Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9182 |
| ensemblid | ENSG00000198774.5 |
| hgncid | 15739 |
| symbol | RASSF9 |
| name | Ras association domain family member 9 |
| refseq_nuc | NM_005447.4 |
| refseq_prot | NP_005438.2 |
| ensembl_nuc | ENST00000361228.5 |
| ensembl_prot | ENSP00000354884.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 85800703 |
| end | 85836409 |
| strand | - |
| ver | v1.2 |
| region | chr12:85800703-85836409 |
| region5000 | chr12:85795703-85841409 |
| regionname0 | RASSF9_chr12_85800703_85836409 |
| regionname5000 | RASSF9_chr12_85795703_85841409 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 435 | 299 | 79 | 58 | 106 | 14 | 40 | 72 | RASSF9_chr12_85795703_85841409 | RASSF9 | MAPFG others(430): Show |
chr12 | 85795703 | 85841409 |
| a0002 | 0/0 | 435 | 38 | 4 | 14 | 18 | 2 | 0 | 14 | RASSF9_chr12_85795703_85841409 | RASSF9 | MAPFG others(430): Show |
chr12 | 85795703 | 85841409 |
| a0003 | 0/0 | 435 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | MAPFG others(430): Show |
chr12 | 85795703 | 85841409 |
| a0004 | 0/0 | 435 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | MAPFG others(430): Show |
chr12 | 85795703 | 85841409 |
| a0005 | 0/0 | 435 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | MAPFG others(430): Show |
chr12 | 85795703 | 85841409 |
| a0006 | 0/0 | 435 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | MAPFG others(430): Show |
chr12 | 85795703 | 85841409 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1305 | 289 | 73 | 58 | 102 | 14 | 40 | RASSF9_chr12_85795703_85841409 | RASSF9 | ATGGC others(1300): Show |
chr12 | 85795703 | 85841409 | ||
| a0001c0003 | 0/0 | 1305 | 5 | 5 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ATGGC others(1300): Show |
chr12 | 85795703 | 85841409 | ||
| a0001c0004 | 0/0 | 1305 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ATGGC others(1300): Show |
chr12 | 85795703 | 85841409 | ||
| a0001c0009 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ATGGC others(1300): Show |
chr12 | 85795703 | 85841409 | ||
| a0002c0002 | 0/0 | 1305 | 38 | 4 | 14 | 18 | 2 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ATGGC others(1300): Show |
chr12 | 85795703 | 85841409 | ||
| a0003c0005 | 0/0 | 1305 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ATGGC others(1300): Show |
chr12 | 85795703 | 85841409 | ||
| a0004c0006 | 0/0 | 1305 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ATGGC others(1300): Show |
chr12 | 85795703 | 85841409 | ||
| a0005c0007 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ATGGC others(1300): Show |
chr12 | 85795703 | 85841409 | ||
| a0006c0008 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ATGGC others(1300): Show |
chr12 | 85795703 | 85841409 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5515 | 191 | 33 | 40 | 86 | 6 | 25 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0002 | 0/1 | 5515 | 23 | 3 | 13 | 0 | 3 | 3 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0005 | 0/0 | 5516 | 9 | 8 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5511): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0006 | 0/0 | 5515 | 8 | 0 | 0 | 8 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0007 | 0/0 | 5517 | 6 | 3 | 0 | 0 | 0 | 3 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5512): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0008 | 0/0 | 5515 | 6 | 6 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0009 | 0/0 | 5515 | 4 | 0 | 2 | 0 | 2 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0011 | 0/0 | 5515 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0015 | 0/0 | 5514 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5509): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0016 | 0/0 | 5515 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0017 | 0/0 | 5515 | 3 | 0 | 0 | 0 | 1 | 2 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0018 | 0/0 | 5515 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0020 | 0/0 | 5515 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0021 | 0/0 | 5515 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0022 | 0/0 | 5515 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0024 | 0/0 | 5515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0025 | 0/0 | 5515 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0026 | 0/0 | 5517 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5512): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0027 | 0/0 | 5515 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0029 | 0/0 | 5515 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0030 | 0/0 | 5515 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0031 | 0/0 | 5515 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0032 | 0/0 | 5515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0033 | 0/0 | 5515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0034 | 0/0 | 5515 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0035 | 0/0 | 5515 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0036 | 0/0 | 5515 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0037 | 0/0 | 5515 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0038 | 0/0 | 5515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0039 | 0/0 | 5458 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5453): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0040 | 0/0 | 5515 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0041 | 0/0 | 5515 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0042 | 0/0 | 5515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0043 | 0/0 | 5515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0044 | 0/0 | 5515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0045 | 0/0 | 5515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0046 | 0/0 | 5516 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5511): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0047 | 0/0 | 5515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0001t0048 | 0/0 | 5515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0003t0012 | 0/0 | 5516 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5511): Show |
chr12 | 85795703 | 85841409 |
| a0001c0003t0019 | 0/0 | 5516 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5511): Show |
chr12 | 85795703 | 85841409 |
| a0001c0004t0010 | 0/0 | 5515 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0001c0009t0013 | 0/0 | 5517 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5512): Show |
chr12 | 85795703 | 85841409 |
| a0002c0002t0003 | 0/0 | 5515 | 22 | 1 | 14 | 5 | 2 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0002c0002t0004 | 0/0 | 5515 | 13 | 0 | 0 | 13 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0002c0002t0014 | 0/0 | 5515 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0003c0005t0013 | 0/0 | 5517 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5512): Show |
chr12 | 85795703 | 85841409 |
| a0003c0005t0028 | 0/0 | 5517 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5512): Show |
chr12 | 85795703 | 85841409 |
| a0004c0006t0001 | 0/0 | 5515 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0005c0007t0001 | 0/0 | 5515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| a0006c0008t0023 | 0/0 | 5515 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | ACAAC others(5510): Show |
chr12 | 85795703 | 85841409 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 0 | 7 | 3 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0002 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 4 | 1 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0008 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0015 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0016 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 7 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0002g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0005g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0006g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0006g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0007g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0007g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0009g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0009g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0009g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0011g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0011g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0015g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0015g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0016g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0016g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0017g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0017g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0018g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0018g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0020g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0021g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0022g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0024g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0025g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0026g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0027g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0029g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0030g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0031g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0032g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0033g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0034g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0035g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0036g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0037g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0038g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0039g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0040g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0041g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0042g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0043g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0044g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0045g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0046g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0047g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0001t0048g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0003t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0003t0012g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0003t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0003t0019g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0004t0010g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0004t0010g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0004t0010g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0001c0009t0013g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0007 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0004g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0014g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0002c0002t0014g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0003c0005t0013g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0003c0005t0013g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0003c0005t0028g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0004c0006t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0004c0006t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0005c0007t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| a0006c0008t0023g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0069 | EUR | GBR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00099 | hp2 | a0001 | c0001 | t0017 | g0220 | EUR | GBR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00140 | hp1 | a0002 | c0002 | t0003 | g0007 | EUR | GBR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00280 | hp1 | a0001 | c0001 | t0027 | g0093 | EUR | FIN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00280 | hp2 | a0002 | c0002 | t0003 | g0057 | EUR | FIN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00408 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00438 | hp2 | a0002 | c0002 | t0004 | g0058 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00639 | hp1 | a0001 | c0001 | t0029 | g0227 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0243 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00642 | hp2 | a0002 | c0002 | t0003 | g0021 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00733 | hp2 | a0002 | c0002 | t0003 | g0022 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG00741 | hp2 | a0001 | c0001 | t0009 | g0230 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01081 | hp1 | a0001 | c0001 | t0036 | g0191 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0007 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01192 | hp1 | a0002 | c0002 | t0003 | g0050 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01243 | hp1 | a0002 | c0002 | t0003 | g0022 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0023 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01261 | hp2 | a0002 | c0002 | t0003 | g0054 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01358 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0229 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01515 | hp1 | a0001 | c0001 | t0009 | g0043 | EUR | IBS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0067 | EUR | IBS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01517 | hp1 | a0001 | c0001 | t0009 | g0043 | EUR | IBS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01884 | hp2 | a0001 | c0001 | t0042 | g0045 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01891 | hp1 | a0005 | c0007 | t0001 | g0154 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01891 | hp2 | a0002 | c0002 | t0003 | g0007 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01934 | hp2 | a0002 | c0002 | t0003 | g0052 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0051 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01981 | hp2 | a0002 | c0002 | t0003 | g0023 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02004 | hp1 | a0002 | c0002 | t0003 | g0055 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02027 | hp1 | a0001 | c0001 | t0037 | g0114 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02055 | hp1 | a0004 | c0006 | t0001 | g0147 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02055 | hp2 | a0003 | c0005 | t0013 | g0094 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02071 | hp1 | a0001 | c0001 | t0041 | g0196 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02071 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0205 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02145 | hp1 | a0001 | c0001 | t0038 | g0059 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02148 | hp1 | a0002 | c0002 | t0003 | g0021 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02257 | hp2 | a0001 | c0003 | t0012 | g0169 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02258 | hp1 | a0001 | c0001 | t0016 | g0026 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02280 | hp2 | a0002 | c0002 | t0014 | g0025 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02293 | hp2 | a0002 | c0002 | t0003 | g0056 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02602 | hp1 | a0001 | c0001 | t0007 | g0237 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0128 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0247 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02622 | hp2 | a0001 | c0001 | t0043 | g0073 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02630 | hp1 | a0003 | c0005 | t0028 | g0086 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02647 | hp2 | a0002 | c0002 | t0014 | g0025 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02683 | hp2 | a0001 | c0001 | t0040 | g0166 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02698 | hp1 | a0001 | c0001 | t0007 | g0103 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02698 | hp2 | a0001 | c0001 | t0020 | g0032 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0079 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0245 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0076 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02895 | hp2 | a0001 | c0003 | t0019 | g0027 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02897 | hp2 | a0001 | c0003 | t0019 | g0027 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02922 | hp1 | a0006 | c0008 | t0023 | g0153 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02922 | hp2 | a0001 | c0001 | t0048 | g0248 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02965 | hp2 | a0001 | c0001 | t0016 | g0087 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0246 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0148 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03041 | hp1 | a0001 | c0001 | t0046 | g0241 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03041 | hp2 | a0001 | c0001 | t0032 | g0142 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0020 | AFR | MSL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03098 | hp2 | a0001 | c0001 | t0016 | g0026 | AFR | MSL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03130 | hp1 | a0001 | c0001 | t0015 | g0072 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03130 | hp2 | a0001 | c0001 | t0015 | g0033 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0242 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0081 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03195 | hp1 | a0001 | c0001 | t0015 | g0033 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0240 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0020 | AFR | MSL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03209 | hp2 | a0001 | c0001 | t0011 | g0106 | AFR | MSL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0089 | AFR | MSL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03486 | hp2 | a0001 | c0009 | t0013 | g0092 | AFR | MSL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03491 | hp2 | a0001 | c0001 | t0017 | g0039 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03492 | hp1 | a0001 | c0001 | t0025 | g0065 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03492 | hp2 | a0001 | c0001 | t0017 | g0039 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03516 | hp1 | a0001 | c0003 | t0012 | g0173 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | ESN | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03540 | hp1 | a0001 | c0001 | t0045 | g0080 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03540 | hp2 | a0003 | c0005 | t0013 | g0085 | AFR | GWD | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03579 | hp1 | a0001 | c0003 | t0012 | g0175 | AFR | MSL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03654 | hp1 | a0001 | c0001 | t0020 | g0032 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03704 | hp2 | a0001 | c0001 | t0035 | g0180 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | BEB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG04115 | hp1 | a0001 | c0001 | t0026 | g0126 | SAS | STU | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG04228 | hp2 | a0001 | c0001 | t0021 | g0138 | SAS | STU | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18747 | hp2 | a0001 | c0001 | t0034 | g0223 | EAS | CHB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18939 | hp1 | a0002 | c0002 | t0004 | g0053 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18941 | hp1 | a0001 | c0001 | t0031 | g0202 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18942 | hp2 | a0001 | c0001 | t0006 | g0211 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18947 | hp1 | a0001 | c0004 | t0010 | g0129 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18947 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18966 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18968 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18971 | hp2 | a0001 | c0001 | t0018 | g0146 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18973 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18979 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18984 | hp2 | a0001 | c0004 | t0010 | g0030 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18990 | hp1 | a0002 | c0002 | t0003 | g0046 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18992 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18993 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18998 | hp1 | a0001 | c0004 | t0010 | g0125 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18998 | hp2 | a0001 | c0001 | t0030 | g0145 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18999 | hp2 | a0001 | c0001 | t0018 | g0152 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19007 | hp2 | a0001 | c0004 | t0010 | g0030 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19009 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19010 | hp1 | a0002 | c0002 | t0004 | g0187 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19030 | hp1 | a0001 | c0001 | t0047 | g0244 | AFR | LWK | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19082 | hp2 | a0002 | c0002 | t0004 | g0047 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19084 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19089 | hp1 | a0001 | c0001 | t0039 | g0204 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19090 | hp1 | a0002 | c0002 | t0004 | g0049 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19240 | hp1 | a0004 | c0006 | t0001 | g0141 | AFR | YRI | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0078 | AFR | YRI | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | TSI | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA20805 | hp1 | a0001 | c0001 | t0022 | g0232 | EUR | TSI | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | TSI | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | GIH | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | GIH | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02109 | hp2 | a0002 | c0002 | t0014 | g0074 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02559 | hp1 | a0001 | c0001 | t0044 | g0077 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0098 | AFR | MSL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG03471 | hp2 | a0001 | c0001 | t0033 | g0075 | AFR | MSL | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | USA | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | USA | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA18955 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | USA | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | USA | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| NA21309 | hp2 | a0001 | c0001 | t0024 | g0060 | AFR | LWK | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0068 | REF | REF | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0172 | REF | REF | RASSF9_chr12_85795703_85841409 | RASSF9 | chr12 | 85795703 | 85841409 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:85804757 | T | G | 1 | a0005 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1253A>C | p.Asn418Thr | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1461/5515 | 1253/1308 | 418/435 | chr12 | 85804757 | |||
| chr12:85804953 | T | G | 1 | a0004 | 2 | HG02055.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.1057A>C | p.Lys353Gln | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1265/5515 | 1057/1308 | 353/435 | chr12 | 85804953 | |||
| chr12:85804995 | T | C | 1 | a0006 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1015A>G | p.Ile339Val | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1223/5515 | 1015/1308 | 339/435 | chr12 | 85804995 | |||
| chr12:85805076 | T | C | 1 | a0003 | 3 | HG02055.hp2 HG02630.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.934A>G | p.Ser312Gly | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1142/5515 | 934/1308 | 312/435 | chr12 | 85805076 | |||
| chr12:85805157 | C | T | 1 | a0002 | 38 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(35): Show |
missense_variant | MODERATE | c.853G>A | p.Ala285Thr | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1061/5515 | 853/1308 | 285/435 | chr12 | 85805157 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:85804816 | A | G | 1 | a0002c0002 | 38 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(35): Show |
synonymous_variant | LOW | c.1194T>C | p.Thr398Thr | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1402/5515 | 1194/1308 | 398/435 | chr12 | 85804816 | |||
| chr12:85804951 | T | C | 1 | a0004c0006 | 2 | HG02055.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.1059A>G | p.Lys353Lys | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1267/5515 | 1059/1308 | 353/435 | chr12 | 85804951 | |||
| chr12:85805374 | T | C | 1 | a0001c0004 | 4 | NA18947.hp1 NA18984.hp2 NA18998.hp1 others(1): Show |
synonymous_variant | LOW | c.636A>G | p.Glu212Glu | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 844/5515 | 636/1308 | 212/435 | chr12 | 85805374 | |||
| chr12:85805659 | T | C | 1 | a0001c0003 | 5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
synonymous_variant | LOW | c.351A>G | p.Ala117Ala | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 559/5515 | 351/1308 | 117/435 | chr12 | 85805659 | |||
| chr12:85805758 | T | C | 1 | a0001c0009 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.252A>G | p.Arg84Arg | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 460/5515 | 252/1308 | 84/435 | chr12 | 85805758 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:85800797 | A | G | 1 | a0001c0001t0029 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3905T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3905 | chr12 | 85800797 | ||||||
| chr12:85800979 | TA | T | 1 | a0001c0001t0015 | 3 | HG03130.hp1 HG03130.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3722delT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3722 | chr12 | 85800979 | ||||||
| chr12:85801089 | C | A | 1 | a0001c0001t0024 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3613G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3613 | chr12 | 85801089 | ||||||
| chr12:85801160 | C | A | 6 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0024 others(3): Show |
32 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3542G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3542 | chr12 | 85801160 | ||||||
| chr12:85801269 | C | A | 1 | a0001c0001t0045 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3433G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3433 | chr12 | 85801269 | ||||||
| chr12:85801360 | A | C | 1 | a0001c0001t0048 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3342T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3342 | chr12 | 85801360 | ||||||
| chr12:85801390 | A | AAC | 9 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0026 others(6): Show |
26 | HG00639.hp2 HG01884.hp1 HG02055.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3310_*3311dupGT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3311 | chr12 | 85801390 | ||||||
| chr12:85801534 | C | A | 1 | a0001c0004t0010 | 4 | NA18947.hp1 NA18984.hp2 NA18998.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3168G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3168 | chr12 | 85801534 | ||||||
| chr12:85801539 | A | G | 1 | a0001c0001t0027 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3163T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3163 | chr12 | 85801539 | ||||||
| chr12:85801564 | G | A | 1 | a0001c0001t0035 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3138C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3138 | chr12 | 85801564 | ||||||
| chr12:85801578 | C | T | 1 | a0001c0001t0042 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3124G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3124 | chr12 | 85801578 | ||||||
| chr12:85801579 | A | G | 1 | a0001c0001t0042 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3123T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3123 | chr12 | 85801579 | ||||||
| chr12:85801582 | A | G | 1 | a0001c0001t0042 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3120T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3120 | chr12 | 85801582 | ||||||
| chr12:85801583 | C | T | 1 | a0001c0001t0042 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3119G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3119 | chr12 | 85801583 | ||||||
| chr12:85801587 | T | C | 1 | a0001c0001t0042 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3115A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3115 | chr12 | 85801587 | ||||||
| chr12:85801595 | A | G | 1 | a0001c0001t0042 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3107T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3107 | chr12 | 85801595 | ||||||
| chr12:85801603 | G | A | 1 | a0001c0001t0042 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3099C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3099 | chr12 | 85801603 | ||||||
| chr12:85801605 | C | G | 1 | a0001c0001t0042 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3097G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3097 | chr12 | 85801605 | ||||||
| chr12:85801629 | G | A | 1 | a0001c0003t0019 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3073C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3073 | chr12 | 85801629 | ||||||
| chr12:85801654 | A | C | 1 | a0001c0001t0034 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3048T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3048 | chr12 | 85801654 | ||||||
| chr12:85801672 | T | G | 1 | a0003c0005t0028 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3030A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 3030 | chr12 | 85801672 | ||||||
| chr12:85801718 | G | A | 1 | a0001c0001t0036 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2984C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2984 | chr12 | 85801718 | ||||||
| chr12:85801725 | A | G | 11 | a0001c0001t0009 a0001c0001t0029 a0001c0001t0038 others(8): Show |
53 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2977T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2977 | chr12 | 85801725 | ||||||
| chr12:85801738 | C | A | 1 | a0001c0001t0033 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2964G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2964 | chr12 | 85801738 | ||||||
| chr12:85801770 | G | A | 1 | a0001c0001t0037 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2932C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2932 | chr12 | 85801770 | ||||||
| chr12:85801816 | AG | A | 4 | a0001c0001t0005 a0001c0001t0046 a0001c0003t0012 others(1): Show |
15 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2885delC | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2885 | chr12 | 85801816 | ||||||
| chr12:85801817 | GGA | G | 10 | a0001c0001t0009 a0001c0001t0029 a0001c0001t0038 others(7): Show |
49 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2883_*2884delTC | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2883 | chr12 | 85801817 | ||||||
| chr12:85801823 | A | G | 2 | a0001c0001t0009 a0001c0001t0029 |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2879T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2879 | chr12 | 85801823 | ||||||
| chr12:85801829 | T | A | 14 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0029 others(11): Show |
64 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2873A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2873 | chr12 | 85801829 | ||||||
| chr12:85802009 | G | A | 1 | a0001c0001t0016 | 3 | HG02258.hp1 HG02965.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2693C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2693 | chr12 | 85802009 | ||||||
| chr12:85802050 | A | C | 1 | a0001c0001t0033 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2652T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2652 | chr12 | 85802050 | ||||||
| chr12:85802160 | A | G | 1 | a0001c0001t0040 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2542T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2542 | chr12 | 85802160 | ||||||
| chr12:85802170 | A | G | 10 | a0001c0001t0009 a0001c0001t0029 a0001c0003t0012 others(7): Show |
52 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2532T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2532 | chr12 | 85802170 | ||||||
| chr12:85802173 | A | C | 1 | a0001c0001t0032 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2529T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2529 | chr12 | 85802173 | ||||||
| chr12:85802195 | A | G | 10 | a0001c0001t0009 a0001c0001t0029 a0001c0003t0012 others(7): Show |
52 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2507T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2507 | chr12 | 85802195 | ||||||
| chr12:85802268 | A | T | 10 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(7): Show |
38 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2434T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2434 | chr12 | 85802268 | ||||||
| chr12:85802393 | A | G | 1 | a0001c0001t0031 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2309T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2309 | chr12 | 85802393 | ||||||
| chr12:85802402 | G | C | 5 | a0001c0003t0012 a0001c0003t0019 a0001c0009t0013 others(2): Show |
9 | HG02055.hp2 HG02257.hp2 HG02630.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2300C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2300 | chr12 | 85802402 | ||||||
| chr12:85802411 | C | T | 1 | a0001c0001t0044 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2291G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2291 | chr12 | 85802411 | ||||||
| chr12:85802561 | T | C | 1 | a0001c0001t0025 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2141A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 2141 | chr12 | 85802561 | ||||||
| chr12:85802875 | T | C | 1 | a0002c0002t0014 | 3 | HG02109.hp2 HG02280.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1827A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1827 | chr12 | 85802875 | ||||||
| chr12:85802888 | A | T | 1 | a0001c0001t0030 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1814T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1814 | chr12 | 85802888 | ||||||
| chr12:85803027 | A | G | 2 | a0001c0003t0012 a0001c0003t0019 |
5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1675T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1675 | chr12 | 85803027 | ||||||
| chr12:85803091 | G | A | 8 | a0001c0003t0012 a0001c0003t0019 a0001c0009t0013 others(5): Show |
47 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1611C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1611 | chr12 | 85803091 | ||||||
| chr12:85803094 | G | A | 2 | a0001c0001t0009 a0001c0001t0029 |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1608C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1608 | chr12 | 85803094 | ||||||
| chr12:85803159 | T | C | 1 | a0001c0001t0020 | 2 | HG02698.hp2 HG03654.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1543A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1543 | chr12 | 85803159 | ||||||
| chr12:85803165 | T | C | 1 | a0002c0002t0014 | 3 | HG02109.hp2 HG02280.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1537A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1537 | chr12 | 85803165 | ||||||
| chr12:85803226 | AAACCTGC others(50): Show |
A | 1 | a0001c0001t0039 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1419_*1475delGTCC others(53): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1419 | chr12 | 85803226 | ||||||
| chr12:85803261 | G | A | 8 | a0001c0003t0012 a0001c0003t0019 a0001c0009t0013 others(5): Show |
47 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1441C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1441 | chr12 | 85803261 | ||||||
| chr12:85803281 | G | A | 1 | a0001c0001t0001 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1421C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1421 | chr12 | 85803281 | ||||||
| chr12:85803392 | C | T | 22 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(19): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1310G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 1310 | chr12 | 85803392 | ||||||
| chr12:85803718 | C | A | 2 | a0001c0001t0006 a0001c0001t0039 |
9 | HG02015.hp1 HG02074.hp1 HG02135.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*984G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 984 | chr12 | 85803718 | ||||||
| chr12:85803732 | T | C | 2 | a0002c0002t0003 a0002c0002t0004 |
35 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*970A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 970 | chr12 | 85803732 | ||||||
| chr12:85803981 | G | T | 1 | a0002c0002t0004 | 13 | HG00408.hp2 HG00438.hp2 HG02071.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*721C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 721 | chr12 | 85803981 | ||||||
| chr12:85803989 | A | T | 1 | a0001c0001t0018 | 2 | NA18971.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*713T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 713 | chr12 | 85803989 | ||||||
| chr12:85804064 | C | A | 2 | a0001c0001t0017 a0001c0001t0040 |
4 | HG00099.hp2 HG02683.hp2 HG03491.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*638G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 638 | chr12 | 85804064 | ||||||
| chr12:85804100 | G | A | 1 | a0001c0001t0041 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*602C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 602 | chr12 | 85804100 | ||||||
| chr12:85804194 | A | G | 1 | a0001c0001t0026 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*508T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 508 | chr12 | 85804194 | ||||||
| chr12:85804195 | C | T | 4 | a0001c0001t0002 a0001c0001t0024 a0001c0001t0025 others(1): Show |
25 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*507G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 507 | chr12 | 85804195 | ||||||
| chr12:85804254 | C | G | 1 | a0001c0001t0022 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*448G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 448 | chr12 | 85804254 | ||||||
| chr12:85804257 | T | C | 1 | a0001c0001t0020 | 2 | HG02698.hp2 HG03654.hp1 |
3_prime_UTR_variant | MODIFIER | c.*445A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 445 | chr12 | 85804257 | ||||||
| chr12:85804262 | C | G | 1 | a0001c0001t0043 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 440 | chr12 | 85804262 | ||||||
| chr12:85804464 | T | A | 1 | a0001c0001t0042 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*238A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 238 | chr12 | 85804464 | ||||||
| chr12:85804469 | C | T | 2 | a0001c0001t0021 a0001c0001t0046 |
2 | HG03041.hp1 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*233G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 233 | chr12 | 85804469 | ||||||
| chr12:85804501 | T | G | 4 | a0001c0001t0008 a0001c0001t0043 a0001c0001t0044 others(1): Show |
9 | HG02559.hp1 HG02622.hp2 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*201A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 2/2 | 201 | chr12 | 85804501 | ||||||
| chr12:85836210 | G | A | 4 | a0001c0001t0005 a0001c0001t0046 a0001c0001t0047 others(1): Show |
12 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-9C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/2 | chr12 | 85836210 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:85805969 | G | GA | 3 | a0001c0001t0016g0026 a0001c0001t0016g0087 a0001c0001t0039g0204 |
4 | HG02258.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.48-8dupT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85805969 | |||||||
| chr12:85806072 | A | AT | 12 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(9): Show |
15 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.48-111dupA | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806072 | |||||||
| chr12:85806109 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0189 |
2 | NA18993.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.48-147G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806109 | |||||||
| chr12:85806110 | G | T | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-148C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806110 | |||||||
| chr12:85806112 | T | C | 8 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(5): Show |
10 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.48-150A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806112 | |||||||
| chr12:85806138 | T | C | 56 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0024 others(53): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-176A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806138 | |||||||
| chr12:85806148 | G | T | 1 | a0001c0001t0001g0108 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.48-186C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806148 | |||||||
| chr12:85806213 | A | AT | 31 | a0001c0001t0001g0044 a0001c0001t0001g0115 a0001c0001t0001g0189 others(28): Show |
41 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.48-252dupA | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806213 | |||||||
| chr12:85806265 | T | C | 4 | a0001c0003t0012g0169 a0001c0003t0012g0173 a0001c0003t0012g0175 others(1): Show |
5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-303A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806265 | |||||||
| chr12:85806325 | C | T | 3 | a0003c0005t0013g0085 a0003c0005t0013g0094 a0003c0005t0028g0086 |
3 | HG02055.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.48-363G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806325 | |||||||
| chr12:85806329 | C | T | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-367G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806329 | |||||||
| chr12:85806378 | G | C | 56 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0024 others(53): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-416C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806378 | |||||||
| chr12:85806445 | G | A | 19 | a0002c0002t0003g0007 a0002c0002t0003g0011 a0002c0002t0003g0021 others(16): Show |
34 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.48-483C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806445 | |||||||
| chr12:85806672 | C | CA | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(73): Show |
108 | HG00323.hp1 HG00423.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.48-711dupT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806672 | |||||||
| chr12:85806672 | C | CAA | 18 | a0001c0001t0001g0008 a0001c0001t0001g0071 a0001c0001t0001g0104 others(15): Show |
21 | HG00438.hp1 HG00673.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.48-712_48-711dupTT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806672 | |||||||
| chr12:85806672 | CA | C | 15 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(12): Show |
17 | HG01361.hp2 HG01433.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.48-711delT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806672 | |||||||
| chr12:85806672 | CAA | C | 5 | a0001c0001t0001g0235 a0001c0001t0009g0043 a0001c0001t0009g0230 others(2): Show |
7 | HG00741.hp2 HG01258.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.48-712_48-711delTT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806672 | |||||||
| chr12:85806672 | CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0008g0076 a0001c0001t0008g0078 a0001c0001t0008g0079 others(4): Show |
7 | HG02622.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.48-719_48-711delTT others(7): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806672 | |||||||
| chr12:85806672 | CAAAAAAA others(3): Show |
C | 6 | a0001c0001t0008g0098 a0001c0001t0011g0020 a0001c0001t0011g0106 others(3): Show |
7 | HG00280.hp1 HG02559.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.48-720_48-711delTT others(8): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806672 | |||||||
| chr12:85806672 | CAAAAAAA others(4): Show |
C | 22 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0024 others(19): Show |
34 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.48-721_48-711delTT others(9): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806672 | |||||||
| chr12:85806672 | CAAAAAAA others(5): Show |
C | 21 | a0001c0003t0012g0169 a0001c0003t0012g0173 a0001c0003t0012g0175 others(18): Show |
36 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.48-722_48-711delTT others(10): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85806672 | |||||||
| chr12:85807086 | A | T | 56 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0024 others(53): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-1124T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85807086 | |||||||
| chr12:85807109 | G | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0143 a0001c0001t0032g0142 |
3 | HG02622.hp1 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.48-1147C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85807109 | |||||||
| chr12:85807243 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.48-1281C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85807243 | |||||||
| chr12:85807292 | G | A | 1 | a0002c0002t0003g0022 | 2 | HG00733.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.48-1330C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85807292 | |||||||
| chr12:85807377 | C | G | 27 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0024 others(24): Show |
38 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.48-1415G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85807377 | |||||||
| chr12:85807385 | GTGTTAGC | G | 3 | a0003c0005t0013g0085 a0003c0005t0013g0094 a0003c0005t0028g0086 |
3 | HG02055.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.48-1430_48-1424del others(7): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85807385 | |||||||
| chr12:85807593 | A | T | 21 | a0002c0002t0003g0007 a0002c0002t0003g0011 a0002c0002t0003g0021 others(18): Show |
37 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.48-1631T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85807593 | |||||||
| chr12:85807645 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.48-1683C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85807645 | |||||||
| chr12:85807689 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.48-1727C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85807689 | |||||||
| chr12:85807725 | C | G | 1 | a0006c0008t0023g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.48-1763G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85807725 | |||||||
| chr12:85807925 | T | C | 27 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0024 others(24): Show |
38 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.48-1963A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85807925 | |||||||
| chr12:85807933 | C | T | 1 | a0001c0001t0005g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-1971G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85807933 | |||||||
| chr12:85807972 | T | A | 21 | a0002c0002t0003g0007 a0002c0002t0003g0011 a0002c0002t0003g0021 others(18): Show |
37 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.48-2010A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85807972 | |||||||
| chr12:85808072 | C | T | 19 | a0002c0002t0003g0007 a0002c0002t0003g0011 a0002c0002t0003g0021 others(16): Show |
34 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.48-2110G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808072 | |||||||
| chr12:85808144 | T | C | 5 | a0001c0001t0001g0137 a0001c0001t0001g0140 a0001c0001t0001g0150 others(2): Show |
5 | HG00323.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.48-2182A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808144 | |||||||
| chr12:85808165 | TTAAC | T | 5 | a0001c0001t0001g0119 a0001c0001t0009g0043 a0001c0001t0009g0229 others(2): Show |
6 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.48-2207_48-2204del others(4): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808165 | |||||||
| chr12:85808169 | C | T | 3 | a0001c0004t0010g0030 a0001c0004t0010g0125 a0001c0004t0010g0129 |
4 | NA18947.hp1 NA18984.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-2207G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808169 | |||||||
| chr12:85808215 | A | G | 37 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0024 others(34): Show |
50 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.48-2253T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808215 | |||||||
| chr12:85808366 | T | A | 60 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0024 others(57): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.48-2404A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808366 | |||||||
| chr12:85808400 | C | G | 1 | a0001c0001t0001g0193 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.48-2438G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808400 | |||||||
| chr12:85808540 | T | A | 68 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0024 others(65): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.48-2578A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808540 | |||||||
| chr12:85808595 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.48-2633T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808595 | |||||||
| chr12:85808712 | CAT | C | 21 | a0002c0002t0003g0007 a0002c0002t0003g0011 a0002c0002t0003g0021 others(18): Show |
37 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.48-2752_48-2751del others(2): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808712 | |||||||
| chr12:85808727 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0097 a0001c0001t0001g0119 others(3): Show |
15 | HG00621.hp2 HG00733.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.48-2765G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808727 | |||||||
| chr12:85808777 | G | A | 4 | a0001c0003t0012g0169 a0001c0003t0012g0173 a0001c0003t0012g0175 others(1): Show |
5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-2815C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808777 | |||||||
| chr12:85808826 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.48-2864T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808826 | |||||||
| chr12:85808836 | G | A | 8 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(5): Show |
10 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.48-2874C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808836 | |||||||
| chr12:85808905 | G | A | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-2943C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808905 | |||||||
| chr12:85808985 | C | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0208 |
2 | HG01934.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.48-3023G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85808985 | |||||||
| chr12:85809032 | T | C | 1 | a0001c0001t0007g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.48-3070A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809032 | |||||||
| chr12:85809214 | T | C | 3 | a0001c0001t0011g0020 a0001c0001t0011g0106 a0001c0001t0042g0045 |
4 | HG01884.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-3252A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809214 | |||||||
| chr12:85809265 | T | C | 8 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(5): Show |
10 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.48-3303A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809265 | |||||||
| chr12:85809300 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.48-3338G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809300 | |||||||
| chr12:85809380 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.48-3418G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809380 | |||||||
| chr12:85809665 | AATAATGA others(14): Show |
A | 21 | a0002c0002t0003g0007 a0002c0002t0003g0011 a0002c0002t0003g0021 others(18): Show |
37 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.48-3724_48-3704del others(21): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809665 | |||||||
| chr12:85809668 | A | AATG | 10 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0100 others(7): Show |
12 | HG01123.hp2 HG01891.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.48-3709_48-3707dup others(3): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809668 | |||||||
| chr12:85809668 | AATG | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0015 others(15): Show |
18 | HG00323.hp1 HG00738.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.48-3709_48-3707del others(3): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809668 | |||||||
| chr12:85809668 | AATGATG | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(11): Show |
20 | HG00639.hp2 HG00673.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.48-3712_48-3707del others(6): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809668 | |||||||
| chr12:85809668 | AATGATGA others(2): Show |
A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(17): Show |
26 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.48-3715_48-3707del others(9): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809668 | |||||||
| chr12:85809668 | AATGATGA others(5): Show |
A | 1 | a0001c0001t0029g0227 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.48-3718_48-3707del others(12): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809668 | |||||||
| chr12:85809668 | AATGATGA others(14): Show |
A | 29 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0024 others(26): Show |
40 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.48-3727_48-3707del others(21): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809668 | |||||||
| chr12:85809879 | C | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(237): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.48-3917G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809879 | |||||||
| chr12:85809951 | CT | C | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-3990delA | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85809951 | |||||||
| chr12:85810054 | C | A | 13 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0024 others(10): Show |
23 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.48-4092G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810054 | |||||||
| chr12:85810086 | T | C | 1 | a0001c0001t0038g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.48-4124A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810086 | |||||||
| chr12:85810100 | C | T | 26 | a0001c0001t0001g0071 a0001c0001t0002g0004 a0001c0001t0002g0012 others(23): Show |
37 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.48-4138G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810100 | |||||||
| chr12:85810185 | A | G | 1 | a0001c0001t0015g0033 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.48-4223T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810185 | |||||||
| chr12:85810224 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.48-4262T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810224 | |||||||
| chr12:85810312 | T | C | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-4350A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810312 | |||||||
| chr12:85810342 | G | A | 27 | a0001c0001t0001g0071 a0001c0001t0002g0004 a0001c0001t0002g0012 others(24): Show |
38 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.48-4380C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810342 | |||||||
| chr12:85810398 | C | T | 3 | a0001c0001t0008g0089 a0001c0001t0033g0075 a0001c0009t0013g0092 |
3 | HG03453.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.48-4436G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810398 | |||||||
| chr12:85810613 | C | T | 1 | a0001c0009t0013g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.48-4651G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810613 | |||||||
| chr12:85810614 | G | A | 1 | a0001c0003t0019g0027 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.48-4652C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810614 | |||||||
| chr12:85810660 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.48-4698T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810660 | |||||||
| chr12:85810679 | T | C | 53 | a0001c0001t0001g0071 a0001c0001t0002g0004 a0001c0001t0002g0012 others(50): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.48-4717A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810679 | |||||||
| chr12:85810747 | A | G | 9 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(6): Show |
11 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.48-4785T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810747 | |||||||
| chr12:85810918 | A | ACTTTG | 45 | a0001c0001t0001g0071 a0001c0001t0002g0004 a0001c0001t0002g0012 others(42): Show |
59 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.48-4961_48-4957dup others(5): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810918 | |||||||
| chr12:85810923 | G | GCTT | 21 | a0002c0002t0003g0007 a0002c0002t0003g0011 a0002c0002t0003g0021 others(18): Show |
37 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.48-4962_48-4961ins others(3): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85810923 | |||||||
| chr12:85811021 | T | G | 21 | a0002c0002t0003g0007 a0002c0002t0003g0011 a0002c0002t0003g0021 others(18): Show |
37 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.48-5059A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85811021 | |||||||
| chr12:85811036 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.48-5074G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85811036 | |||||||
| chr12:85811220 | C | G | 5 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0067 others(2): Show |
14 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.48-5258G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85811220 | |||||||
| chr12:85811398 | A | G | 2 | a0003c0005t0013g0085 a0003c0005t0028g0086 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.48-5436T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85811398 | |||||||
| chr12:85811407 | C | G | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-5445G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85811407 | |||||||
| chr12:85811511 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.48-5549C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85811511 | |||||||
| chr12:85811588 | C | T | 1 | a0001c0001t0005g0242 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.48-5626G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85811588 | |||||||
| chr12:85811855 | A | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0017 others(38): Show |
57 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.48-5893T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85811855 | |||||||
| chr12:85811862 | T | G | 1 | a0001c0001t0043g0073 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.48-5900A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85811862 | |||||||
| chr12:85811919 | C | G | 1 | a0001c0001t0038g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.48-5957G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85811919 | |||||||
| chr12:85811999 | A | G | 1 | a0002c0002t0003g0055 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.48-6037T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85811999 | |||||||
| chr12:85812021 | T | C | 2 | a0001c0001t0016g0026 a0001c0001t0016g0087 |
3 | HG02258.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48-6059A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85812021 | |||||||
| chr12:85812201 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.48-6239A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85812201 | |||||||
| chr12:85812359 | T | C | 4 | a0001c0001t0001g0207 a0001c0001t0001g0213 a0001c0001t0001g0215 others(1): Show |
4 | HG00738.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-6397A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85812359 | |||||||
| chr12:85812372 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): Show |
8 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.48-6410G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85812372 | |||||||
| chr12:85812394 | A | G | 1 | a0001c0003t0019g0027 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.48-6432T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85812394 | |||||||
| chr12:85812521 | A | G | 76 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(73): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.48-6559T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85812521 | |||||||
| chr12:85812572 | T | A | 2 | a0001c0001t0008g0089 a0001c0001t0033g0075 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.48-6610A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85812572 | |||||||
| chr12:85812674 | A | G | 1 | a0002c0002t0003g0051 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.48-6712T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85812674 | |||||||
| chr12:85812688 | G | A | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-6726C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85812688 | |||||||
| chr12:85812748 | T | C | 1 | a0005c0007t0001g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.48-6786A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85812748 | |||||||
| chr12:85812771 | A | C | 1 | a0001c0001t0001g0231 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.48-6809T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85812771 | |||||||
| chr12:85812773 | T | C | 2 | a0001c0001t0008g0076 a0001c0001t0008g0079 |
2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.48-6811A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85812773 | |||||||
| chr12:85813097 | G | A | 1 | a0001c0001t0027g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.48-7135C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813097 | |||||||
| chr12:85813207 | G | C | 2 | a0003c0005t0013g0085 a0003c0005t0028g0086 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.48-7245C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813207 | |||||||
| chr12:85813371 | A | G | 10 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0181 others(7): Show |
15 | HG01928.hp2 HG01934.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.48-7409T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813371 | |||||||
| chr12:85813510 | G | A | 3 | a0001c0001t0016g0026 a0001c0001t0016g0087 a0003c0005t0013g0094 |
4 | HG02055.hp2 HG02258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-7548C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813510 | |||||||
| chr12:85813558 | G | C | 2 | a0003c0005t0013g0085 a0003c0005t0028g0086 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.48-7596C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813558 | |||||||
| chr12:85813579 | A | T | 2 | a0002c0002t0014g0025 a0002c0002t0014g0074 |
3 | HG02109.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.48-7617T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813579 | |||||||
| chr12:85813647 | A | C | 1 | a0001c0001t0027g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.48-7685T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813647 | |||||||
| chr12:85813662 | T | C | 2 | a0001c0001t0008g0089 a0001c0001t0033g0075 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.48-7700A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813662 | |||||||
| chr12:85813769 | G | T | 57 | a0001c0001t0001g0071 a0001c0001t0002g0004 a0001c0001t0002g0012 others(54): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.48-7807C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813769 | |||||||
| chr12:85813832 | C | T | 3 | a0001c0001t0011g0020 a0001c0001t0027g0093 a0001c0001t0042g0045 |
4 | HG00280.hp1 HG01884.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-7870G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813832 | |||||||
| chr12:85813846 | G | A | 5 | a0001c0001t0008g0089 a0001c0001t0033g0075 a0001c0009t0013g0092 others(2): Show |
5 | HG02630.hp1 HG03453.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-7884C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813846 | |||||||
| chr12:85813850 | A | G | 6 | a0001c0001t0006g0010 a0001c0001t0006g0038 a0001c0001t0006g0205 others(3): Show |
10 | HG02015.hp1 HG02074.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.48-7888T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813850 | |||||||
| chr12:85813893 | A | T | 1 | a0001c0001t0015g0072 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.48-7931T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813893 | |||||||
| chr12:85813940 | T | C | 1 | a0004c0006t0001g0141 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.48-7978A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85813940 | |||||||
| chr12:85814026 | C | T | 2 | a0001c0001t0008g0089 a0001c0001t0033g0075 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.48-8064G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85814026 | |||||||
| chr12:85814150 | T | C | 3 | a0001c0001t0001g0127 a0001c0001t0007g0128 a0001c0001t0026g0126 |
3 | HG02602.hp2 HG03239.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.48-8188A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85814150 | |||||||
| chr12:85814311 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.48-8349C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85814311 | |||||||
| chr12:85814323 | A | G | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-8361T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85814323 | |||||||
| chr12:85814404 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0139 a0001c0001t0020g0032 |
6 | HG02698.hp2 HG03654.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.48-8442T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85814404 | |||||||
| chr12:85814500 | C | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0017 others(38): Show |
57 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.48-8538G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85814500 | |||||||
| chr12:85814659 | A | AT | 15 | a0001c0001t0001g0071 a0001c0001t0001g0238 a0001c0001t0002g0069 others(12): Show |
16 | HG00099.hp1 HG00280.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.48-8698dupA | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85814659 | |||||||
| chr12:85814659 | A | ATT | 14 | a0001c0001t0001g0088 a0001c0001t0002g0004 a0001c0001t0002g0012 others(11): Show |
24 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.48-8699_48-8698dup others(2): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85814659 | |||||||
| chr12:85814659 | AT | A | 7 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0163 others(4): Show |
8 | HG00438.hp1 HG00639.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.48-8698delA | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85814659 | |||||||
| chr12:85814667 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.48-8705A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85814667 | |||||||
| chr12:85814703 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0181 others(7): Show |
15 | HG01928.hp2 HG01934.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.48-8741G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85814703 | |||||||
| chr12:85814919 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.48-8957T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85814919 | |||||||
| chr12:85815128 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.48-9166T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815128 | |||||||
| chr12:85815160 | G | A | 9 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(6): Show |
11 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.48-9198C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815160 | |||||||
| chr12:85815184 | A | C | 28 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0002g0004 others(25): Show |
39 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.48-9222T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815184 | |||||||
| chr12:85815393 | A | G | 3 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-9431T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815393 | |||||||
| chr12:85815395 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.48-9433C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815395 | |||||||
| chr12:85815498 | G | C | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-9536C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815498 | |||||||
| chr12:85815529 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.48-9567T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815529 | |||||||
| chr12:85815700 | G | A | 5 | a0001c0001t0008g0089 a0001c0001t0033g0075 a0001c0009t0013g0092 others(2): Show |
5 | HG02630.hp1 HG03453.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-9738C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815700 | |||||||
| chr12:85815718 | C | T | 69 | a0001c0001t0001g0071 a0001c0001t0001g0104 a0001c0001t0001g0143 others(66): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.48-9756G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815718 | |||||||
| chr12:85815719 | GC | G | 75 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(72): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.48-9758delG | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815719 | |||||||
| chr12:85815721 | A | G | 75 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(72): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.48-9759T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815721 | |||||||
| chr12:85815802 | T | C | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-9840A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815802 | |||||||
| chr12:85815858 | A | G | 1 | a0001c0001t0038g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.48-9896T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815858 | |||||||
| chr12:85815908 | C | A | 19 | a0002c0002t0003g0007 a0002c0002t0003g0011 a0002c0002t0003g0021 others(16): Show |
34 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.48-9946G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85815908 | |||||||
| chr12:85816096 | C | A | 9 | a0001c0001t0008g0089 a0001c0001t0009g0043 a0001c0001t0009g0229 others(6): Show |
10 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.48-10134G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816096 | |||||||
| chr12:85816198 | A | G | 3 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-10236T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816198 | |||||||
| chr12:85816309 | T | TA | 46 | a0001c0001t0001g0071 a0001c0001t0002g0004 a0001c0001t0002g0012 others(43): Show |
73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.48-10348dupT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816309 | |||||||
| chr12:85816309 | TA | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
11 | HG00639.hp1 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.48-10348delT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816309 | |||||||
| chr12:85816324 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.48-10362C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816324 | |||||||
| chr12:85816376 | A | G | 66 | a0001c0001t0001g0071 a0001c0001t0002g0004 a0001c0001t0002g0012 others(63): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.48-10414T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816376 | |||||||
| chr12:85816429 | C | T | 1 | a0001c0009t0013g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.48-10467G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816429 | |||||||
| chr12:85816500 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.48-10538G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816500 | |||||||
| chr12:85816523 | T | G | 2 | a0001c0001t0011g0020 a0001c0001t0042g0045 |
3 | HG01884.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.48-10561A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816523 | |||||||
| chr12:85816558 | G | A | 2 | a0001c0001t0008g0089 a0001c0001t0033g0075 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.48-10596C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816558 | |||||||
| chr12:85816660 | T | A | 21 | a0002c0002t0003g0007 a0002c0002t0003g0011 a0002c0002t0003g0021 others(18): Show |
37 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.48-10698A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816660 | |||||||
| chr12:85816663 | A | G | 30 | a0001c0001t0008g0089 a0001c0001t0009g0043 a0001c0001t0009g0229 others(27): Show |
47 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.48-10701T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816663 | |||||||
| chr12:85816703 | G | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(45): Show |
68 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.48-10741C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816703 | |||||||
| chr12:85816853 | T | A | 10 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(7): Show |
10 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.48-10891A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816853 | |||||||
| chr12:85816854 | C | A | 5 | a0001c0001t0008g0089 a0001c0001t0033g0075 a0001c0009t0013g0092 others(2): Show |
5 | HG02630.hp1 HG03453.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-10892G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816854 | |||||||
| chr12:85816936 | C | G | 1 | a0004c0006t0001g0141 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.48-10974G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85816936 | |||||||
| chr12:85817079 | T | C | 30 | a0001c0001t0008g0089 a0001c0001t0009g0043 a0001c0001t0009g0229 others(27): Show |
47 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.48-11117A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85817079 | |||||||
| chr12:85817233 | G | A | 1 | a0003c0005t0013g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.48-11271C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85817233 | |||||||
| chr12:85817455 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0038g0059 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.48-11493A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85817455 | |||||||
| chr12:85817457 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.48-11495A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85817457 | |||||||
| chr12:85817537 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0038g0059 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.48-11575G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85817537 | |||||||
| chr12:85817545 | A | G | 1 | a0001c0001t0001g0017 | 3 | HG01496.hp1 HG01952.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.48-11583T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85817545 | |||||||
| chr12:85817778 | A | G | 1 | a0006c0008t0023g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.48-11816T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85817778 | |||||||
| chr12:85818167 | A | G | 1 | a0001c0001t0009g0043 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.48-12205T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818167 | |||||||
| chr12:85818409 | T | C | 1 | a0001c0001t0008g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.48-12447A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818409 | |||||||
| chr12:85818474 | A | G | 28 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0002g0004 others(25): Show |
39 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.48-12512T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818474 | |||||||
| chr12:85818491 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0038g0059 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.48-12529A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818491 | |||||||
| chr12:85818698 | C | T | 1 | a0002c0002t0003g0056 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.48-12736G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818698 | |||||||
| chr12:85818800 | A | AAT | 2 | a0001c0001t0002g0024 a0001c0001t0002g0066 |
3 | HG03017.hp1 HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.48-12839_48-12838i others(4): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818800 | |||||||
| chr12:85818804 | C | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0066 |
3 | HG03017.hp1 HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.48-12842G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818804 | |||||||
| chr12:85818806 | T | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0066 |
3 | HG03017.hp1 HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.48-12844A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818806 | |||||||
| chr12:85818825 | G | A | 9 | a0001c0001t0008g0089 a0001c0001t0009g0043 a0001c0001t0009g0229 others(6): Show |
10 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.48-12863C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818825 | |||||||
| chr12:85818873 | G | C | 3 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-12911C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818873 | |||||||
| chr12:85818914 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.48-12952C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818914 | |||||||
| chr12:85818956 | C | CA | 34 | a0001c0001t0001g0013 a0001c0001t0001g0083 a0001c0001t0001g0095 others(31): Show |
46 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.48-12995dupT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818956 | |||||||
| chr12:85818956 | C | CAA | 7 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0002g0070 others(4): Show |
7 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.48-12996_48-12995d others(4): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818956 | |||||||
| chr12:85818956 | CA | C | 23 | a0001c0001t0001g0009 a0001c0001t0001g0183 a0001c0001t0001g0192 others(20): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.48-12995delT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818956 | |||||||
| chr12:85818995 | A | C | 22 | a0001c0001t0048g0248 a0002c0002t0003g0007 a0002c0002t0003g0011 others(19): Show |
38 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.48-13033T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85818995 | |||||||
| chr12:85819072 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0157 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.48-13110T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85819072 | |||||||
| chr12:85819115 | CA | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(1): Show |
6 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.48-13154delT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85819115 | |||||||
| chr12:85819209 | C | A | 2 | a0003c0005t0013g0085 a0003c0005t0028g0086 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.48-13247G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85819209 | |||||||
| chr12:85819210 | AT | A | 61 | a0001c0001t0001g0018 a0001c0001t0001g0041 a0001c0001t0001g0044 others(58): Show |
77 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.48-13249delA | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85819210 | |||||||
| chr12:85819247 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG00609.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.48-13285T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85819247 | |||||||
| chr12:85819259 | C | T | 3 | a0001c0001t0008g0089 a0001c0001t0033g0075 a0001c0009t0013g0092 |
3 | HG03453.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.48-13297G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85819259 | |||||||
| chr12:85819375 | G | A | 1 | a0002c0002t0003g0056 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.48-13413C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85819375 | |||||||
| chr12:85819393 | T | C | 1 | a0001c0001t0027g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.48-13431A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85819393 | |||||||
| chr12:85819406 | C | A | 74 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(71): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.48-13444G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85819406 | |||||||
| chr12:85819562 | T | G | 1 | a0001c0009t0013g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.48-13600A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85819562 | |||||||
| chr12:85819700 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.48-13738A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85819700 | |||||||
| chr12:85819782 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.48-13820T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85819782 | |||||||
| chr12:85819886 | C | A | 27 | a0001c0001t0001g0071 a0001c0001t0002g0004 a0001c0001t0002g0012 others(24): Show |
38 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.48-13924G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85819886 | |||||||
| chr12:85820066 | T | G | 1 | a0001c0001t0020g0032 | 2 | HG02698.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.48-14104A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85820066 | |||||||
| chr12:85820203 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.48-14241G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85820203 | |||||||
| chr12:85820280 | G | T | 27 | a0001c0001t0001g0071 a0001c0001t0002g0004 a0001c0001t0002g0012 others(24): Show |
38 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.48-14318C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85820280 | |||||||
| chr12:85820444 | C | T | 2 | a0001c0001t0008g0089 a0001c0001t0033g0075 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.48-14482G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85820444 | |||||||
| chr12:85820534 | A | C | 1 | a0001c0001t0001g0091 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.48-14572T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85820534 | |||||||
| chr12:85820571 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.48-14609T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85820571 | |||||||
| chr12:85820588 | AT | A | 22 | a0001c0001t0048g0248 a0002c0002t0003g0007 a0002c0002t0003g0011 others(19): Show |
38 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.48-14627delA | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85820588 | |||||||
| chr12:85820709 | A | T | 3 | a0001c0001t0005g0240 a0001c0001t0005g0245 a0001c0001t0046g0241 |
3 | HG02723.hp1 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.48-14747T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85820709 | |||||||
| chr12:85821068 | C | T | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.47+15087G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821068 | |||||||
| chr12:85821069 | G | A | 1 | a0001c0001t0033g0075 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.47+15086C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821069 | |||||||
| chr12:85821079 | C | G | 9 | a0001c0001t0008g0089 a0001c0001t0009g0043 a0001c0001t0009g0229 others(6): Show |
10 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.47+15076G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821079 | |||||||
| chr12:85821101 | G | T | 1 | a0001c0009t0013g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47+15054C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821101 | |||||||
| chr12:85821142 | A | T | 1 | a0001c0001t0001g0091 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.47+15013T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821142 | |||||||
| chr12:85821163 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.47+14992T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821163 | |||||||
| chr12:85821375 | C | G | 1 | a0001c0003t0012g0169 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.47+14780G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821375 | |||||||
| chr12:85821558 | TTAA | T | 9 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(6): Show |
11 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.47+14594_47+14596d others(5): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821558 | |||||||
| chr12:85821577 | C | T | 1 | a0001c0001t0017g0039 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.47+14578G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821577 | |||||||
| chr12:85821660 | AGT | A | 3 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+14493_47+14494d others(4): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821660 | |||||||
| chr12:85821696 | C | T | 9 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(6): Show |
11 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.47+14459G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821696 | |||||||
| chr12:85821726 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.47+14429C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821726 | |||||||
| chr12:85821830 | G | A | 2 | a0003c0005t0013g0085 a0003c0005t0028g0086 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.47+14325C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821830 | |||||||
| chr12:85821854 | A | T | 1 | a0001c0001t0021g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.47+14301T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821854 | |||||||
| chr12:85821902 | C | T | 1 | a0002c0002t0003g0054 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.47+14253G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821902 | |||||||
| chr12:85821974 | C | G | 1 | a0001c0009t0013g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47+14181G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821974 | |||||||
| chr12:85821997 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | NA18966.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.47+14158C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85821997 | |||||||
| chr12:85822065 | C | CA | 6 | a0001c0001t0001g0035 a0001c0001t0001g0116 a0001c0001t0001g0118 others(3): Show |
7 | HG00423.hp2 HG00621.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+14089dupT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822065 | |||||||
| chr12:85822065 | CA | C | 4 | a0001c0001t0001g0091 a0001c0001t0048g0248 a0002c0002t0014g0025 others(1): Show |
5 | HG02109.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.47+14089delT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822065 | |||||||
| chr12:85822180 | T | C | 11 | a0002c0002t0003g0007 a0002c0002t0003g0021 a0002c0002t0003g0022 others(8): Show |
17 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.47+13975A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822180 | |||||||
| chr12:85822275 | TC | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0031 others(32): Show |
49 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.47+13879delG | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822275 | |||||||
| chr12:85822315 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): Show |
8 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.47+13840C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822315 | |||||||
| chr12:85822366 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.47+13789C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822366 | |||||||
| chr12:85822422 | C | A | 1 | a0001c0001t0001g0091 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.47+13733G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822422 | |||||||
| chr12:85822431 | G | T | 1 | a0002c0002t0014g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.47+13724C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822431 | |||||||
| chr12:85822533 | C | T | 1 | a0001c0001t0048g0248 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.47+13622G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822533 | |||||||
| chr12:85822546 | T | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(4): Show |
10 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.47+13609A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822546 | |||||||
| chr12:85822569 | T | TTATTCTT others(4): Show |
1 | a0001c0001t0021g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.47+13575_47+13585d others(13): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822569 | |||||||
| chr12:85822581 | A | T | 1 | a0001c0001t0021g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.47+13574T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822581 | |||||||
| chr12:85822582 | C | T | 1 | a0001c0001t0021g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.47+13573G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822582 | |||||||
| chr12:85822658 | A | T | 1 | a0001c0001t0048g0248 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.47+13497T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822658 | |||||||
| chr12:85822676 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.47+13479T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822676 | |||||||
| chr12:85822688 | G | C | 2 | a0001c0001t0016g0026 a0001c0001t0016g0087 |
3 | HG02258.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.47+13467C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822688 | |||||||
| chr12:85822793 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.47+13362G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822793 | |||||||
| chr12:85822816 | C | G | 1 | a0001c0009t0013g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47+13339G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85822816 | |||||||
| chr12:85823052 | T | C | 13 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(10): Show |
14 | HG00280.hp1 HG01884.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.47+13103A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823052 | |||||||
| chr12:85823067 | T | G | 76 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(73): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.47+13088A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823067 | |||||||
| chr12:85823127 | G | C | 32 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0024 others(29): Show |
57 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.47+13028C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823127 | |||||||
| chr12:85823199 | C | CA | 28 | a0001c0001t0001g0016 a0001c0001t0001g0088 a0001c0001t0001g0107 others(25): Show |
34 | HG00609.hp2 HG00642.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.47+12955dupT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823199 | |||||||
| chr12:85823199 | C | CAA | 9 | a0001c0001t0001g0135 a0001c0001t0011g0020 a0001c0001t0016g0026 others(6): Show |
11 | HG00280.hp1 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.47+12954_47+12955d others(4): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823199 | |||||||
| chr12:85823199 | CA | C | 10 | a0001c0001t0001g0091 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG00323.hp1 HG00741.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.47+12955delT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823199 | |||||||
| chr12:85823199 | CAA | C | 10 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(7): Show |
10 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.47+12954_47+12955d others(4): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823199 | |||||||
| chr12:85823339 | T | C | 2 | a0003c0005t0013g0085 a0003c0005t0028g0086 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.47+12816A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823339 | |||||||
| chr12:85823364 | A | G | 1 | a0001c0001t0029g0227 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.47+12791T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823364 | |||||||
| chr12:85823479 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0038g0059 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.47+12676A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823479 | |||||||
| chr12:85823575 | T | C | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.47+12580A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823575 | |||||||
| chr12:85823623 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0038g0059 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.47+12532T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823623 | |||||||
| chr12:85823755 | C | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0017 others(38): Show |
57 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.47+12400G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823755 | |||||||
| chr12:85823771 | A | G | 2 | a0002c0002t0014g0025 a0002c0002t0014g0074 |
3 | HG02109.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.47+12384T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823771 | |||||||
| chr12:85823786 | A | G | 13 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(10): Show |
14 | HG00280.hp1 HG01884.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.47+12369T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823786 | |||||||
| chr12:85823834 | C | T | 1 | a0001c0001t0048g0248 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.47+12321G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85823834 | |||||||
| chr12:85824097 | A | G | 1 | a0001c0001t0035g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.47+12058T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824097 | |||||||
| chr12:85824319 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.47+11836G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824319 | |||||||
| chr12:85824326 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02523.hp1 NA18966.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.47+11829G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824326 | |||||||
| chr12:85824382 | A | G | 1 | a0002c0002t0003g0046 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.47+11773T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824382 | |||||||
| chr12:85824504 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.47+11651G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824504 | |||||||
| chr12:85824522 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0091 a0001c0001t0001g0097 others(28): Show |
41 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.47+11633G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824522 | |||||||
| chr12:85824557 | T | G | 1 | a0001c0001t0008g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.47+11598A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824557 | |||||||
| chr12:85824571 | C | A | 7 | a0001c0001t0008g0076 a0001c0001t0008g0078 a0001c0001t0008g0079 others(4): Show |
7 | HG02559.hp1 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+11584G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824571 | |||||||
| chr12:85824712 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.47+11443A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824712 | |||||||
| chr12:85824761 | C | T | 1 | a0003c0005t0013g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.47+11394G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824761 | |||||||
| chr12:85824764 | C | A | 56 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(53): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.47+11391G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824764 | |||||||
| chr12:85824819 | C | A | 1 | a0001c0001t0005g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.47+11336G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824819 | |||||||
| chr12:85824824 | C | G | 1 | a0001c0001t0027g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.47+11331G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824824 | |||||||
| chr12:85824845 | T | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(7): Show |
14 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.47+11310A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824845 | |||||||
| chr12:85824981 | G | C | 63 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(60): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.47+11174C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85824981 | |||||||
| chr12:85825060 | T | G | 1 | a0001c0001t0027g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.47+11095A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825060 | |||||||
| chr12:85825066 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.47+11089C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825066 | |||||||
| chr12:85825387 | G | A | 13 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(10): Show |
14 | HG00280.hp1 HG01884.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.47+10768C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825387 | |||||||
| chr12:85825472 | C | T | 10 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(7): Show |
14 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.47+10683G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825472 | |||||||
| chr12:85825498 | A | G | 1 | a0001c0001t0048g0248 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.47+10657T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825498 | |||||||
| chr12:85825576 | A | G | 1 | a0001c0001t0001g0189 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.47+10579T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825576 | |||||||
| chr12:85825650 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.47+10505T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825650 | |||||||
| chr12:85825758 | C | A | 56 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(53): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.47+10397G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825758 | |||||||
| chr12:85825783 | T | TAC | 12 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0158 others(9): Show |
13 | HG01167.hp2 HG01169.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+10370_47+10371d others(4): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825783 | |||||||
| chr12:85825783 | TAC | T | 8 | a0001c0001t0001g0118 a0001c0001t0001g0163 a0001c0001t0001g0178 others(5): Show |
9 | HG00438.hp1 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.47+10370_47+10371d others(4): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825783 | |||||||
| chr12:85825783 | TACAC | T | 26 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0002g0004 others(23): Show |
39 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.47+10368_47+10371d others(6): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825783 | |||||||
| chr12:85825783 | TACACAC | T | 47 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(44): Show |
67 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.47+10366_47+10371d others(8): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825783 | |||||||
| chr12:85825814 | A | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02027.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.47+10341T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825814 | |||||||
| chr12:85825815 | C | CA | 3 | a0001c0001t0001g0165 a0001c0001t0001g0188 a0001c0001t0001g0212 |
3 | HG03927.hp2 NA19001.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.47+10339_47+10340i others(3): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825815 | |||||||
| chr12:85825843 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.47+10312T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825843 | |||||||
| chr12:85825987 | G | C | 2 | a0003c0005t0013g0085 a0003c0005t0028g0086 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.47+10168C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85825987 | |||||||
| chr12:85826109 | A | C | 1 | a0001c0001t0035g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.47+10046T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826109 | |||||||
| chr12:85826284 | G | C | 2 | a0001c0001t0001g0160 a0001c0001t0037g0114 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.47+9871C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826284 | |||||||
| chr12:85826318 | C | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(227): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.47+9837G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826318 | |||||||
| chr12:85826447 | A | AT | 23 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0071 others(20): Show |
26 | HG00609.hp2 HG00639.hp1 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.47+9707dupA | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826447 | |||||||
| chr12:85826447 | A | ATTTTTT | 4 | a0001c0001t0008g0089 a0001c0001t0016g0026 a0001c0001t0033g0075 others(1): Show |
6 | HG02258.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+9702_47+9707dup others(6): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826447 | |||||||
| chr12:85826447 | AT | A | 45 | a0001c0001t0001g0088 a0001c0001t0001g0161 a0001c0001t0001g0164 others(42): Show |
70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.47+9707delA | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826447 | |||||||
| chr12:85826449 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.47+9706A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826449 | |||||||
| chr12:85826494 | C | G | 1 | a0003c0005t0013g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.47+9661G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826494 | |||||||
| chr12:85826496 | A | G | 59 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(56): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.47+9659T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826496 | |||||||
| chr12:85826549 | G | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.47+9606C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826549 | |||||||
| chr12:85826596 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(227): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.47+9559A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826596 | |||||||
| chr12:85826613 | A | C | 12 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(9): Show |
13 | HG00280.hp1 HG01884.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+9542T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826613 | |||||||
| chr12:85826615 | T | C | 12 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(9): Show |
13 | HG00280.hp1 HG01884.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+9540A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826615 | |||||||
| chr12:85826616 | T | C | 12 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(9): Show |
13 | HG00280.hp1 HG01884.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+9539A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826616 | |||||||
| chr12:85826619 | T | G | 12 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(9): Show |
13 | HG00280.hp1 HG01884.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+9536A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826619 | |||||||
| chr12:85826620 | T | TTCACCCA others(11): Show |
12 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(9): Show |
13 | HG00280.hp1 HG01884.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+9534_47+9535ins others(18): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826620 | |||||||
| chr12:85826621 | G | A | 12 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(9): Show |
13 | HG00280.hp1 HG01884.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+9534C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826621 | |||||||
| chr12:85826626 | T | C | 12 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(9): Show |
13 | HG00280.hp1 HG01884.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+9529A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826626 | |||||||
| chr12:85826627 | T | TCTCAACC others(3): Show |
12 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(9): Show |
13 | HG00280.hp1 HG01884.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+9527_47+9528ins others(10): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826627 | |||||||
| chr12:85826666 | A | G | 12 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(9): Show |
13 | HG00280.hp1 HG01884.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+9489T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826666 | |||||||
| chr12:85826733 | G | A | 3 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+9422C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826733 | |||||||
| chr12:85826752 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.47+9403G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826752 | |||||||
| chr12:85826911 | G | A | 1 | a0001c0009t0013g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47+9244C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826911 | |||||||
| chr12:85826949 | C | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(9): Show |
17 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.47+9206G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826949 | |||||||
| chr12:85826966 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.47+9189T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826966 | |||||||
| chr12:85826976 | T | C | 2 | a0002c0002t0014g0025 a0002c0002t0014g0074 |
3 | HG02109.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.47+9179A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85826976 | |||||||
| chr12:85827102 | C | A | 2 | a0002c0002t0014g0025 a0002c0002t0014g0074 |
3 | HG02109.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.47+9053G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85827102 | |||||||
| chr12:85827276 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0038g0059 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.47+8879T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85827276 | |||||||
| chr12:85827331 | T | A | 1 | a0001c0001t0001g0162 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.47+8824A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85827331 | |||||||
| chr12:85827428 | C | T | 19 | a0002c0002t0003g0007 a0002c0002t0003g0011 a0002c0002t0003g0021 others(16): Show |
34 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.47+8727G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85827428 | |||||||
| chr12:85827435 | G | C | 59 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(56): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.47+8720C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85827435 | |||||||
| chr12:85827447 | C | G | 9 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(6): Show |
11 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.47+8708G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85827447 | |||||||
| chr12:85827698 | C | A | 1 | a0002c0002t0003g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.47+8457G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85827698 | |||||||
| chr12:85827701 | T | C | 46 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0002g0004 others(43): Show |
72 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.47+8454A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85827701 | |||||||
| chr12:85827979 | G | A | 3 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+8176C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85827979 | |||||||
| chr12:85828066 | T | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG00438.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.47+8089A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85828066 | |||||||
| chr12:85828130 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.47+8025T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85828130 | |||||||
| chr12:85828160 | G | A | 2 | a0003c0005t0013g0085 a0003c0005t0028g0086 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.47+7995C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85828160 | |||||||
| chr12:85828358 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(6): Show |
13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+7797C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85828358 | |||||||
| chr12:85828380 | G | A | 1 | a0001c0001t0048g0248 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.47+7775C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85828380 | |||||||
| chr12:85828401 | G | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(9): Show |
17 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.47+7754C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85828401 | |||||||
| chr12:85828463 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.47+7692A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85828463 | |||||||
| chr12:85828475 | A | T | 46 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0002g0004 others(43): Show |
72 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.47+7680T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85828475 | |||||||
| chr12:85828778 | G | A | 1 | a0001c0001t0038g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.47+7377C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85828778 | |||||||
| chr12:85828826 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.47+7329C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85828826 | |||||||
| chr12:85828969 | G | A | 32 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0024 others(29): Show |
57 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.47+7186C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85828969 | |||||||
| chr12:85829241 | G | A | 9 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(6): Show |
9 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.47+6914C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85829241 | |||||||
| chr12:85829332 | T | C | 1 | a0001c0009t0013g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47+6823A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85829332 | |||||||
| chr12:85829424 | T | C | 1 | a0001c0001t0029g0227 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.47+6731A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85829424 | |||||||
| chr12:85829502 | T | A | 1 | a0001c0001t0038g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.47+6653A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85829502 | |||||||
| chr12:85829503 | A | T | 1 | a0001c0001t0038g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.47+6652T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85829503 | |||||||
| chr12:85829891 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG00408.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.47+6264C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85829891 | |||||||
| chr12:85829951 | G | A | 1 | a0003c0005t0013g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.47+6204C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85829951 | |||||||
| chr12:85830076 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG00408.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.47+6079C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830076 | |||||||
| chr12:85830088 | C | T | 9 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(6): Show |
11 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.47+6067G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830088 | |||||||
| chr12:85830116 | C | G | 1 | a0001c0001t0011g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.47+6039G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830116 | |||||||
| chr12:85830305 | G | A | 1 | a0001c0001t0017g0220 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.47+5850C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830305 | |||||||
| chr12:85830360 | T | C | 1 | a0002c0002t0004g0058 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.47+5795A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830360 | |||||||
| chr12:85830521 | A | C | 1 | a0001c0009t0013g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47+5634T>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830521 | |||||||
| chr12:85830528 | C | T | 58 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(55): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.47+5627G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830528 | |||||||
| chr12:85830554 | T | A | 1 | a0001c0001t0048g0248 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.47+5601A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830554 | |||||||
| chr12:85830588 | A | G | 3 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+5567T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830588 | |||||||
| chr12:85830804 | A | G | 1 | a0001c0001t0034g0223 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.47+5351T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830804 | |||||||
| chr12:85830840 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.47+5315C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830840 | |||||||
| chr12:85830845 | G | A | 45 | a0001c0001t0001g0071 a0001c0001t0002g0004 a0001c0001t0002g0012 others(42): Show |
71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.47+5310C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830845 | |||||||
| chr12:85830884 | T | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG00609.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.47+5271A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830884 | |||||||
| chr12:85830919 | A | G | 1 | a0001c0001t0048g0248 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.47+5236T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830919 | |||||||
| chr12:85830928 | T | G | 1 | a0001c0001t0034g0223 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.47+5227A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830928 | |||||||
| chr12:85830957 | A | G | 1 | a0001c0001t0040g0166 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.47+5198T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85830957 | |||||||
| chr12:85831036 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.47+5119G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85831036 | |||||||
| chr12:85831049 | G | T | 2 | a0003c0005t0013g0085 a0003c0005t0028g0086 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.47+5106C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85831049 | |||||||
| chr12:85831072 | G | T | 2 | a0001c0001t0016g0026 a0001c0001t0016g0087 |
3 | HG02258.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.47+5083C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85831072 | |||||||
| chr12:85831135 | C | T | 2 | a0001c0001t0008g0089 a0001c0001t0033g0075 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.47+5020G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85831135 | |||||||
| chr12:85831137 | T | C | 1 | a0003c0005t0013g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.47+5018A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85831137 | |||||||
| chr12:85831284 | C | A | 1 | a0001c0001t0001g0224 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.47+4871G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85831284 | |||||||
| chr12:85831285 | G | C | 12 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(9): Show |
17 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.47+4870C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85831285 | |||||||
| chr12:85831533 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG03491.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.47+4622A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85831533 | |||||||
| chr12:85831637 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.47+4518G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85831637 | |||||||
| chr12:85831875 | C | T | 1 | a0001c0001t0038g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.47+4280G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85831875 | |||||||
| chr12:85831926 | C | T | 2 | a0001c0001t0001g0102 a0001c0001t0007g0103 |
2 | HG02698.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.47+4229G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85831926 | |||||||
| chr12:85831927 | C | G | 1 | a0001c0001t0029g0227 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.47+4228G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85831927 | |||||||
| chr12:85832132 | T | A | 1 | a0003c0005t0013g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.47+4023A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85832132 | |||||||
| chr12:85832201 | T | C | 12 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(9): Show |
17 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.47+3954A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85832201 | |||||||
| chr12:85832236 | A | G | 1 | a0001c0001t0042g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.47+3919T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85832236 | |||||||
| chr12:85832257 | G | T | 9 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(6): Show |
11 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.47+3898C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85832257 | |||||||
| chr12:85832280 | C | T | 1 | a0001c0001t0008g0089 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.47+3875G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85832280 | |||||||
| chr12:85832305 | C | A | 1 | a0001c0001t0016g0087 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.47+3850G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85832305 | |||||||
| chr12:85832378 | T | C | 1 | a0001c0001t0029g0227 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.47+3777A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85832378 | |||||||
| chr12:85832471 | T | G | 1 | a0001c0001t0001g0165 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.47+3684A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85832471 | |||||||
| chr12:85832714 | A | G | 1 | a0001c0001t0009g0229 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.47+3441T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85832714 | |||||||
| chr12:85832803 | T | C | 1 | a0001c0009t0013g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47+3352A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85832803 | |||||||
| chr12:85832961 | C | A | 74 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(71): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.47+3194G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85832961 | |||||||
| chr12:85833098 | GA | G | 45 | a0001c0001t0001g0071 a0001c0001t0002g0004 a0001c0001t0002g0012 others(42): Show |
71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.47+3056delT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85833098 | |||||||
| chr12:85833215 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(82): Show |
119 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.47+2940G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85833215 | |||||||
| chr12:85833241 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG03239.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.47+2914G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85833241 | |||||||
| chr12:85833248 | T | A | 12 | a0001c0001t0001g0071 a0001c0001t0008g0076 a0001c0001t0008g0078 others(9): Show |
13 | HG00280.hp1 HG01884.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+2907A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85833248 | |||||||
| chr12:85833390 | C | A | 3 | a0001c0001t0011g0020 a0001c0001t0027g0093 a0001c0001t0042g0045 |
4 | HG00280.hp1 HG01884.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+2765G>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85833390 | |||||||
| chr12:85833399 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.47+2756G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85833399 | |||||||
| chr12:85833461 | A | T | 1 | a0001c0001t0008g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.47+2694T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85833461 | |||||||
| chr12:85833688 | A | G | 1 | a0001c0001t0002g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.47+2467T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85833688 | |||||||
| chr12:85833781 | A | T | 3 | a0001c0001t0011g0020 a0001c0001t0027g0093 a0001c0001t0042g0045 |
4 | HG00280.hp1 HG01884.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+2374T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85833781 | |||||||
| chr12:85833805 | A | T | 19 | a0002c0002t0003g0007 a0002c0002t0003g0011 a0002c0002t0003g0021 others(16): Show |
34 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.47+2350T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85833805 | |||||||
| chr12:85833918 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.47+2237C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85833918 | |||||||
| chr12:85833998 | G | C | 1 | a0001c0001t0005g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.47+2157C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85833998 | |||||||
| chr12:85834057 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0095 a0001c0001t0001g0096 |
4 | HG01928.hp1 HG02451.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.47+2098G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85834057 | |||||||
| chr12:85834073 | G | C | 10 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(7): Show |
12 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.47+2082C>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85834073 | |||||||
| chr12:85834096 | T | G | 10 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(7): Show |
12 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.47+2059A>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85834096 | |||||||
| chr12:85834135 | C | T | 74 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0082 others(71): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.47+2020G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85834135 | |||||||
| chr12:85834165 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.47+1990G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85834165 | |||||||
| chr12:85834283 | G | T | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.47+1872C>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85834283 | |||||||
| chr12:85834284 | CG | C | 4 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.47+1870delC | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85834284 | |||||||
| chr12:85834285 | G | A | 1 | a0001c0001t0011g0020 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.47+1870C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85834285 | |||||||
| chr12:85834837 | A | T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(17): Show |
25 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.47+1318T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85834837 | |||||||
| chr12:85835165 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.47+990A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835165 | |||||||
| chr12:85835198 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.47+957T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835198 | |||||||
| chr12:85835269 | T | C | 1 | a0001c0001t0008g0081 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.47+886A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835269 | |||||||
| chr12:85835290 | A | T | 10 | a0001c0001t0001g0090 a0001c0001t0005g0019 a0001c0001t0005g0240 others(7): Show |
12 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.47+865T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835290 | |||||||
| chr12:85835342 | G | A | 3 | a0001c0001t0009g0043 a0001c0001t0009g0229 a0001c0001t0009g0230 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+813C>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835342 | |||||||
| chr12:85835493 | GTAA | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 |
5 | HG02109.hp1 HG02145.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.47+659_47+661delTT others(1): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835493 | |||||||
| chr12:85835569 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.47+586A>T | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835569 | |||||||
| chr12:85835607 | G | GTGTT | 10 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(7): Show |
12 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.47+544_47+547dupAA others(2): Show |
RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835607 | |||||||
| chr12:85835785 | A | G | 39 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0002g0004 others(36): Show |
65 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.47+370T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835785 | |||||||
| chr12:85835910 | C | G | 8 | a0001c0001t0008g0076 a0001c0001t0008g0078 a0001c0001t0008g0079 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.47+245G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835910 | |||||||
| chr12:85835920 | T | C | 10 | a0001c0001t0005g0019 a0001c0001t0005g0240 a0001c0001t0005g0242 others(7): Show |
12 | HG00639.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.47+235A>G | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835920 | |||||||
| chr12:85835944 | C | G | 39 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0002g0004 others(36): Show |
65 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.47+211G>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835944 | |||||||
| chr12:85835962 | A | T | 17 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0083 others(14): Show |
21 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.47+193T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835962 | |||||||
| chr12:85835965 | A | T | 2 | a0001c0001t0011g0020 a0001c0001t0042g0045 |
3 | HG01884.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.47+190T>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85835965 | |||||||
| chr12:85836006 | A | G | 2 | a0002c0002t0014g0025 a0002c0002t0014g0074 |
3 | HG02109.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.47+149T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85836006 | |||||||
| chr12:85836065 | C | T | 38 | a0001c0001t0001g0071 a0001c0001t0002g0004 a0001c0001t0002g0012 others(35): Show |
64 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.47+90G>A | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85836065 | |||||||
| chr12:85836068 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.47+87T>C | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85836068 | |||||||
| chr12:85836102 | G | GAC | 8 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(5): Show |
8 | HG01258.hp1 HG01361.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.47+51_47+52dupGT | RASSF9 | ENSG00000198774.5 | transcript | ENST00000361228.5 | protein_coding | 1/1 | chr12 | 85836102 |