Item | Value |
---|---|
geneid | 9770 |
ensemblid | ENSG00000101265.16 |
hgncid | 9883 |
symbol | RASSF2 |
name | Ras association domain family member 2 |
refseq_nuc | NM_014737.3 |
refseq_prot | NP_055552.1 |
ensembl_nuc | ENST00000379400.8 |
ensembl_prot | ENSP00000368710.3 |
mane_status | MANE Select |
chr | chr20 |
start | 4780023 |
end | 4823608 |
strand | - |
ver | v1.2 |
region | chr20:4780023-4823608 |
region5000 | chr20:4775023-4828608 |
regionname0 | RASSF2_chr20_4780023_4823608 |
regionname5000 | RASSF2_chr20_4775023_4828608 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 326 | 426 | 93 | 73 | 192 | 18 | 48 | 144 | RASSF2_chr20_4775023_4828608 | RASSF2 | MDYSH others(321): Show |
chr20 | 4775023 | 4828608 |
a0002 | 0/0 | 326 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | MDYSH others(321): Show |
chr20 | 4775023 | 4828608 |
a0003 | 0/0 | 326 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | MDYSH others(321): Show |
chr20 | 4775023 | 4828608 |
a0004 | 0/0 | 326 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | MDYSH others(321): Show |
chr20 | 4775023 | 4828608 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 978 | 393 | 77 | 71 | 177 | 18 | 48 | RASSF2_chr20_4775023_4828608 | RASSF2 | ATGGA others(973): Show |
chr20 | 4775023 | 4828608 | ||
a0001c0002 | 0/0 | 978 | 17 | 16 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | ATGGA others(973): Show |
chr20 | 4775023 | 4828608 | ||
a0001c0003 | 0/0 | 978 | 14 | 0 | 0 | 14 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | ATGGA others(973): Show |
chr20 | 4775023 | 4828608 | ||
a0001c0006 | 0/0 | 978 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | ATGGA others(973): Show |
chr20 | 4775023 | 4828608 | ||
a0001c0007 | 0/0 | 978 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | ATGGA others(973): Show |
chr20 | 4775023 | 4828608 | ||
a0002c0004 | 0/0 | 978 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | ATGGA others(973): Show |
chr20 | 4775023 | 4828608 | ||
a0003c0008 | 0/0 | 978 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | ATGGA others(973): Show |
chr20 | 4775023 | 4828608 | ||
a0004c0005 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | ATGGA others(973): Show |
chr20 | 4775023 | 4828608 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5391 | 74 | 4 | 9 | 50 | 6 | 5 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0002 | 0/0 | 5391 | 68 | 7 | 14 | 39 | 1 | 7 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0003 | 0/0 | 5390 | 30 | 5 | 3 | 15 | 3 | 4 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0004 | 0/0 | 5392 | 35 | 3 | 6 | 23 | 1 | 2 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5387): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0005 | 0/0 | 5390 | 17 | 4 | 1 | 9 | 0 | 3 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0006 | 0/0 | 5390 | 13 | 2 | 7 | 0 | 0 | 4 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0007 | 1/1 | 5390 | 12 | 0 | 1 | 3 | 0 | 6 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0008 | 0/0 | 5390 | 12 | 3 | 1 | 2 | 2 | 4 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0009 | 0/0 | 5391 | 11 | 0 | 3 | 7 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0010 | 0/0 | 5389 | 10 | 9 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5384): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0011 | 0/0 | 5390 | 8 | 1 | 4 | 0 | 2 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0012 | 0/0 | 5392 | 5 | 5 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5387): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0013 | 0/0 | 5390 | 6 | 0 | 5 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0014 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0015 | 0/0 | 5391 | 4 | 0 | 1 | 3 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0016 | 0/0 | 5391 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0017 | 0/0 | 5392 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5387): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0018 | 0/0 | 5392 | 3 | 1 | 2 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5387): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0019 | 0/0 | 5391 | 3 | 2 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0020 | 0/0 | 5390 | 3 | 0 | 2 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0021 | 0/0 | 5377 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5372): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0022 | 0/0 | 5390 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0023 | 0/0 | 5391 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0024 | 0/0 | 5391 | 3 | 2 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0025 | 0/0 | 5391 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0027 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0029 | 0/0 | 5390 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0030 | 0/0 | 5390 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0031 | 0/0 | 5390 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0033 | 0/0 | 5390 | 2 | 0 | 0 | 0 | 1 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0034 | 0/0 | 5391 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0035 | 0/0 | 5389 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5384): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0036 | 0/0 | 5391 | 2 | 1 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0037 | 0/0 | 5391 | 2 | 0 | 0 | 0 | 2 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0038 | 0/0 | 5391 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0039 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0040 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0041 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0042 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0043 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0044 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0045 | 0/0 | 5392 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5387): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0046 | 0/0 | 5392 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5387): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0047 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0048 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0049 | 0/0 | 5392 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5387): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0052 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0053 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0055 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0057 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0058 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0059 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0060 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0061 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0062 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0063 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0064 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0065 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0066 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0067 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0068 | 0/0 | 5392 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5387): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0069 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0070 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0071 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0072 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0073 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0074 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0075 | 0/0 | 5391 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0076 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0077 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0001t0078 | 0/0 | 5391 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0002t0001 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0002t0012 | 0/0 | 5392 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5387): Show |
chr20 | 4775023 | 4828608 |
a0001c0002t0014 | 0/0 | 5390 | 4 | 3 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0002t0026 | 0/0 | 5392 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5387): Show |
chr20 | 4775023 | 4828608 |
a0001c0002t0027 | 0/0 | 5390 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0002t0028 | 0/0 | 5391 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0001c0002t0032 | 0/0 | 5390 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0003t0003 | 0/0 | 5390 | 12 | 0 | 0 | 12 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0003t0054 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0003t0056 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0006t0005 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
a0001c0007t0002 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0002c0004t0050 | 0/0 | 5378 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5373): Show |
chr20 | 4775023 | 4828608 |
a0002c0004t0051 | 0/0 | 5379 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5374): Show |
chr20 | 4775023 | 4828608 |
a0003c0008t0002 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5386): Show |
chr20 | 4775023 | 4828608 |
a0004c0005t0003 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | AGAGT others(5385): Show |
chr20 | 4775023 | 4828608 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0002g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0003g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0004g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0005g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0006g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0006g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0006g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0006g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0007g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0007g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0007g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0007g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0007g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0007g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0008g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0008g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0008g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0008g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0008g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0008g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0008g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0008g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0008g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0008g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0009g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0009g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0009g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0009g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0009g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0009g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0009g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0009g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0009g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0010g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0010g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0010g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0010g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0011g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0011g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0011g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0011g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0011g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0011g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0011g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0011g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0012g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0012g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0012g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0012g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0013g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0013g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0013g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0013g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0013g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0014g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0015g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0015g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0016g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0016g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0016g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0017g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0017g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0017g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0017g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0018g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0018g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0018g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0019g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0019g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0019g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0020g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0020g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0020g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0021g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0021g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0022g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0022g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0022g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0023g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0023g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0023g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0024g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0024g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0024g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0025g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0025g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0027g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0029g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0030g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0030g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0031g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0031g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0033g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0033g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0034g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0035g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0035g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0036g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0036g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0037g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0037g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0038g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0039g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0040g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0041g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0042g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0043g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0044g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0045g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0046g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0047g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0048g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0049g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0052g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0053g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0055g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0057g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0058g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0059g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0060g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0061g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0062g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0063g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0064g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0065g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0066g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0067g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0068g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0069g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0070g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0071g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0072g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0073g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0074g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0075g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0076g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0077g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0001t0078g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0012g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0014g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0014g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0014g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0014g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0026g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0026g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0026g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0027g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0027g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0028g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0028g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0028g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0032g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0002t0032g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0003t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0003t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0003t0003g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0003t0054g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0003t0056g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0006t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0001c0007t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0002c0004t0050g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0002c0004t0051g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0003c0008t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
a0004c0005t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00099 | hp2 | a0001 | c0001 | t0008 | g0234 | EUR | GBR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00140 | hp1 | a0001 | c0001 | t0011 | g0203 | EUR | GBR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0261 | EUR | GBR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00280 | hp1 | a0001 | c0001 | t0008 | g0195 | EUR | FIN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00323 | hp1 | a0001 | c0001 | t0011 | g0341 | EUR | FIN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0279 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00423 | hp2 | a0001 | c0003 | t0054 | g0272 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00438 | hp1 | a0001 | c0001 | t0019 | g0174 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00544 | hp1 | a0001 | c0001 | t0007 | g0064 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00558 | hp2 | a0001 | c0001 | t0062 | g0218 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0358 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00609 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0345 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0250 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0342 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0379 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00733 | hp2 | a0001 | c0001 | t0020 | g0173 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00735 | hp1 | a0001 | c0001 | t0067 | g0193 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0145 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00738 | hp2 | a0001 | c0001 | t0009 | g0068 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00741 | hp1 | a0001 | c0001 | t0031 | g0078 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG00741 | hp2 | a0001 | c0001 | t0044 | g0073 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01070 | hp1 | a0001 | c0001 | t0013 | g0319 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01070 | hp2 | a0001 | c0001 | t0034 | g0017 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01071 | hp1 | a0001 | c0001 | t0034 | g0017 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01071 | hp2 | a0001 | c0001 | t0009 | g0062 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0361 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01074 | hp2 | a0001 | c0001 | t0011 | g0376 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01081 | hp2 | a0001 | c0001 | t0011 | g0165 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0253 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01106 | hp1 | a0001 | c0001 | t0007 | g0074 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01109 | hp1 | a0001 | c0001 | t0010 | g0155 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0328 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01168 | hp1 | a0001 | c0001 | t0018 | g0066 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01168 | hp2 | a0001 | c0001 | t0036 | g0267 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01169 | hp2 | a0001 | c0001 | t0018 | g0067 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0135 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01243 | hp1 | a0001 | c0001 | t0008 | g0302 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01243 | hp2 | a0001 | c0002 | t0014 | g0153 | AMR | PUR | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01255 | hp1 | a0001 | c0001 | t0009 | g0060 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01255 | hp2 | a0001 | c0001 | t0063 | g0240 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01256 | hp2 | a0001 | c0007 | t0002 | g0259 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01261 | hp1 | a0001 | c0001 | t0031 | g0036 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01261 | hp2 | a0001 | c0001 | t0006 | g0027 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01346 | hp1 | a0001 | c0001 | t0006 | g0151 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01346 | hp2 | a0001 | c0001 | t0013 | g0030 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01358 | hp1 | a0001 | c0001 | t0057 | g0301 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01496 | hp1 | a0001 | c0001 | t0043 | g0076 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0378 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01515 | hp1 | a0001 | c0001 | t0037 | g0139 | EUR | IBS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01517 | hp1 | a0001 | c0001 | t0037 | g0141 | EUR | IBS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0375 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01891 | hp2 | a0001 | c0001 | t0010 | g0126 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01928 | hp1 | a0001 | c0001 | t0006 | g0179 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0330 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01943 | hp2 | a0001 | c0001 | t0020 | g0137 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01975 | hp2 | a0001 | c0001 | t0006 | g0027 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01978 | hp2 | a0001 | c0001 | t0013 | g0030 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01981 | hp1 | a0001 | c0001 | t0011 | g0268 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01981 | hp2 | a0003 | c0008 | t0002 | g0096 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0349 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0298 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02040 | hp2 | a0001 | c0001 | t0023 | g0353 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02055 | hp1 | a0001 | c0001 | t0016 | g0004 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02055 | hp2 | a0001 | c0002 | t0032 | g0152 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02056 | hp1 | a0001 | c0001 | t0059 | g0322 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02074 | hp2 | a0001 | c0001 | t0005 | g0299 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02080 | hp2 | a0001 | c0001 | t0025 | g0320 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02083 | hp1 | a0001 | c0001 | t0022 | g0365 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0288 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02135 | hp1 | a0001 | c0001 | t0007 | g0046 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02145 | hp1 | a0001 | c0001 | t0017 | g0127 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02145 | hp2 | a0001 | c0001 | t0012 | g0371 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02148 | hp1 | a0001 | c0001 | t0013 | g0101 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0143 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0300 | EAS | CDX | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0278 | EAS | CDX | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | CDX | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0382 | EAS | CDX | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02257 | hp1 | a0001 | c0001 | t0014 | g0167 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0260 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02258 | hp1 | a0001 | c0001 | t0010 | g0333 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0351 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02280 | hp1 | a0001 | c0001 | t0016 | g0042 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02280 | hp2 | a0001 | c0001 | t0017 | g0160 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02293 | hp2 | a0001 | c0001 | t0013 | g0327 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02300 | hp1 | a0001 | c0001 | t0015 | g0315 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0238 | AMR | PEL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02451 | hp1 | a0001 | c0002 | t0014 | g0125 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02451 | hp2 | a0001 | c0002 | t0012 | g0035 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0381 | EAS | KHV | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02572 | hp2 | a0001 | c0001 | t0061 | g0119 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02602 | hp1 | a0001 | c0001 | t0075 | g0134 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02615 | hp1 | a0001 | c0001 | t0017 | g0163 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02615 | hp2 | a0001 | c0001 | t0019 | g0037 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02622 | hp1 | a0001 | c0001 | t0010 | g0162 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02630 | hp2 | a0001 | c0001 | t0017 | g0128 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02683 | hp2 | a0001 | c0001 | t0053 | g0111 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02698 | hp1 | a0001 | c0001 | t0078 | g0136 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0281 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0011 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02717 | hp2 | a0001 | c0001 | t0073 | g0106 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02723 | hp1 | a0001 | c0001 | t0046 | g0286 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02723 | hp2 | a0001 | c0001 | t0042 | g0053 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02735 | hp1 | a0001 | c0001 | t0011 | g0370 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0354 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0374 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0383 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02809 | hp1 | a0001 | c0001 | t0035 | g0161 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02809 | hp2 | a0001 | c0001 | t0016 | g0038 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02818 | hp1 | a0001 | c0002 | t0028 | g0122 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02818 | hp2 | a0001 | c0001 | t0041 | g0077 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02886 | hp1 | a0001 | c0001 | t0012 | g0011 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02886 | hp2 | a0002 | c0004 | t0051 | g0166 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02895 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02895 | hp2 | a0001 | c0001 | t0019 | g0045 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0293 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0294 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0392 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02976 | hp1 | a0001 | c0002 | t0014 | g0369 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02976 | hp2 | a0001 | c0002 | t0028 | g0123 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0331 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03041 | hp1 | a0001 | c0001 | t0027 | g0110 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0366 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03098 | hp1 | a0001 | c0001 | t0012 | g0130 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03098 | hp2 | a0001 | c0001 | t0024 | g0044 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03130 | hp1 | a0001 | c0001 | t0011 | g0377 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03130 | hp2 | a0001 | c0002 | t0032 | g0132 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03139 | hp1 | a0001 | c0001 | t0038 | g0013 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03139 | hp2 | a0001 | c0001 | t0021 | g0014 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03195 | hp1 | a0001 | c0002 | t0026 | g0158 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03195 | hp2 | a0001 | c0002 | t0028 | g0292 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03209 | hp1 | a0001 | c0001 | t0021 | g0014 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03209 | hp2 | a0001 | c0002 | t0014 | g0104 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03225 | hp1 | a0001 | c0001 | t0076 | g0168 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03225 | hp2 | a0001 | c0002 | t0027 | g0107 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03239 | hp1 | a0001 | c0001 | t0007 | g0075 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0057 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0015 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03486 | hp1 | a0001 | c0002 | t0026 | g0156 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03486 | hp2 | a0001 | c0001 | t0024 | g0039 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0269 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03490 | hp2 | a0001 | c0001 | t0030 | g0050 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03491 | hp1 | a0001 | c0001 | t0007 | g0058 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03491 | hp2 | a0001 | c0001 | t0029 | g0005 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03492 | hp1 | a0001 | c0001 | t0029 | g0005 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03492 | hp2 | a0001 | c0001 | t0030 | g0051 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0169 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03579 | hp1 | a0001 | c0001 | t0010 | g0118 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03579 | hp2 | a0001 | c0001 | t0069 | g0182 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0372 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0146 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03669 | hp1 | a0001 | c0001 | t0008 | g0239 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03669 | hp2 | a0001 | c0001 | t0007 | g0069 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | STU | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03688 | hp2 | a0001 | c0001 | t0008 | g0262 | SAS | STU | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03704 | hp1 | a0001 | c0001 | t0033 | g0308 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03704 | hp2 | a0001 | c0001 | t0009 | g0172 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03710 | hp1 | a0001 | c0001 | t0020 | g0138 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03710 | hp2 | a0001 | c0001 | t0008 | g0207 | SAS | PJL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0275 | SAS | BEB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0205 | SAS | BEB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0282 | SAS | BEB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03942 | hp1 | a0001 | c0001 | t0008 | g0264 | SAS | BEB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0283 | SAS | BEB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG04115 | hp1 | a0001 | c0001 | t0006 | g0080 | SAS | STU | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0363 | SAS | STU | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0255 | SAS | BEB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | BEB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | STU | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG04204 | hp1 | a0001 | c0001 | t0040 | g0056 | SAS | STU | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0047 | SAS | STU | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG04228 | hp1 | a0001 | c0001 | t0064 | g0336 | SAS | STU | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG04228 | hp2 | a0001 | c0001 | t0006 | g0280 | SAS | STU | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18522 | hp1 | a0001 | c0001 | t0010 | g0105 | AFR | YRI | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18522 | hp2 | a0001 | c0002 | t0026 | g0040 | AFR | YRI | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18612 | hp2 | a0001 | c0003 | t0003 | g0095 | EAS | CHB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | CHB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | YRI | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18906 | hp2 | a0001 | c0001 | t0021 | g0296 | AFR | YRI | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18941 | hp1 | a0001 | c0001 | t0008 | g0311 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18942 | hp2 | a0001 | c0001 | t0004 | g0350 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0343 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18944 | hp1 | a0001 | c0001 | t0009 | g0063 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18946 | hp1 | a0001 | c0001 | t0022 | g0190 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18952 | hp1 | a0001 | c0001 | t0007 | g0052 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0347 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0389 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18954 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18956 | hp2 | a0001 | c0001 | t0005 | g0321 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18957 | hp2 | a0001 | c0003 | t0003 | g0216 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0386 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18963 | hp1 | a0001 | c0001 | t0023 | g0355 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0387 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18964 | hp1 | a0001 | c0001 | t0023 | g0225 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18965 | hp1 | a0001 | c0001 | t0025 | g0031 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18969 | hp1 | a0001 | c0001 | t0077 | g0192 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18969 | hp2 | a0001 | c0001 | t0071 | g0194 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18972 | hp1 | a0001 | c0001 | t0009 | g0072 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18972 | hp2 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18973 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18980 | hp1 | a0001 | c0001 | t0049 | g0227 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18981 | hp1 | a0001 | c0003 | t0056 | g0221 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18981 | hp2 | a0001 | c0001 | t0009 | g0049 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18982 | hp1 | a0001 | c0001 | t0009 | g0059 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18982 | hp2 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18988 | hp1 | a0001 | c0006 | t0005 | g0271 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18992 | hp1 | a0001 | c0001 | t0005 | g0324 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18992 | hp2 | a0001 | c0001 | t0065 | g0230 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18994 | hp2 | a0001 | c0001 | t0074 | g0089 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18997 | hp2 | a0001 | c0001 | t0058 | g0309 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18999 | hp1 | a0001 | c0003 | t0003 | g0222 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19002 | hp2 | a0001 | c0001 | t0024 | g0092 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19003 | hp2 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19004 | hp2 | a0001 | c0001 | t0009 | g0061 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19007 | hp2 | a0001 | c0001 | t0068 | g0334 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19011 | hp1 | a0001 | c0001 | t0072 | g0348 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0385 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | LWK | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19030 | hp2 | a0001 | c0001 | t0070 | g0154 | AFR | LWK | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | LWK | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19043 | hp2 | a0001 | c0001 | t0012 | g0171 | AFR | LWK | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19056 | hp2 | a0001 | c0001 | t0013 | g0316 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19057 | hp2 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19062 | hp1 | a0001 | c0003 | t0003 | g0220 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19063 | hp1 | a0001 | c0001 | t0009 | g0048 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19065 | hp1 | a0001 | c0003 | t0003 | g0208 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19067 | hp2 | a0001 | c0001 | t0005 | g0212 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19068 | hp1 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19070 | hp1 | a0001 | c0001 | t0048 | g0226 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19070 | hp2 | a0001 | c0001 | t0025 | g0031 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19074 | hp2 | a0001 | c0001 | t0008 | g0224 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19077 | hp2 | a0001 | c0001 | t0055 | g0303 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19078 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0380 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19079 | hp2 | a0001 | c0001 | t0009 | g0071 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19080 | hp1 | a0001 | c0003 | t0003 | g0384 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19081 | hp2 | a0001 | c0001 | t0066 | g0231 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19082 | hp2 | a0001 | c0001 | t0039 | g0176 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0388 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0356 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19084 | hp1 | a0001 | c0003 | t0003 | g0217 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19085 | hp2 | a0001 | c0001 | t0022 | g0276 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0390 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19091 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA19240 | hp2 | a0001 | c0001 | t0010 | g0159 | AFR | YRI | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA20129 | hp1 | a0001 | c0002 | t0027 | g0157 | AFR | ASW | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA20129 | hp2 | a0001 | c0002 | t0012 | g0035 | AFR | ASW | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0117 | EUR | TSI | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0249 | EUR | TSI | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA20805 | hp1 | a0001 | c0001 | t0033 | g0133 | EUR | TSI | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0200 | EUR | TSI | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | GIH | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0055 | SAS | GIH | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01123 | hp1 | a0001 | c0001 | t0060 | g0112 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG01123 | hp2 | a0001 | c0001 | t0011 | g0084 | AMR | CLM | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02109 | hp1 | a0001 | c0001 | t0052 | g0085 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02109 | hp2 | a0001 | c0001 | t0047 | g0373 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02486 | hp1 | a0002 | c0004 | t0050 | g0121 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02486 | hp2 | a0004 | c0005 | t0003 | g0116 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02559 | hp1 | a0001 | c0001 | t0018 | g0287 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG02559 | hp2 | a0001 | c0001 | t0016 | g0004 | AFR | ACB | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03471 | hp1 | a0001 | c0001 | t0038 | g0013 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG03471 | hp2 | a0001 | c0001 | t0045 | g0065 | AFR | MSL | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG06807 | hp1 | a0001 | c0001 | t0010 | g0120 | AFR | USA | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
HG06807 | hp2 | a0001 | c0001 | t0036 | g0367 | AFR | USA | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0199 | AFR | USA | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0391 | AFR | USA | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA21309 | hp1 | a0001 | c0001 | t0035 | g0197 | AFR | LWK | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0368 | AFR | LWK | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0070 | REF | REF | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0054 | REF | REF | RASSF2_chr20_4775023_4828608 | RASSF2 | chr20 | 4775023 | 4828608 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:4790536 | C | T | 1 | a0004 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.452G>A | p.Arg151His | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 7/12 | 611/5390 | 452/981 | 151/326 | chr20 | 4790536 | |||
chr20:4790587 | T | A | 1 | a0002 | 2 | HG02486.hp1 HG02886.hp2 |
missense_variant | MODERATE | c.401A>T | p.Gln134Leu | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 7/12 | 560/5390 | 401/981 | 134/326 | chr20 | 4790587 | |||
chr20:4792562 | C | A | 1 | a0003 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.353G>T | p.Gly118Val | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/12 | 512/5390 | 353/981 | 118/326 | chr20 | 4792562 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:4786287 | G | A | 1 | a0001c0006 | 1 | NA18988.hp1 | synonymous_variant | LOW | c.855C>T | p.Ser285Ser | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/12 | 1014/5390 | 855/981 | 285/326 | chr20 | 4786287 | |||
chr20:4787636 | G | A | 1 | a0001c0002 | 17 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(14): Show |
synonymous_variant | LOW | c.810C>T | p.Tyr270Tyr | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/12 | 969/5390 | 810/981 | 270/326 | chr20 | 4787636 | |||
chr20:4789629 | T | G | 1 | a0001c0007 | 1 | HG01256.hp2 | synonymous_variant | LOW | c.606A>C | p.Pro202Pro | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/12 | 765/5390 | 606/981 | 202/326 | chr20 | 4789629 | |||
chr20:4792567 | C | T | 1 | a0001c0003 | 14 | HG00423.hp2 NA18612.hp2 NA18954.hp1 others(11): Show |
synonymous_variant | LOW | c.348G>A | p.Pro116Pro | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/12 | 507/5390 | 348/981 | 116/326 | chr20 | 4792567 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:4780175 | T | C | 1 | a0001c0001t0040 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4098A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 4098 | chr20 | 4780175 | ||||||
chr20:4780358 | C | T | 1 | a0001c0001t0066 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3915G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3915 | chr20 | 4780358 | ||||||
chr20:4780403 | C | T | 3 | a0001c0001t0011 a0001c0001t0021 a0001c0001t0031 |
13 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3870G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3870 | chr20 | 4780403 | ||||||
chr20:4780413 | C | T | 2 | a0001c0001t0013 a0001c0001t0015 |
10 | HG01070.hp1 HG01346.hp2 HG01978.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3860G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3860 | chr20 | 4780413 | ||||||
chr20:4780417 | C | T | 1 | a0001c0001t0074 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3856G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3856 | chr20 | 4780417 | ||||||
chr20:4780616 | T | C | 2 | a0001c0001t0010 a0001c0001t0035 |
12 | HG01109.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3657A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3657 | chr20 | 4780616 | ||||||
chr20:4780684 | T | C | 1 | a0001c0001t0061 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3589A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3589 | chr20 | 4780684 | ||||||
chr20:4780825 | C | T | 3 | a0001c0001t0017 a0001c0001t0038 a0001c0001t0045 |
7 | HG02145.hp1 HG02280.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3448G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3448 | chr20 | 4780825 | ||||||
chr20:4780829 | C | T | 1 | a0001c0001t0073 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3444G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3444 | chr20 | 4780829 | ||||||
chr20:4780860 | T | C | 1 | a0001c0001t0067 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3413A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3413 | chr20 | 4780860 | ||||||
chr20:4780901 | G | A | 1 | a0001c0001t0037 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3372C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3372 | chr20 | 4780901 | ||||||
chr20:4780932 | G | T | 1 | a0001c0001t0030 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3341C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3341 | chr20 | 4780932 | ||||||
chr20:4780956 | C | T | 1 | a0001c0001t0065 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3317G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3317 | chr20 | 4780956 | ||||||
chr20:4780968 | C | CA | 18 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0016 others(15): Show |
67 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*3304dupT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3304 | chr20 | 4780968 | ||||||
chr20:4780979 | A | AG | 2 | a0001c0001t0017 a0001c0001t0045 |
5 | HG02145.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3293_*3294insC | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3293 | chr20 | 4780979 | ||||||
chr20:4781231 | T | G | 1 | a0001c0001t0061 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3042A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3042 | chr20 | 4781231 | ||||||
chr20:4781231 | T | TG | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(39): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*3041dupC | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3041 | chr20 | 4781231 | ||||||
chr20:4781231 | TG | T | 2 | a0001c0001t0010 a0001c0001t0035 |
12 | HG01109.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3041delC | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3041 | chr20 | 4781231 | ||||||
chr20:4781233 | G | T | 1 | a0001c0003t0054 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3040C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3040 | chr20 | 4781233 | ||||||
chr20:4781234 | G | T | 2 | a0001c0001t0010 a0001c0001t0035 |
12 | HG01109.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3039C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 3039 | chr20 | 4781234 | ||||||
chr20:4781476 | T | C | 1 | a0001c0001t0075 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2797A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 2797 | chr20 | 4781476 | ||||||
chr20:4781712 | A | G | 1 | a0001c0001t0048 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2561T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 2561 | chr20 | 4781712 | ||||||
chr20:4781715 | C | T | 1 | a0001c0001t0072 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2558G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 2558 | chr20 | 4781715 | ||||||
chr20:4781802 | C | T | 2 | a0001c0001t0029 a0001c0001t0033 |
4 | HG03491.hp2 HG03492.hp1 HG03704.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2471G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 2471 | chr20 | 4781802 | ||||||
chr20:4781806 | A | G | 1 | a0001c0001t0047 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2467T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 2467 | chr20 | 4781806 | ||||||
chr20:4781931 | C | G | 20 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0016 others(17): Show |
107 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2342G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 2342 | chr20 | 4781931 | ||||||
chr20:4782055 | A | G | 63 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(60): Show |
361 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*2218T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 2218 | chr20 | 4782055 | ||||||
chr20:4782090 | G | C | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(56): Show |
353 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(350): Show |
3_prime_UTR_variant | MODIFIER | c.*2183C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 2183 | chr20 | 4782090 | ||||||
chr20:4782111 | C | T | 1 | a0001c0001t0071 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2162G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 2162 | chr20 | 4782111 | ||||||
chr20:4782182 | C | A | 1 | a0001c0001t0025 | 3 | HG02080.hp2 NA18965.hp1 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2091G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 2091 | chr20 | 4782182 | ||||||
chr20:4782223 | G | A | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(43): Show |
285 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*2050C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 2050 | chr20 | 4782223 | ||||||
chr20:4782438 | G | C | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(50): Show |
291 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*1835C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1835 | chr20 | 4782438 | ||||||
chr20:4782447 | T | C | 14 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(11): Show |
112 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1826A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1826 | chr20 | 4782447 | ||||||
chr20:4782462 | G | A | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(50): Show |
291 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*1811C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1811 | chr20 | 4782462 | ||||||
chr20:4782509 | C | T | 3 | a0001c0001t0011 a0001c0001t0031 a0001c0001t0078 |
11 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1764G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1764 | chr20 | 4782509 | ||||||
chr20:4782653 | C | G | 12 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0015 others(9): Show |
61 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1620G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1620 | chr20 | 4782653 | ||||||
chr20:4782665 | G | A | 12 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0015 others(9): Show |
61 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1608C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1608 | chr20 | 4782665 | ||||||
chr20:4782710 | T | C | 1 | a0001c0001t0076 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1563A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1563 | chr20 | 4782710 | ||||||
chr20:4782792 | G | T | 12 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0015 others(9): Show |
61 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1481C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1481 | chr20 | 4782792 | ||||||
chr20:4782891 | ATCTGTCT others(6): Show |
A | 3 | a0001c0001t0021 a0002c0004t0050 a0002c0004t0051 |
5 | HG02486.hp1 HG02886.hp2 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1369_*1381delGGAG others(9): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1369 | chr20 | 4782891 | ||||||
chr20:4782899 | C | T | 1 | a0001c0001t0010 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1374G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1374 | chr20 | 4782899 | ||||||
chr20:4783041 | C | A | 1 | a0001c0001t0059 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1232G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1232 | chr20 | 4783041 | ||||||
chr20:4783172 | T | C | 13 | a0001c0001t0011 a0001c0001t0012 a0001c0001t0014 others(10): Show |
35 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1101A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1101 | chr20 | 4783172 | ||||||
chr20:4783218 | G | A | 11 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0015 others(8): Show |
60 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1055C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1055 | chr20 | 4783218 | ||||||
chr20:4783258 | G | C | 12 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0015 others(9): Show |
61 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1015C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 1015 | chr20 | 4783258 | ||||||
chr20:4783357 | C | T | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(34): Show |
223 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*916G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 916 | chr20 | 4783357 | ||||||
chr20:4783380 | C | T | 2 | a0001c0001t0014 a0001c0002t0014 |
5 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*893G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 893 | chr20 | 4783380 | ||||||
chr20:4783607 | C | T | 1 | a0001c0001t0060 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*666G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 666 | chr20 | 4783607 | ||||||
chr20:4783683 | G | A | 1 | a0001c0001t0077 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*590C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 590 | chr20 | 4783683 | ||||||
chr20:4783895 | T | C | 1 | a0001c0003t0056 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 378 | chr20 | 4783895 | ||||||
chr20:4783930 | C | T | 13 | a0001c0001t0011 a0001c0001t0012 a0001c0001t0014 others(10): Show |
35 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*343G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 343 | chr20 | 4783930 | ||||||
chr20:4783983 | G | A | 22 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0011 others(19): Show |
100 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*290C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 290 | chr20 | 4783983 | ||||||
chr20:4784036 | T | C | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(34): Show |
223 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*237A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 237 | chr20 | 4784036 | ||||||
chr20:4784102 | G | C | 13 | a0001c0001t0011 a0001c0001t0012 a0001c0001t0014 others(10): Show |
35 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*171C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 12/12 | 171 | chr20 | 4784102 | ||||||
chr20:4822340 | G | C | 71 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(68): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
5_prime_UTR_variant | MODIFIER | c.-44C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/12 | 21310 | chr20 | 4822340 | ||||||
chr20:4822340 | G | T | 1 | a0001c0001t0039 | 1 | NA19082.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/12 | 21310 | chr20 | 4822340 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:4784359 | G | A | 2 | a0001c0001t0021g0014 a0001c0001t0021g0296 |
3 | HG03139.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.912-17C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784359 | |||||||
chr20:4784388 | C | A | 51 | a0001c0001t0003g0022 a0001c0001t0003g0082 a0001c0001t0003g0083 others(48): Show |
56 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.912-46G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784388 | |||||||
chr20:4784564 | T | C | 54 | a0001c0001t0003g0022 a0001c0001t0003g0082 a0001c0001t0003g0083 others(51): Show |
61 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.912-222A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784564 | |||||||
chr20:4784592 | C | CA | 8 | a0001c0001t0003g0088 a0001c0001t0003g0219 a0001c0001t0003g0235 others(5): Show |
8 | HG02071.hp2 HG02135.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.912-251dupT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784592 | |||||||
chr20:4784592 | CA | C | 15 | a0001c0001t0003g0215 a0001c0001t0003g0229 a0001c0001t0003g0293 others(12): Show |
17 | HG02015.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.912-251delT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784592 | |||||||
chr20:4784592 | CAA | C | 138 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(135): Show |
154 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.912-252_912-251del others(2): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784592 | |||||||
chr20:4784592 | CAAA | C | 97 | a0001c0001t0001g0201 a0001c0001t0001g0354 a0001c0001t0002g0002 others(94): Show |
105 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.912-253_912-251del others(3): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784592 | |||||||
chr20:4784592 | CAAAAAAA others(4): Show |
C | 8 | a0001c0001t0010g0015 a0001c0001t0010g0105 a0001c0001t0010g0118 others(5): Show |
9 | HG01891.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.912-261_912-251del others(11): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784592 | |||||||
chr20:4784592 | CAAAAAAA others(5): Show |
C | 45 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0124 others(42): Show |
47 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.912-262_912-251del others(12): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784592 | |||||||
chr20:4784620 | A | G | 11 | a0001c0001t0011g0084 a0001c0001t0011g0165 a0001c0001t0011g0203 others(8): Show |
11 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.912-278T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784620 | |||||||
chr20:4784627 | A | C | 1 | a0001c0001t0001g0201 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.912-285T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784627 | |||||||
chr20:4784663 | G | A | 54 | a0001c0001t0003g0022 a0001c0001t0003g0082 a0001c0001t0003g0083 others(51): Show |
61 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.912-321C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784663 | |||||||
chr20:4784768 | C | T | 1 | a0001c0001t0008g0239 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.912-426G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784768 | |||||||
chr20:4784840 | G | A | 203 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(200): Show |
224 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.912-498C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784840 | |||||||
chr20:4784859 | G | A | 1 | a0001c0001t0004g0243 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.912-517C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784859 | |||||||
chr20:4784880 | G | C | 16 | a0001c0001t0005g0007 a0001c0001t0005g0212 a0001c0001t0005g0246 others(13): Show |
18 | HG02027.hp1 HG02040.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.912-538C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4784880 | |||||||
chr20:4785101 | G | A | 2 | a0001c0001t0021g0014 a0001c0001t0021g0296 |
3 | HG03139.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.912-759C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785101 | |||||||
chr20:4785125 | C | G | 1 | a0001c0001t0069g0182 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.912-783G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785125 | |||||||
chr20:4785139 | G | A | 1 | a0001c0001t0004g0124 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.912-797C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785139 | |||||||
chr20:4785155 | C | CA | 156 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(153): Show |
171 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.912-814dupT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785155 | |||||||
chr20:4785155 | C | CAA | 39 | a0001c0001t0001g0086 a0001c0001t0001g0258 a0001c0001t0001g0266 others(36): Show |
42 | HG00140.hp1 HG00323.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.912-815_912-814dup others(2): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785155 | |||||||
chr20:4785155 | CA | C | 9 | a0001c0001t0002g0254 a0001c0001t0002g0305 a0001c0001t0002g0338 others(6): Show |
10 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.912-814delT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785155 | |||||||
chr20:4785299 | T | A | 54 | a0001c0001t0003g0022 a0001c0001t0003g0082 a0001c0001t0003g0083 others(51): Show |
61 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.911+932A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785299 | |||||||
chr20:4785364 | A | G | 204 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(201): Show |
225 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.911+867T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785364 | |||||||
chr20:4785445 | G | A | 1 | a0003c0008t0002g0096 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.911+786C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785445 | |||||||
chr20:4785551 | G | A | 87 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(84): Show |
99 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.911+680C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785551 | |||||||
chr20:4785559 | C | T | 20 | a0001c0001t0004g0041 a0001c0001t0005g0007 a0001c0001t0005g0016 others(17): Show |
23 | HG02027.hp1 HG02040.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.911+672G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785559 | |||||||
chr20:4785596 | A | G | 2 | a0001c0003t0003g0023 a0001c0003t0056g0221 |
3 | NA18981.hp1 NA19057.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.911+635T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785596 | |||||||
chr20:4785604 | A | G | 2 | a0001c0001t0011g0370 a0001c0001t0078g0136 |
2 | HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.911+627T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785604 | |||||||
chr20:4785657 | A | C | 1 | a0001c0001t0052g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.911+574T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785657 | |||||||
chr20:4785698 | C | T | 1 | a0001c0001t0055g0303 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.911+533G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785698 | |||||||
chr20:4785747 | T | C | 57 | a0001c0001t0001g0379 a0001c0001t0003g0022 a0001c0001t0003g0082 others(54): Show |
65 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.911+484A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785747 | |||||||
chr20:4785810 | C | T | 107 | a0001c0001t0001g0379 a0001c0001t0003g0022 a0001c0001t0003g0082 others(104): Show |
120 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.911+421G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785810 | |||||||
chr20:4785920 | C | G | 1 | a0001c0001t0041g0077 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.911+311G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785920 | |||||||
chr20:4785921 | T | C | 33 | a0001c0001t0011g0084 a0001c0001t0011g0203 a0001c0001t0011g0268 others(30): Show |
36 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.911+310A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785921 | |||||||
chr20:4785923 | T | C | 41 | a0001c0001t0001g0129 a0001c0001t0004g0018 a0001c0001t0004g0019 others(38): Show |
43 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.911+308A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4785923 | |||||||
chr20:4786120 | G | A | 6 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0001c0001t0002g0359 others(3): Show |
6 | NA18941.hp2 NA18988.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.911+111C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4786120 | |||||||
chr20:4786173 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.911+58C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 11/11 | chr20 | 4786173 | |||||||
chr20:4786361 | C | T | 4 | a0001c0001t0012g0011 a0001c0001t0012g0371 a0001c0001t0027g0110 others(1): Show |
5 | HG02145.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.814-33G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4786361 | |||||||
chr20:4786429 | A | C | 2 | a0001c0001t0005g0081 a0001c0001t0021g0014 |
3 | HG03139.hp2 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.814-101T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4786429 | |||||||
chr20:4786518 | G | C | 2 | a0001c0001t0003g0109 a0001c0001t0035g0161 |
2 | HG02293.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.814-190C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4786518 | |||||||
chr20:4786550 | T | C | 2 | a0001c0001t0002g0339 a0001c0001t0002g0340 |
2 | NA18994.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.814-222A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4786550 | |||||||
chr20:4786572 | A | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(96): Show |
114 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.814-244T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4786572 | |||||||
chr20:4786598 | A | C | 1 | a0001c0001t0001g0012 | 2 | HG00597.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.814-270T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4786598 | |||||||
chr20:4786700 | C | T | 47 | a0001c0001t0001g0129 a0001c0001t0002g0187 a0001c0001t0002g0188 others(44): Show |
50 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.814-372G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4786700 | |||||||
chr20:4786707 | C | T | 3 | a0001c0001t0004g0041 a0001c0001t0005g0016 a0001c0001t0005g0169 |
4 | HG02965.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.814-379G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4786707 | |||||||
chr20:4786834 | G | A | 98 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(95): Show |
113 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.814-506C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4786834 | |||||||
chr20:4786974 | G | T | 94 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(91): Show |
106 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.814-646C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4786974 | |||||||
chr20:4786979 | G | A | 94 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(91): Show |
106 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.814-651C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4786979 | |||||||
chr20:4787058 | A | C | 100 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0129 others(97): Show |
110 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.813+575T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4787058 | |||||||
chr20:4787295 | G | A | 1 | a0001c0001t0053g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.813+338C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4787295 | |||||||
chr20:4787330 | A | G | 93 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(90): Show |
105 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.813+303T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4787330 | |||||||
chr20:4787401 | C | A | 2 | a0001c0001t0006g0146 a0001c0001t0007g0075 |
2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.813+232G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4787401 | |||||||
chr20:4787490 | T | C | 208 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0129 others(205): Show |
226 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.813+143A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4787490 | |||||||
chr20:4787537 | G | A | 91 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(88): Show |
103 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.813+96C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 10/11 | chr20 | 4787537 | |||||||
chr20:4787829 | A | AAGGGACT | 249 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(246): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.692-76_692-75insAG others(5): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 9/11 | chr20 | 4787829 | |||||||
chr20:4787889 | C | T | 1 | a0001c0002t0001g0170 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.692-135G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 9/11 | chr20 | 4787889 | |||||||
chr20:4788002 | C | G | 2 | a0001c0001t0001g0362 a0001c0001t0001g0364 |
2 | NA18956.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.691+215G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 9/11 | chr20 | 4788002 | |||||||
chr20:4788069 | A | G | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0265 |
3 | HG02132.hp1 NA18747.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.691+148T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 9/11 | chr20 | 4788069 | |||||||
chr20:4788200 | GT | G | 49 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(46): Show |
56 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.691+16delA | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 9/11 | chr20 | 4788200 | |||||||
chr20:4788316 | C | T | 1 | a0001c0001t0002g0375 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.640-48G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4788316 | |||||||
chr20:4788463 | A | C | 1 | a0001c0001t0005g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.640-195T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4788463 | |||||||
chr20:4788531 | G | C | 155 | a0001c0001t0001g0129 a0001c0001t0001g0213 a0001c0001t0001g0214 others(152): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.640-263C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4788531 | |||||||
chr20:4788537 | G | A | 320 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(317): Show |
354 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(351): Show |
intron_variant | MODIFIER | c.640-269C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4788537 | |||||||
chr20:4788619 | A | G | 146 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(143): Show |
166 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.640-351T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4788619 | |||||||
chr20:4788728 | T | C | 173 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0129 others(170): Show |
187 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.640-460A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4788728 | |||||||
chr20:4789008 | C | A | 1 | a0001c0001t0002g0223 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.639+588G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4789008 | |||||||
chr20:4789031 | A | G | 1 | a0001c0001t0012g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.639+565T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4789031 | |||||||
chr20:4789148 | A | G | 146 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(143): Show |
166 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.639+448T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4789148 | |||||||
chr20:4789149 | C | T | 53 | a0001c0001t0001g0129 a0001c0001t0002g0187 a0001c0001t0002g0188 others(50): Show |
56 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.639+447G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4789149 | |||||||
chr20:4789150 | G | A | 146 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(143): Show |
166 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.639+446C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4789150 | |||||||
chr20:4789188 | C | A | 103 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0263 others(100): Show |
110 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.639+408G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4789188 | |||||||
chr20:4789251 | C | G | 146 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(143): Show |
166 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.639+345G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4789251 | |||||||
chr20:4789298 | G | A | 1 | a0001c0001t0008g0239 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.639+298C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4789298 | |||||||
chr20:4789328 | T | A | 1 | a0001c0001t0012g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.639+268A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4789328 | |||||||
chr20:4789333 | G | A | 1 | a0001c0001t0003g0219 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.639+263C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4789333 | |||||||
chr20:4789413 | C | T | 7 | a0001c0001t0003g0022 a0001c0001t0003g0091 a0001c0001t0003g0184 others(4): Show |
8 | HG00558.hp2 HG01975.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.639+183G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4789413 | |||||||
chr20:4789457 | G | A | 4 | a0001c0001t0012g0011 a0001c0001t0012g0371 a0001c0001t0027g0110 others(1): Show |
5 | HG02145.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.639+139C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4789457 | |||||||
chr20:4789475 | G | A | 1 | a0001c0001t0049g0227 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.639+121C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 8/11 | chr20 | 4789475 | |||||||
chr20:4789718 | C | T | 3 | a0001c0001t0016g0004 a0001c0001t0016g0038 a0001c0001t0016g0042 |
4 | HG02055.hp1 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.538-21G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 7/11 | chr20 | 4789718 | |||||||
chr20:4789765 | G | A | 1 | a0001c0001t0035g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.538-68C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 7/11 | chr20 | 4789765 | |||||||
chr20:4789773 | G | A | 1 | a0001c0001t0012g0011 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.538-76C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 7/11 | chr20 | 4789773 | |||||||
chr20:4789794 | G | A | 350 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(347): Show |
385 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(382): Show |
intron_variant | MODIFIER | c.538-97C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 7/11 | chr20 | 4789794 | |||||||
chr20:4789821 | G | A | 15 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0329 others(12): Show |
19 | HG02027.hp1 HG02056.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.538-124C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 7/11 | chr20 | 4789821 | |||||||
chr20:4789869 | A | G | 2 | a0001c0001t0003g0293 a0001c0001t0003g0294 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.538-172T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 7/11 | chr20 | 4789869 | |||||||
chr20:4789911 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0346 a0001c0001t0001g0354 others(1): Show |
5 | HG02735.hp2 NA18944.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.538-214C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 7/11 | chr20 | 4789911 | |||||||
chr20:4789963 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.538-266G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 7/11 | chr20 | 4789963 | |||||||
chr20:4789967 | G | A | 16 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0329 others(13): Show |
20 | HG02027.hp1 HG02056.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.538-270C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 7/11 | chr20 | 4789967 | |||||||
chr20:4790016 | T | A | 3 | a0001c0001t0016g0004 a0001c0001t0016g0038 a0001c0001t0016g0042 |
4 | HG02055.hp1 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.538-319A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 7/11 | chr20 | 4790016 | |||||||
chr20:4790690 | G | T | 56 | a0001c0001t0001g0129 a0001c0001t0002g0187 a0001c0001t0002g0188 others(53): Show |
59 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.377-79C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4790690 | |||||||
chr20:4790725 | T | C | 3 | a0001c0001t0010g0155 a0001c0001t0010g0333 a0001c0001t0061g0119 |
3 | HG01109.hp1 HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.377-114A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4790725 | |||||||
chr20:4790745 | G | A | 1 | a0001c0001t0001g0314 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377-134C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4790745 | |||||||
chr20:4790828 | G | T | 3 | a0001c0001t0035g0197 a0002c0004t0050g0121 a0002c0004t0051g0166 |
3 | HG02486.hp1 HG02886.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.377-217C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4790828 | |||||||
chr20:4790910 | A | G | 1 | a0001c0001t0021g0014 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.377-299T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4790910 | |||||||
chr20:4790929 | G | A | 14 | a0001c0001t0002g0149 a0001c0001t0002g0164 a0001c0001t0002g0342 others(11): Show |
14 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.377-318C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4790929 | |||||||
chr20:4790997 | T | C | 192 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(189): Show |
218 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.377-386A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4790997 | |||||||
chr20:4791024 | A | G | 270 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(267): Show |
302 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(299): Show |
intron_variant | MODIFIER | c.377-413T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791024 | |||||||
chr20:4791049 | C | T | 1 | a0001c0001t0004g0347 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.377-438G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791049 | |||||||
chr20:4791092 | T | C | 30 | a0001c0001t0002g0149 a0001c0001t0002g0164 a0001c0001t0002g0342 others(27): Show |
31 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.377-481A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791092 | |||||||
chr20:4791134 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.377-523G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791134 | |||||||
chr20:4791214 | G | A | 2 | a0001c0001t0030g0050 a0001c0001t0030g0051 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.377-603C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791214 | |||||||
chr20:4791226 | A | T | 109 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0263 others(106): Show |
116 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.377-615T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791226 | |||||||
chr20:4791252 | A | G | 16 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0329 others(13): Show |
20 | HG02027.hp1 HG02056.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.377-641T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791252 | |||||||
chr20:4791312 | T | C | 9 | a0001c0001t0002g0020 a0001c0001t0002g0028 a0001c0001t0002g0144 others(6): Show |
11 | HG00735.hp1 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.377-701A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791312 | |||||||
chr20:4791327 | A | G | 30 | a0001c0001t0002g0149 a0001c0001t0002g0164 a0001c0001t0002g0342 others(27): Show |
31 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.377-716T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791327 | |||||||
chr20:4791400 | T | C | 144 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0032 others(141): Show |
159 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.377-789A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791400 | |||||||
chr20:4791477 | A | G | 1 | a0001c0001t0012g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.377-866T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791477 | |||||||
chr20:4791497 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.377-886G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791497 | |||||||
chr20:4791532 | T | C | 286 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(283): Show |
317 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.377-921A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791532 | |||||||
chr20:4791541 | C | T | 141 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0263 others(138): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.377-930G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791541 | |||||||
chr20:4791547 | T | G | 1 | a0001c0001t0004g0251 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.377-936A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791547 | |||||||
chr20:4791710 | G | A | 175 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(172): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.376+829C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791710 | |||||||
chr20:4791732 | G | A | 2 | a0001c0001t0005g0016 a0001c0001t0005g0169 |
3 | HG02965.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.376+807C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791732 | |||||||
chr20:4791743 | C | T | 1 | a0001c0001t0035g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.376+796G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791743 | |||||||
chr20:4791786 | G | A | 156 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0213 others(153): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.376+753C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791786 | |||||||
chr20:4791798 | T | G | 1 | a0001c0001t0005g0283 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.376+741A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791798 | |||||||
chr20:4791872 | A | G | 5 | a0001c0001t0001g0244 a0001c0001t0001g0312 a0001c0001t0001g0313 others(2): Show |
5 | NA18949.hp1 NA18970.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+667T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791872 | |||||||
chr20:4791909 | A | G | 7 | a0001c0001t0003g0183 a0001c0001t0003g0249 a0001c0001t0003g0269 others(4): Show |
7 | HG00639.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.376+630T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791909 | |||||||
chr20:4791999 | C | T | 145 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(142): Show |
166 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.376+540G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4791999 | |||||||
chr20:4792076 | A | G | 3 | a0001c0001t0004g0041 a0001c0001t0005g0016 a0001c0001t0005g0169 |
4 | HG02965.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.376+463T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792076 | |||||||
chr20:4792192 | A | T | 145 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(142): Show |
166 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.376+347T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792192 | |||||||
chr20:4792213 | C | T | 2 | a0001c0001t0003g0293 a0001c0001t0003g0294 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.376+326G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792213 | |||||||
chr20:4792226 | GAGGGAGA others(10): Show |
G | 1 | a0001c0001t0004g0131 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.376+296_376+312del others(17): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792226 | |||||||
chr20:4792256 | A | AGGAGG | 92 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(89): Show |
105 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.376+278_376+282dup others(5): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792256 | |||||||
chr20:4792256 | A | AGGAGGGG others(3): Show |
47 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(44): Show |
54 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.376+273_376+282dup others(10): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792256 | |||||||
chr20:4792256 | A | AGGAGGGG others(8): Show |
2 | a0001c0001t0005g0016 a0001c0001t0005g0169 |
3 | HG02965.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.376+268_376+282dup others(15): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792256 | |||||||
chr20:4792256 | A | AGGAGGGG others(13): Show |
1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.376+263_376+282dup others(20): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792256 | |||||||
chr20:4792256 | AGGAGG | A | 142 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0263 others(139): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.376+278_376+282del others(5): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792256 | |||||||
chr20:4792256 | AGGAGGGG others(3): Show |
A | 1 | a0001c0001t0006g0331 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.376+273_376+282del others(10): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792256 | |||||||
chr20:4792270 | G | A | 1 | a0001c0001t0005g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.376+269C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792270 | |||||||
chr20:4792284 | A | AGGGGAGG others(4): Show |
1 | a0001c0001t0003g0215 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.376+254_376+255ins others(11): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792284 | |||||||
chr20:4792371 | G | A | 16 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0329 others(13): Show |
20 | HG02027.hp1 HG02056.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.376+168C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792371 | |||||||
chr20:4792409 | A | C | 1 | a0001c0001t0043g0076 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.376+130T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 6/11 | chr20 | 4792409 | |||||||
chr20:4792686 | G | C | 49 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(46): Show |
56 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.288-59C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4792686 | |||||||
chr20:4792692 | G | A | 161 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(158): Show |
186 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.288-65C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4792692 | |||||||
chr20:4792693 | C | T | 1 | a0001c0001t0022g0190 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.288-66G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4792693 | |||||||
chr20:4792799 | C | G | 1 | a0001c0001t0005g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.288-172G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4792799 | |||||||
chr20:4792807 | G | C | 3 | a0001c0002t0028g0122 a0001c0002t0028g0123 a0001c0002t0028g0292 |
3 | HG02818.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.288-180C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4792807 | |||||||
chr20:4792854 | C | T | 17 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0329 others(14): Show |
21 | HG02027.hp1 HG02056.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.288-227G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4792854 | |||||||
chr20:4792951 | T | C | 307 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(304): Show |
342 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.288-324A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4792951 | |||||||
chr20:4793047 | A | G | 1 | a0001c0001t0002g0318 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.288-420T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4793047 | |||||||
chr20:4793134 | G | C | 1 | a0001c0001t0004g0252 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.288-507C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4793134 | |||||||
chr20:4793351 | T | G | 15 | a0001c0001t0001g0380 a0001c0001t0002g0009 a0001c0001t0002g0093 others(12): Show |
16 | HG00673.hp1 HG01981.hp2 NA18940.hp2 others(13): Show |
intron_variant | MODIFIER | c.288-724A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4793351 | |||||||
chr20:4793525 | T | G | 145 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(142): Show |
166 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.288-898A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4793525 | |||||||
chr20:4793636 | A | T | 1 | a0001c0001t0002g0285 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.288-1009T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4793636 | |||||||
chr20:4793643 | T | A | 84 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(81): Show |
95 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.288-1016A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4793643 | |||||||
chr20:4793644 | T | A | 1 | a0001c0001t0002g0270 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.288-1017A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4793644 | |||||||
chr20:4793646 | T | A | 1 | a0001c0001t0041g0077 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.288-1019A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4793646 | |||||||
chr20:4793648 | TA | T | 3 | a0001c0001t0008g0010 a0001c0001t0008g0392 a0001c0002t0014g0369 |
4 | HG02895.hp1 HG02897.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.288-1022delT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4793648 | |||||||
chr20:4793649 | A | T | 2 | a0001c0001t0027g0110 a0001c0001t0046g0286 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.288-1022T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4793649 | |||||||
chr20:4793654 | A | T | 162 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(159): Show |
187 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.288-1027T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4793654 | |||||||
chr20:4793656 | T | A | 145 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(142): Show |
166 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.288-1029A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4793656 | |||||||
chr20:4794039 | G | T | 96 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(93): Show |
110 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.288-1412C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4794039 | |||||||
chr20:4794083 | T | C | 1 | a0001c0001t0077g0192 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.288-1456A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4794083 | |||||||
chr20:4794433 | G | A | 1 | a0001c0001t0007g0064 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.287+1382C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4794433 | |||||||
chr20:4794492 | G | A | 1 | a0001c0001t0012g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.287+1323C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4794492 | |||||||
chr20:4794515 | C | T | 1 | a0001c0001t0035g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.287+1300G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4794515 | |||||||
chr20:4794521 | C | T | 2 | a0001c0001t0008g0010 a0001c0001t0008g0392 |
3 | HG02895.hp1 HG02897.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.287+1294G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4794521 | |||||||
chr20:4794620 | G | T | 1 | a0001c0001t0002g0093 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.287+1195C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4794620 | |||||||
chr20:4794753 | G | A | 3 | a0001c0001t0016g0004 a0001c0001t0016g0038 a0001c0001t0016g0042 |
4 | HG02055.hp1 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.287+1062C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4794753 | |||||||
chr20:4794970 | G | T | 17 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0329 others(14): Show |
21 | HG02027.hp1 HG02056.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.287+845C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4794970 | |||||||
chr20:4794972 | T | A | 1 | a0001c0001t0012g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.287+843A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4794972 | |||||||
chr20:4794993 | A | T | 145 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(142): Show |
166 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.287+822T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4794993 | |||||||
chr20:4795004 | G | C | 1 | a0001c0001t0005g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.287+811C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795004 | |||||||
chr20:4795108 | C | T | 4 | a0001c0001t0019g0037 a0001c0001t0019g0045 a0001c0001t0045g0065 others(1): Show |
4 | HG02615.hp2 HG02895.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.287+707G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795108 | |||||||
chr20:4795216 | C | T | 165 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(162): Show |
191 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.287+599G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795216 | |||||||
chr20:4795258 | A | C | 166 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(163): Show |
192 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.287+557T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795258 | |||||||
chr20:4795420 | T | A | 2 | a0002c0004t0050g0121 a0002c0004t0051g0166 |
2 | HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.287+395A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795420 | |||||||
chr20:4795432 | T | C | 1 | a0001c0001t0012g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.287+383A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795432 | |||||||
chr20:4795437 | C | T | 1 | a0001c0001t0011g0341 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.287+378G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795437 | |||||||
chr20:4795652 | T | C | 166 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(163): Show |
192 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.287+163A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795652 | |||||||
chr20:4795653 | G | C | 166 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(163): Show |
192 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.287+162C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795653 | |||||||
chr20:4795674 | T | C | 201 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(198): Show |
228 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.287+141A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795674 | |||||||
chr20:4795721 | G | C | 73 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0087 others(70): Show |
87 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.287+94C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795721 | |||||||
chr20:4795721 | G | T | 93 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(90): Show |
105 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.287+94C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795721 | |||||||
chr20:4795741 | C | G | 146 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(143): Show |
167 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.287+74G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795741 | |||||||
chr20:4795799 | G | A | 166 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(163): Show |
192 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.287+16C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 5/11 | chr20 | 4795799 | |||||||
chr20:4796013 | G | A | 104 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0263 others(101): Show |
111 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.136-47C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796013 | |||||||
chr20:4796072 | C | A | 166 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(163): Show |
192 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.136-106G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796072 | |||||||
chr20:4796118 | G | C | 166 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(163): Show |
192 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.136-152C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796118 | |||||||
chr20:4796141 | G | A | 4 | a0001c0001t0017g0127 a0001c0001t0017g0128 a0001c0001t0017g0160 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-175C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796141 | |||||||
chr20:4796143 | C | A | 81 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0087 others(78): Show |
96 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.136-177G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796143 | |||||||
chr20:4796306 | T | C | 81 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0087 others(78): Show |
96 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.136-340A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796306 | |||||||
chr20:4796352 | C | T | 81 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0087 others(78): Show |
96 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.136-386G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796352 | |||||||
chr20:4796395 | C | T | 13 | a0001c0002t0014g0104 a0001c0002t0014g0125 a0001c0002t0014g0153 others(10): Show |
13 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.136-429G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796395 | |||||||
chr20:4796477 | G | A | 16 | a0001c0001t0001g0380 a0001c0001t0002g0009 a0001c0001t0002g0093 others(13): Show |
17 | HG00673.hp1 HG01981.hp2 NA18940.hp2 others(14): Show |
intron_variant | MODIFIER | c.136-511C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796477 | |||||||
chr20:4796575 | C | T | 1 | a0001c0001t0010g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.136-609G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796575 | |||||||
chr20:4796586 | A | G | 1 | a0001c0001t0005g0282 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.136-620T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796586 | |||||||
chr20:4796618 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0007g0047 |
2 | HG04204.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.136-652C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796618 | |||||||
chr20:4796703 | G | A | 108 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0087 others(105): Show |
123 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.136-737C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796703 | |||||||
chr20:4796791 | C | T | 6 | a0001c0001t0002g0008 a0001c0001t0002g0043 a0001c0001t0002g0150 others(3): Show |
7 | HG01071.hp2 HG01361.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-825G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796791 | |||||||
chr20:4796814 | A | G | 2 | a0001c0001t0008g0010 a0001c0001t0008g0392 |
3 | HG02895.hp1 HG02897.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.136-848T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796814 | |||||||
chr20:4796902 | G | A | 77 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0087 others(74): Show |
91 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.136-936C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796902 | |||||||
chr20:4796947 | A | G | 109 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0087 others(106): Show |
124 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.136-981T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796947 | |||||||
chr20:4796969 | C | T | 2 | a0001c0001t0004g0228 a0001c0001t0023g0225 |
2 | NA18964.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.136-1003G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796969 | |||||||
chr20:4796982 | A | G | 78 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0087 others(75): Show |
92 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.136-1016T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4796982 | |||||||
chr20:4797094 | C | T | 29 | a0001c0001t0002g0149 a0001c0001t0002g0164 a0001c0001t0002g0342 others(26): Show |
30 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.135+916G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4797094 | |||||||
chr20:4797404 | C | T | 1 | a0001c0001t0002g0372 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.135+606G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4797404 | |||||||
chr20:4797511 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.135+499C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4797511 | |||||||
chr20:4797564 | C | A | 78 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0087 others(75): Show |
92 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.135+446G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4797564 | |||||||
chr20:4797565 | ACTATCAG others(8): Show |
A | 78 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0087 others(75): Show |
92 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.135+430_135+444del others(15): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4797565 | |||||||
chr20:4797581 | C | G | 78 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0087 others(75): Show |
92 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.135+429G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4797581 | |||||||
chr20:4797640 | C | A | 1 | a0001c0002t0026g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.135+370G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4797640 | |||||||
chr20:4797724 | C | T | 62 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(59): Show |
72 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.135+286G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4797724 | |||||||
chr20:4797832 | T | C | 7 | a0001c0001t0010g0015 a0001c0001t0010g0105 a0001c0001t0010g0118 others(4): Show |
8 | HG01891.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+178A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4797832 | |||||||
chr20:4797871 | C | A | 29 | a0001c0001t0002g0149 a0001c0001t0002g0164 a0001c0001t0002g0342 others(26): Show |
30 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.135+139G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4797871 | |||||||
chr20:4797955 | A | T | 1 | a0001c0001t0008g0224 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.135+55T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4797955 | |||||||
chr20:4797965 | A | G | 1 | a0001c0001t0004g0250 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.135+45T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 4/11 | chr20 | 4797965 | |||||||
chr20:4798108 | A | G | 62 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(59): Show |
72 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.60-23T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798108 | |||||||
chr20:4798153 | CTT | C | 24 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0142 others(21): Show |
26 | HG00621.hp1 HG00673.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.60-70_60-69delAA | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798153 | |||||||
chr20:4798229 | C | A | 1 | a0001c0001t0001g0313 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.60-144G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798229 | |||||||
chr20:4798249 | A | G | 63 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(60): Show |
73 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.60-164T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798249 | |||||||
chr20:4798314 | G | A | 3 | a0001c0001t0004g0238 a0001c0001t0004g0250 a0001c0001t0004g0261 |
3 | HG00140.hp2 HG00639.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.60-229C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798314 | |||||||
chr20:4798348 | C | G | 1 | a0001c0001t0041g0077 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.60-263G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798348 | |||||||
chr20:4798351 | G | T | 1 | a0001c0001t0011g0377 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.60-266C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798351 | |||||||
chr20:4798355 | C | T | 1 | a0001c0001t0029g0005 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.60-270G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798355 | |||||||
chr20:4798356 | G | A | 1 | a0001c0002t0027g0157 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.60-271C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798356 | |||||||
chr20:4798362 | C | G | 2 | a0001c0002t0014g0125 a0001c0002t0014g0369 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.60-277G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798362 | |||||||
chr20:4798367 | A | G | 1 | a0001c0001t0002g0232 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.60-282T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798367 | |||||||
chr20:4798422 | G | A | 63 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(60): Show |
73 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.60-337C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798422 | |||||||
chr20:4798474 | T | C | 63 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(60): Show |
73 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.60-389A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798474 | |||||||
chr20:4798548 | C | G | 63 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(60): Show |
73 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.60-463G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798548 | |||||||
chr20:4798579 | C | T | 20 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0329 others(17): Show |
24 | HG02027.hp1 HG02056.hp1 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.60-494G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798579 | |||||||
chr20:4798609 | A | G | 63 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(60): Show |
73 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.60-524T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798609 | |||||||
chr20:4798724 | G | T | 18 | a0001c0001t0002g0149 a0001c0001t0002g0164 a0001c0001t0002g0342 others(15): Show |
18 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.60-639C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798724 | |||||||
chr20:4798758 | A | AGAGGTTG others(398): Show |
1 | a0001c0003t0003g0095 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.60-674_60-673insCA others(403): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798758 | |||||||
chr20:4798758 | A | AGAGGTTG others(398): Show |
49 | a0001c0001t0002g0149 a0001c0001t0002g0164 a0001c0001t0002g0342 others(46): Show |
51 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.60-674_60-673insCA others(403): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798758 | |||||||
chr20:4798758 | A | AGAGGTTG others(398): Show |
5 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0329 others(2): Show |
8 | HG02080.hp2 NA18965.hp1 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.60-674_60-673insCA others(403): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798758 | |||||||
chr20:4798765 | G | GCAGTGAG others(397): Show |
54 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(51): Show |
63 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.60-681_60-680insGA others(402): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798765 | |||||||
chr20:4798765 | G | GCAGTGAG others(397): Show |
1 | a0001c0001t0052g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.60-681_60-680insGA others(402): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798765 | |||||||
chr20:4798765 | G | GCAGTGAG others(397): Show |
7 | a0001c0001t0010g0015 a0001c0001t0010g0105 a0001c0001t0010g0118 others(4): Show |
8 | HG01891.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.60-681_60-680insGA others(402): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798765 | |||||||
chr20:4798780 | C | T | 1 | a0003c0008t0002g0096 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.60-695G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798780 | |||||||
chr20:4798807 | A | C | 63 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(60): Show |
73 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.60-722T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798807 | |||||||
chr20:4798829 | A | C | 6 | a0001c0001t0010g0015 a0001c0001t0010g0105 a0001c0001t0010g0118 others(3): Show |
7 | HG02257.hp1 HG02622.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.60-744T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798829 | |||||||
chr20:4798829 | A | G | 1 | a0004c0005t0003g0116 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.60-744T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798829 | |||||||
chr20:4798841 | C | CA | 3 | a0001c0001t0002g0284 a0001c0001t0009g0072 a0001c0001t0024g0092 |
3 | HG01361.hp2 NA18972.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.60-757dupT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798841 | |||||||
chr20:4798844 | AC | A | 5 | a0001c0001t0002g0009 a0001c0001t0017g0127 a0001c0001t0017g0128 others(2): Show |
6 | HG02145.hp1 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-760delG | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798844 | |||||||
chr20:4798845 | C | A | 81 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0263 others(78): Show |
87 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.60-760G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798845 | |||||||
chr20:4798845 | CA | C | 52 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0329 others(49): Show |
57 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.60-761delT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798845 | |||||||
chr20:4798848 | A | AC | 7 | a0001c0001t0010g0015 a0001c0001t0010g0105 a0001c0001t0010g0118 others(4): Show |
8 | HG01891.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.60-764_60-763insG | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798848 | |||||||
chr20:4798849 | A | C | 82 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0090 others(79): Show |
94 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.60-764T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798849 | |||||||
chr20:4798853 | A | C | 1 | a0001c0001t0011g0377 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.60-768T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798853 | |||||||
chr20:4798891 | C | A | 134 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0213 others(131): Show |
145 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.60-806G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798891 | |||||||
chr20:4798923 | T | C | 66 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(63): Show |
76 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.60-838A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798923 | |||||||
chr20:4798931 | G | A | 1 | a0001c0001t0057g0301 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.60-846C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798931 | |||||||
chr20:4798963 | G | T | 56 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0181 others(53): Show |
65 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.60-878C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4798963 | |||||||
chr20:4799007 | G | A | 1 | a0001c0001t0002g0202 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.60-922C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799007 | |||||||
chr20:4799054 | G | T | 63 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0329 others(60): Show |
71 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.60-969C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799054 | |||||||
chr20:4799072 | G | C | 17 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0329 others(14): Show |
21 | HG02027.hp1 HG02056.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.60-987C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799072 | |||||||
chr20:4799128 | G | A | 129 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0108 others(126): Show |
141 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.60-1043C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799128 | |||||||
chr20:4799179 | A | G | 24 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0329 others(21): Show |
29 | HG01070.hp1 HG01346.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.60-1094T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799179 | |||||||
chr20:4799213 | C | T | 14 | a0001c0001t0012g0171 a0001c0001t0016g0004 a0001c0001t0016g0038 others(11): Show |
16 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.60-1128G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799213 | |||||||
chr20:4799277 | G | A | 1 | a0001c0001t0070g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.60-1192C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799277 | |||||||
chr20:4799301 | C | G | 4 | a0001c0001t0001g0247 a0001c0001t0001g0374 a0001c0001t0003g0383 others(1): Show |
4 | HG02602.hp2 HG02738.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-1216G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799301 | |||||||
chr20:4799343 | C | T | 7 | a0001c0001t0010g0015 a0001c0001t0010g0105 a0001c0001t0010g0118 others(4): Show |
8 | HG01891.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.60-1258G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799343 | |||||||
chr20:4799637 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0004g0378 a0001c0001t0024g0039 |
3 | HG01496.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.59+1335G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799637 | |||||||
chr20:4799734 | G | A | 1 | a0001c0001t0002g0241 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.59+1238C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799734 | |||||||
chr20:4799842 | T | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0346 a0001c0001t0001g0354 others(1): Show |
5 | HG02735.hp2 NA18944.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+1130A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799842 | |||||||
chr20:4799845 | C | T | 1 | a0001c0001t0052g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.59+1127G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799845 | |||||||
chr20:4799849 | C | T | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.59+1123G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799849 | |||||||
chr20:4799884 | G | A | 1 | a0001c0001t0044g0073 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.59+1088C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799884 | |||||||
chr20:4799922 | A | G | 358 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(355): Show |
395 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(392): Show |
intron_variant | MODIFIER | c.59+1050T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799922 | |||||||
chr20:4799969 | G | T | 1 | a0001c0001t0005g0324 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.59+1003C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4799969 | |||||||
chr20:4800103 | G | T | 188 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0026 others(185): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.59+869C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800103 | |||||||
chr20:4800110 | TA | T | 23 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0142 others(20): Show |
25 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.59+861delT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800110 | |||||||
chr20:4800123 | A | AG | 2 | a0001c0001t0008g0010 a0001c0001t0008g0392 |
3 | HG02895.hp1 HG02897.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.59+848_59+849insC | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800123 | |||||||
chr20:4800123 | A | G | 3 | a0001c0001t0002g0202 a0001c0001t0012g0130 a0001c0001t0027g0110 |
3 | HG03041.hp1 HG03098.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.59+849T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800123 | |||||||
chr20:4800156 | A | G | 1 | a0001c0001t0004g0238 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.59+816T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800156 | |||||||
chr20:4800184 | A | G | 1 | a0001c0001t0003g0205 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.59+788T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800184 | |||||||
chr20:4800300 | C | T | 1 | a0001c0001t0005g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.59+672G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800300 | |||||||
chr20:4800301 | T | C | 148 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0026 others(145): Show |
162 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.59+671A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800301 | |||||||
chr20:4800369 | C | T | 16 | a0001c0001t0002g0164 a0001c0001t0002g0342 a0001c0001t0002g0372 others(13): Show |
17 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.59+603G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800369 | |||||||
chr20:4800432 | G | C | 1 | a0001c0001t0047g0373 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.59+540C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800432 | |||||||
chr20:4800514 | G | A | 1 | a0001c0001t0011g0268 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.59+458C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800514 | |||||||
chr20:4800515 | C | T | 1 | a0001c0001t0002g0270 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.59+457G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800515 | |||||||
chr20:4800526 | C | T | 2 | a0001c0001t0005g0016 a0001c0001t0005g0169 |
3 | HG02965.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.59+446G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800526 | |||||||
chr20:4800552 | T | C | 250 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0024 others(247): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.59+420A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800552 | |||||||
chr20:4800584 | C | T | 2 | a0001c0001t0002g0339 a0001c0001t0002g0340 |
2 | NA18994.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.59+388G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800584 | |||||||
chr20:4800643 | C | T | 28 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0317 others(25): Show |
35 | HG01070.hp1 HG01346.hp1 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.59+329G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800643 | |||||||
chr20:4800662 | A | G | 1 | a0001c0001t0002g0093 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.59+310T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800662 | |||||||
chr20:4800674 | ACTC | A | 6 | a0001c0001t0007g0047 a0001c0001t0007g0055 a0001c0001t0007g0057 others(3): Show |
6 | HG03239.hp1 HG03239.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.59+295_59+297delGA others(1): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800674 | |||||||
chr20:4800678 | C | T | 2 | a0001c0001t0037g0139 a0001c0001t0037g0141 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.59+294G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800678 | |||||||
chr20:4800743 | C | T | 1 | a0001c0001t0021g0014 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.59+229G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800743 | |||||||
chr20:4800774 | G | A | 1 | a0001c0001t0052g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.59+198C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800774 | |||||||
chr20:4800794 | G | A | 2 | a0001c0001t0018g0287 a0004c0005t0003g0116 |
2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.59+178C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800794 | |||||||
chr20:4800828 | A | G | 1 | a0001c0001t0006g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.59+144T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800828 | |||||||
chr20:4800850 | T | C | 74 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0108 others(71): Show |
87 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.59+122A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800850 | |||||||
chr20:4800968 | T | C | 1 | a0001c0001t0012g0011 | 2 | HG02717.hp1 HG02886.hp1 |
splice_region_variant&intron_variant | LOW | c.59+4A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 3/11 | chr20 | 4800968 | |||||||
chr20:4801066 | C | T | 1 | a0001c0001t0013g0319 | 1 | HG01070.hp1 | splice_region_variant&intron_variant | LOW | c.-32-4G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4801066 | |||||||
chr20:4801098 | A | G | 1 | a0001c0001t0013g0327 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-32-36T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4801098 | |||||||
chr20:4801156 | G | T | 1 | a0001c0001t0002g0093 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-32-94C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4801156 | |||||||
chr20:4801169 | G | A | 3 | a0001c0001t0005g0081 a0002c0004t0050g0121 a0002c0004t0051g0166 |
3 | HG02486.hp1 HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-32-107C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4801169 | |||||||
chr20:4801338 | G | C | 193 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0024 others(190): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-32-276C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4801338 | |||||||
chr20:4801388 | G | A | 85 | a0001c0001t0001g0021 a0001c0001t0001g0213 a0001c0001t0001g0214 others(82): Show |
93 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-32-326C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4801388 | |||||||
chr20:4801437 | A | C | 85 | a0001c0001t0001g0021 a0001c0001t0001g0213 a0001c0001t0001g0214 others(82): Show |
93 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-32-375T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4801437 | |||||||
chr20:4801454 | G | A | 85 | a0001c0001t0001g0021 a0001c0001t0001g0213 a0001c0001t0001g0214 others(82): Show |
93 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-32-392C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4801454 | |||||||
chr20:4801554 | TATAAC | T | 29 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0317 others(26): Show |
36 | HG01070.hp1 HG01346.hp1 HG01346.hp2 others(33): Show |
intron_variant | MODIFIER | c.-32-497_-32-493del others(5): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4801554 | |||||||
chr20:4801634 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0002g0366 |
2 | HG03041.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-32-572G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4801634 | |||||||
chr20:4801644 | C | T | 3 | a0001c0002t0028g0122 a0001c0002t0028g0123 a0001c0002t0028g0292 |
3 | HG02818.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-32-582G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4801644 | |||||||
chr20:4801840 | G | A | 2 | a0001c0002t0012g0035 a0001c0002t0026g0040 |
3 | HG02451.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-778C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4801840 | |||||||
chr20:4801875 | A | G | 15 | a0001c0001t0001g0129 a0001c0001t0004g0124 a0001c0001t0004g0378 others(12): Show |
16 | HG00741.hp1 HG01123.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.-32-813T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4801875 | |||||||
chr20:4802084 | T | C | 1 | a0001c0001t0010g0159 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-32-1022A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802084 | |||||||
chr20:4802181 | C | A | 4 | a0001c0001t0002g0020 a0001c0001t0002g0028 a0001c0001t0002g0144 others(1): Show |
6 | HG00735.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-1119G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802181 | |||||||
chr20:4802183 | C | T | 15 | a0001c0001t0001g0129 a0001c0001t0004g0124 a0001c0001t0004g0378 others(12): Show |
16 | HG00741.hp1 HG01123.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.-32-1121G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802183 | |||||||
chr20:4802196 | C | T | 1 | a0001c0001t0011g0377 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-32-1134G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802196 | |||||||
chr20:4802197 | G | A | 1 | a0001c0001t0006g0080 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-32-1135C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802197 | |||||||
chr20:4802216 | T | C | 29 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0317 others(26): Show |
36 | HG01070.hp1 HG01346.hp1 HG01346.hp2 others(33): Show |
intron_variant | MODIFIER | c.-32-1154A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802216 | |||||||
chr20:4802330 | C | CA | 12 | a0001c0001t0002g0043 a0001c0001t0005g0081 a0001c0001t0016g0004 others(9): Show |
15 | HG01123.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-32-1269dupT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802330 | |||||||
chr20:4802537 | C | A | 1 | a0001c0001t0001g0191 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-32-1475G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802537 | |||||||
chr20:4802579 | C | T | 2 | a0001c0001t0010g0159 a0001c0001t0010g0162 |
2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-32-1517G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802579 | |||||||
chr20:4802724 | T | A | 1 | a0001c0001t0001g0026 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-32-1662A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802724 | |||||||
chr20:4802756 | G | A | 1 | a0001c0001t0012g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-32-1694C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802756 | |||||||
chr20:4802868 | G | A | 1 | a0001c0001t0057g0301 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-32-1806C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802868 | |||||||
chr20:4802882 | G | A | 1 | a0001c0001t0016g0004 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-32-1820C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802882 | |||||||
chr20:4802882 | G | GTA | 16 | a0001c0001t0001g0129 a0001c0001t0004g0124 a0001c0001t0004g0378 others(13): Show |
16 | HG00741.hp1 HG01123.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.-32-1822_-32-1821d others(4): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802882 | |||||||
chr20:4802882 | G | GTATA | 86 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0001g0181 others(83): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.-32-1824_-32-1821d others(6): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802882 | |||||||
chr20:4802895 | T | C | 1 | a0001c0001t0015g0315 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-32-1833A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802895 | |||||||
chr20:4802897 | C | T | 74 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0033 others(71): Show |
80 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.-32-1835G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802897 | |||||||
chr20:4802897 | CAT | C | 5 | a0001c0001t0002g0094 a0001c0001t0002g0100 a0001c0001t0002g0388 others(2): Show |
5 | HG00544.hp1 HG02109.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-1837_-32-1836d others(4): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802897 | |||||||
chr20:4802897 | CATAT | C | 17 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0142 others(14): Show |
19 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.-32-1839_-32-1836d others(6): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802897 | |||||||
chr20:4802899 | T | C | 6 | a0001c0001t0008g0010 a0001c0001t0008g0392 a0001c0001t0047g0373 others(3): Show |
7 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-1837A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802899 | |||||||
chr20:4802901 | T | C | 61 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
65 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.-32-1839A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802901 | |||||||
chr20:4802903 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0360 |
3 | HG00597.hp1 HG02071.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.-32-1841A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802903 | |||||||
chr20:4802909 | TATA | T | 18 | a0001c0001t0002g0164 a0001c0001t0002g0256 a0001c0001t0002g0284 others(15): Show |
20 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.-32-1850_-32-1848d others(5): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802909 | |||||||
chr20:4802911 | TA | T | 4 | a0001c0001t0016g0004 a0001c0001t0016g0042 a0001c0001t0021g0014 others(1): Show |
5 | HG01123.hp1 HG02055.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-1850delT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802911 | |||||||
chr20:4802911 | TATA | T | 86 | a0001c0001t0001g0021 a0001c0001t0001g0213 a0001c0001t0001g0214 others(83): Show |
96 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.-32-1852_-32-1850d others(5): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802911 | |||||||
chr20:4802912 | A | AT | 4 | a0001c0001t0003g0293 a0001c0001t0003g0294 a0001c0001t0008g0010 others(1): Show |
5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-1851dupA | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802912 | |||||||
chr20:4802912 | A | ATT | 3 | a0001c0001t0005g0081 a0002c0004t0050g0121 a0002c0004t0051g0166 |
3 | HG02486.hp1 HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-32-1851_-32-1850i others(4): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802912 | |||||||
chr20:4802912 | A | ATTT | 4 | a0001c0001t0004g0332 a0001c0001t0005g0299 a0001c0001t0012g0371 others(1): Show |
4 | HG02056.hp1 HG02074.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-1851_-32-1850i others(5): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802912 | |||||||
chr20:4802912 | A | T | 14 | a0001c0001t0001g0129 a0001c0001t0002g0043 a0001c0001t0002g0150 others(11): Show |
14 | HG00741.hp1 HG01261.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.-32-1850T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802912 | |||||||
chr20:4802913 | TA | T | 2 | a0001c0002t0012g0035 a0001c0002t0026g0040 |
3 | HG02451.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-1852delT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802913 | |||||||
chr20:4802914 | A | AT | 64 | a0001c0001t0001g0181 a0001c0001t0001g0185 a0001c0001t0001g0244 others(61): Show |
67 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.-32-1853dupA | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802914 | |||||||
chr20:4802914 | A | ATAT | 36 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(33): Show |
40 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-32-1853_-32-1852i others(5): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802914 | |||||||
chr20:4802914 | A | ATATTT | 10 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0295 others(7): Show |
10 | HG02040.hp2 HG03516.hp2 HG03540.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-1853_-32-1852i others(7): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802914 | |||||||
chr20:4802914 | A | ATT | 6 | a0001c0001t0001g0201 a0001c0001t0004g0350 a0001c0001t0004g0390 others(3): Show |
6 | HG01516.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-1854_-32-1853d others(4): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802914 | |||||||
chr20:4802914 | A | ATTT | 31 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0177 others(28): Show |
35 | HG00673.hp2 HG01070.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.-32-1855_-32-1853d others(5): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802914 | |||||||
chr20:4802914 | A | T | 58 | a0001c0001t0001g0129 a0001c0001t0002g0043 a0001c0001t0002g0150 others(55): Show |
64 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-32-1852T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802914 | |||||||
chr20:4802915 | T | TA | 14 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0003g0091 others(11): Show |
18 | HG00099.hp1 HG01257.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.-32-1854_-32-1853i others(3): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802915 | |||||||
chr20:4802915 | T | TATA | 9 | a0001c0001t0001g0310 a0001c0001t0001g0312 a0001c0001t0001g0313 others(6): Show |
9 | HG02615.hp2 HG02895.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-1854_-32-1853i others(5): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802915 | |||||||
chr20:4802916 | T | A | 2 | a0001c0001t0007g0075 a0001c0001t0008g0195 |
2 | HG00280.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-32-1854A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802916 | |||||||
chr20:4802917 | T | A | 1 | a0001c0003t0003g0217 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-32-1855A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4802917 | |||||||
chr20:4803124 | C | T | 2 | a0001c0001t0010g0120 a0001c0001t0061g0119 |
2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-32-2062G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4803124 | |||||||
chr20:4803174 | G | T | 156 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0024 others(153): Show |
169 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.-32-2112C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4803174 | |||||||
chr20:4803306 | C | T | 70 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0029 others(67): Show |
80 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.-32-2244G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4803306 | |||||||
chr20:4803307 | G | A | 90 | a0001c0001t0001g0021 a0001c0001t0001g0213 a0001c0001t0001g0214 others(87): Show |
101 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-32-2245C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4803307 | |||||||
chr20:4803346 | C | T | 1 | a0001c0001t0016g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-32-2284G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4803346 | |||||||
chr20:4803356 | G | T | 1 | a0001c0001t0002g0318 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-32-2294C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4803356 | |||||||
chr20:4803465 | T | C | 1 | a0001c0001t0002g0270 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-32-2403A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4803465 | |||||||
chr20:4803692 | G | A | 1 | a0001c0001t0007g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-32-2630C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4803692 | |||||||
chr20:4803784 | C | T | 1 | a0001c0001t0013g0101 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-32-2722G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4803784 | |||||||
chr20:4803913 | C | T | 1 | a0001c0001t0004g0349 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-32-2851G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4803913 | |||||||
chr20:4803916 | G | A | 37 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0001g0087 others(34): Show |
42 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.-32-2854C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4803916 | |||||||
chr20:4803929 | G | A | 2 | a0001c0002t0012g0035 a0001c0002t0026g0040 |
3 | HG02451.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-2867C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4803929 | |||||||
chr20:4803983 | G | A | 1 | a0001c0001t0006g0080 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-32-2921C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4803983 | |||||||
chr20:4804049 | C | T | 2 | a0001c0002t0012g0035 a0001c0002t0026g0040 |
3 | HG02451.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-2987G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804049 | |||||||
chr20:4804057 | A | G | 2 | a0001c0001t0001g0310 a0001c0001t0058g0309 |
2 | NA18997.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-32-2995T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804057 | |||||||
chr20:4804141 | G | A | 2 | a0001c0001t0002g0339 a0001c0001t0002g0340 |
2 | NA18994.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-32-3079C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804141 | |||||||
chr20:4804150 | G | A | 1 | a0001c0001t0018g0287 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-32-3088C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804150 | |||||||
chr20:4804216 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0002g0366 |
2 | HG03041.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-32-3154A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804216 | |||||||
chr20:4804226 | T | C | 1 | a0001c0002t0026g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-32-3164A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804226 | |||||||
chr20:4804308 | C | T | 5 | a0001c0001t0002g0178 a0001c0001t0004g0018 a0001c0001t0004g0180 others(2): Show |
6 | HG01928.hp1 HG02165.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32-3246G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804308 | |||||||
chr20:4804353 | C | CT | 133 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0026 others(130): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-32-3292dupA | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804353 | |||||||
chr20:4804353 | C | CTT | 32 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0329 others(29): Show |
36 | HG00544.hp2 HG00733.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.-32-3293_-32-3292d others(4): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804353 | |||||||
chr20:4804353 | C | CTTT | 23 | a0001c0001t0001g0129 a0001c0001t0001g0295 a0001c0001t0001g0317 others(20): Show |
24 | HG01123.hp2 HG01167.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.-32-3294_-32-3292d others(5): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804353 | |||||||
chr20:4804353 | C | CTTTT | 76 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0001g0090 others(73): Show |
83 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-32-3295_-32-3292d others(6): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804353 | |||||||
chr20:4804353 | C | CTTTTT | 61 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
66 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-32-3296_-32-3292d others(7): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804353 | |||||||
chr20:4804353 | C | CTTTTTT | 16 | a0001c0001t0001g0012 a0001c0001t0001g0113 a0001c0001t0001g0115 others(13): Show |
17 | HG00597.hp1 HG00735.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-32-3297_-32-3292d others(8): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804353 | |||||||
chr20:4804392 | C | T | 24 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0317 others(21): Show |
28 | HG01070.hp1 HG01346.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.-32-3330G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804392 | |||||||
chr20:4804504 | A | AT | 5 | a0001c0002t0012g0035 a0001c0002t0026g0040 a0001c0002t0026g0158 others(2): Show |
6 | HG02055.hp2 HG02451.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-3443dupA | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804504 | |||||||
chr20:4804527 | C | T | 2 | a0001c0001t0018g0066 a0001c0001t0018g0067 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-32-3465G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804527 | |||||||
chr20:4804626 | C | A | 170 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0024 others(167): Show |
184 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.-32-3564G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804626 | |||||||
chr20:4804669 | G | A | 172 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0024 others(169): Show |
186 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-32-3607C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804669 | |||||||
chr20:4804700 | T | G | 245 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0024 others(242): Show |
269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.-32-3638A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804700 | |||||||
chr20:4804713 | A | G | 172 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0024 others(169): Show |
186 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-32-3651T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804713 | |||||||
chr20:4804759 | C | T | 145 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0024 others(142): Show |
158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.-32-3697G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804759 | |||||||
chr20:4804870 | G | A | 5 | a0001c0002t0012g0035 a0001c0002t0026g0040 a0001c0002t0026g0158 others(2): Show |
6 | HG02055.hp2 HG02451.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-3808C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804870 | |||||||
chr20:4804909 | G | A | 1 | a0001c0002t0014g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-32-3847C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4804909 | |||||||
chr20:4805004 | G | A | 1 | a0001c0001t0002g0304 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-32-3942C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805004 | |||||||
chr20:4805008 | G | T | 8 | a0001c0001t0002g0043 a0001c0001t0005g0081 a0001c0001t0016g0004 others(5): Show |
9 | HG01123.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-3946C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805008 | |||||||
chr20:4805050 | C | G | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0265 others(1): Show |
4 | HG02132.hp1 NA18747.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-3988G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805050 | |||||||
chr20:4805104 | G | T | 6 | a0001c0001t0010g0159 a0001c0001t0010g0162 a0001c0001t0047g0373 others(3): Show |
6 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-4042C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805104 | |||||||
chr20:4805197 | T | G | 1 | a0001c0001t0010g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-32-4135A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805197 | |||||||
chr20:4805220 | C | T | 142 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0024 others(139): Show |
152 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-32-4158G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805220 | |||||||
chr20:4805246 | G | A | 1 | a0001c0001t0052g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-32-4184C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805246 | |||||||
chr20:4805265 | C | T | 142 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0024 others(139): Show |
152 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-32-4203G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805265 | |||||||
chr20:4805434 | T | C | 223 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0024 others(220): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.-32-4372A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805434 | |||||||
chr20:4805455 | G | A | 5 | a0001c0001t0010g0120 a0001c0001t0061g0119 a0001c0002t0028g0122 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-4393C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805455 | |||||||
chr20:4805510 | A | G | 19 | a0001c0001t0001g0129 a0001c0001t0004g0124 a0001c0001t0004g0131 others(16): Show |
20 | HG00741.hp1 HG01123.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-32-4448T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805510 | |||||||
chr20:4805550 | A | G | 31 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0142 others(28): Show |
34 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.-32-4488T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805550 | |||||||
chr20:4805574 | G | A | 3 | a0001c0002t0028g0122 a0001c0002t0028g0123 a0001c0002t0028g0292 |
3 | HG02818.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-32-4512C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805574 | |||||||
chr20:4805678 | C | T | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0265 others(1): Show |
4 | HG02132.hp1 NA18747.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-4616G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805678 | |||||||
chr20:4805721 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-32-4659C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805721 | |||||||
chr20:4805793 | G | A | 4 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0236 others(1): Show |
4 | NA18970.hp2 NA18984.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-4731C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805793 | |||||||
chr20:4805847 | C | T | 283 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(280): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.-32-4785G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805847 | |||||||
chr20:4805875 | G | A | 2 | a0001c0001t0004g0261 a0001c0001t0006g0260 |
2 | HG00140.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-32-4813C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805875 | |||||||
chr20:4805993 | G | C | 283 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(280): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.-32-4931C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4805993 | |||||||
chr20:4806038 | G | A | 1 | a0001c0001t0045g0065 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-32-4976C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806038 | |||||||
chr20:4806057 | G | A | 3 | a0001c0002t0012g0035 a0001c0002t0026g0158 a0001c0002t0027g0157 |
4 | HG02451.hp2 HG03195.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-4995C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806057 | |||||||
chr20:4806064 | A | G | 283 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(280): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.-32-5002T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806064 | |||||||
chr20:4806220 | T | C | 53 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0129 others(50): Show |
57 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-32-5158A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806220 | |||||||
chr20:4806261 | T | C | 2 | a0001c0001t0006g0199 a0001c0001t0008g0207 |
2 | HG03710.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-32-5199A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806261 | |||||||
chr20:4806323 | G | A | 1 | a0001c0001t0005g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-32-5261C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806323 | |||||||
chr20:4806339 | C | T | 1 | a0001c0001t0002g0285 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-32-5277G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806339 | |||||||
chr20:4806340 | G | A | 1 | a0001c0001t0010g0120 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-32-5278C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806340 | |||||||
chr20:4806352 | C | T | 1 | a0001c0001t0004g0279 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-32-5290G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806352 | |||||||
chr20:4806373 | A | C | 322 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(319): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.-32-5311T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806373 | |||||||
chr20:4806378 | T | A | 209 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0032 others(206): Show |
226 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.-32-5316A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806378 | |||||||
chr20:4806389 | C | T | 209 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0032 others(206): Show |
226 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.-32-5327G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806389 | |||||||
chr20:4806468 | G | A | 56 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0129 others(53): Show |
60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-32-5406C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806468 | |||||||
chr20:4806586 | T | C | 300 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(297): Show |
331 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(328): Show |
intron_variant | MODIFIER | c.-32-5524A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806586 | |||||||
chr20:4806600 | T | C | 14 | a0001c0001t0002g0043 a0001c0001t0005g0081 a0001c0001t0011g0084 others(11): Show |
16 | HG01123.hp1 HG01123.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-32-5538A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806600 | |||||||
chr20:4806709 | A | G | 3 | a0001c0002t0028g0122 a0001c0002t0028g0123 a0001c0002t0028g0292 |
3 | HG02818.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-32-5647T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806709 | |||||||
chr20:4806802 | G | A | 8 | a0001c0001t0002g0043 a0001c0001t0005g0081 a0001c0001t0016g0004 others(5): Show |
9 | HG01123.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-5740C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806802 | |||||||
chr20:4806901 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-32-5839G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4806901 | |||||||
chr20:4807031 | C | T | 66 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0129 others(63): Show |
72 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-32-5969G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807031 | |||||||
chr20:4807050 | T | C | 55 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0129 others(52): Show |
59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-32-5988A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807050 | |||||||
chr20:4807078 | C | T | 55 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0129 others(52): Show |
59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-32-6016G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807078 | |||||||
chr20:4807180 | G | A | 1 | a0001c0001t0005g0324 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-32-6118C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807180 | |||||||
chr20:4807185 | C | T | 8 | a0001c0001t0002g0043 a0001c0001t0005g0081 a0001c0001t0016g0004 others(5): Show |
9 | HG01123.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-32-6123G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807185 | |||||||
chr20:4807211 | T | G | 1 | a0001c0001t0001g0129 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-32-6149A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807211 | |||||||
chr20:4807330 | G | GA | 51 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0129 others(48): Show |
54 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.-32-6269dupT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807330 | |||||||
chr20:4807330 | GA | G | 21 | a0001c0001t0001g0115 a0001c0001t0001g0374 a0001c0001t0002g0043 others(18): Show |
23 | HG01123.hp1 HG01123.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-32-6269delT | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807330 | |||||||
chr20:4807413 | G | C | 11 | a0001c0001t0001g0129 a0001c0001t0004g0378 a0001c0001t0008g0010 others(8): Show |
12 | HG01496.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32-6351C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807413 | |||||||
chr20:4807438 | A | G | 57 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0129 others(54): Show |
61 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-32-6376T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807438 | |||||||
chr20:4807484 | A | G | 56 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0129 others(53): Show |
60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-32-6422T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807484 | |||||||
chr20:4807525 | A | G | 220 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0025 others(217): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.-32-6463T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807525 | |||||||
chr20:4807622 | C | T | 2 | a0001c0001t0004g0041 a0001c0001t0069g0182 |
2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-32-6560G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807622 | |||||||
chr20:4807626 | T | C | 13 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0086 others(10): Show |
15 | HG00408.hp1 HG00597.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-32-6564A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807626 | |||||||
chr20:4807655 | T | C | 1 | a0001c0001t0008g0207 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-32-6593A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807655 | |||||||
chr20:4807798 | A | G | 2 | a0001c0002t0027g0107 a0001c0002t0032g0132 |
2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-32-6736T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807798 | |||||||
chr20:4807880 | G | A | 4 | a0001c0001t0002g0198 a0001c0001t0009g0049 a0001c0001t0009g0071 others(1): Show |
4 | HG00673.hp1 NA18972.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-6818C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4807880 | |||||||
chr20:4808010 | G | A | 1 | a0001c0001t0012g0371 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-32-6948C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808010 | |||||||
chr20:4808069 | G | T | 18 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0209 others(15): Show |
20 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.-32-7007C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808069 | |||||||
chr20:4808161 | C | T | 2 | a0001c0001t0030g0050 a0001c0001t0030g0051 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-32-7099G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808161 | |||||||
chr20:4808163 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-32-7101A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808163 | |||||||
chr20:4808440 | A | C | 16 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0002g0144 others(13): Show |
18 | HG00735.hp2 HG01109.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-32-7378T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808440 | |||||||
chr20:4808441 | G | A | 15 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0002g0144 others(12): Show |
17 | HG00735.hp2 HG01109.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-32-7379C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808441 | |||||||
chr20:4808449 | A | G | 2 | a0001c0001t0038g0013 a0001c0002t0014g0153 |
3 | HG01243.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-32-7387T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808449 | |||||||
chr20:4808486 | C | CT | 147 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0032 others(144): Show |
166 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.-32-7425dupA | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808486 | |||||||
chr20:4808486 | C | CTT | 9 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0002g0093 others(6): Show |
10 | HG00099.hp1 HG01257.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-7426_-32-7425d others(4): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808486 | |||||||
chr20:4808486 | C | CTTT | 24 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0248 others(21): Show |
27 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.-32-7427_-32-7425d others(5): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808486 | |||||||
chr20:4808486 | CT | C | 39 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0002g0043 others(36): Show |
44 | HG00140.hp1 HG00323.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-32-7425delA | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808486 | |||||||
chr20:4808550 | G | A | 4 | a0001c0001t0002g0150 a0001c0001t0002g0375 a0001c0001t0005g0016 others(1): Show |
5 | HG01884.hp2 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-7488C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808550 | |||||||
chr20:4808574 | C | T | 1 | a0001c0001t0003g0274 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-32-7512G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808574 | |||||||
chr20:4808637 | C | A | 281 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(278): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.-32-7575G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808637 | |||||||
chr20:4808642 | A | G | 31 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0266 others(28): Show |
35 | HG01070.hp1 HG01346.hp1 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.-32-7580T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808642 | |||||||
chr20:4808704 | T | C | 3 | a0001c0001t0008g0239 a0001c0001t0009g0068 a0001c0001t0063g0240 |
3 | HG00738.hp2 HG01255.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-32-7642A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4808704 | |||||||
chr20:4809219 | G | A | 48 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0266 others(45): Show |
54 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.-32-8157C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809219 | |||||||
chr20:4809262 | T | A | 65 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0266 others(62): Show |
73 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.-32-8200A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809262 | |||||||
chr20:4809265 | A | G | 65 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0266 others(62): Show |
73 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.-32-8203T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809265 | |||||||
chr20:4809267 | G | A | 31 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0266 others(28): Show |
35 | HG01070.hp1 HG01346.hp1 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.-32-8205C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809267 | |||||||
chr20:4809274 | T | G | 2 | a0001c0001t0002g0241 a0001c0001t0003g0242 |
2 | HG00733.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-32-8212A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809274 | |||||||
chr20:4809284 | A | G | 342 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(339): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.-32-8222T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809284 | |||||||
chr20:4809291 | A | T | 2 | a0001c0001t0046g0286 a0001c0001t0070g0154 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-32-8229T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809291 | |||||||
chr20:4809485 | G | A | 1 | a0001c0001t0007g0058 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-32-8423C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809485 | |||||||
chr20:4809503 | C | A | 168 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(165): Show |
185 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.-32-8441G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809503 | |||||||
chr20:4809565 | C | T | 2 | a0001c0001t0017g0160 a0001c0001t0021g0014 |
3 | HG02280.hp2 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-32-8503G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809565 | |||||||
chr20:4809675 | G | A | 4 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0003g0088 others(1): Show |
4 | NA18994.hp2 NA19009.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-8613C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809675 | |||||||
chr20:4809697 | A | G | 5 | a0001c0001t0001g0129 a0001c0001t0004g0378 a0001c0001t0012g0130 others(2): Show |
5 | HG01496.hp2 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-8635T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809697 | |||||||
chr20:4809797 | C | G | 140 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(137): Show |
150 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.-32-8735G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809797 | |||||||
chr20:4809928 | A | C | 46 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0001g0295 others(43): Show |
51 | HG00140.hp1 HG01074.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.-32-8866T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809928 | |||||||
chr20:4809934 | C | A | 91 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0033 others(88): Show |
99 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.-32-8872G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809934 | |||||||
chr20:4809934 | C | T | 8 | a0001c0001t0001g0206 a0001c0001t0001g0310 a0001c0001t0001g0312 others(5): Show |
8 | HG00621.hp1 NA18941.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-8872G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809934 | |||||||
chr20:4809966 | G | A | 4 | a0001c0001t0001g0129 a0001c0001t0012g0130 a0001c0001t0017g0127 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-8904C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4809966 | |||||||
chr20:4810067 | T | A | 3 | a0001c0001t0010g0162 a0001c0001t0011g0377 a0001c0002t0032g0132 |
3 | HG02622.hp1 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-32-9005A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810067 | |||||||
chr20:4810137 | C | T | 4 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0001c0001t0002g0307 others(1): Show |
4 | NA18988.hp2 NA19003.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-9075G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810137 | |||||||
chr20:4810175 | C | A | 166 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(163): Show |
183 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.-32-9113G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810175 | |||||||
chr20:4810190 | G | A | 129 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(126): Show |
142 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-32-9128C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810190 | |||||||
chr20:4810222 | C | T | 165 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(162): Show |
182 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-32-9160G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810222 | |||||||
chr20:4810236 | A | G | 2 | a0001c0001t0002g0339 a0001c0001t0002g0340 |
2 | NA18994.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-32-9174T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810236 | |||||||
chr20:4810408 | C | T | 1 | a0001c0001t0058g0309 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-32-9346G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810408 | |||||||
chr20:4810428 | A | G | 163 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(160): Show |
179 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-32-9366T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810428 | |||||||
chr20:4810472 | G | A | 1 | a0001c0001t0012g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-32-9410C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810472 | |||||||
chr20:4810480 | A | G | 163 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(160): Show |
179 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-32-9418T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810480 | |||||||
chr20:4810488 | G | T | 1 | a0001c0001t0009g0062 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-32-9426C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810488 | |||||||
chr20:4810544 | G | A | 159 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(156): Show |
175 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.-32-9482C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810544 | |||||||
chr20:4810551 | G | A | 1 | a0001c0001t0004g0180 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-32-9489C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810551 | |||||||
chr20:4810592 | T | C | 164 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(161): Show |
180 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.-32-9530A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810592 | |||||||
chr20:4810612 | C | A | 3 | a0001c0001t0010g0159 a0001c0002t0026g0158 a0001c0002t0027g0157 |
3 | HG03195.hp1 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-32-9550G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810612 | |||||||
chr20:4810651 | G | A | 163 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(160): Show |
179 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-32-9589C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810651 | |||||||
chr20:4810668 | G | C | 163 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(160): Show |
179 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-32-9606C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810668 | |||||||
chr20:4810711 | T | C | 163 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(160): Show |
179 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-32-9649A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810711 | |||||||
chr20:4810714 | G | A | 163 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(160): Show |
179 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-32-9652C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810714 | |||||||
chr20:4810723 | G | A | 31 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0266 others(28): Show |
35 | HG01070.hp1 HG01346.hp1 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.-32-9661C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810723 | |||||||
chr20:4810746 | C | G | 2 | a0001c0001t0017g0160 a0001c0001t0021g0014 |
3 | HG02280.hp2 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-32-9684G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810746 | |||||||
chr20:4810774 | G | A | 163 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(160): Show |
179 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-32-9712C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810774 | |||||||
chr20:4810801 | C | A | 163 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(160): Show |
179 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-32-9739G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810801 | |||||||
chr20:4810975 | A | G | 5 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0012g0130 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-9913T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4810975 | |||||||
chr20:4811031 | G | A | 163 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(160): Show |
179 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-32-9969C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811031 | |||||||
chr20:4811112 | C | G | 1 | a0001c0001t0011g0370 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-32-10050G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811112 | |||||||
chr20:4811176 | A | G | 167 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(164): Show |
183 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.-32-10114T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811176 | |||||||
chr20:4811189 | A | C | 1 | a0001c0001t0020g0173 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-32-10127T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811189 | |||||||
chr20:4811191 | A | T | 1 | a0001c0001t0077g0192 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-32-10129T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811191 | |||||||
chr20:4811224 | G | GCCTGTAG others(55): Show |
30 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0142 others(27): Show |
32 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.-32-10163_-32-1016 others(66): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811224 | |||||||
chr20:4811224 | G | GCCTGTAG others(86): Show |
133 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0029 others(130): Show |
147 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.-32-10163_-32-1016 others(97): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811224 | |||||||
chr20:4811296 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0008g0262 |
2 | HG00323.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-32-10234G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811296 | |||||||
chr20:4811297 | G | A | 161 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(158): Show |
177 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.-32-10235C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811297 | |||||||
chr20:4811353 | A | G | 161 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(158): Show |
177 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.-32-10291T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811353 | |||||||
chr20:4811478 | A | T | 2 | a0001c0001t0002g0289 a0001c0001t0002g0290 |
2 | HG00738.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.-32-10416T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811478 | |||||||
chr20:4811542 | G | A | 162 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(159): Show |
178 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-32-10480C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811542 | |||||||
chr20:4811616 | C | A | 50 | a0001c0001t0001g0374 a0001c0001t0002g0043 a0001c0001t0002g0150 others(47): Show |
55 | HG00140.hp1 HG00741.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.-32-10554G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811616 | |||||||
chr20:4811724 | G | A | 6 | a0001c0001t0001g0380 a0001c0001t0002g0385 a0001c0001t0002g0386 others(3): Show |
6 | NA18953.hp2 NA18959.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+10605C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811724 | |||||||
chr20:4811758 | G | A | 1 | a0001c0001t0020g0173 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-33+10571C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811758 | |||||||
chr20:4811770 | A | C | 162 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(159): Show |
178 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-33+10559T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811770 | |||||||
chr20:4811789 | C | T | 38 | a0001c0001t0001g0295 a0001c0001t0001g0374 a0001c0001t0002g0043 others(35): Show |
43 | HG00140.hp1 HG01074.hp2 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.-33+10540G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811789 | |||||||
chr20:4811847 | C | A | 31 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0266 others(28): Show |
35 | HG01070.hp1 HG01346.hp1 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.-33+10482G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811847 | |||||||
chr20:4811894 | G | T | 1 | a0001c0001t0015g0315 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-33+10435C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811894 | |||||||
chr20:4811913 | G | T | 162 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(159): Show |
178 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-33+10416C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4811913 | |||||||
chr20:4812203 | T | A | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+10126A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812203 | |||||||
chr20:4812269 | C | T | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+10060G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812269 | |||||||
chr20:4812424 | C | T | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+9905G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812424 | |||||||
chr20:4812427 | G | C | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+9902C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812427 | |||||||
chr20:4812515 | T | C | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+9814A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812515 | |||||||
chr20:4812528 | A | T | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+9801T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812528 | |||||||
chr20:4812559 | T | C | 11 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0010g0120 others(8): Show |
11 | HG02145.hp1 HG02451.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-33+9770A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812559 | |||||||
chr20:4812655 | T | G | 31 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0266 others(28): Show |
35 | HG01070.hp1 HG01346.hp1 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.-33+9674A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812655 | |||||||
chr20:4812731 | T | C | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+9598A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812731 | |||||||
chr20:4812738 | G | A | 1 | a0001c0001t0003g0274 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-33+9591C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812738 | |||||||
chr20:4812792 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-33+9537C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812792 | |||||||
chr20:4812824 | T | G | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+9505A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812824 | |||||||
chr20:4812848 | C | T | 2 | a0001c0001t0010g0120 a0001c0001t0061g0119 |
2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-33+9481G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812848 | |||||||
chr20:4812865 | C | T | 166 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(163): Show |
182 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-33+9464G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812865 | |||||||
chr20:4812874 | G | T | 31 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0266 others(28): Show |
35 | HG01070.hp1 HG01346.hp1 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.-33+9455C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812874 | |||||||
chr20:4812893 | G | A | 2 | a0001c0001t0010g0120 a0001c0001t0061g0119 |
2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-33+9436C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812893 | |||||||
chr20:4812928 | T | C | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+9401A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4812928 | |||||||
chr20:4813032 | G | A | 131 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(128): Show |
143 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-33+9297C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813032 | |||||||
chr20:4813049 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-33+9280G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813049 | |||||||
chr20:4813088 | G | A | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+9241C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813088 | |||||||
chr20:4813109 | A | G | 31 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0266 others(28): Show |
35 | HG01070.hp1 HG01346.hp1 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.-33+9220T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813109 | |||||||
chr20:4813122 | T | C | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+9207A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813122 | |||||||
chr20:4813134 | G | A | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+9195C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813134 | |||||||
chr20:4813164 | A | G | 100 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0033 others(97): Show |
110 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-33+9165T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813164 | |||||||
chr20:4813228 | G | A | 1 | a0001c0001t0012g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-33+9101C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813228 | |||||||
chr20:4813231 | G | A | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+9098C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813231 | |||||||
chr20:4813272 | A | G | 6 | a0001c0001t0010g0120 a0001c0001t0027g0110 a0001c0001t0061g0119 others(3): Show |
6 | HG02451.hp1 HG02572.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+9057T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813272 | |||||||
chr20:4813284 | A | G | 2 | a0001c0001t0010g0120 a0001c0001t0061g0119 |
2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-33+9045T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813284 | |||||||
chr20:4813289 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-33+9040C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813289 | |||||||
chr20:4813371 | C | T | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+8958G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813371 | |||||||
chr20:4813412 | T | C | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+8917A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813412 | |||||||
chr20:4813427 | A | T | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+8902T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813427 | |||||||
chr20:4813430 | G | A | 1 | a0001c0001t0004g0243 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-33+8899C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813430 | |||||||
chr20:4813465 | G | A | 1 | a0001c0001t0010g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-33+8864C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813465 | |||||||
chr20:4813544 | A | G | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+8785T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813544 | |||||||
chr20:4813582 | T | C | 351 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(348): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.-33+8747A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813582 | |||||||
chr20:4813585 | C | T | 5 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0012g0130 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+8744G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813585 | |||||||
chr20:4813597 | C | T | 132 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(129): Show |
144 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.-33+8732G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813597 | |||||||
chr20:4813659 | G | C | 9 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0012g0130 others(6): Show |
9 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33+8670C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813659 | |||||||
chr20:4813666 | G | A | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+8663C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813666 | |||||||
chr20:4813673 | C | T | 1 | a0002c0004t0051g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-33+8656G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813673 | |||||||
chr20:4813678 | C | T | 3 | a0001c0002t0028g0122 a0001c0002t0028g0123 a0002c0004t0050g0121 |
3 | HG02486.hp1 HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-33+8651G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813678 | |||||||
chr20:4813782 | CGT | C | 169 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(166): Show |
185 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.-33+8545_-33+8546d others(4): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813782 | |||||||
chr20:4813847 | A | G | 4 | a0001c0001t0027g0110 a0001c0002t0014g0125 a0001c0002t0014g0369 others(1): Show |
4 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+8482T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813847 | |||||||
chr20:4813981 | G | A | 5 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0012g0130 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+8348C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4813981 | |||||||
chr20:4814131 | A | T | 2 | a0001c0001t0038g0013 a0001c0002t0014g0153 |
3 | HG01243.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-33+8198T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814131 | |||||||
chr20:4814198 | G | A | 30 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0266 others(27): Show |
34 | HG01070.hp1 HG01346.hp1 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.-33+8131C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814198 | |||||||
chr20:4814302 | C | T | 1 | a0001c0001t0019g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-33+8027G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814302 | |||||||
chr20:4814343 | G | A | 132 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(129): Show |
144 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-33+7986C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814343 | |||||||
chr20:4814481 | G | A | 125 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0025 others(122): Show |
137 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-33+7848C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814481 | |||||||
chr20:4814506 | G | A | 36 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0002g0385 others(33): Show |
39 | HG00140.hp2 HG01099.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.-33+7823C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814506 | |||||||
chr20:4814736 | G | A | 268 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0024 others(265): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.-33+7593C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814736 | |||||||
chr20:4814823 | G | C | 1 | a0001c0001t0009g0062 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-33+7506C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814823 | |||||||
chr20:4814852 | A | G | 39 | a0001c0001t0001g0086 a0001c0001t0002g0009 a0001c0001t0002g0093 others(36): Show |
46 | HG00544.hp2 HG01175.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.-33+7477T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814852 | |||||||
chr20:4814931 | C | T | 32 | a0001c0001t0001g0032 a0001c0001t0001g0310 a0001c0001t0001g0312 others(29): Show |
35 | HG01070.hp1 HG01109.hp2 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.-33+7398G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814931 | |||||||
chr20:4814946 | C | T | 2 | a0001c0001t0010g0120 a0001c0001t0061g0119 |
2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-33+7383G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814946 | |||||||
chr20:4814972 | G | C | 59 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0191 others(56): Show |
65 | HG00140.hp2 HG00741.hp1 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.-33+7357C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814972 | |||||||
chr20:4814975 | C | T | 2 | a0001c0001t0003g0082 a0001c0001t0005g0081 |
2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-33+7354G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814975 | |||||||
chr20:4814980 | A | G | 233 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(230): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-33+7349T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4814980 | |||||||
chr20:4815033 | T | C | 1 | a0001c0001t0002g0330 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-33+7296A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815033 | |||||||
chr20:4815057 | T | C | 360 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(357): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.-33+7272A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815057 | |||||||
chr20:4815079 | C | G | 172 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(169): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-33+7250G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815079 | |||||||
chr20:4815085 | C | T | 3 | a0001c0001t0031g0036 a0001c0001t0031g0078 a0001c0001t0041g0077 |
3 | HG00741.hp1 HG01261.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-33+7244G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815085 | |||||||
chr20:4815110 | G | A | 1 | a0001c0001t0020g0173 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-33+7219C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815110 | |||||||
chr20:4815175 | C | A | 127 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(124): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.-33+7154G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815175 | |||||||
chr20:4815253 | C | T | 34 | a0001c0001t0001g0295 a0001c0001t0001g0368 a0001c0001t0001g0374 others(31): Show |
36 | HG00642.hp2 HG01074.hp2 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.-33+7076G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815253 | |||||||
chr20:4815272 | A | G | 1 | a0001c0001t0002g0028 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-33+7057T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815272 | |||||||
chr20:4815290 | G | A | 7 | a0001c0001t0001g0129 a0001c0001t0004g0124 a0001c0001t0010g0126 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+7039C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815290 | |||||||
chr20:4815295 | T | G | 7 | a0001c0001t0001g0129 a0001c0001t0004g0124 a0001c0001t0010g0126 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+7034A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815295 | |||||||
chr20:4815352 | A | G | 7 | a0001c0001t0001g0129 a0001c0001t0004g0124 a0001c0001t0010g0126 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+6977T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815352 | |||||||
chr20:4815388 | TACC | T | 131 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(128): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-33+6938_-33+6940d others(5): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815388 | |||||||
chr20:4815424 | A | G | 259 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(256): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-33+6905T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815424 | |||||||
chr20:4815447 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0079 |
3 | HG00099.hp1 HG01257.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-33+6882G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815447 | |||||||
chr20:4815453 | C | T | 1 | a0001c0001t0077g0192 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-33+6876G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815453 | |||||||
chr20:4815536 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-33+6793C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815536 | |||||||
chr20:4815592 | G | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(133): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.-33+6737C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815592 | |||||||
chr20:4815757 | C | T | 3 | a0001c0001t0001g0191 a0001c0001t0002g0285 a0001c0001t0022g0190 |
3 | NA18946.hp1 NA18947.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-33+6572G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815757 | |||||||
chr20:4815759 | A | C | 2 | a0001c0001t0010g0120 a0001c0001t0061g0119 |
2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-33+6570T>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815759 | |||||||
chr20:4815870 | G | T | 2 | a0001c0001t0018g0287 a0001c0001t0046g0286 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-33+6459C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815870 | |||||||
chr20:4815872 | T | C | 7 | a0001c0001t0001g0129 a0001c0001t0004g0124 a0001c0001t0010g0126 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+6457A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815872 | |||||||
chr20:4815946 | A | G | 7 | a0001c0001t0001g0129 a0001c0001t0004g0124 a0001c0001t0010g0126 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+6383T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815946 | |||||||
chr20:4815948 | A | G | 1 | a0001c0001t0007g0046 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-33+6381T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815948 | |||||||
chr20:4815984 | T | C | 64 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0087 others(61): Show |
71 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.-33+6345A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815984 | |||||||
chr20:4815994 | A | G | 1 | a0004c0005t0003g0116 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-33+6335T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4815994 | |||||||
chr20:4816026 | G | T | 10 | a0001c0001t0002g0043 a0001c0001t0004g0041 a0001c0001t0012g0171 others(7): Show |
11 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-33+6303C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4816026 | |||||||
chr20:4816073 | G | A | 1 | a0001c0001t0004g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-33+6256C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4816073 | |||||||
chr20:4816210 | G | A | 138 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(135): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.-33+6119C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4816210 | |||||||
chr20:4816384 | T | C | 1 | a0001c0001t0043g0076 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-33+5945A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4816384 | |||||||
chr20:4816472 | G | C | 1 | a0001c0001t0017g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-33+5857C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4816472 | |||||||
chr20:4816637 | C | T | 1 | a0001c0001t0016g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-33+5692G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4816637 | |||||||
chr20:4816638 | A | G | 264 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(261): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.-33+5691T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4816638 | |||||||
chr20:4816743 | C | T | 1 | a0001c0001t0052g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-33+5586G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4816743 | |||||||
chr20:4816763 | A | G | 264 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(261): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.-33+5566T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4816763 | |||||||
chr20:4816922 | G | A | 152 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(149): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.-33+5407C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4816922 | |||||||
chr20:4817030 | G | A | 2 | a0001c0001t0002g0359 a0001c0001t0004g0356 |
2 | NA18941.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-33+5299C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4817030 | |||||||
chr20:4817135 | G | A | 3 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0005g0081 |
3 | HG03540.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-33+5194C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4817135 | |||||||
chr20:4817194 | G | A | 64 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0087 others(61): Show |
71 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.-33+5135C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4817194 | |||||||
chr20:4817249 | T | C | 1 | a0001c0001t0022g0276 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-33+5080A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4817249 | |||||||
chr20:4817433 | T | C | 5 | a0001c0001t0008g0010 a0001c0001t0010g0155 a0001c0001t0038g0013 others(2): Show |
7 | HG01109.hp1 HG01243.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+4896A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4817433 | |||||||
chr20:4817647 | G | C | 78 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0087 others(75): Show |
87 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.-33+4682C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4817647 | |||||||
chr20:4817806 | A | G | 350 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(347): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.-33+4523T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4817806 | |||||||
chr20:4817842 | T | TGTATAGA others(5): Show |
1 | a0001c0001t0022g0365 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-33+4475_-33+4486d others(14): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4817842 | |||||||
chr20:4817982 | A | G | 94 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(91): Show |
105 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.-33+4347T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4817982 | |||||||
chr20:4817987 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-33+4342G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4817987 | |||||||
chr20:4818041 | T | C | 4 | a0001c0001t0031g0036 a0001c0001t0031g0078 a0001c0001t0041g0077 others(1): Show |
4 | HG00741.hp1 HG01261.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+4288A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4818041 | |||||||
chr20:4818137 | T | G | 2 | a0001c0001t0018g0287 a0001c0001t0046g0286 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-33+4192A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4818137 | |||||||
chr20:4818149 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0006g0080 |
4 | HG00099.hp1 HG01257.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+4180G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4818149 | |||||||
chr20:4818182 | G | A | 3 | a0001c0001t0007g0069 a0001c0001t0007g0074 a0001c0001t0044g0073 |
3 | HG00741.hp2 HG01106.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-33+4147C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4818182 | |||||||
chr20:4818245 | C | T | 1 | a0001c0001t0003g0291 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-33+4084G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4818245 | |||||||
chr20:4818296 | C | G | 68 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0087 others(65): Show |
75 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.-33+4033G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4818296 | |||||||
chr20:4818322 | G | A | 2 | a0001c0001t0004g0278 a0001c0001t0004g0279 |
2 | HG00423.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-33+4007C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4818322 | |||||||
chr20:4818540 | C | T | 1 | a0001c0002t0026g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-33+3789G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4818540 | |||||||
chr20:4818622 | C | T | 3 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0006g0027 |
4 | HG00738.hp1 HG01167.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+3707G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4818622 | |||||||
chr20:4818676 | C | T | 70 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0087 others(67): Show |
77 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.-33+3653G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4818676 | |||||||
chr20:4818700 | A | G | 4 | a0001c0001t0031g0036 a0001c0001t0031g0078 a0001c0001t0041g0077 others(1): Show |
4 | HG00741.hp1 HG01261.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+3629T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4818700 | |||||||
chr20:4818738 | C | T | 1 | a0001c0001t0061g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-33+3591G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4818738 | |||||||
chr20:4818923 | C | A | 1 | a0001c0002t0032g0152 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-33+3406G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4818923 | |||||||
chr20:4819152 | G | A | 2 | a0001c0001t0017g0160 a0001c0001t0021g0014 |
3 | HG02280.hp2 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-33+3177C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4819152 | |||||||
chr20:4819157 | T | G | 4 | a0001c0001t0008g0392 a0001c0001t0010g0162 a0001c0001t0017g0163 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+3172A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4819157 | |||||||
chr20:4819159 | C | T | 129 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(126): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-33+3170G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4819159 | |||||||
chr20:4819391 | C | T | 74 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0087 others(71): Show |
81 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.-33+2938G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4819391 | |||||||
chr20:4819766 | T | C | 1 | a0001c0001t0006g0280 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-33+2563A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4819766 | |||||||
chr20:4819854 | G | A | 3 | a0001c0001t0010g0015 a0001c0001t0014g0167 a0002c0004t0051g0166 |
4 | HG02257.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+2475C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4819854 | |||||||
chr20:4819875 | C | T | 138 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(135): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.-33+2454G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4819875 | |||||||
chr20:4819882 | C | G | 1 | a0001c0001t0003g0184 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-33+2447G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4819882 | |||||||
chr20:4819902 | C | T | 3 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0005g0081 |
3 | HG03540.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-33+2427G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4819902 | |||||||
chr20:4819998 | TAG | T | 3 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0005g0081 |
3 | HG03540.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-33+2329_-33+2330d others(4): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4819998 | |||||||
chr20:4820003 | T | C | 15 | a0001c0001t0001g0129 a0001c0001t0004g0124 a0001c0001t0010g0126 others(12): Show |
15 | HG00741.hp1 HG01261.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-33+2326A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4820003 | |||||||
chr20:4820109 | C | T | 1 | a0001c0001t0003g0183 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-33+2220G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4820109 | |||||||
chr20:4820415 | G | A | 4 | a0001c0001t0002g0178 a0001c0001t0004g0018 a0001c0001t0004g0180 others(1): Show |
5 | HG01928.hp1 NA18945.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+1914C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4820415 | |||||||
chr20:4820516 | T | A | 20 | a0001c0001t0001g0129 a0001c0001t0003g0082 a0001c0001t0003g0083 others(17): Show |
21 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.-33+1813A>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4820516 | |||||||
chr20:4820533 | A | T | 6 | a0001c0001t0008g0392 a0001c0001t0010g0162 a0001c0001t0017g0160 others(3): Show |
7 | HG02280.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+1796T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4820533 | |||||||
chr20:4820614 | G | C | 349 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(346): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.-33+1715C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4820614 | |||||||
chr20:4820656 | T | C | 1 | a0001c0002t0001g0170 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-33+1673A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4820656 | |||||||
chr20:4820769 | C | T | 2 | a0001c0001t0018g0287 a0001c0001t0046g0286 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-33+1560G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4820769 | |||||||
chr20:4820938 | A | G | 1 | a0001c0001t0069g0182 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-33+1391T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4820938 | |||||||
chr20:4821219 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-33+1110G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4821219 | |||||||
chr20:4821231 | G | A | 16 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0005g0081 others(13): Show |
16 | HG00741.hp1 HG01261.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-33+1098C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4821231 | |||||||
chr20:4821276 | C | G | 1 | a0001c0001t0019g0045 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-33+1053G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4821276 | |||||||
chr20:4821338 | G | A | 3 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0005g0081 |
3 | HG03540.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-33+991C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4821338 | |||||||
chr20:4821343 | G | C | 207 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(204): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.-33+986C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4821343 | |||||||
chr20:4821360 | T | G | 330 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(327): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.-33+969A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4821360 | |||||||
chr20:4821718 | G | A | 3 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0005g0081 |
3 | HG03540.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-33+611C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4821718 | |||||||
chr20:4821840 | G | GCC | 354 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(351): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.-33+487_-33+488dup others(2): Show |
RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4821840 | |||||||
chr20:4822099 | T | C | 65 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0087 others(62): Show |
71 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.-33+230A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4822099 | |||||||
chr20:4822218 | T | G | 2 | a0001c0001t0018g0287 a0001c0001t0046g0286 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-33+111A>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4822218 | |||||||
chr20:4822219 | C | T | 1 | a0001c0001t0005g0288 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-33+110G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4822219 | |||||||
chr20:4822279 | T | C | 2 | a0001c0001t0007g0074 a0001c0001t0044g0073 |
2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-33+50A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 2/11 | chr20 | 4822279 | |||||||
chr20:4822412 | T | C | 2 | a0001c0001t0007g0075 a0001c0001t0043g0076 |
2 | HG01496.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-107-9A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822412 | |||||||
chr20:4822426 | CT | C | 279 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0024 others(276): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-107-24delA | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822426 | |||||||
chr20:4822500 | G | A | 19 | a0001c0001t0001g0129 a0001c0001t0004g0124 a0001c0001t0004g0131 others(16): Show |
20 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-107-97C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822500 | |||||||
chr20:4822581 | G | C | 1 | a0001c0001t0002g0284 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-107-178C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822581 | |||||||
chr20:4822627 | C | A | 11 | a0001c0001t0005g0016 a0001c0001t0005g0169 a0001c0001t0010g0155 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-107-224G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822627 | |||||||
chr20:4822633 | C | T | 8 | a0001c0001t0002g0043 a0001c0001t0004g0041 a0001c0001t0016g0004 others(5): Show |
9 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-107-230G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822633 | |||||||
chr20:4822683 | C | G | 1 | a0001c0001t0011g0084 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-107-280G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822683 | |||||||
chr20:4822694 | A | T | 3 | a0001c0001t0010g0159 a0001c0002t0026g0158 a0001c0002t0027g0157 |
3 | HG03195.hp1 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-107-291T>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822694 | |||||||
chr20:4822699 | C | T | 2 | a0001c0001t0010g0120 a0001c0001t0061g0119 |
2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-107-296G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822699 | |||||||
chr20:4822781 | G | A | 29 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(26): Show |
33 | HG00544.hp2 HG01123.hp2 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.-107-378C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822781 | |||||||
chr20:4822794 | G | C | 64 | a0001c0001t0001g0012 a0001c0001t0001g0113 a0001c0001t0001g0114 others(61): Show |
69 | HG00597.hp1 HG00735.hp2 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.-107-391C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822794 | |||||||
chr20:4822799 | G | A | 253 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(250): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.-107-396C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822799 | |||||||
chr20:4822806 | G | A | 20 | a0001c0001t0005g0016 a0001c0001t0005g0169 a0001c0001t0008g0392 others(17): Show |
23 | HG01109.hp1 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.-107-403C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822806 | |||||||
chr20:4822848 | C | T | 265 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(262): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.-107-445G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822848 | |||||||
chr20:4822881 | C | G | 1 | a0001c0001t0019g0037 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-107-478G>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822881 | |||||||
chr20:4822946 | G | T | 132 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(129): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.-107-543C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822946 | |||||||
chr20:4822949 | T | C | 6 | a0001c0001t0002g0385 a0001c0001t0002g0386 a0001c0001t0002g0387 others(3): Show |
6 | NA18953.hp2 NA18959.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.-107-546A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822949 | |||||||
chr20:4822962 | C | T | 244 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(241): Show |
270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.-107-559G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4822962 | |||||||
chr20:4823004 | G | C | 31 | a0001c0001t0001g0129 a0001c0001t0004g0124 a0001c0001t0004g0131 others(28): Show |
34 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.-108+553C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4823004 | |||||||
chr20:4823093 | G | T | 14 | a0001c0001t0001g0129 a0001c0001t0004g0124 a0001c0001t0004g0131 others(11): Show |
14 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-108+464C>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4823093 | |||||||
chr20:4823143 | A | G | 1 | a0001c0001t0034g0017 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-108+414T>C | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4823143 | |||||||
chr20:4823160 | G | A | 1 | a0001c0001t0004g0390 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-108+397C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4823160 | |||||||
chr20:4823173 | C | T | 1 | a0001c0001t0020g0173 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-108+384G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4823173 | |||||||
chr20:4823256 | G | C | 241 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(238): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.-108+301C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4823256 | |||||||
chr20:4823299 | G | C | 1 | a0001c0001t0002g0391 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-108+258C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4823299 | |||||||
chr20:4823357 | C | T | 2 | a0001c0001t0010g0120 a0001c0001t0061g0119 |
2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-108+200G>A | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4823357 | |||||||
chr20:4823412 | G | A | 2 | a0001c0001t0002g0164 a0001c0001t0011g0165 |
2 | HG01081.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-108+145C>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4823412 | |||||||
chr20:4823448 | G | C | 8 | a0001c0001t0005g0016 a0001c0001t0005g0169 a0001c0001t0010g0015 others(5): Show |
10 | HG02257.hp1 HG02886.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-108+109C>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4823448 | |||||||
chr20:4823462 | T | C | 58 | a0001c0001t0001g0129 a0001c0001t0001g0142 a0001c0001t0001g0147 others(55): Show |
62 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.-108+95A>G | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4823462 | |||||||
chr20:4823485 | C | A | 243 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(240): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.-108+72G>T | RASSF2 | ENSG00000101265.16 | transcript | ENST00000379400.8 | protein_coding | 1/11 | chr20 | 4823485 |