HG02273.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.66-5743C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604461 | |||||||
| chr4:73604468 | T | C | 1 | a0001c0001t0003g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.66-5750A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604468 | |||||||
| chr4:73604474 | A | AAAAAC | 9 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0163 others(6): Show |
11 | HG01243.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.66-5761_66-5757dup others(5): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604474 | |||||||
| chr4:73604490 | A | C | 4 | a0002c0002t0006g0018 a0002c0002t0006g0051 a0002c0002t0006g0052 others(1): Show |
5 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.66-5772T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604490 | |||||||
| chr4:73604864 | C | A | 1 | a0002c0002t0027g0059 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.66-6146G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604864 | |||||||
| chr4:73604884 | C | CT | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(101): Show |
152 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.66-6167dupA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604884 | |||||||
| chr4:73604920 | G | A | 1 | a0002c0002t0002g0093 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.66-6202C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604920 | |||||||
| chr4:73605215 | G | A | 1 | a0002c0002t0002g0086 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.66-6497C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605215 | |||||||
| chr4:73605260 | C | T | 7 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(4): Show |
7 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.65+6471G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605260 | |||||||
| chr4:73605608 | T | G | 2 | a0002c0002t0002g0071 a0002c0002t0002g0072 |
2 | HG02735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.65+6123A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605608 | |||||||
| chr4:73605614 | G | A | 1 | a0002c0002t0004g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.65+6117C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605614 | |||||||
| chr4:73605615 | A | C | 1 | a0002c0002t0004g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.65+6116T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605615 | |||||||
| chr4:73605881 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(30): Show |
49 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.65+5850T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605881 | |||||||
| chr4:73605998 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.65+5733G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605998 | |||||||
| chr4:73606021 | C | G | 4 | a0001c0001t0002g0045 a0001c0001t0002g0053 a0001c0001t0002g0054 others(1): Show |
4 | HG02258.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.65+5710G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606021 | |||||||
| chr4:73606227 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(124): Show |
165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.65+5504A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606227 | |||||||
| chr4:73606280 | C | T | 2 | a0001c0001t0002g0044 a0001c0001t0002g0047 |
2 | HG00323.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.65+5451G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606280 | |||||||
| chr4:73606364 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(124): Show |
165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.65+5367G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606364 | |||||||
| chr4:73606397 | A | G | 1 | a0001c0001t0003g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.65+5334T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606397 | |||||||
| chr4:73606434 | C | G | 3 | a0002c0002t0002g0087 a0002c0002t0002g0094 a0002c0002t0002g0096 |
3 | HG02083.hp1 NA18985.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.65+5297G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606434 | |||||||
| chr4:73606496 | C | A | 1 | a0001c0001t0001g0135 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.65+5235G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606496 | |||||||
| chr4:73606551 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(122): Show |
163 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.65+5180C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606551 | |||||||
| chr4:73606639 | GT | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(105): Show |
156 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.65+5091delA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606639 | |||||||
| chr4:73606639 | GTT | G | 7 | a0001c0001t0002g0044 a0001c0001t0002g0047 a0001c0001t0003g0131 others(4): Show |
8 | HG00323.hp2 HG01069.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.65+5090_65+5091del others(2): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606639 | |||||||
| chr4:73606639 | GTTTTTT | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(124): Show |
165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.65+5086_65+5091del others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606639 | |||||||
| chr4:73607066 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.65+4665A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607066 | |||||||
| chr4:73607089 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65+4642A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607089 | |||||||
| chr4:73607119 | G | C | 1 | a0001c0001t0003g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.65+4612C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607119 | |||||||
| chr4:73607159 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(124): Show |
165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.65+4572T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607159 | |||||||
| chr4:73607179 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(124): Show |
165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.65+4552T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607179 | |||||||
| chr4:73607197 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65+4534A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607197 | |||||||
| chr4:73607419 | C | T | 14 | a0001c0001t0007g0023 a0001c0001t0007g0100 a0002c0002t0005g0024 others(11): Show |
19 | HG01070.hp2 HG01071.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.65+4312G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607419 | |||||||
| chr4:73607598 | G | A | 11 | a0002c0002t0005g0024 a0002c0002t0005g0043 a0002c0002t0005g0106 others(8): Show |
15 | HG02027.hp1 HG02056.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.65+4133C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607598 | |||||||
| chr4:73607722 | T | C | 1 | a0002c0002t0004g0063 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65+4009A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607722 | |||||||
| chr4:73607729 | TA | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.65+4001delT | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607729 | |||||||
| chr4:73607734 | AACCCTCC | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.65+3990_65+3996del others(7): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607734 | |||||||
| chr4:73607740 | C | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3991G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607740 | |||||||
| chr4:73607741 | C | T | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3990G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607741 | |||||||
| chr4:73607742 | A | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.65+3989T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607742 | |||||||
| chr4:73607753 | C | T | 1 | a0001c0001t0003g0148 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.65+3978G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607753 | |||||||
| chr4:73607757 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.65+3974T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607757 | |||||||
| chr4:73607766 | T | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3965A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607766 | |||||||
| chr4:73607780 | T | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3951A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607780 | |||||||
| chr4:73607784 | A | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3947T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607784 | |||||||
| chr4:73607785 | T | A | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3946A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607785 | |||||||
| chr4:73607789 | A | T | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3942T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607789 | |||||||
| chr4:73607793 | T | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3938A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607793 | |||||||
| chr4:73607795 | C | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3936G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607795 | |||||||
| chr4:73607801 | A | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3930T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607801 | |||||||
| chr4:73607805 | G | T | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3926C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607805 | |||||||
| chr4:73607811 | C | T | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3920G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607811 | |||||||
| chr4:73607813 | ACCTCCTC others(22): Show |
A | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3889_65+3917del others(29): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607813 | |||||||
| chr4:73607814 | C | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.65+3917G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607814 | |||||||
| chr4:73607843 | C | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3888G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607843 | |||||||
| chr4:73607845 | T | A | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3886A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607845 | |||||||
| chr4:73607846 | A | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3885T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607846 | |||||||
| chr4:73607848 | C | A | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3883G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607848 | |||||||
| chr4:73607849 | C | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3882G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607849 | |||||||
| chr4:73607850 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.65+3881G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607850 | |||||||
| chr4:73607858 | T | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3873A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607858 | |||||||
| chr4:73607861 | T | C | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3870A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607861 | |||||||
| chr4:73607862 | C | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3869G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607862 | |||||||
| chr4:73607863 | T | A | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3868A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607863 | |||||||
| chr4:73607864 | T | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3867A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607864 | |||||||
| chr4:73607866 | T | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3865A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607866 | |||||||
| chr4:73607868 | C | A | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3863G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607868 | |||||||
| chr4:73607869 | C | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3862G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607869 | |||||||
| chr4:73607879 | C | T | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3852G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607879 | |||||||
| chr4:73607880 | T | C | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3851A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607880 | |||||||
| chr4:73607889 | ACCCCTCC others(61): Show |
A | 1 | a0002c0002t0002g0005 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.65+3774_65+3841del others(68): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607889 | |||||||
| chr4:73607895 | C | A | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3836G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607895 | |||||||
| chr4:73607899 | T | A | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3832A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607899 | |||||||
| chr4:73607902 | C | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3829G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607902 | |||||||
| chr4:73607904 | T | C | 3 | a0001c0001t0003g0146 a0001c0001t0003g0158 a0001c0001t0003g0175 |
3 | NA18960.hp2 NA18983.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.65+3827A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607904 | |||||||
| chr4:73607905 | C | T | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3826G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607905 | |||||||
| chr4:73607907 | T | G | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3824A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607907 | |||||||
| chr4:73607974 | CTCTCTAC others(6): Show |
C | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3744_65+3756del others(13): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607974 | |||||||
| chr4:73607987 | TTCCTCTC others(8): Show |
T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
332 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.65+3729_65+3743del others(15): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607987 | |||||||
| chr4:73607994 | C | A | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3737G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607994 | |||||||
| chr4:73607996 | C | T | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3735G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607996 | |||||||
| chr4:73608015 | C | T | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3716G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608015 | |||||||
| chr4:73608016 | T | C | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3715A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608016 | |||||||
| chr4:73608017 | C | T | 1 | a0001c0001t0003g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3714G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608017 | |||||||
| chr4:73608143 | G | A | 45 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0027 others(42): Show |
54 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.65+3588C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608143 | |||||||
| chr4:73608144 | C | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.65+3587G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608144 | |||||||
| chr4:73608409 | A | G | 2 | a0001c0001t0019g0113 a0001c0001t0029g0138 |
2 | HG02004.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.65+3322T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608409 | |||||||
| chr4:73608547 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(30): Show |
49 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.65+3184T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608547 | |||||||
| chr4:73608760 | T | C | 1 | a0002c0002t0004g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65+2971A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608760 | |||||||
| chr4:73608780 | G | A | 1 | a0002c0002t0002g0066 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.65+2951C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608780 | |||||||
| chr4:73608836 | T | C | 11 | a0002c0002t0005g0024 a0002c0002t0005g0043 a0002c0002t0005g0106 others(8): Show |
15 | HG02027.hp1 HG02056.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.65+2895A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608836 | |||||||
| chr4:73609152 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.65+2579T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609152 | |||||||
| chr4:73609377 | A | T | 1 | a0001c0001t0002g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.65+2354T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609377 | |||||||
| chr4:73609534 | A | T | 2 | a0001c0001t0019g0113 a0001c0001t0029g0138 |
2 | HG02004.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.65+2197T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609534 | |||||||
| chr4:73609542 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.65+2189G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609542 | |||||||
| chr4:73609703 | G | A | 1 | a0002c0002t0004g0061 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.65+2028C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609703 | |||||||
| chr4:73609752 | C | T | 2 | a0001c0001t0019g0113 a0001c0001t0029g0138 |
2 | HG02004.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.65+1979G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609752 | |||||||
| chr4:73609792 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0239 |
2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.65+1939G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609792 | |||||||
| chr4:73610077 | C | T | 43 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(40): Show |
65 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.65+1654G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610077 | |||||||
| chr4:73610078 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.65+1653C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610078 | |||||||
| chr4:73610149 | C | A | 1 | a0001c0001t0003g0159 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.65+1582G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610149 | |||||||
| chr4:73610203 | C | A | 1 | a0002c0002t0010g0025 | 2 | HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.65+1528G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610203 | |||||||
| chr4:73610689 | C | T | 1 | a0001c0001t0003g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.65+1042G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610689 | |||||||
| chr4:73610809 | T | C | 1 | a0001c0001t0028g0238 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.65+922A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610809 | |||||||
| chr4:73610948 | C | T | 1 | a0001c0001t0003g0190 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.65+783G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610948 | |||||||
| chr4:73610986 | C | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.65+745G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610986 | |||||||
| chr4:73611110 | T | A | 1 | a0001c0001t0002g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.65+621A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611110 | |||||||
| chr4:73611165 | C | T | 1 | a0001c0001t0001g0027 | 2 | NA19010.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.65+566G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611165 | |||||||
| chr4:73611207 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(125): Show |
167 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.65+524T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611207 | |||||||
| chr4:73611276 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.65+455G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611276 | |||||||
| chr4:73611306 | A | G | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.65+425T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611306 | |||||||
| chr4:73611418 | T | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(123): Show |
164 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.65+313A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611418 | |||||||
| chr4:73611475 | T | G | 17 | a0002c0002t0004g0007 a0002c0002t0004g0017 a0002c0002t0004g0048 others(14): Show |
23 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.65+256A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611475 | |||||||
| chr4:73611663 | A | C | 1 | a0002c0002t0002g0084 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.65+68T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611663 | |||||||
| chr4:73611703 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | NA18964.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.65+28G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611703 | |||||||
| chr4:73612100 | T | G | 2 | a0001c0001t0019g0113 a0001c0001t0029g0138 |
2 | HG02004.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-34-271A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612100 | |||||||
| chr4:73612122 | G | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-34-293C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612122 | |||||||
| chr4:73612184 | G | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-34-355C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612184 | |||||||
| chr4:73612358 | A | G | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-34-529T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612358 | |||||||
| chr4:73612377 | C | A | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-34-548G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612377 | |||||||
| chr4:73612483 | T | TC | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(140): Show |
202 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.-34-655_-34-654ins others(1): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612483 | |||||||
| chr4:73612484 | T | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(94): Show |
125 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-34-655A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612484 | |||||||
| chr4:73612492 | TTTTAAAA | T | 45 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0027 others(42): Show |
54 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-34-670_-34-664del others(7): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612492 | |||||||
| chr4:73612496 | A | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
280 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.-34-667T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612496 | |||||||
| chr4:73612497 | A | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
279 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.-34-668T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612497 | |||||||
| chr4:73612498 | A | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
279 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.-34-669T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612498 | |||||||
| chr4:73612499 | A | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
248 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.-34-670T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612499 | |||||||
| chr4:73612634 | A | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0241 |
5 | HG01257.hp2 HG02735.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-805T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612634 | |||||||
| chr4:73612685 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(31): Show |
50 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-34-856T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612685 | |||||||
| chr4:73612831 | A | C | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-34-1002T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612831 | |||||||
| chr4:73612908 | C | G | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-34-1079G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612908 | |||||||
| chr4:73613004 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-34-1175C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73613004 | |||||||
| chr4:73613170 | T | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-34-1341A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73613170 | |||||||
| chr4:73613464 | T | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.-34-1635A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73613464 | |||||||
| chr4:73613532 | G | A | 5 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0053 others(2): Show |
5 | HG02258.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-1703C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73613532 | |||||||
| chr4:73613663 | C | A | 1 | a0001c0001t0003g0177 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-34-1834G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73613663 | |||||||
| chr4:73613997 | C | T | 1 | a0002c0002t0002g0095 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-34-2168G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73613997 | |||||||
| chr4:73614237 | T | C | 1 | a0001c0001t0032g0247 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-34-2408A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73614237 | |||||||
| chr4:73614302 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-34-2473G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73614302 | |||||||
| chr4:73614725 | G | A | 1 | a0002c0002t0002g0082 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-34-2896C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73614725 | |||||||
| chr4:73614783 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-34-2954G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73614783 | |||||||
| chr4:73614817 | A | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-34-2988T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73614817 | |||||||
| chr4:73614997 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-34-3168A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73614997 | |||||||
| chr4:73615066 | C | A | 1 | a0001c0001t0002g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-34-3237G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615066 | |||||||
| chr4:73615117 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-34-3288A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615117 | |||||||
| chr4:73615125 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-34-3296C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615125 | |||||||
| chr4:73615178 | C | CAA | 7 | a0001c0001t0001g0036 a0001c0001t0001g0201 a0001c0001t0007g0100 others(4): Show |
8 | HG00609.hp1 HG02135.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34-3351_-34-3350d others(4): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615178 | |||||||
| chr4:73615178 | C | CAAA | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
240 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.-34-3352_-34-3350d others(5): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615178 | |||||||
| chr4:73615178 | C | CAAAA | 57 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0137 others(54): Show |
82 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.-34-3353_-34-3350d others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615178 | |||||||
| chr4:73615198 | G | A | 2 | a0002c0002t0002g0071 a0002c0002t0002g0072 |
2 | HG02735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-34-3369C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615198 | |||||||
| chr4:73615242 | A | G | 1 | a0002c0002t0004g0058 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-34-3413T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615242 | |||||||
| chr4:73615358 | G | GTAGA | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.-34-3533_-34-3530d others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615358 | |||||||
| chr4:73615366 | A | C | 1 | a0001c0001t0032g0247 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-34-3537T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615366 | |||||||
| chr4:73615430 | C | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-34-3601G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615430 | |||||||
| chr4:73615509 | T | G | 1 | a0001c0001t0001g0132 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-34-3680A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615509 | |||||||
| chr4:73615560 | C | A | 13 | a0001c0001t0007g0023 a0001c0001t0007g0100 a0002c0002t0005g0024 others(10): Show |
18 | HG01070.hp2 HG01071.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-34-3731G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615560 | |||||||
| chr4:73615562 | A | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(31): Show |
50 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-34-3733T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615562 | |||||||
| chr4:73615737 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-34-3908T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615737 | |||||||
| chr4:73615790 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-34-3961C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615790 | |||||||
| chr4:73616096 | C | T | 2 | a0001c0001t0002g0044 a0001c0001t0002g0047 |
2 | HG00323.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-35+4192G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616096 | |||||||
| chr4:73616221 | A | ATATC | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(21): Show |
25 | HG00639.hp1 HG00741.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.-35+4063_-35+4066d others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616221 | |||||||
| chr4:73616221 | A | ATATCTAT others(1): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0031g0141 |
4 | HG03195.hp2 HG03927.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+4059_-35+4066d others(10): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616221 | |||||||
| chr4:73616221 | ATATC | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(67): Show |
81 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+4063_-35+4066d others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616221 | |||||||
| chr4:73616221 | ATATCTAT others(1): Show |
A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0034 others(10): Show |
16 | HG00733.hp1 HG02071.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.-35+4059_-35+4066d others(10): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616221 | |||||||
| chr4:73616221 | ATATCTAT others(5): Show |
A | 1 | a0001c0001t0003g0173 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-35+4055_-35+4066d others(14): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616221 | |||||||
| chr4:73616247 | A | G | 1 | a0002c0002t0004g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-35+4041T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616247 | |||||||
| chr4:73616600 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-35+3688A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616600 | |||||||
| chr4:73616668 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(31): Show |
50 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-35+3620G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616668 | |||||||
| chr4:73616679 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-35+3609C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616679 | |||||||
| chr4:73616952 | C | G | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-35+3336G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616952 | |||||||
| chr4:73616989 | T | A | 1 | a0002c0002t0002g0084 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-35+3299A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616989 | |||||||
| chr4:73617337 | C | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-35+2951G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73617337 | |||||||
| chr4:73617360 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(70): Show |
102 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-35+2928G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73617360 | |||||||
| chr4:73617793 | A | C | 1 | a0001c0001t0003g0150 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-35+2495T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73617793 | |||||||
| chr4:73617853 | T | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-35+2435A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73617853 | |||||||
| chr4:73617891 | C | A | 3 | a0002c0002t0002g0029 a0002c0002t0002g0162 a0002c0002t0002g0179 |
4 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+2397G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73617891 | |||||||
| chr4:73617937 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-35+2351G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73617937 | |||||||
| chr4:73618022 | T | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(31): Show |
50 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-35+2266A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618022 | |||||||
| chr4:73618252 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-35+2036C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618252 | |||||||
| chr4:73618300 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-35+1988C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618300 | |||||||
| chr4:73618301 | T | TCTATCTA others(14): Show |
1 | a0001c0001t0001g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-35+1986_-35+1987i others(23): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | |||||||
| chr4:73618301 | T | TTATC | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-35+1983_-35+1986d others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | |||||||
| chr4:73618301 | T | TTATCTAT others(1): Show |
16 | a0001c0001t0001g0033 a0001c0001t0001g0187 a0001c0001t0001g0188 others(13): Show |
21 | HG01243.hp1 HG02027.hp1 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.-35+1979_-35+1986d others(10): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | |||||||
| chr4:73618301 | T | TTATCTAT others(5): Show |
1 | a0002c0002t0002g0066 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-35+1975_-35+1986d others(14): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | |||||||
| chr4:73618301 | T | TTATCTAT others(9): Show |
36 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0027 others(33): Show |
49 | HG00544.hp2 HG01070.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-35+1971_-35+1986d others(18): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | |||||||
| chr4:73618301 | T | TTATCTAT others(13): Show |
85 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(82): Show |
119 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-35+1967_-35+1986d others(22): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | |||||||
| chr4:73618301 | T | TTATCTAT others(17): Show |
89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(86): Show |
122 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.-35+1986_-35+1987i others(26): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | |||||||
| chr4:73618301 | T | TTATCTAT others(21): Show |
16 | a0001c0001t0001g0041 a0001c0001t0001g0133 a0001c0001t0001g0134 others(13): Show |
17 | HG00438.hp1 HG00741.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.-35+1986_-35+1987i others(30): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | |||||||
| chr4:73618301 | T | TTATCTAT others(25): Show |
2 | a0001c0001t0025g0242 a0002c0002t0002g0098 |
2 | HG01952.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-35+1986_-35+1987i others(34): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | |||||||
| chr4:73618327 | A | G | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-35+1961T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618327 | |||||||
| chr4:73618412 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0186 a0001c0001t0021g0185 |
4 | HG02572.hp2 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+1876G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618412 | |||||||
| chr4:73618629 | C | T | 1 | a0001c0001t0018g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-35+1659G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618629 | |||||||
| chr4:73618927 | C | G | 1 | a0001c0001t0029g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-35+1361G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618927 | |||||||
| chr4:73618971 | T | C | 4 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | NA18964.hp2 NA18971.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+1317A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618971 | |||||||
| chr4:73618982 | A | C | 2 | a0001c0007t0014g0143 a0001c0007t0014g0144 |
2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-35+1306T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618982 | |||||||
| chr4:73619066 | C | A | 1 | a0001c0001t0029g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-35+1222G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619066 | |||||||
| chr4:73619090 | A | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-35+1198T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619090 | |||||||
| chr4:73619108 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-35+1180A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619108 | |||||||
| chr4:73619131 | A | G | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-35+1157T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619131 | |||||||
| chr4:73619170 | C | T | 1 | a0001c0001t0004g0183 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-35+1118G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619170 | |||||||
| chr4:73619255 | T | G | 1 | a0001c0001t0003g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35+1033A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619255 | |||||||
| chr4:73619408 | G | A | 3 | a0001c0001t0015g0140 a0001c0001t0015g0142 a0001c0001t0031g0141 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-35+880C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619408 | |||||||
| chr4:73619773 | G | A | 2 | a0001c0007t0014g0143 a0001c0007t0014g0144 |
2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-35+515C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619773 | |||||||
| chr4:73619790 | A | AT | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0027 others(48): Show |
60 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.-35+497dupA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619790 | |||||||
| chr4:73619792 | T | G | 2 | a0001c0007t0014g0143 a0001c0007t0014g0144 |
2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-35+496A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619792 | |||||||
| chr4:73619867 | T | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-35+421A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619867 | |||||||
| chr4:73619947 | G | A | 43 | a0002c0002t0001g0077 a0002c0002t0001g0092 a0002c0002t0002g0005 others(40): Show |
65 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.-35+341C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619947 | |||||||
| chr4:73620059 | C | T | 2 | a0001c0001t0007g0023 a0001c0001t0007g0100 |
3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-35+229G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73620059 | |||||||
| chr4:73620151 | C | T | 69 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(66): Show |
97 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.-35+137G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73620151 | |||||||
| chr4:73620179 | C | A | 1 | a0001c0001t0001g0145 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-35+109G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73620179 | |||||||
| chr4:73620197 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-35+91A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73620197 | |||||||
| chr4:73620268 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(122): Show |
163 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.-35+20A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73620268 | |||||||
| chr4:73620278 | C | T | 1 | a0001c0001t0003g0042 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-35+10G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73620278 |