Item | Value |
---|---|
geneid | 11228 |
ensemblid | ENSG00000123094.16 |
hgncid | 13232 |
symbol | RASSF8 |
name | Ras association domain family member 8 |
refseq_nuc | NM_001394098.1 |
refseq_prot | NP_001381027.1 |
ensembl_nuc | ENST00000689635.1 |
ensembl_prot | ENSP00000510086.1 |
mane_status | MANE Select |
chr | chr12 |
start | 25958682 |
end | 26072869 |
strand | + |
ver | v1.2 |
region | chr12:25958682-26072869 |
region5000 | chr12:25953682-26077869 |
regionname0 | RASSF8_chr12_25958682_26072869 |
regionname5000 | RASSF8_chr12_25953682_26077869 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 419 | 389 | 90 | 60 | 189 | 12 | 36 | 147 | RASSF8_chr12_25953682_26077869 | RASSF8 | MELKV others(414): Show |
chr12 | 25953682 | 26077869 |
a0002 | 0/0 | 419 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | MELKV others(414): Show |
chr12 | 25953682 | 26077869 |
a0003 | 0/0 | 419 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | MELKV others(414): Show |
chr12 | 25953682 | 26077869 |
a0004 | 0/0 | 419 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | MELKV others(414): Show |
chr12 | 25953682 | 26077869 |
a0005 | 0/0 | 419 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | MELKV others(414): Show |
chr12 | 25953682 | 26077869 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1257 | 292 | 78 | 54 | 116 | 12 | 30 | RASSF8_chr12_25953682_26077869 | RASSF8 | ATGGA others(1252): Show |
chr12 | 25953682 | 26077869 | ||
a0001c0002 | 0/0 | 1257 | 79 | 0 | 6 | 68 | 0 | 5 | RASSF8_chr12_25953682_26077869 | RASSF8 | ATGGA others(1252): Show |
chr12 | 25953682 | 26077869 | ||
a0001c0003 | 0/0 | 1257 | 6 | 0 | 0 | 5 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | ATGGA others(1252): Show |
chr12 | 25953682 | 26077869 | ||
a0001c0004 | 0/0 | 1257 | 5 | 5 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | ATGGA others(1252): Show |
chr12 | 25953682 | 26077869 | ||
a0001c0005 | 0/0 | 1257 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | ATGGA others(1252): Show |
chr12 | 25953682 | 26077869 | ||
a0001c0006 | 0/0 | 1257 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | ATGGA others(1252): Show |
chr12 | 25953682 | 26077869 | ||
a0002c0007 | 0/0 | 1257 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | ATGGA others(1252): Show |
chr12 | 25953682 | 26077869 | ||
a0003c0008 | 0/0 | 1257 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | ATGGA others(1252): Show |
chr12 | 25953682 | 26077869 | ||
a0004c0010 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | ATGGA others(1252): Show |
chr12 | 25953682 | 26077869 | ||
a0005c0009 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | ATGGA others(1252): Show |
chr12 | 25953682 | 26077869 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/1 | 5978 | 40 | 8 | 10 | 3 | 4 | 14 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5973): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0003 | 0/0 | 5979 | 42 | 5 | 14 | 17 | 0 | 6 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0004 | 0/0 | 5980 | 36 | 0 | 10 | 20 | 2 | 4 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0005 | 0/0 | 5968 | 35 | 0 | 0 | 35 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5963): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0006 | 0/0 | 5979 | 31 | 8 | 3 | 14 | 4 | 2 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0007 | 0/0 | 5980 | 12 | 6 | 3 | 3 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0008 | 0/0 | 5979 | 10 | 9 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0009 | 0/0 | 5979 | 10 | 4 | 1 | 4 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0010 | 0/0 | 5980 | 7 | 4 | 3 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0011 | 0/0 | 5979 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0012 | 0/0 | 5979 | 5 | 5 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0013 | 1/0 | 5980 | 5 | 4 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0015 | 0/0 | 5980 | 3 | 1 | 1 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0016 | 0/0 | 5979 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0017 | 0/0 | 5980 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0018 | 0/0 | 5978 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5973): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0019 | 0/0 | 5979 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0020 | 0/0 | 5980 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0021 | 0/0 | 5969 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5964): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0022 | 0/0 | 5980 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0023 | 0/0 | 5978 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5973): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0024 | 0/0 | 5979 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0025 | 0/0 | 5979 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0027 | 0/0 | 5978 | 2 | 0 | 1 | 0 | 1 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5973): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0028 | 0/0 | 5981 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5976): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0029 | 0/0 | 5979 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0030 | 0/0 | 5980 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0031 | 0/0 | 5978 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5973): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0032 | 0/0 | 5969 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5964): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0033 | 0/0 | 5979 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0034 | 0/0 | 5997 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5992): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0036 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0038 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0039 | 0/0 | 5979 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0040 | 0/0 | 5979 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0041 | 0/0 | 5978 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5973): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0042 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0043 | 0/0 | 5980 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0044 | 0/0 | 5979 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0046 | 0/0 | 5981 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5976): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0048 | 0/0 | 5980 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0050 | 0/0 | 5979 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0051 | 0/0 | 5979 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0052 | 0/0 | 5979 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0053 | 0/0 | 5978 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5973): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0055 | 0/0 | 5970 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5965): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0056 | 0/0 | 5969 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5964): Show |
chr12 | 25953682 | 26077869 |
a0001c0001t0058 | 0/0 | 5978 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5973): Show |
chr12 | 25953682 | 26077869 |
a0001c0002t0001 | 0/0 | 5980 | 63 | 0 | 3 | 58 | 0 | 2 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0002t0002 | 0/0 | 5978 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5973): Show |
chr12 | 25953682 | 26077869 |
a0001c0002t0004 | 0/0 | 5980 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0002t0006 | 0/0 | 5979 | 2 | 0 | 0 | 1 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0002t0014 | 0/0 | 5980 | 4 | 0 | 3 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0002t0016 | 0/0 | 5979 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0002t0045 | 0/0 | 5979 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0002t0047 | 0/0 | 5980 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0002t0049 | 0/0 | 5980 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0002t0059 | 0/0 | 5997 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5992): Show |
chr12 | 25953682 | 26077869 |
a0001c0002t0060 | 0/0 | 6065 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(6060): Show |
chr12 | 25953682 | 26077869 |
a0001c0003t0004 | 0/0 | 5980 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0003t0011 | 0/0 | 5979 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0003t0020 | 0/0 | 5980 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0003t0026 | 0/0 | 5980 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0004t0011 | 0/0 | 5979 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0004t0015 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0004t0037 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0005t0002 | 0/0 | 5978 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5973): Show |
chr12 | 25953682 | 26077869 |
a0001c0005t0006 | 0/0 | 5979 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0001c0006t0007 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0006t0035 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0001c0006t0057 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
a0002c0007t0005 | 0/0 | 5968 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5963): Show |
chr12 | 25953682 | 26077869 |
a0003c0008t0019 | 0/0 | 5979 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0004c0010t0061 | 0/0 | 5979 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5974): Show |
chr12 | 25953682 | 26077869 |
a0005c0009t0054 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | AGAGG others(5975): Show |
chr12 | 25953682 | 26077869 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0004g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0006g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0007g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0007g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0007g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0007g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0008g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0008g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0008g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0009g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0009g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0009g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0009g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0009g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0009g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0009g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0009g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0009g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0009g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0010g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0010g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0010g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0010g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0010g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0011g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0011g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0012g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0012g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0012g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0012g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0013g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0013g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0013g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0013g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0013g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0015g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0015g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0015g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0016g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0016g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0016g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0017g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0017g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0017g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0018g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0018g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0018g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0019g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0020g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0020g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0021g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0021g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0022g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0022g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0023g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0023g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0024g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0024g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0025g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0025g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0027g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0027g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0028g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0028g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0029g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0029g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0030g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0030g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0031g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0031g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0032g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0032g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0033g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0034g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0036g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0038g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0039g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0040g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0041g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0042g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0043g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0044g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0046g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0048g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0050g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0051g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0052g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0053g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0055g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0056g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0001t0058g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0004g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0004g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0006g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0014g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0014g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0014g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0014g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0016g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0045g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0047g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0049g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0059g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0002t0060g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0003t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0003t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0003t0011g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0003t0020g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0003t0026g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0003t0026g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0004t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0004t0011g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0004t0011g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0004t0015g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0004t0037g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0005t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0005t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0005t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0005t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0006t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0006t0035g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0001c0006t0057g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0002c0007t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0002c0007t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0002c0007t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0003c0008t0019g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0003c0008t0019g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0004c0010t0061g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
a0005c0009t0054g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0027 | g0163 | EUR | GBR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00099 | hp2 | a0001 | c0001 | t0006 | g0286 | EUR | GBR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0167 | EUR | FIN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00323 | hp2 | a0001 | c0001 | t0048 | g0136 | EUR | FIN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00408 | hp1 | a0001 | c0001 | t0009 | g0306 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00423 | hp2 | a0001 | c0001 | t0016 | g0290 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00438 | hp1 | a0002 | c0007 | t0005 | g0158 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0375 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00544 | hp2 | a0001 | c0001 | t0016 | g0289 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0361 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00558 | hp2 | a0001 | c0001 | t0018 | g0311 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00597 | hp2 | a0001 | c0001 | t0005 | g0132 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00621 | hp1 | a0001 | c0002 | t0006 | g0185 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00621 | hp2 | a0001 | c0001 | t0018 | g0374 | EAS | CHS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00642 | hp2 | a0001 | c0001 | t0050 | g0212 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00733 | hp1 | a0001 | c0001 | t0020 | g0250 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00738 | hp1 | a0001 | c0001 | t0015 | g0092 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00738 | hp2 | a0001 | c0001 | t0010 | g0270 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00741 | hp1 | a0001 | c0001 | t0008 | g0035 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0226 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0248 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0217 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01070 | hp2 | a0001 | c0001 | t0006 | g0278 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01074 | hp1 | a0001 | c0001 | t0043 | g0251 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0333 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0332 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0347 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01109 | hp1 | a0001 | c0001 | t0020 | g0155 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01109 | hp2 | a0001 | c0002 | t0014 | g0335 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01167 | hp1 | a0001 | c0001 | t0007 | g0243 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01167 | hp2 | a0001 | c0001 | t0019 | g0322 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01168 | hp1 | a0001 | c0001 | t0010 | g0014 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01168 | hp2 | a0001 | c0001 | t0007 | g0249 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01169 | hp1 | a0001 | c0001 | t0010 | g0014 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01169 | hp2 | a0001 | c0001 | t0007 | g0244 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0265 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0345 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0235 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0350 | AMR | PUR | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0334 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0133 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01358 | hp1 | a0001 | c0001 | t0030 | g0153 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0348 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01496 | hp1 | a0001 | c0001 | t0027 | g0102 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01516 | hp1 | a0001 | c0001 | t0006 | g0015 | EUR | IBS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0106 | EUR | IBS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0015 | EUR | IBS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0343 | EUR | IBS | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01884 | hp1 | a0001 | c0005 | t0006 | g0255 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0164 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01891 | hp1 | a0001 | c0005 | t0006 | g0257 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01891 | hp2 | a0001 | c0001 | t0010 | g0266 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PEL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0285 | AMR | PEL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PEL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0364 | AMR | PEL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01993 | hp1 | a0001 | c0002 | t0014 | g0356 | AMR | PEL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01993 | hp2 | a0001 | c0001 | t0009 | g0298 | AMR | PEL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0339 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02040 | hp2 | a0001 | c0001 | t0016 | g0288 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02055 | hp1 | a0001 | c0001 | t0022 | g0026 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02055 | hp2 | a0001 | c0001 | t0028 | g0327 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0277 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02071 | hp1 | a0001 | c0001 | t0009 | g0297 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0341 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02074 | hp2 | a0001 | c0001 | t0032 | g0146 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02080 | hp2 | a0001 | c0001 | t0005 | g0154 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02083 | hp1 | a0001 | c0001 | t0052 | g0187 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0126 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02129 | hp1 | a0001 | c0001 | t0005 | g0135 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0365 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02135 | hp2 | a0001 | c0001 | t0005 | g0166 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02145 | hp1 | a0001 | c0001 | t0008 | g0033 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02145 | hp2 | a0001 | c0001 | t0028 | g0326 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02165 | hp1 | a0001 | c0003 | t0004 | g0293 | EAS | CDX | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02165 | hp2 | a0001 | c0001 | t0056 | g0145 | EAS | CDX | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02257 | hp1 | a0001 | c0006 | t0057 | g0295 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0234 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02258 | hp1 | a0001 | c0005 | t0002 | g0245 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0261 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0258 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02293 | hp2 | a0001 | c0002 | t0014 | g0357 | AMR | PEL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0337 | AMR | PEL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0148 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02523 | hp1 | a0001 | c0003 | t0011 | g0292 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0369 | EAS | KHV | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0279 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0319 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02630 | hp1 | a0001 | c0001 | t0010 | g0223 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02630 | hp2 | a0001 | c0001 | t0009 | g0318 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02647 | hp1 | a0001 | c0001 | t0046 | g0260 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02647 | hp2 | a0001 | c0001 | t0010 | g0269 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0344 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02723 | hp1 | a0001 | c0001 | t0025 | g0321 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02723 | hp2 | a0001 | c0001 | t0007 | g0040 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02735 | hp1 | a0001 | c0001 | t0006 | g0280 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02735 | hp2 | a0001 | c0001 | t0009 | g0299 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0360 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0324 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02818 | hp2 | a0001 | c0001 | t0012 | g0029 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02886 | hp1 | a0001 | c0001 | t0010 | g0274 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0170 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02895 | hp1 | a0001 | c0001 | t0023 | g0032 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02895 | hp2 | a0001 | c0001 | t0029 | g0267 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02896 | hp1 | a0003 | c0008 | t0019 | g0308 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02896 | hp2 | a0001 | c0004 | t0037 | g0323 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02897 | hp1 | a0003 | c0008 | t0019 | g0307 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02897 | hp2 | a0001 | c0001 | t0029 | g0268 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02922 | hp1 | a0001 | c0001 | t0025 | g0320 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02922 | hp2 | a0001 | c0001 | t0053 | g0022 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02965 | hp1 | a0001 | c0006 | t0035 | g0038 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02965 | hp2 | a0001 | c0001 | t0042 | g0239 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0139 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0034 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02976 | hp1 | a0001 | c0001 | t0051 | g0016 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0330 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03017 | hp2 | a0001 | c0001 | t0011 | g0310 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03098 | hp1 | a0001 | c0001 | t0023 | g0028 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03098 | hp2 | a0001 | c0004 | t0011 | g0314 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03130 | hp1 | a0001 | c0001 | t0024 | g0222 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03130 | hp2 | a0001 | c0005 | t0006 | g0256 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03139 | hp1 | a0001 | c0001 | t0033 | g0221 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03195 | hp1 | a0001 | c0001 | t0034 | g0104 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03209 | hp1 | a0001 | c0001 | t0009 | g0316 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03209 | hp2 | a0001 | c0001 | t0058 | g0294 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03225 | hp2 | a0001 | c0001 | t0012 | g0005 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03239 | hp2 | a0001 | c0001 | t0015 | g0068 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0147 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03486 | hp1 | a0001 | c0001 | t0038 | g0317 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03486 | hp2 | a0001 | c0006 | t0007 | g0325 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03491 | hp1 | a0001 | c0001 | t0011 | g0358 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0138 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03516 | hp2 | a0004 | c0010 | t0061 | g0019 | AFR | ESN | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0247 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03579 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03688 | hp1 | a0001 | c0003 | t0020 | g0203 | SAS | STU | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | STU | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0273 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0227 | SAS | BEB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0376 | SAS | BEB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | BEB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | BEB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | BEB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0271 | SAS | BEB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG04115 | hp1 | a0001 | c0002 | t0006 | g0098 | SAS | STU | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | STU | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | BEB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG04184 | hp2 | a0001 | c0002 | t0014 | g0305 | SAS | BEB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | STU | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | STU | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | STU | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG04228 | hp2 | a0001 | c0001 | t0006 | g0282 | SAS | STU | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | YRI | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18522 | hp2 | a0001 | c0001 | t0024 | g0202 | AFR | YRI | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | CHB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18612 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | CHB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18747 | hp1 | a0001 | c0003 | t0026 | g0304 | EAS | CHB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18747 | hp2 | a0002 | c0007 | t0005 | g0159 | EAS | CHB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18906 | hp1 | a0001 | c0001 | t0013 | g0241 | AFR | YRI | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18906 | hp2 | a0001 | c0004 | t0011 | g0312 | AFR | YRI | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18939 | hp2 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0368 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18941 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18942 | hp1 | a0001 | c0001 | t0005 | g0140 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18942 | hp2 | a0001 | c0001 | t0007 | g0254 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18943 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0351 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18944 | hp2 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18945 | hp1 | a0001 | c0001 | t0006 | g0189 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18946 | hp1 | a0001 | c0001 | t0006 | g0281 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18947 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18949 | hp2 | a0001 | c0001 | t0005 | g0115 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18950 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18954 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18960 | hp1 | a0001 | c0001 | t0009 | g0296 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18960 | hp2 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0355 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18962 | hp1 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18962 | hp2 | a0001 | c0002 | t0049 | g0072 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18963 | hp1 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18964 | hp1 | a0001 | c0001 | t0017 | g0340 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18964 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18965 | hp1 | a0001 | c0002 | t0004 | g0346 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18966 | hp2 | a0001 | c0001 | t0009 | g0301 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18967 | hp2 | a0001 | c0001 | t0018 | g0367 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18968 | hp1 | a0002 | c0007 | t0005 | g0107 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18970 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18972 | hp1 | a0001 | c0002 | t0004 | g0371 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18975 | hp1 | a0001 | c0001 | t0021 | g0011 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18979 | hp1 | a0001 | c0001 | t0007 | g0253 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18979 | hp2 | a0001 | c0002 | t0045 | g0090 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0342 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18982 | hp1 | a0001 | c0001 | t0006 | g0180 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18982 | hp2 | a0001 | c0003 | t0026 | g0303 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18983 | hp2 | a0001 | c0001 | t0006 | g0283 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18984 | hp1 | a0001 | c0003 | t0004 | g0291 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18984 | hp2 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18987 | hp2 | a0001 | c0001 | t0006 | g0186 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0173 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18989 | hp1 | a0001 | c0001 | t0055 | g0119 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18990 | hp2 | a0001 | c0001 | t0005 | g0168 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18991 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18992 | hp2 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18993 | hp1 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18995 | hp1 | a0001 | c0002 | t0059 | g0023 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18995 | hp2 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0359 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19003 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19003 | hp2 | a0001 | c0001 | t0006 | g0287 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0157 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0372 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19006 | hp2 | a0001 | c0001 | t0006 | g0188 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19007 | hp1 | a0001 | c0001 | t0004 | g0366 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0349 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19012 | hp1 | a0001 | c0001 | t0021 | g0141 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19012 | hp2 | a0001 | c0001 | t0039 | g0302 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0259 | AFR | LWK | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | LWK | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19043 | hp1 | a0005 | c0009 | t0054 | g0236 | AFR | LWK | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19043 | hp2 | a0001 | c0001 | t0041 | g0309 | AFR | LWK | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19056 | hp1 | a0001 | c0001 | t0044 | g0190 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19057 | hp2 | a0001 | c0001 | t0040 | g0300 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19058 | hp2 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19064 | hp1 | a0001 | c0001 | t0007 | g0252 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19064 | hp2 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19065 | hp2 | a0001 | c0002 | t0016 | g0088 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19067 | hp2 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0352 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19070 | hp2 | a0001 | c0001 | t0017 | g0354 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19074 | hp1 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19074 | hp2 | a0001 | c0002 | t0060 | g0076 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19077 | hp2 | a0001 | c0001 | t0006 | g0182 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19079 | hp1 | a0001 | c0001 | t0006 | g0275 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19079 | hp2 | a0001 | c0001 | t0017 | g0353 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0373 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19083 | hp1 | a0001 | c0001 | t0032 | g0134 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0370 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0362 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19090 | hp1 | a0001 | c0002 | t0004 | g0363 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19091 | hp2 | a0001 | c0001 | t0021 | g0011 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19240 | hp1 | a0001 | c0001 | t0022 | g0027 | AFR | YRI | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0137 | AFR | YRI | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA20129 | hp1 | a0001 | c0001 | t0013 | g0242 | AFR | ASW | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA20129 | hp2 | a0001 | c0001 | t0009 | g0315 | AFR | ASW | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0042 | EUR | TSI | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0284 | EUR | TSI | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0338 | EUR | TSI | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0111 | EUR | TSI | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | GIH | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA20905 | hp2 | a0001 | c0002 | t0047 | g0058 | SAS | GIH | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0336 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG01123 | hp2 | a0001 | c0001 | t0030 | g0152 | AMR | CLM | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02109 | hp1 | a0001 | c0001 | t0013 | g0238 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02109 | hp2 | a0001 | c0001 | t0012 | g0025 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02486 | hp1 | a0001 | c0001 | t0015 | g0059 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02486 | hp2 | a0001 | c0001 | t0031 | g0020 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02559 | hp1 | a0001 | c0001 | t0013 | g0246 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG02559 | hp2 | a0001 | c0004 | t0015 | g0262 | AFR | ACB | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03471 | hp1 | a0001 | c0004 | t0011 | g0313 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0024 | AFR | MSL | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG06807 | hp1 | a0001 | c0001 | t0031 | g0021 | AFR | USA | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
HG06807 | hp2 | a0001 | c0001 | t0036 | g0039 | AFR | USA | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18955 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA18955 | hp2 | a0001 | c0001 | t0006 | g0276 | EAS | JPT | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | USA | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0229 | AFR | USA | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA21309 | hp1 | a0001 | c0001 | t0008 | g0237 | AFR | LWK | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | LWK | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0175 | REF | REF | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
homoSapiens | grch38p0 | a0001 | c0001 | t0013 | g0240 | REF | REF | RASSF8_chr12_25953682_26077869 | RASSF8 | chr12 | 25953682 | 26077869 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:26065047 | T | C | 1 | a0003 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.653T>C | p.Val218Ala | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/6 | 1322/5980 | 653/1260 | 218/419 | chr12 | 26065047 | |||
chr12:26065230 | G | A | 1 | a0002 | 3 | HG00438.hp1 NA18747.hp2 NA18968.hp1 |
missense_variant | MODERATE | c.836G>A | p.Arg279Gln | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/6 | 1505/5980 | 836/1260 | 279/419 | chr12 | 26065230 | |||
chr12:26065280 | G | A | 1 | a0005 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.886G>A | p.Gly296Ser | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/6 | 1555/5980 | 886/1260 | 296/419 | chr12 | 26065280 | |||
chr12:26068721 | T | A | 1 | a0004 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.1163T>A | p.Leu388Gln | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 1832/5980 | 1163/1260 | 388/419 | chr12 | 26068721 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:26064634 | T | C | 1 | a0001c0002 | 79 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
synonymous_variant | LOW | c.240T>C | p.Thr80Thr | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/6 | 909/5980 | 240/1260 | 80/419 | chr12 | 26064634 | |||
chr12:26064706 | G | A | 1 | a0001c0006 | 3 | HG02257.hp1 HG02965.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.312G>A | p.Gln104Gln | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/6 | 981/5980 | 312/1260 | 104/419 | chr12 | 26064706 | |||
chr12:26064919 | G | A | 1 | a0001c0005 | 4 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(1): Show |
synonymous_variant | LOW | c.525G>A | p.Glu175Glu | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/6 | 1194/5980 | 525/1260 | 175/419 | chr12 | 26064919 | |||
chr12:26065264 | G | A | 1 | a0001c0003 | 6 | HG02165.hp1 HG02523.hp1 HG03688.hp1 others(3): Show |
synonymous_variant | LOW | c.870G>A | p.Glu290Glu | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/6 | 1539/5980 | 870/1260 | 290/419 | chr12 | 26065264 | |||
chr12:26067658 | C | T | 1 | a0001c0004 | 5 | HG02559.hp2 HG02896.hp2 HG03098.hp2 others(2): Show |
synonymous_variant | LOW | c.1083C>T | p.Thr361Thr | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 5/6 | 1752/5980 | 1083/1260 | 361/419 | chr12 | 26067658 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:25958715 | G | A | 1 | a0001c0001t0033 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-636G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/6 | 96629 | chr12 | 25958715 | ||||||
chr12:25958716 | A | ACTCCTAC others(10): Show |
1 | a0001c0001t0034 | 1 | HG03195.hp1 | 5_prime_UTR_variant | MODIFIER | c.-617_-601dupCTCCTA others(11): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/6 | 96593 | INFO_REALIGN_3_PRIME | chr12 | 25958716 | |||||
chr12:25958739 | A | ACGCCCGC others(10): Show |
1 | a0001c0002t0059 | 1 | NA18995.hp1 | 5_prime_UTR_variant | MODIFIER | c.-606_-590dupGCGCTC others(11): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/6 | 96582 | INFO_REALIGN_3_PRIME | chr12 | 25958739 | |||||
chr12:25958739 | A | ACGCCCGC others(78): Show |
1 | a0001c0002t0060 | 1 | NA19074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-590_-589insGCGCTC others(79): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/6 | 96582 | INFO_REALIGN_3_PRIME | chr12 | 25958739 | |||||
chr12:25958762 | C | T | 1 | a0004c0010t0061 | 1 | HG03516.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-589C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/6 | chr12 | 25958762 | |||||||
chr12:25958807 | C | T | 2 | a0001c0001t0058 a0001c0006t0057 |
2 | HG02257.hp1 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-544C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/6 | 96537 | chr12 | 25958807 | ||||||
chr12:25958847 | C | A | 6 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0022 others(3): Show |
22 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-504C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/6 | 96497 | chr12 | 25958847 | ||||||
chr12:25958990 | G | A | 21 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0011 others(18): Show |
81 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(78): Show |
5_prime_UTR_variant | MODIFIER | c.-361G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/6 | 96354 | chr12 | 25958990 | ||||||
chr12:25959005 | G | A | 1 | a0001c0001t0017 | 3 | NA18964.hp1 NA19070.hp2 NA19079.hp2 |
5_prime_UTR_variant | MODIFIER | c.-346G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/6 | 96339 | chr12 | 25959005 | ||||||
chr12:25959007 | GCGGGGAG others(3): Show |
G | 6 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0032 others(3): Show |
45 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-336_-327delCGCCGG others(4): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/6 | 96320 | INFO_REALIGN_3_PRIME | chr12 | 25959007 | |||||
chr12:25959008 | C | T | 2 | a0001c0001t0031 a0001c0001t0053 |
3 | HG02486.hp2 HG02922.hp2 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-343C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/6 | 96336 | chr12 | 25959008 | ||||||
chr12:25959015 | C | CGCCGGGG others(3): Show |
1 | a0001c0001t0003 | 1 | HG03831.hp1 | 5_prime_UTR_variant | MODIFIER | c.-323_-314dupCGGGGA others(4): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/6 | 96306 | INFO_REALIGN_3_PRIME | chr12 | 25959015 | |||||
chr12:25959131 | G | A | 1 | a0001c0001t0042 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-220G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/6 | 96213 | chr12 | 25959131 | ||||||
chr12:25995106 | G | T | 1 | a0004c0010t0061 | 1 | HG03516.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-133G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/6 | chr12 | 25995106 | |||||||
chr12:26055335 | C | T | 1 | a0005c0009t0054 | 1 | NA19043.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-9C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/6 | chr12 | 26055335 | |||||||
chr12:26068880 | G | C | 1 | a0001c0001t0043 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*62G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 62 | chr12 | 26068880 | ||||||
chr12:26068933 | T | A | 2 | a0001c0001t0022 a0001c0006t0057 |
3 | HG02055.hp1 HG02257.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*115T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 115 | chr12 | 26068933 | ||||||
chr12:26069173 | T | C | 1 | a0001c0001t0044 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*355T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 355 | chr12 | 26069173 | ||||||
chr12:26069190 | A | G | 3 | a0001c0001t0031 a0001c0001t0041 a0001c0001t0053 |
4 | HG02486.hp2 HG02922.hp2 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*372A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 372 | chr12 | 26069190 | ||||||
chr12:26069225 | CTT | C | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(11): Show |
99 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*408_*409delTT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 408 | chr12 | 26069225 | ||||||
chr12:26069230 | C | G | 1 | a0001c0003t0026 | 2 | NA18747.hp1 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*412C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 412 | chr12 | 26069230 | ||||||
chr12:26069337 | C | T | 1 | a0001c0001t0052 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*519C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 519 | chr12 | 26069337 | ||||||
chr12:26069554 | G | A | 1 | a0001c0002t0045 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*736G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 736 | chr12 | 26069554 | ||||||
chr12:26069571 | T | G | 2 | a0001c0001t0010 a0001c0006t0035 |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*753T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 753 | chr12 | 26069571 | ||||||
chr12:26069799 | G | A | 6 | a0001c0001t0007 a0001c0001t0034 a0001c0001t0036 others(3): Show |
17 | HG01074.hp1 HG01167.hp1 HG01168.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*981G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 981 | chr12 | 26069799 | ||||||
chr12:26069812 | A | C | 52 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(49): Show |
252 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*994A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 994 | chr12 | 26069812 | ||||||
chr12:26069835 | A | G | 15 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(12): Show |
70 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1017A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 1017 | chr12 | 26069835 | ||||||
chr12:26070110 | G | A | 1 | a0001c0001t0050 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1292G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 1292 | chr12 | 26070110 | ||||||
chr12:26070184 | G | A | 1 | a0001c0002t0047 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1366G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 1366 | chr12 | 26070184 | ||||||
chr12:26070228 | T | G | 1 | a0001c0001t0027 | 2 | HG00099.hp1 HG01496.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1410T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 1410 | chr12 | 26070228 | ||||||
chr12:26070505 | G | A | 50 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(47): Show |
249 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1687G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 1687 | chr12 | 26070505 | ||||||
chr12:26070526 | G | A | 4 | a0001c0001t0010 a0001c0001t0031 a0001c0001t0041 others(1): Show |
11 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1708G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 1708 | chr12 | 26070526 | ||||||
chr12:26070620 | G | T | 1 | a0001c0001t0040 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1802G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 1802 | chr12 | 26070620 | ||||||
chr12:26070650 | A | T | 6 | a0001c0002t0001 a0001c0002t0014 a0001c0002t0047 others(3): Show |
71 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1832A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 1832 | chr12 | 26070650 | ||||||
chr12:26070729 | G | GA | 16 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(13): Show |
102 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1912dupA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 1913 | INFO_REALIGN_3_PRIME | chr12 | 26070729 | |||||
chr12:26070731 | G | C | 16 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(13): Show |
102 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1913G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 1913 | chr12 | 26070731 | ||||||
chr12:26070735 | T | C | 16 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(13): Show |
102 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1917T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 1917 | chr12 | 26070735 | ||||||
chr12:26070933 | A | T | 14 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(11): Show |
68 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2115A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 2115 | chr12 | 26070933 | ||||||
chr12:26071062 | A | C | 7 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0039 others(4): Show |
18 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2244A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 2244 | chr12 | 26071062 | ||||||
chr12:26071077 | G | A | 1 | a0001c0001t0029 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2259G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 2259 | chr12 | 26071077 | ||||||
chr12:26071100 | T | A | 63 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(60): Show |
335 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(332): Show |
3_prime_UTR_variant | MODIFIER | c.*2282T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 2282 | chr12 | 26071100 | ||||||
chr12:26071198 | G | A | 1 | a0001c0001t0025 | 2 | HG02723.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2380G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 2380 | chr12 | 26071198 | ||||||
chr12:26071263 | A | C | 1 | a0001c0001t0022 | 2 | HG02055.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2445A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 2445 | chr12 | 26071263 | ||||||
chr12:26071301 | G | A | 3 | a0001c0001t0039 a0001c0001t0040 a0001c0002t0045 |
3 | NA18979.hp2 NA19012.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2483G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 2483 | chr12 | 26071301 | ||||||
chr12:26071409 | T | TA | 8 | a0001c0001t0007 a0001c0001t0021 a0001c0001t0034 others(5): Show |
21 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2591_*2592insA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 2592 | chr12 | 26071409 | ||||||
chr12:26071410 | T | A | 56 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(53): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*2592T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 2592 | chr12 | 26071410 | ||||||
chr12:26071625 | A | G | 1 | a0001c0001t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2807A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 2807 | chr12 | 26071625 | ||||||
chr12:26071814 | TA | T | 47 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(44): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
3_prime_UTR_variant | MODIFIER | c.*3006delA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 3006 | INFO_REALIGN_3_PRIME | chr12 | 26071814 | |||||
chr12:26071913 | C | A | 14 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(11): Show |
68 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*3095C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 3095 | chr12 | 26071913 | ||||||
chr12:26071987 | C | T | 1 | a0001c0001t0028 | 2 | HG02055.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3169C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 3169 | chr12 | 26071987 | ||||||
chr12:26072081 | T | G | 70 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(67): Show |
384 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(381): Show |
3_prime_UTR_variant | MODIFIER | c.*3263T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 3263 | chr12 | 26072081 | ||||||
chr12:26072126 | T | G | 73 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(70): Show |
389 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(386): Show |
3_prime_UTR_variant | MODIFIER | c.*3308T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 3308 | chr12 | 26072126 | ||||||
chr12:26072128 | G | A | 1 | a0001c0002t0049 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3310G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 3310 | chr12 | 26072128 | ||||||
chr12:26072400 | G | A | 1 | a0001c0001t0051 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3582G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 3582 | chr12 | 26072400 | ||||||
chr12:26072471 | C | A | 71 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(68): Show |
385 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(382): Show |
3_prime_UTR_variant | MODIFIER | c.*3653C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 3653 | chr12 | 26072471 | ||||||
chr12:26072745 | A | C | 1 | a0001c0001t0038 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3927A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 6/6 | 3927 | chr12 | 26072745 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:25959165 | C | T | 48 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(45): Show |
48 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-203+17C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959165 | |||||||
chr12:25959191 | C | T | 1 | a0001c0001t0002g0328 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-203+43C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959191 | |||||||
chr12:25959197 | C | T | 1 | a0001c0001t0004g0376 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-203+49C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959197 | |||||||
chr12:25959249 | C | T | 3 | a0001c0001t0028g0326 a0001c0001t0028g0327 a0001c0006t0007g0325 |
3 | HG02055.hp2 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-203+101C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959249 | |||||||
chr12:25959278 | C | T | 1 | a0001c0001t0007g0324 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-203+130C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959278 | |||||||
chr12:25959356 | C | G | 28 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(25): Show |
28 | HG00408.hp1 HG00558.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.-203+208C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959356 | |||||||
chr12:25959408 | T | A | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-203+260T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959408 | |||||||
chr12:25959567 | A | T | 2 | a0001c0001t0058g0294 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-203+419A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959567 | |||||||
chr12:25959587 | A | T | 3 | a0001c0003t0004g0291 a0001c0003t0004g0293 a0001c0003t0011g0292 |
3 | HG02165.hp1 HG02523.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-203+439A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959587 | |||||||
chr12:25959656 | G | A | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-203+508G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959656 | |||||||
chr12:25959671 | C | G | 17 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0275 others(14): Show |
18 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.-203+523C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959671 | |||||||
chr12:25959683 | T | C | 1 | a0001c0001t0003g0018 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-203+535T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959683 | |||||||
chr12:25959717 | A | T | 37 | a0001c0001t0002g0149 a0001c0001t0002g0177 a0001c0001t0002g0178 others(34): Show |
38 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-203+569A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959717 | |||||||
chr12:25959874 | T | C | 17 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0275 others(14): Show |
18 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.-203+726T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959874 | |||||||
chr12:25959912 | C | T | 15 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0003g0265 others(12): Show |
16 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-203+764C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959912 | |||||||
chr12:25959992 | T | C | 21 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0275 others(18): Show |
22 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.-203+844T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25959992 | |||||||
chr12:25960048 | T | TA | 17 | a0001c0001t0008g0006 a0001c0001t0008g0030 a0001c0001t0008g0031 others(14): Show |
19 | HG00741.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-203+911dupA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25960048 | ||||||
chr12:25960394 | C | T | 1 | a0001c0001t0006g0261 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-203+1246C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25960394 | |||||||
chr12:25960553 | C | T | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-203+1405C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25960553 | |||||||
chr12:25960762 | C | A | 20 | a0001c0001t0002g0037 a0001c0001t0002g0263 a0001c0001t0002g0264 others(17): Show |
21 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.-203+1614C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25960762 | |||||||
chr12:25960767 | G | A | 18 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0275 others(15): Show |
19 | HG00099.hp2 HG01070.hp2 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.-203+1619G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25960767 | |||||||
chr12:25960912 | A | G | 14 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0275 others(11): Show |
15 | HG00099.hp2 HG01070.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.-203+1764A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25960912 | |||||||
chr12:25960980 | A | C | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-203+1832A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25960980 | |||||||
chr12:25961009 | T | A | 1 | a0001c0001t0007g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-203+1861T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961009 | |||||||
chr12:25961066 | G | A | 1 | a0001c0004t0015g0262 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-203+1918G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961066 | |||||||
chr12:25961086 | G | A | 208 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(205): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-203+1938G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961086 | |||||||
chr12:25961100 | C | T | 1 | a0001c0001t0004g0375 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-203+1952C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961100 | |||||||
chr12:25961162 | AT | A | 14 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0275 others(11): Show |
15 | HG00099.hp2 HG01070.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.-203+2016delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25961162 | ||||||
chr12:25961237 | T | C | 348 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(345): Show |
367 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.-203+2089T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961237 | |||||||
chr12:25961294 | T | G | 43 | a0001c0001t0002g0012 a0001c0001t0003g0004 a0001c0001t0003g0193 others(40): Show |
46 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-203+2146T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961294 | |||||||
chr12:25961436 | T | A | 31 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(28): Show |
31 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.-203+2288T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961436 | |||||||
chr12:25961487 | G | A | 18 | a0001c0001t0002g0037 a0001c0001t0002g0263 a0001c0001t0002g0264 others(15): Show |
19 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-203+2339G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961487 | |||||||
chr12:25961593 | G | C | 4 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 others(1): Show |
4 | HG01433.hp1 HG02280.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-203+2445G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961593 | |||||||
chr12:25961596 | C | T | 1 | a0001c0001t0005g0192 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-203+2448C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961596 | |||||||
chr12:25961597 | G | A | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-203+2449G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961597 | |||||||
chr12:25961675 | G | A | 18 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0275 others(15): Show |
19 | HG00099.hp2 HG01070.hp2 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.-203+2527G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961675 | |||||||
chr12:25961694 | A | G | 1 | a0001c0001t0002g0012 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-203+2546A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961694 | |||||||
chr12:25961715 | C | T | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-203+2567C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961715 | |||||||
chr12:25961974 | C | T | 1 | a0001c0004t0037g0323 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-203+2826C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25961974 | |||||||
chr12:25962054 | GA | G | 266 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(263): Show |
285 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.-203+2916delA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25962054 | ||||||
chr12:25962089 | T | C | 43 | a0001c0001t0002g0012 a0001c0001t0003g0004 a0001c0001t0003g0193 others(40): Show |
46 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-203+2941T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962089 | |||||||
chr12:25962138 | C | A | 1 | a0001c0001t0002g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-203+2990C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962138 | |||||||
chr12:25962184 | A | C | 367 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0037 others(364): Show |
387 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(384): Show |
intron_variant | MODIFIER | c.-203+3036A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962184 | |||||||
chr12:25962184 | A | T | 1 | a0001c0006t0007g0325 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-203+3036A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962184 | |||||||
chr12:25962230 | C | T | 1 | a0001c0002t0001g0191 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-203+3082C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962230 | |||||||
chr12:25962463 | T | A | 20 | a0001c0001t0002g0037 a0001c0001t0002g0263 a0001c0001t0002g0264 others(17): Show |
21 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.-203+3315T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962463 | |||||||
chr12:25962542 | C | G | 1 | a0001c0001t0023g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-203+3394C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962542 | |||||||
chr12:25962569 | A | C | 3 | a0001c0001t0019g0322 a0001c0001t0025g0320 a0001c0001t0025g0321 |
3 | HG01167.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-203+3421A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962569 | |||||||
chr12:25962574 | C | G | 118 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 others(115): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-203+3426C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962574 | |||||||
chr12:25962639 | G | T | 43 | a0001c0001t0002g0012 a0001c0001t0003g0004 a0001c0001t0003g0193 others(40): Show |
46 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-203+3491G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962639 | |||||||
chr12:25962769 | C | T | 1 | a0001c0006t0007g0325 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-203+3621C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962769 | |||||||
chr12:25962892 | C | T | 2 | a0001c0001t0031g0021 a0001c0001t0053g0022 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-203+3744C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962892 | |||||||
chr12:25962898 | A | G | 1 | a0001c0001t0008g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-203+3750A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962898 | |||||||
chr12:25962921 | T | A | 63 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(60): Show |
70 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-203+3773T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962921 | |||||||
chr12:25962986 | A | AT | 31 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(28): Show |
31 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.-203+3845dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25962986 | ||||||
chr12:25962998 | G | A | 1 | a0001c0002t0002g0045 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-203+3850G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25962998 | |||||||
chr12:25963054 | G | A | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-203+3906G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25963054 | |||||||
chr12:25963203 | G | T | 15 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0006g0180 others(12): Show |
15 | HG00621.hp1 HG02074.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-203+4055G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25963203 | |||||||
chr12:25963230 | A | G | 5 | a0001c0001t0009g0315 a0001c0001t0009g0316 a0001c0001t0009g0318 others(2): Show |
5 | HG02615.hp1 HG02630.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+4082A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25963230 | |||||||
chr12:25963246 | T | A | 1 | a0001c0002t0001g0046 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-203+4098T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25963246 | |||||||
chr12:25963247 | T | A | 72 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(69): Show |
80 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-203+4099T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25963247 | |||||||
chr12:25963321 | C | CA | 67 | a0001c0001t0003g0018 a0001c0001t0003g0199 a0001c0001t0003g0200 others(64): Show |
67 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-203+4195dupA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25963321 | ||||||
chr12:25963321 | C | CAA | 9 | a0001c0001t0004g0338 a0001c0001t0018g0311 a0001c0003t0004g0291 others(6): Show |
9 | HG00558.hp2 HG02165.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.-203+4194_-203+419 others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25963321 | ||||||
chr12:25963321 | C | CAAAA | 14 | a0001c0001t0009g0296 a0001c0001t0009g0299 a0001c0001t0009g0301 others(11): Show |
14 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.-203+4192_-203+419 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25963321 | ||||||
chr12:25963321 | C | CAAAAA | 6 | a0001c0001t0009g0297 a0001c0001t0009g0298 a0001c0001t0009g0318 others(3): Show |
6 | HG01993.hp2 HG02071.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-203+4191_-203+419 others(9): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25963321 | ||||||
chr12:25963321 | CA | C | 109 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0103 others(106): Show |
115 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-203+4195delA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25963321 | ||||||
chr12:25963321 | CAAAAA | C | 69 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(66): Show |
77 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.-203+4191_-203+419 others(9): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25963321 | ||||||
chr12:25963569 | T | C | 3 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0049 |
3 | HG02080.hp1 HG02129.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-203+4421T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25963569 | |||||||
chr12:25963661 | C | G | 18 | a0001c0001t0002g0037 a0001c0001t0002g0263 a0001c0001t0002g0264 others(15): Show |
19 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-203+4513C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25963661 | |||||||
chr12:25963734 | G | T | 1 | a0001c0002t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-203+4586G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25963734 | |||||||
chr12:25964041 | C | A | 28 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-203+4893C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25964041 | |||||||
chr12:25964092 | C | T | 3 | a0001c0001t0004g0372 a0001c0001t0004g0373 a0001c0001t0018g0374 |
3 | HG00621.hp2 NA19005.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-203+4944C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25964092 | |||||||
chr12:25964179 | A | G | 42 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-203+5031A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25964179 | |||||||
chr12:25964236 | C | T | 6 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(3): Show |
7 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-203+5088C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25964236 | |||||||
chr12:25964289 | G | GT | 8 | a0001c0001t0004g0370 a0001c0001t0006g0287 a0001c0001t0022g0026 others(5): Show |
8 | HG02055.hp1 HG02165.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.-203+5156dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25964289 | ||||||
chr12:25964289 | GT | G | 58 | a0001c0001t0002g0233 a0001c0001t0003g0004 a0001c0001t0003g0193 others(55): Show |
61 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.-203+5156delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25964289 | ||||||
chr12:25964552 | T | G | 16 | a0001c0001t0002g0233 a0001c0001t0006g0234 a0001c0001t0006g0235 others(13): Show |
17 | HG00741.hp1 HG01167.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.-203+5404T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25964552 | |||||||
chr12:25964637 | A | G | 18 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0275 others(15): Show |
19 | HG00099.hp2 HG01070.hp2 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.-203+5489A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25964637 | |||||||
chr12:25964696 | T | G | 2 | a0001c0001t0006g0234 a0001c0001t0006g0235 |
2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-203+5548T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25964696 | |||||||
chr12:25964857 | A | C | 79 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(76): Show |
79 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-203+5709A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25964857 | |||||||
chr12:25964899 | G | T | 15 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(12): Show |
16 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-203+5751G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25964899 | |||||||
chr12:25964952 | A | T | 6 | a0001c0001t0011g0310 a0001c0001t0018g0311 a0001c0001t0041g0309 others(3): Show |
6 | HG00558.hp2 HG03017.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-203+5804A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25964952 | |||||||
chr12:25964969 | G | A | 1 | a0001c0001t0002g0013 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-203+5821G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25964969 | |||||||
chr12:25965003 | C | T | 42 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-203+5855C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965003 | |||||||
chr12:25965027 | C | G | 3 | a0001c0001t0005g0003 a0001c0001t0005g0173 a0001c0001t0005g0174 |
5 | NA18955.hp1 NA18988.hp1 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+5879C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965027 | |||||||
chr12:25965028 | C | T | 1 | a0001c0001t0044g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-203+5880C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965028 | |||||||
chr12:25965060 | A | C | 101 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(98): Show |
106 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-203+5912A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965060 | |||||||
chr12:25965153 | G | A | 28 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-203+6005G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965153 | |||||||
chr12:25965168 | C | A | 1 | a0001c0001t0004g0329 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-203+6020C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965168 | |||||||
chr12:25965183 | C | T | 2 | a0003c0008t0019g0307 a0003c0008t0019g0308 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-203+6035C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965183 | |||||||
chr12:25965184 | G | A | 1 | a0001c0001t0006g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-203+6036G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965184 | |||||||
chr12:25965190 | C | T | 1 | a0001c0001t0012g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-203+6042C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965190 | |||||||
chr12:25965200 | C | G | 3 | a0001c0004t0011g0312 a0001c0004t0011g0313 a0001c0004t0011g0314 |
3 | HG03098.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-203+6052C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965200 | |||||||
chr12:25965239 | C | T | 87 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(84): Show |
96 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.-203+6091C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965239 | |||||||
chr12:25965248 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-203+6100G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965248 | |||||||
chr12:25965271 | C | T | 1 | a0001c0001t0006g0286 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-203+6123C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965271 | |||||||
chr12:25965290 | C | G | 42 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-203+6142C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965290 | |||||||
chr12:25965363 | C | CT | 129 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0171 others(126): Show |
131 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.-203+6235dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25965363 | ||||||
chr12:25965363 | C | CTT | 18 | a0001c0001t0003g0017 a0001c0001t0003g0279 a0001c0001t0004g0368 others(15): Show |
19 | HG00099.hp2 HG00423.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.-203+6234_-203+623 others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25965363 | ||||||
chr12:25965363 | C | T | 1 | a0001c0003t0004g0291 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-203+6215C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965363 | |||||||
chr12:25965367 | T | C | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0101 |
3 | NA19007.hp2 NA19060.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-203+6219T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965367 | |||||||
chr12:25965368 | T | TC | 14 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0006g0234 others(11): Show |
16 | HG00741.hp1 HG01192.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-203+6220_-203+622 others(5): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965368 | |||||||
chr12:25965387 | A | G | 1 | a0004c0010t0061g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-203+6239A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965387 | |||||||
chr12:25965389 | A | C | 1 | a0001c0001t0003g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-203+6241A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965389 | |||||||
chr12:25965469 | A | G | 1 | a0001c0001t0007g0258 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-203+6321A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965469 | |||||||
chr12:25965486 | C | T | 1 | a0001c0001t0008g0036 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-203+6338C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965486 | |||||||
chr12:25965584 | C | G | 355 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(352): Show |
374 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.-203+6436C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965584 | |||||||
chr12:25965635 | C | T | 104 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(101): Show |
109 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-203+6487C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965635 | |||||||
chr12:25965647 | T | C | 351 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(348): Show |
370 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(367): Show |
intron_variant | MODIFIER | c.-203+6499T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965647 | |||||||
chr12:25965725 | G | C | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-203+6577G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965725 | |||||||
chr12:25965950 | T | A | 355 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(352): Show |
374 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.-203+6802T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965950 | |||||||
chr12:25965999 | C | T | 9 | a0001c0001t0008g0006 a0001c0001t0008g0030 a0001c0001t0008g0031 others(6): Show |
10 | HG00741.hp1 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-203+6851C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25965999 | |||||||
chr12:25966011 | G | A | 8 | a0001c0001t0003g0004 a0001c0001t0003g0194 a0001c0001t0003g0195 others(5): Show |
10 | NA18947.hp1 NA18948.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.-203+6863G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25966011 | |||||||
chr12:25966127 | T | C | 3 | a0001c0001t0007g0040 a0001c0001t0007g0247 a0001c0001t0013g0246 |
3 | HG02559.hp1 HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-203+6979T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25966127 | |||||||
chr12:25966154 | A | G | 1 | a0001c0001t0006g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-203+7006A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25966154 | |||||||
chr12:25966202 | A | T | 42 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-203+7054A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25966202 | |||||||
chr12:25966320 | A | G | 63 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(60): Show |
70 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-203+7172A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25966320 | |||||||
chr12:25966336 | T | C | 6 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(3): Show |
7 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-203+7188T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25966336 | |||||||
chr12:25966449 | G | T | 48 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(45): Show |
48 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-203+7301G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25966449 | |||||||
chr12:25966540 | AC | A | 3 | a0001c0001t0031g0020 a0001c0001t0031g0021 a0001c0001t0053g0022 |
3 | HG02486.hp2 HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-203+7393delC | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25966540 | |||||||
chr12:25966541 | C | T | 2 | a0001c0001t0058g0294 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-203+7393C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25966541 | |||||||
chr12:25966655 | T | A | 1 | a0001c0006t0035g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-203+7507T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25966655 | |||||||
chr12:25966739 | C | T | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-203+7591C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25966739 | |||||||
chr12:25966832 | G | A | 63 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(60): Show |
70 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-203+7684G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25966832 | |||||||
chr12:25966937 | A | G | 367 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0037 others(364): Show |
387 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(384): Show |
intron_variant | MODIFIER | c.-203+7789A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25966937 | |||||||
chr12:25967075 | T | C | 4 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0055 others(1): Show |
4 | NA18953.hp2 NA18983.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.-203+7927T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967075 | |||||||
chr12:25967109 | G | A | 4 | a0001c0001t0007g0040 a0001c0001t0007g0247 a0001c0001t0013g0246 others(1): Show |
4 | HG02559.hp1 HG02723.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-203+7961G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967109 | |||||||
chr12:25967132 | A | T | 1 | a0001c0001t0006g0189 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-203+7984A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967132 | |||||||
chr12:25967319 | A | G | 17 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0006g0234 others(14): Show |
19 | HG00741.hp1 HG01167.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-203+8171A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967319 | |||||||
chr12:25967322 | A | G | 101 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(98): Show |
106 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-203+8174A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967322 | |||||||
chr12:25967363 | A | C | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-203+8215A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967363 | |||||||
chr12:25967413 | T | C | 12 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(9): Show |
13 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-203+8265T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967413 | |||||||
chr12:25967418 | T | C | 1 | a0001c0001t0009g0297 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-203+8270T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967418 | |||||||
chr12:25967458 | T | A | 3 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0005c0009t0054g0236 |
3 | HG01192.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-203+8310T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967458 | |||||||
chr12:25967643 | G | T | 70 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(67): Show |
78 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.-203+8495G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967643 | |||||||
chr12:25967677 | C | A | 1 | a0001c0001t0041g0309 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-203+8529C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967677 | |||||||
chr12:25967848 | A | C | 1 | a0001c0001t0009g0319 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-203+8700A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967848 | |||||||
chr12:25967872 | A | G | 18 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0275 others(15): Show |
19 | HG00099.hp2 HG01070.hp2 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.-203+8724A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967872 | |||||||
chr12:25967951 | G | A | 1 | a0001c0001t0023g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-203+8803G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967951 | |||||||
chr12:25967975 | A | T | 1 | a0001c0001t0002g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-203+8827A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25967975 | |||||||
chr12:25968014 | T | C | 347 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(344): Show |
366 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.-203+8866T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968014 | |||||||
chr12:25968027 | T | C | 3 | a0001c0004t0011g0312 a0001c0004t0011g0313 a0001c0004t0011g0314 |
3 | HG03098.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-203+8879T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968027 | |||||||
chr12:25968132 | C | G | 3 | a0001c0005t0006g0255 a0001c0005t0006g0256 a0001c0005t0006g0257 |
3 | HG01884.hp1 HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-203+8984C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968132 | |||||||
chr12:25968175 | C | T | 1 | a0001c0001t0008g0229 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-203+9027C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968175 | |||||||
chr12:25968350 | T | C | 1 | a0001c0001t0044g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-203+9202T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968350 | |||||||
chr12:25968353 | A | T | 1 | a0001c0001t0002g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-203+9205A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968353 | |||||||
chr12:25968377 | C | T | 1 | a0005c0009t0054g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-203+9229C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968377 | |||||||
chr12:25968382 | G | A | 103 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(100): Show |
108 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.-203+9234G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968382 | |||||||
chr12:25968620 | A | G | 3 | a0001c0003t0004g0291 a0001c0003t0004g0293 a0001c0003t0011g0292 |
3 | HG02165.hp1 HG02523.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-203+9472A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968620 | |||||||
chr12:25968632 | T | C | 86 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(83): Show |
95 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.-203+9484T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968632 | |||||||
chr12:25968687 | T | C | 347 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(344): Show |
366 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.-203+9539T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968687 | |||||||
chr12:25968779 | T | G | 2 | a0001c0001t0006g0015 a0001c0001t0006g0278 |
3 | HG01070.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-203+9631T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968779 | |||||||
chr12:25968797 | C | T | 70 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(67): Show |
78 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.-203+9649C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968797 | |||||||
chr12:25968861 | A | G | 1 | a0001c0001t0005g0168 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-203+9713A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968861 | |||||||
chr12:25968925 | A | G | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-203+9777A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968925 | |||||||
chr12:25968998 | G | C | 121 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(118): Show |
127 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.-203+9850G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25968998 | |||||||
chr12:25969085 | G | A | 14 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0006g0234 others(11): Show |
16 | HG00741.hp1 HG01192.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-203+9937G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969085 | |||||||
chr12:25969101 | A | G | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-203+9953A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969101 | |||||||
chr12:25969242 | C | T | 103 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(100): Show |
108 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.-203+10094C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969242 | |||||||
chr12:25969244 | C | T | 3 | a0001c0001t0031g0020 a0001c0001t0031g0021 a0001c0001t0053g0022 |
3 | HG02486.hp2 HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-203+10096C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969244 | |||||||
chr12:25969245 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-203+10097A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969245 | |||||||
chr12:25969266 | C | T | 121 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(118): Show |
127 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.-203+10118C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969266 | |||||||
chr12:25969333 | C | T | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-203+10185C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969333 | |||||||
chr12:25969358 | T | C | 1 | a0001c0001t0034g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-203+10210T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969358 | |||||||
chr12:25969526 | G | A | 1 | a0001c0004t0037g0323 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-203+10378G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969526 | |||||||
chr12:25969620 | G | T | 51 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(48): Show |
51 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.-203+10472G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969620 | |||||||
chr12:25969654 | G | T | 1 | a0001c0001t0018g0311 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-203+10506G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969654 | |||||||
chr12:25969792 | A | G | 3 | a0001c0001t0019g0322 a0001c0001t0025g0320 a0001c0001t0025g0321 |
3 | HG01167.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-203+10644A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969792 | |||||||
chr12:25969880 | T | C | 354 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(351): Show |
373 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.-203+10732T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969880 | |||||||
chr12:25969955 | G | A | 1 | a0001c0001t0004g0331 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-203+10807G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969955 | |||||||
chr12:25969968 | C | T | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-203+10820C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25969968 | |||||||
chr12:25970005 | G | A | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-203+10857G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970005 | |||||||
chr12:25970097 | C | CT | 52 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0195 others(49): Show |
55 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-203+10963dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25970097 | ||||||
chr12:25970120 | G | T | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-203+10972G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970120 | |||||||
chr12:25970228 | A | G | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-203+11080A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970228 | |||||||
chr12:25970312 | G | A | 1 | a0001c0001t0003g0265 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-203+11164G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970312 | |||||||
chr12:25970312 | G | T | 48 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(45): Show |
48 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-203+11164G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970312 | |||||||
chr12:25970412 | A | G | 207 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(204): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.-203+11264A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970412 | |||||||
chr12:25970604 | A | G | 17 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0006g0234 others(14): Show |
19 | HG00741.hp1 HG01167.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-203+11456A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970604 | |||||||
chr12:25970627 | G | T | 1 | a0001c0001t0005g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-203+11479G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970627 | |||||||
chr12:25970641 | G | T | 21 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(18): Show |
21 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.-203+11493G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970641 | |||||||
chr12:25970670 | A | T | 16 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(13): Show |
17 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-203+11522A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970670 | |||||||
chr12:25970716 | G | A | 1 | a0001c0002t0059g0023 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-203+11568G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970716 | |||||||
chr12:25970758 | T | C | 14 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-203+11610T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970758 | |||||||
chr12:25970901 | C | T | 48 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(45): Show |
48 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-203+11753C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970901 | |||||||
chr12:25970908 | C | T | 7 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-203+11760C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970908 | |||||||
chr12:25970917 | A | C | 12 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(9): Show |
13 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-203+11769A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970917 | |||||||
chr12:25970918 | A | G | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-203+11770A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25970918 | |||||||
chr12:25971125 | G | A | 1 | a0001c0001t0005g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-203+11977G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25971125 | |||||||
chr12:25971216 | T | C | 1 | a0001c0004t0037g0323 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-203+12068T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25971216 | |||||||
chr12:25971227 | T | TG | 7 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-203+12081dupG | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25971227 | ||||||
chr12:25971482 | T | A | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-203+12334T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25971482 | |||||||
chr12:25971490 | C | G | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-203+12342C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25971490 | |||||||
chr12:25971541 | A | G | 3 | a0001c0005t0006g0255 a0001c0005t0006g0256 a0001c0005t0006g0257 |
3 | HG01884.hp1 HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-203+12393A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25971541 | |||||||
chr12:25971547 | C | T | 3 | a0001c0001t0002g0165 a0001c0001t0007g0164 a0001c0001t0034g0104 |
3 | HG01884.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-203+12399C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25971547 | |||||||
chr12:25971570 | GA | G | 63 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(60): Show |
70 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-203+12430delA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25971570 | ||||||
chr12:25971570 | GAAAAAAA others(3): Show |
G | 2 | a0001c0001t0058g0294 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-203+12434_-203+12 others(16): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25971570 | ||||||
chr12:25971615 | T | A | 63 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(60): Show |
70 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-203+12467T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25971615 | |||||||
chr12:25971619 | A | T | 2 | a0001c0001t0027g0102 a0001c0001t0027g0163 |
2 | HG00099.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-203+12471A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25971619 | |||||||
chr12:25971798 | T | C | 1 | a0001c0002t0001g0057 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-203+12650T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25971798 | |||||||
chr12:25971901 | A | G | 138 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(135): Show |
146 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.-203+12753A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25971901 | |||||||
chr12:25972189 | T | G | 16 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(13): Show |
17 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-203+13041T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25972189 | |||||||
chr12:25972650 | A | G | 42 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-203+13502A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25972650 | |||||||
chr12:25972729 | A | T | 1 | a0001c0002t0001g0201 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-203+13581A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25972729 | |||||||
chr12:25972775 | A | G | 86 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(83): Show |
95 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.-203+13627A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25972775 | |||||||
chr12:25973010 | A | G | 1 | a0001c0001t0023g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-203+13862A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973010 | |||||||
chr12:25973036 | T | A | 70 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(67): Show |
78 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.-203+13888T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973036 | |||||||
chr12:25973044 | A | T | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-203+13896A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973044 | |||||||
chr12:25973046 | T | A | 1 | a0001c0001t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-203+13898T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973046 | |||||||
chr12:25973085 | G | A | 1 | a0001c0002t0006g0098 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-203+13937G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973085 | |||||||
chr12:25973142 | T | G | 1 | a0001c0001t0003g0018 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-203+13994T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973142 | |||||||
chr12:25973192 | A | G | 1 | a0004c0010t0061g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-203+14044A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973192 | |||||||
chr12:25973200 | C | T | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-203+14052C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973200 | |||||||
chr12:25973204 | A | AT | 13 | a0001c0001t0002g0162 a0001c0001t0003g0265 a0001c0001t0003g0271 others(10): Show |
14 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-203+14070dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25973204 | ||||||
chr12:25973204 | AT | A | 128 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0003g0004 others(125): Show |
132 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.-203+14070delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25973204 | ||||||
chr12:25973210 | T | G | 1 | a0001c0002t0001g0201 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-203+14062T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973210 | |||||||
chr12:25973225 | A | G | 3 | a0001c0001t0002g0103 a0001c0001t0002g0161 a0001c0001t0002g0169 |
3 | HG03239.hp1 HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-203+14077A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973225 | |||||||
chr12:25973285 | G | A | 1 | a0001c0001t0024g0202 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-203+14137G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973285 | |||||||
chr12:25973305 | T | C | 7 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-203+14157T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973305 | |||||||
chr12:25973351 | A | G | 14 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0006g0234 others(11): Show |
16 | HG00741.hp1 HG01192.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-203+14203A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973351 | |||||||
chr12:25973411 | T | G | 70 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(67): Show |
78 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.-203+14263T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973411 | |||||||
chr12:25973465 | G | A | 138 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(135): Show |
146 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.-203+14317G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973465 | |||||||
chr12:25973521 | A | T | 1 | a0001c0006t0057g0295 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-203+14373A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973521 | |||||||
chr12:25973686 | C | T | 72 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(69): Show |
80 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-203+14538C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973686 | |||||||
chr12:25973755 | A | C | 1 | a0001c0002t0001g0201 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-203+14607A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973755 | |||||||
chr12:25973756 | T | C | 3 | a0001c0001t0006g0275 a0001c0001t0006g0276 a0001c0001t0006g0287 |
3 | NA18955.hp2 NA19003.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-203+14608T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973756 | |||||||
chr12:25973960 | A | G | 63 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(60): Show |
70 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-203+14812A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25973960 | |||||||
chr12:25974012 | C | T | 28 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-203+14864C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25974012 | |||||||
chr12:25974049 | A | G | 1 | a0001c0001t0009g0318 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-203+14901A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25974049 | |||||||
chr12:25974110 | G | A | 103 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(100): Show |
108 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.-203+14962G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25974110 | |||||||
chr12:25974224 | A | AT | 3 | a0001c0005t0006g0255 a0001c0005t0006g0256 a0001c0005t0006g0257 |
3 | HG01884.hp1 HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-203+15081dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25974224 | ||||||
chr12:25974245 | G | A | 2 | a0001c0001t0005g0009 a0001c0001t0005g0105 |
3 | NA18964.hp2 NA19003.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-203+15097G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25974245 | |||||||
chr12:25974295 | C | T | 86 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(83): Show |
95 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.-203+15147C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25974295 | |||||||
chr12:25974297 | C | T | 14 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0275 others(11): Show |
15 | HG00099.hp2 HG01070.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.-203+15149C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25974297 | |||||||
chr12:25974388 | T | C | 21 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(18): Show |
21 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.-203+15240T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25974388 | |||||||
chr12:25974495 | ACC | A | 6 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(3): Show |
7 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-203+15348_-203+15 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25974495 | |||||||
chr12:25974497 | CT | C | 6 | a0001c0001t0003g0017 a0001c0001t0003g0197 a0001c0001t0003g0214 others(3): Show |
6 | HG01070.hp1 HG02293.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-203+15365delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25974497 | ||||||
chr12:25974497 | CTT | C | 125 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0003g0265 others(122): Show |
129 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.-203+15364_-203+15 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25974497 | ||||||
chr12:25974497 | CTTT | C | 108 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(105): Show |
113 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.-203+15363_-203+15 others(9): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25974497 | ||||||
chr12:25974499 | T | C | 6 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(3): Show |
7 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-203+15351T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25974499 | |||||||
chr12:25974730 | A | G | 3 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0228 |
3 | HG01069.hp1 HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-203+15582A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25974730 | |||||||
chr12:25974833 | G | A | 1 | a0001c0001t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-203+15685G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25974833 | |||||||
chr12:25974934 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-203+15786A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25974934 | |||||||
chr12:25975044 | C | A | 1 | a0001c0001t0002g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-203+15896C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975044 | |||||||
chr12:25975115 | T | C | 1 | a0001c0001t0002g0012 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-203+15967T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975115 | |||||||
chr12:25975200 | G | A | 48 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(45): Show |
48 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-203+16052G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975200 | |||||||
chr12:25975249 | A | G | 1 | a0001c0001t0003g0225 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-203+16101A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975249 | |||||||
chr12:25975341 | A | G | 2 | a0001c0002t0001g0096 a0001c0002t0001g0097 |
2 | HG00642.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.-203+16193A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975341 | |||||||
chr12:25975497 | G | A | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-203+16349G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975497 | |||||||
chr12:25975514 | G | T | 101 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(98): Show |
106 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-203+16366G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975514 | |||||||
chr12:25975540 | T | C | 1 | a0001c0001t0015g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-203+16392T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975540 | |||||||
chr12:25975595 | A | G | 1 | a0004c0010t0061g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-203+16447A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975595 | |||||||
chr12:25975768 | C | G | 1 | a0001c0004t0037g0323 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-203+16620C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975768 | |||||||
chr12:25975791 | A | G | 5 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-203+16643A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975791 | |||||||
chr12:25975834 | G | T | 1 | a0001c0002t0002g0045 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-203+16686G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975834 | |||||||
chr12:25975864 | A | G | 1 | a0004c0010t0061g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-203+16716A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975864 | |||||||
chr12:25975901 | G | A | 1 | a0001c0001t0041g0309 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-203+16753G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975901 | |||||||
chr12:25975986 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-203+16838A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25975986 | |||||||
chr12:25976009 | C | T | 14 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-203+16861C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976009 | |||||||
chr12:25976042 | A | G | 42 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-203+16894A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976042 | |||||||
chr12:25976085 | C | G | 3 | a0001c0001t0006g0284 a0001c0001t0006g0285 a0001c0001t0006g0286 |
3 | HG00099.hp2 HG01934.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-203+16937C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976085 | |||||||
chr12:25976154 | C | T | 4 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(1): Show |
4 | HG01175.hp2 HG03710.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.-203+17006C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976154 | |||||||
chr12:25976220 | T | C | 1 | a0001c0006t0057g0295 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-203+17072T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976220 | |||||||
chr12:25976248 | C | T | 2 | a0002c0007t0005g0158 a0002c0007t0005g0159 |
2 | HG00438.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-203+17100C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976248 | |||||||
chr12:25976257 | C | T | 1 | a0001c0001t0004g0366 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-203+17109C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976257 | |||||||
chr12:25976379 | G | T | 1 | a0001c0001t0053g0022 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-203+17231G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976379 | |||||||
chr12:25976418 | CTT | C | 48 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(45): Show |
48 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-203+17272_-203+17 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25976418 | ||||||
chr12:25976673 | T | G | 1 | a0001c0003t0020g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-203+17525T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976673 | |||||||
chr12:25976721 | G | T | 1 | a0001c0001t0007g0258 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-203+17573G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976721 | |||||||
chr12:25976830 | C | G | 101 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(98): Show |
106 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-203+17682C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976830 | |||||||
chr12:25976876 | A | G | 1 | a0001c0001t0019g0322 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-203+17728A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976876 | |||||||
chr12:25976906 | C | T | 1 | a0001c0001t0012g0029 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-203+17758C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976906 | |||||||
chr12:25976907 | G | A | 8 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0060 others(5): Show |
11 | HG01074.hp2 NA18939.hp1 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.-203+17759G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976907 | |||||||
chr12:25976968 | A | T | 35 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0003g0279 others(32): Show |
38 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-203+17820A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25976968 | |||||||
chr12:25977020 | G | T | 1 | a0001c0001t0003g0224 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-203+17872G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25977020 | |||||||
chr12:25977243 | T | C | 3 | a0001c0001t0006g0261 a0001c0001t0007g0259 a0001c0001t0046g0260 |
3 | HG02258.hp2 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-202-17794T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25977243 | |||||||
chr12:25977248 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-202-17789G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25977248 | |||||||
chr12:25977435 | A | G | 7 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-202-17602A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25977435 | |||||||
chr12:25977457 | C | T | 35 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0003g0279 others(32): Show |
38 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-202-17580C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25977457 | |||||||
chr12:25977482 | A | AT | 6 | a0001c0001t0011g0310 a0001c0001t0018g0311 a0001c0001t0041g0309 others(3): Show |
6 | HG00558.hp2 HG03017.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-202-17545dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25977482 | ||||||
chr12:25977522 | T | C | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-202-17515T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25977522 | |||||||
chr12:25977643 | T | C | 18 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0275 others(15): Show |
19 | HG00099.hp2 HG01070.hp2 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.-202-17394T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25977643 | |||||||
chr12:25977671 | C | CA | 45 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0003g0265 others(42): Show |
52 | HG00738.hp2 HG00741.hp1 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.-202-17354dupA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25977671 | ||||||
chr12:25977671 | C | CAA | 57 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(54): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-202-17355_-202-17 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25977671 | ||||||
chr12:25977847 | A | G | 28 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-202-17190A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25977847 | |||||||
chr12:25977866 | A | G | 1 | a0001c0002t0001g0093 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-202-17171A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25977866 | |||||||
chr12:25977889 | A | C | 101 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(98): Show |
106 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-202-17148A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25977889 | |||||||
chr12:25977964 | G | A | 36 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(33): Show |
38 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-202-17073G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25977964 | |||||||
chr12:25978012 | G | A | 224 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(221): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.-202-17025G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25978012 | |||||||
chr12:25978122 | G | A | 1 | a0001c0001t0003g0204 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-202-16915G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25978122 | |||||||
chr12:25978124 | G | A | 28 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-202-16913G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25978124 | |||||||
chr12:25978271 | G | A | 14 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-202-16766G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25978271 | |||||||
chr12:25978429 | A | G | 1 | a0001c0001t0051g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-202-16608A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25978429 | |||||||
chr12:25978481 | C | T | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-202-16556C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25978481 | |||||||
chr12:25978528 | T | G | 2 | a0001c0002t0001g0201 a0001c0002t0001g0205 |
2 | NA18987.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-202-16509T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25978528 | |||||||
chr12:25978612 | A | G | 42 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-202-16425A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25978612 | |||||||
chr12:25978684 | A | AT | 17 | a0001c0001t0003g0017 a0001c0001t0003g0265 a0001c0001t0006g0261 others(14): Show |
18 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-202-16339dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25978684 | ||||||
chr12:25978684 | AT | A | 11 | a0001c0001t0002g0106 a0001c0001t0003g0226 a0001c0001t0003g0248 others(8): Show |
11 | HG01069.hp1 HG01069.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.-202-16339delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25978684 | ||||||
chr12:25978903 | T | C | 1 | a0001c0001t0003g0271 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-202-16134T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25978903 | |||||||
chr12:25978907 | A | G | 63 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(60): Show |
70 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-202-16130A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25978907 | |||||||
chr12:25978982 | A | G | 6 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(3): Show |
7 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-202-16055A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25978982 | |||||||
chr12:25979144 | C | T | 1 | a0001c0001t0041g0309 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-202-15893C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25979144 | |||||||
chr12:25979365 | A | G | 1 | a0001c0001t0005g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-202-15672A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25979365 | |||||||
chr12:25979389 | G | A | 86 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(83): Show |
95 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.-202-15648G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25979389 | |||||||
chr12:25979395 | A | T | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-202-15642A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25979395 | |||||||
chr12:25979667 | G | A | 3 | a0001c0001t0019g0322 a0001c0001t0025g0320 a0001c0001t0025g0321 |
3 | HG01167.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-202-15370G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25979667 | |||||||
chr12:25979689 | G | C | 42 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-202-15348G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25979689 | |||||||
chr12:25979717 | T | C | 347 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(344): Show |
366 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.-202-15320T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25979717 | |||||||
chr12:25979840 | T | G | 3 | a0001c0001t0019g0322 a0001c0001t0025g0320 a0001c0001t0025g0321 |
3 | HG01167.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-202-15197T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25979840 | |||||||
chr12:25979845 | A | AGT | 86 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(83): Show |
95 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.-202-15191_-202-15 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25979845 | ||||||
chr12:25979852 | G | A | 101 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(98): Show |
106 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-202-15185G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25979852 | |||||||
chr12:25979987 | G | T | 14 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0006g0234 others(11): Show |
16 | HG00741.hp1 HG01192.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-202-15050G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25979987 | |||||||
chr12:25980033 | T | G | 51 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(48): Show |
51 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.-202-15004T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25980033 | |||||||
chr12:25980066 | A | G | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-202-14971A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25980066 | |||||||
chr12:25980077 | C | G | 138 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(135): Show |
146 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.-202-14960C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25980077 | |||||||
chr12:25980084 | C | T | 7 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-202-14953C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25980084 | |||||||
chr12:25980113 | C | T | 14 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-202-14924C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25980113 | |||||||
chr12:25980204 | C | T | 63 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(60): Show |
70 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-202-14833C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25980204 | |||||||
chr12:25980486 | C | T | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-202-14551C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25980486 | |||||||
chr12:25980655 | G | C | 163 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(160): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-202-14382G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25980655 | |||||||
chr12:25980790 | A | G | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-202-14247A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25980790 | |||||||
chr12:25980837 | A | G | 1 | a0001c0001t0005g0157 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-202-14200A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25980837 | |||||||
chr12:25980992 | A | G | 63 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(60): Show |
70 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-202-14045A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25980992 | |||||||
chr12:25981085 | C | T | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-202-13952C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25981085 | |||||||
chr12:25981144 | T | G | 350 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(347): Show |
369 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.-202-13893T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25981144 | |||||||
chr12:25981207 | A | G | 14 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-202-13830A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25981207 | |||||||
chr12:25981335 | G | C | 5 | a0001c0001t0004g0333 a0001c0001t0004g0334 a0001c0001t0004g0336 others(2): Show |
5 | HG01081.hp2 HG01109.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-13702G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25981335 | |||||||
chr12:25981482 | C | T | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-202-13555C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25981482 | |||||||
chr12:25981531 | T | G | 12 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(9): Show |
13 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-202-13506T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25981531 | |||||||
chr12:25981555 | G | T | 1 | a0005c0009t0054g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-202-13482G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25981555 | |||||||
chr12:25981606 | G | T | 2 | a0001c0001t0003g0193 a0001c0001t0003g0219 |
2 | NA18941.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-202-13431G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25981606 | |||||||
chr12:25981649 | G | T | 2 | a0001c0001t0006g0234 a0001c0001t0006g0235 |
2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-202-13388G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25981649 | |||||||
chr12:25981938 | C | G | 103 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(100): Show |
108 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.-202-13099C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25981938 | |||||||
chr12:25981960 | C | T | 14 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0006g0234 others(11): Show |
16 | HG00741.hp1 HG01192.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-202-13077C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25981960 | |||||||
chr12:25982029 | G | A | 268 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(265): Show |
287 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-202-13008G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25982029 | |||||||
chr12:25982048 | G | A | 1 | a0001c0001t0003g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-202-12989G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25982048 | |||||||
chr12:25982053 | T | C | 1 | a0001c0001t0004g0338 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-202-12984T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25982053 | |||||||
chr12:25982305 | T | C | 1 | a0001c0001t0023g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-202-12732T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25982305 | |||||||
chr12:25982338 | A | G | 224 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(221): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.-202-12699A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25982338 | |||||||
chr12:25982580 | G | C | 42 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-202-12457G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25982580 | |||||||
chr12:25982641 | C | A | 368 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0037 others(365): Show |
388 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(385): Show |
intron_variant | MODIFIER | c.-202-12396C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25982641 | |||||||
chr12:25982711 | G | A | 138 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(135): Show |
146 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.-202-12326G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25982711 | |||||||
chr12:25982746 | G | A | 35 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0003g0279 others(32): Show |
38 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-202-12291G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25982746 | |||||||
chr12:25982877 | T | C | 51 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(48): Show |
51 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.-202-12160T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25982877 | |||||||
chr12:25982928 | G | A | 3 | a0001c0001t0031g0020 a0001c0001t0031g0021 a0001c0001t0053g0022 |
3 | HG02486.hp2 HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-202-12109G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25982928 | |||||||
chr12:25982937 | A | G | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-202-12100A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25982937 | |||||||
chr12:25983093 | T | G | 1 | a0001c0001t0002g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-202-11944T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25983093 | |||||||
chr12:25983242 | C | CA | 344 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(341): Show |
363 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(360): Show |
intron_variant | MODIFIER | c.-202-11787dupA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25983242 | ||||||
chr12:25983254 | G | GAAAA | 347 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(344): Show |
366 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.-202-11780_-202-11 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25983254 | ||||||
chr12:25983255 | A | G | 1 | a0001c0001t0007g0258 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-202-11782A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25983255 | |||||||
chr12:25983268 | C | A | 1 | a0001c0001t0002g0108 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-202-11769C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25983268 | |||||||
chr12:25983414 | A | G | 347 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(344): Show |
366 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.-202-11623A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25983414 | |||||||
chr12:25983443 | A | G | 63 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0100 others(60): Show |
70 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-202-11594A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25983443 | |||||||
chr12:25983588 | C | T | 28 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-202-11449C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25983588 | |||||||
chr12:25983611 | G | A | 1 | a0001c0001t0004g0339 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-202-11426G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25983611 | |||||||
chr12:25983707 | C | A | 60 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0015g0059 others(57): Show |
67 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-202-11330C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25983707 | |||||||
chr12:25983824 | G | C | 44 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0193 others(41): Show |
46 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-202-11213G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25983824 | |||||||
chr12:25983871 | A | G | 138 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(135): Show |
146 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.-202-11166A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25983871 | |||||||
chr12:25983902 | G | A | 6 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(3): Show |
7 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-202-11135G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25983902 | |||||||
chr12:25983936 | C | T | 1 | a0001c0001t0043g0251 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-202-11101C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25983936 | |||||||
chr12:25984037 | C | T | 347 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(344): Show |
366 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.-202-11000C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984037 | |||||||
chr12:25984224 | C | CT | 110 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0003g0200 others(107): Show |
118 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-202-10787dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25984224 | ||||||
chr12:25984224 | C | CTT | 19 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0004g0362 others(16): Show |
19 | HG00738.hp1 HG01175.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.-202-10788_-202-10 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25984224 | ||||||
chr12:25984224 | CT | C | 9 | a0001c0001t0002g0171 a0001c0001t0003g0017 a0001c0001t0003g0220 others(6): Show |
9 | HG01081.hp1 HG01168.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-202-10787delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25984224 | ||||||
chr12:25984244 | T | C | 105 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(102): Show |
110 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-202-10793T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984244 | |||||||
chr12:25984244 | T | TC | 34 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0003g0279 others(31): Show |
37 | HG00099.hp2 HG01070.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.-202-10793_-202-10 others(7): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984244 | |||||||
chr12:25984374 | G | A | 61 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0015g0059 others(58): Show |
68 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-202-10663G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984374 | |||||||
chr12:25984456 | C | T | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-202-10581C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984456 | |||||||
chr12:25984487 | C | T | 1 | a0001c0002t0016g0088 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-202-10550C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984487 | |||||||
chr12:25984520 | T | G | 1 | a0001c0001t0025g0320 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-202-10517T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984520 | |||||||
chr12:25984579 | G | C | 1 | a0001c0001t0002g0012 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-202-10458G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984579 | |||||||
chr12:25984647 | A | G | 21 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(18): Show |
21 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.-202-10390A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984647 | |||||||
chr12:25984663 | G | A | 44 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0193 others(41): Show |
46 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-202-10374G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984663 | |||||||
chr12:25984703 | G | A | 103 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(100): Show |
108 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.-202-10334G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984703 | |||||||
chr12:25984914 | C | A | 2 | a0001c0001t0002g0171 a0001c0001t0002g0172 |
2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-202-10123C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984914 | |||||||
chr12:25984950 | A | C | 44 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0193 others(41): Show |
46 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-202-10087A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984950 | |||||||
chr12:25984952 | T | G | 12 | a0001c0001t0002g0013 a0001c0001t0003g0248 a0001c0001t0007g0040 others(9): Show |
13 | HG00733.hp1 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.-202-10085T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984952 | |||||||
chr12:25984961 | C | G | 1 | a0001c0001t0020g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-202-10076C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984961 | |||||||
chr12:25984992 | G | A | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-202-10045G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25984992 | |||||||
chr12:25985098 | T | G | 3 | a0001c0001t0019g0322 a0001c0001t0025g0320 a0001c0001t0025g0321 |
3 | HG01167.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-202-9939T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25985098 | |||||||
chr12:25985228 | T | G | 9 | a0001c0001t0010g0274 a0001c0001t0011g0310 a0001c0001t0018g0311 others(6): Show |
9 | HG00558.hp2 HG02886.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-202-9809T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25985228 | |||||||
chr12:25985402 | C | T | 1 | a0001c0001t0012g0029 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-202-9635C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25985402 | |||||||
chr12:25985772 | T | C | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-202-9265T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25985772 | |||||||
chr12:25985808 | T | TC | 42 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-202-9229_-202-922 others(5): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25985808 | |||||||
chr12:25985817 | T | G | 3 | a0001c0003t0004g0291 a0001c0003t0004g0293 a0001c0003t0011g0292 |
3 | HG02165.hp1 HG02523.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-202-9220T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25985817 | |||||||
chr12:25986039 | T | C | 6 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0301 others(3): Show |
6 | HG00423.hp2 HG00544.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.-202-8998T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986039 | |||||||
chr12:25986058 | A | G | 2 | a0001c0002t0001g0055 a0001c0002t0001g0056 |
2 | NA18953.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-202-8979A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986058 | |||||||
chr12:25986125 | A | G | 61 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0015g0059 others(58): Show |
68 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-202-8912A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986125 | |||||||
chr12:25986154 | G | A | 1 | a0001c0001t0002g0012 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-202-8883G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986154 | |||||||
chr12:25986188 | C | T | 44 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0193 others(41): Show |
46 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-202-8849C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986188 | |||||||
chr12:25986241 | C | A | 1 | a0001c0001t0031g0020 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-202-8796C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986241 | |||||||
chr12:25986252 | C | T | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-202-8785C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986252 | |||||||
chr12:25986470 | A | G | 48 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(45): Show |
48 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-202-8567A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986470 | |||||||
chr12:25986589 | A | G | 140 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(137): Show |
148 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.-202-8448A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986589 | |||||||
chr12:25986645 | G | A | 1 | a0001c0004t0037g0323 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-202-8392G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986645 | |||||||
chr12:25986718 | C | A | 140 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(137): Show |
148 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.-202-8319C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986718 | |||||||
chr12:25986759 | C | T | 1 | a0001c0001t0003g0225 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-202-8278C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986759 | |||||||
chr12:25986778 | C | T | 1 | a0001c0001t0005g0154 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-202-8259C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986778 | |||||||
chr12:25986849 | A | G | 2 | a0001c0001t0030g0152 a0001c0001t0030g0153 |
2 | HG01123.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-202-8188A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986849 | |||||||
chr12:25986871 | G | A | 2 | a0001c0001t0006g0234 a0001c0001t0006g0235 |
2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-202-8166G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986871 | |||||||
chr12:25986917 | G | A | 1 | a0001c0001t0031g0020 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-202-8120G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986917 | |||||||
chr12:25986922 | T | TTTTG | 38 | a0001c0001t0002g0012 a0001c0001t0002g0142 a0001c0001t0002g0143 others(35): Show |
39 | HG00621.hp1 HG00639.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.-202-8112_-202-811 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25986922 | ||||||
chr12:25986922 | T | TTTTGTTT others(1): Show |
55 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(52): Show |
56 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.-202-8112_-202-811 others(12): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25986922 | ||||||
chr12:25986922 | T | TTTTGTTT others(5): Show |
15 | a0001c0001t0002g0103 a0001c0001t0002g0109 a0001c0001t0002g0111 others(12): Show |
19 | HG03239.hp1 HG03491.hp2 HG04184.hp1 others(16): Show |
intron_variant | MODIFIER | c.-202-8112_-202-811 others(16): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25986922 | ||||||
chr12:25986922 | T | TTTTGTTT others(9): Show |
1 | a0001c0001t0002g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-202-8112_-202-811 others(20): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25986922 | ||||||
chr12:25986926 | T | G | 226 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0037 others(223): Show |
243 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.-202-8111T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986926 | |||||||
chr12:25986926 | T | TG | 3 | a0001c0001t0006g0261 a0001c0002t0001g0050 a0001c0005t0002g0245 |
3 | HG02258.hp1 HG02258.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.-202-8111_-202-811 others(5): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986926 | |||||||
chr12:25986926 | T | TGTTTG | 42 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(39): Show |
42 | HG00544.hp1 HG00621.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.-202-8111_-202-811 others(9): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986926 | |||||||
chr12:25986926 | T | TGTTTGTT others(6): Show |
1 | a0001c0001t0005g0151 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-202-8111_-202-811 others(17): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986926 | |||||||
chr12:25986926 | T | TTTTG | 61 | a0001c0001t0003g0213 a0001c0001t0003g0214 a0001c0001t0003g0215 others(58): Show |
62 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.-202-8087_-202-808 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25986926 | ||||||
chr12:25986926 | T | TTTTGTTT others(1): Show |
20 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(17): Show |
22 | HG00423.hp1 HG00438.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.-202-8091_-202-808 others(12): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25986926 | ||||||
chr12:25986926 | T | TTTTTG | 8 | a0001c0001t0004g0332 a0001c0001t0004g0333 a0001c0001t0004g0334 others(5): Show |
8 | HG00558.hp1 HG01081.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-202-8108_-202-810 others(9): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25986926 | ||||||
chr12:25986947 | T | G | 1 | a0001c0002t0001g0067 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-202-8090T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986947 | |||||||
chr12:25986950 | G | GGTTT | 68 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0012g0005 others(65): Show |
76 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.-202-8087_-202-808 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986950 | |||||||
chr12:25986950 | G | GTTTGT | 16 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(13): Show |
17 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-202-8084_-202-808 others(9): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25986950 | ||||||
chr12:25986950 | G | GTTTT | 15 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0008g0006 others(12): Show |
16 | HG00741.hp1 HG01167.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.-202-8086_-202-808 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25986950 | ||||||
chr12:25986960 | G | A | 2 | a0002c0007t0005g0158 a0002c0007t0005g0159 |
2 | HG00438.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-202-8077G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986960 | |||||||
chr12:25986968 | G | A | 3 | a0001c0001t0002g0233 a0001c0001t0028g0326 a0001c0001t0028g0327 |
3 | HG02055.hp2 HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-202-8069G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25986968 | |||||||
chr12:25987013 | G | A | 14 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0006g0234 others(11): Show |
16 | HG00741.hp1 HG01192.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-202-8024G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25987013 | |||||||
chr12:25987018 | CTCGCCTC others(6): Show |
C | 16 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(13): Show |
17 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-202-8016_-202-800 others(17): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25987018 | ||||||
chr12:25987021 | G | T | 1 | a0001c0001t0002g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-202-8016G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25987021 | |||||||
chr12:25987057 | C | T | 6 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(3): Show |
7 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-202-7980C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25987057 | |||||||
chr12:25987188 | C | G | 3 | a0001c0001t0002g0037 a0001c0001t0002g0263 a0001c0001t0002g0264 |
3 | HG01243.hp1 HG01258.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-202-7849C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25987188 | |||||||
chr12:25987471 | G | A | 140 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(137): Show |
148 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.-202-7566G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25987471 | |||||||
chr12:25987515 | A | G | 9 | a0001c0001t0008g0006 a0001c0001t0008g0030 a0001c0001t0008g0031 others(6): Show |
10 | HG00741.hp1 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-202-7522A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25987515 | |||||||
chr12:25987720 | C | A | 1 | a0001c0001t0025g0320 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-202-7317C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25987720 | |||||||
chr12:25987840 | G | T | 1 | a0001c0001t0004g0359 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-202-7197G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25987840 | |||||||
chr12:25987870 | G | A | 16 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0275 others(13): Show |
17 | HG00099.hp2 HG01070.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.-202-7167G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25987870 | |||||||
chr12:25987883 | ACT | A | 4 | a0001c0001t0007g0040 a0001c0001t0007g0247 a0001c0001t0013g0246 others(1): Show |
4 | HG02559.hp1 HG02723.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-202-7151_-202-715 others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25987883 | ||||||
chr12:25987921 | G | A | 1 | a0001c0002t0001g0061 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-202-7116G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25987921 | |||||||
chr12:25987922 | T | G | 347 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(344): Show |
366 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.-202-7115T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25987922 | |||||||
chr12:25987944 | C | T | 3 | a0001c0001t0019g0322 a0001c0001t0025g0320 a0001c0001t0025g0321 |
3 | HG01167.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-202-7093C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25987944 | |||||||
chr12:25988018 | A | AT | 34 | a0001c0001t0003g0198 a0001c0001t0003g0265 a0001c0001t0003g0271 others(31): Show |
36 | HG00099.hp2 HG00738.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-202-7003dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25988018 | ||||||
chr12:25988228 | C | T | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-202-6809C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25988228 | |||||||
chr12:25988692 | C | G | 14 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(11): Show |
14 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.-202-6345C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25988692 | |||||||
chr12:25988731 | T | A | 12 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(9): Show |
13 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-202-6306T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25988731 | |||||||
chr12:25988746 | A | G | 107 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(104): Show |
112 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.-202-6291A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25988746 | |||||||
chr12:25988824 | C | T | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-202-6213C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25988824 | |||||||
chr12:25989037 | G | T | 1 | a0001c0001t0009g0306 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-202-6000G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25989037 | |||||||
chr12:25989194 | A | G | 1 | a0001c0001t0005g0140 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-202-5843A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25989194 | |||||||
chr12:25989315 | A | T | 1 | a0001c0001t0007g0324 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-202-5722A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25989315 | |||||||
chr12:25989507 | A | G | 3 | a0001c0005t0006g0255 a0001c0005t0006g0256 a0001c0005t0006g0257 |
3 | HG01884.hp1 HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-202-5530A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25989507 | |||||||
chr12:25989650 | T | TTTCTTGT others(110): Show |
1 | a0001c0001t0003g0018 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-202-5384_-202-526 others(121): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25989650 | ||||||
chr12:25989769 | T | C | 3 | a0001c0005t0006g0255 a0001c0005t0006g0256 a0001c0005t0006g0257 |
3 | HG01884.hp1 HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-202-5268T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25989769 | |||||||
chr12:25989882 | A | G | 1 | a0001c0002t0001g0097 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-202-5155A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25989882 | |||||||
chr12:25990060 | C | T | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-202-4977C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990060 | |||||||
chr12:25990060 | CTTATT | C | 13 | a0001c0001t0002g0012 a0001c0001t0006g0234 a0001c0001t0006g0235 others(10): Show |
15 | HG00741.hp1 HG01192.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-202-4975_-202-497 others(9): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25990060 | ||||||
chr12:25990075 | C | A | 62 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0012g0005 others(59): Show |
70 | HG00408.hp2 HG00642.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.-202-4962C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990075 | |||||||
chr12:25990078 | A | G | 22 | a0001c0001t0003g0017 a0001c0001t0003g0265 a0001c0001t0003g0271 others(19): Show |
23 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.-202-4959A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990078 | |||||||
chr12:25990194 | A | G | 43 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(40): Show |
45 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-202-4843A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990194 | |||||||
chr12:25990196 | A | G | 1 | a0001c0002t0001g0057 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-202-4841A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990196 | |||||||
chr12:25990197 | T | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(88): Show |
96 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-202-4840T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990197 | |||||||
chr12:25990340 | A | G | 1 | a0001c0001t0048g0136 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-202-4697A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990340 | |||||||
chr12:25990399 | A | G | 43 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(40): Show |
45 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-202-4638A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990399 | |||||||
chr12:25990510 | A | G | 92 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(89): Show |
97 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-202-4527A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990510 | |||||||
chr12:25990563 | T | G | 8 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(5): Show |
9 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-202-4474T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990563 | |||||||
chr12:25990603 | T | G | 1 | a0001c0001t0007g0324 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-202-4434T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990603 | |||||||
chr12:25990757 | A | G | 271 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(268): Show |
290 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.-202-4280A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990757 | |||||||
chr12:25990801 | A | G | 43 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(40): Show |
45 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-202-4236A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990801 | |||||||
chr12:25990858 | C | G | 85 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0003g0265 others(82): Show |
94 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.-202-4179C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990858 | |||||||
chr12:25990910 | T | TAC | 5 | a0001c0001t0006g0275 a0001c0001t0006g0287 a0001c0001t0007g0324 others(2): Show |
5 | HG02559.hp2 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-202-4111_-202-411 others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25990910 | ||||||
chr12:25990941 | G | A | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-202-4096G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25990941 | |||||||
chr12:25991192 | T | C | 51 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(48): Show |
51 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-202-3845T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25991192 | |||||||
chr12:25991404 | C | T | 9 | a0001c0001t0010g0274 a0001c0001t0012g0005 a0001c0001t0012g0024 others(6): Show |
10 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-202-3633C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25991404 | |||||||
chr12:25991540 | G | A | 2 | a0001c0001t0031g0021 a0001c0001t0053g0022 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-202-3497G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25991540 | |||||||
chr12:25991848 | C | T | 1 | a0001c0001t0005g0154 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-202-3189C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25991848 | |||||||
chr12:25991870 | A | G | 47 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0193 others(44): Show |
49 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-202-3167A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25991870 | |||||||
chr12:25991889 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-202-3148T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25991889 | |||||||
chr12:25991916 | G | A | 43 | a0001c0001t0002g0012 a0001c0001t0003g0279 a0001c0001t0006g0015 others(40): Show |
46 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.-202-3121G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25991916 | |||||||
chr12:25992306 | G | T | 1 | a0001c0002t0001g0078 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-202-2731G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25992306 | |||||||
chr12:25992449 | T | G | 43 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(40): Show |
45 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-202-2588T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25992449 | |||||||
chr12:25992483 | G | T | 1 | a0001c0001t0046g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-202-2554G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25992483 | |||||||
chr12:25992522 | G | T | 1 | a0001c0001t0003g0226 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-202-2515G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25992522 | |||||||
chr12:25992525 | G | A | 2 | a0001c0001t0022g0026 a0001c0001t0022g0027 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-202-2512G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25992525 | |||||||
chr12:25992586 | C | G | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-202-2451C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25992586 | |||||||
chr12:25992615 | C | T | 1 | a0001c0001t0004g0338 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-202-2422C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25992615 | |||||||
chr12:25992716 | A | C | 2 | a0001c0001t0009g0306 a0001c0001t0040g0300 |
2 | HG00408.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-202-2321A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25992716 | |||||||
chr12:25992826 | C | T | 1 | a0001c0002t0014g0305 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-202-2211C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25992826 | |||||||
chr12:25992836 | A | G | 1 | a0001c0002t0001g0084 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-202-2201A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25992836 | |||||||
chr12:25992944 | A | C | 1 | a0001c0002t0001g0050 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-202-2093A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25992944 | |||||||
chr12:25992999 | T | A | 1 | a0001c0002t0001g0050 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-202-2038T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25992999 | |||||||
chr12:25993007 | G | A | 1 | a0001c0004t0015g0262 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-202-2030G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993007 | |||||||
chr12:25993030 | A | G | 363 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0037 others(360): Show |
383 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(380): Show |
intron_variant | MODIFIER | c.-202-2007A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993030 | |||||||
chr12:25993045 | G | T | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-202-1992G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993045 | |||||||
chr12:25993110 | C | T | 350 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(347): Show |
369 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.-202-1927C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993110 | |||||||
chr12:25993124 | C | T | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-202-1913C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993124 | |||||||
chr12:25993128 | C | G | 1 | a0001c0001t0004g0331 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-202-1909C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993128 | |||||||
chr12:25993260 | A | G | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-202-1777A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993260 | |||||||
chr12:25993266 | G | T | 28 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-202-1771G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993266 | |||||||
chr12:25993333 | T | C | 350 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(347): Show |
369 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.-202-1704T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993333 | |||||||
chr12:25993478 | A | G | 1 | a0001c0001t0010g0223 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-202-1559A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993478 | |||||||
chr12:25993488 | A | G | 16 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(13): Show |
17 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-202-1549A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993488 | |||||||
chr12:25993492 | G | A | 1 | a0001c0001t0002g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-202-1545G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993492 | |||||||
chr12:25993587 | G | A | 1 | a0001c0001t0005g0168 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-202-1450G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993587 | |||||||
chr12:25993615 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-202-1422C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993615 | |||||||
chr12:25993882 | C | T | 1 | a0001c0001t0003g0220 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-202-1155C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993882 | |||||||
chr12:25993894 | C | G | 85 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0003g0265 others(82): Show |
94 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.-202-1143C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993894 | |||||||
chr12:25993896 | C | T | 1 | a0001c0001t0003g0265 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-202-1141C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25993896 | |||||||
chr12:25994039 | C | T | 1 | a0004c0010t0061g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-202-998C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994039 | |||||||
chr12:25994201 | G | A | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-202-836G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994201 | |||||||
chr12:25994273 | ATT | A | 9 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(6): Show |
10 | HG01168.hp1 HG01169.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.-202-760_-202-759d others(4): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25994273 | ||||||
chr12:25994276 | TTTA | T | 7 | a0001c0001t0003g0273 a0001c0001t0004g0329 a0001c0001t0004g0341 others(4): Show |
7 | HG00738.hp2 HG02071.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-202-760_-202-758d others(5): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994276 | |||||||
chr12:25994277 | TTA | T | 23 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(20): Show |
23 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-202-759_-202-758d others(4): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994277 | |||||||
chr12:25994277 | TTAA | T | 53 | a0001c0001t0004g0330 a0001c0001t0004g0331 a0001c0001t0004g0332 others(50): Show |
53 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.-202-759_-202-757d others(5): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994277 | |||||||
chr12:25994278 | TA | T | 50 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0193 others(47): Show |
52 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.-202-745delA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25994278 | ||||||
chr12:25994278 | TAA | T | 193 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(190): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-202-746_-202-745d others(4): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25994278 | ||||||
chr12:25994278 | TAAA | T | 14 | a0001c0001t0002g0012 a0001c0001t0006g0180 a0001c0001t0006g0234 others(11): Show |
15 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-202-747_-202-745d others(5): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 25994278 | ||||||
chr12:25994281 | A | T | 152 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(149): Show |
164 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.-202-756A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994281 | |||||||
chr12:25994282 | A | T | 99 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(96): Show |
104 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.-202-755A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994282 | |||||||
chr12:25994335 | A | G | 1 | a0001c0002t0001g0096 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-202-702A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994335 | |||||||
chr12:25994510 | G | A | 1 | a0001c0001t0003g0219 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-202-527G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994510 | |||||||
chr12:25994642 | C | T | 9 | a0001c0001t0008g0006 a0001c0001t0008g0030 a0001c0001t0008g0031 others(6): Show |
10 | HG00741.hp1 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-202-395C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994642 | |||||||
chr12:25994712 | G | A | 3 | a0001c0001t0002g0103 a0001c0001t0002g0161 a0001c0001t0002g0169 |
3 | HG03239.hp1 HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-202-325G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994712 | |||||||
chr12:25994774 | T | A | 61 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0015g0059 others(58): Show |
68 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-202-263T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994774 | |||||||
chr12:25994892 | A | T | 83 | a0001c0001t0003g0017 a0001c0001t0004g0329 a0001c0001t0004g0330 others(80): Show |
83 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-202-145A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994892 | |||||||
chr12:25994911 | A | T | 1 | a0001c0001t0004g0365 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-202-126A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994911 | |||||||
chr12:25994929 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-202-108C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994929 | |||||||
chr12:25994983 | T | C | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-202-54T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994983 | |||||||
chr12:25994996 | C | A | 350 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(347): Show |
369 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.-202-41C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 1/5 | chr12 | 25994996 | |||||||
chr12:25995257 | T | C | 19 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0008g0006 others(16): Show |
20 | HG00741.hp1 HG01192.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-109+127T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25995257 | |||||||
chr12:25995289 | G | A | 5 | a0001c0001t0031g0020 a0001c0005t0006g0255 a0001c0005t0006g0256 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+159G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25995289 | |||||||
chr12:25995348 | T | A | 6 | a0001c0001t0011g0310 a0001c0001t0018g0311 a0001c0001t0041g0309 others(3): Show |
6 | HG00558.hp2 HG03017.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+218T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25995348 | |||||||
chr12:25995368 | A | G | 1 | a0001c0006t0057g0295 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-109+238A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25995368 | |||||||
chr12:25995387 | C | G | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-109+257C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25995387 | |||||||
chr12:25995588 | G | A | 2 | a0001c0001t0015g0059 a0001c0001t0015g0068 |
2 | HG02486.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-109+458G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25995588 | |||||||
chr12:25995656 | A | AG | 13 | a0001c0001t0002g0178 a0001c0001t0003g0265 a0001c0001t0003g0271 others(10): Show |
14 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-109+533dupG | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 25995656 | ||||||
chr12:25995750 | G | A | 1 | a0001c0001t0018g0311 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-109+620G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25995750 | |||||||
chr12:25995803 | A | G | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-109+673A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25995803 | |||||||
chr12:25995881 | G | A | 45 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-109+751G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25995881 | |||||||
chr12:25995885 | CAT | C | 45 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-109+757_-109+758d others(4): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 25995885 | ||||||
chr12:25995919 | T | C | 89 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(86): Show |
94 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-109+789T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25995919 | |||||||
chr12:25995949 | C | T | 45 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-109+819C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25995949 | |||||||
chr12:25996030 | T | G | 1 | a0001c0001t0005g0157 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-109+900T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25996030 | |||||||
chr12:25996205 | A | T | 12 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(9): Show |
13 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-109+1075A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25996205 | |||||||
chr12:25996255 | A | T | 51 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(48): Show |
51 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-109+1125A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25996255 | |||||||
chr12:25996325 | T | C | 1 | a0001c0001t0020g0250 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-109+1195T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25996325 | |||||||
chr12:25996381 | A | G | 30 | a0001c0001t0003g0017 a0001c0001t0009g0296 a0001c0001t0009g0297 others(27): Show |
30 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.-109+1251A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25996381 | |||||||
chr12:25996437 | A | G | 3 | a0001c0005t0006g0255 a0001c0005t0006g0256 a0001c0005t0006g0257 |
3 | HG01884.hp1 HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-109+1307A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25996437 | |||||||
chr12:25996438 | T | C | 6 | a0001c0001t0002g0233 a0001c0001t0012g0005 a0001c0001t0012g0024 others(3): Show |
7 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+1308T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25996438 | |||||||
chr12:25996534 | T | C | 1 | a0001c0001t0034g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-109+1404T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25996534 | |||||||
chr12:25996581 | A | T | 350 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(347): Show |
369 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.-109+1451A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25996581 | |||||||
chr12:25996711 | C | T | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-109+1581C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25996711 | |||||||
chr12:25996746 | A | G | 1 | a0001c0001t0003g0272 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-109+1616A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25996746 | |||||||
chr12:25996770 | A | G | 89 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(86): Show |
94 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-109+1640A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25996770 | |||||||
chr12:25997026 | A | T | 7 | a0001c0001t0011g0310 a0001c0001t0018g0311 a0001c0001t0041g0309 others(4): Show |
7 | HG00558.hp2 HG02896.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+1896A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25997026 | |||||||
chr12:25997038 | A | G | 5 | a0001c0001t0031g0020 a0001c0005t0006g0255 a0001c0005t0006g0256 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+1908A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25997038 | |||||||
chr12:25997241 | G | A | 1 | a0001c0001t0031g0020 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-109+2111G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25997241 | |||||||
chr12:25997554 | C | T | 14 | a0001c0001t0003g0220 a0001c0001t0003g0265 a0001c0001t0003g0271 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-109+2424C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25997554 | |||||||
chr12:25997569 | G | A | 1 | a0001c0001t0023g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-109+2439G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25997569 | |||||||
chr12:25997692 | C | A | 3 | a0001c0001t0023g0028 a0001c0006t0007g0325 a0001c0006t0057g0295 |
3 | HG02257.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-109+2562C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25997692 | |||||||
chr12:25997760 | A | G | 5 | a0001c0001t0031g0020 a0001c0005t0006g0255 a0001c0005t0006g0256 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+2630A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25997760 | |||||||
chr12:25997966 | G | A | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-109+2836G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25997966 | |||||||
chr12:25998022 | A | T | 7 | a0001c0001t0002g0233 a0001c0001t0012g0005 a0001c0001t0012g0024 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-109+2892A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998022 | |||||||
chr12:25998080 | G | A | 1 | a0001c0004t0037g0323 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-109+2950G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998080 | |||||||
chr12:25998245 | C | T | 1 | a0001c0001t0006g0283 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-109+3115C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998245 | |||||||
chr12:25998338 | T | C | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-109+3208T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998338 | |||||||
chr12:25998349 | C | CT | 11 | a0001c0001t0003g0004 a0001c0001t0003g0194 a0001c0001t0003g0195 others(8): Show |
13 | HG02300.hp1 NA18947.hp1 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.-109+3236dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 25998349 | ||||||
chr12:25998349 | CT | C | 109 | a0001c0001t0002g0079 a0001c0001t0002g0109 a0001c0001t0003g0017 others(106): Show |
117 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-109+3236delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 25998349 | ||||||
chr12:25998349 | CTT | C | 16 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(13): Show |
17 | HG00738.hp2 HG01074.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-109+3235_-109+323 others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 25998349 | ||||||
chr12:25998360 | T | G | 1 | a0001c0001t0004g0342 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-109+3230T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998360 | |||||||
chr12:25998391 | C | T | 5 | a0001c0001t0031g0020 a0001c0005t0006g0255 a0001c0005t0006g0256 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+3261C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998391 | |||||||
chr12:25998417 | T | G | 1 | a0001c0004t0015g0262 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-109+3287T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998417 | |||||||
chr12:25998467 | A | G | 64 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0015g0059 others(61): Show |
71 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-109+3337A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998467 | |||||||
chr12:25998545 | C | T | 2 | a0001c0003t0004g0293 a0001c0003t0011g0292 |
2 | HG02165.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-109+3415C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998545 | |||||||
chr12:25998574 | C | G | 1 | a0001c0004t0037g0323 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-109+3444C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998574 | |||||||
chr12:25998589 | C | T | 1 | a0001c0001t0023g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-109+3459C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998589 | |||||||
chr12:25998639 | G | A | 2 | a0001c0001t0002g0142 a0001c0002t0001g0066 |
2 | HG02738.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.-109+3509G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998639 | |||||||
chr12:25998673 | T | C | 3 | a0001c0001t0003g0279 a0001c0001t0006g0280 a0001c0001t0011g0358 |
3 | HG02602.hp1 HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-109+3543T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998673 | |||||||
chr12:25998674 | C | T | 3 | a0001c0001t0003g0279 a0001c0001t0006g0280 a0001c0001t0011g0358 |
3 | HG02602.hp1 HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-109+3544C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998674 | |||||||
chr12:25998783 | C | T | 88 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(85): Show |
93 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-109+3653C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998783 | |||||||
chr12:25998784 | G | A | 1 | a0001c0001t0018g0311 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-109+3654G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998784 | |||||||
chr12:25998798 | A | G | 81 | a0001c0001t0003g0017 a0001c0001t0004g0329 a0001c0001t0004g0330 others(78): Show |
81 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-109+3668A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998798 | |||||||
chr12:25998884 | C | T | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-109+3754C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998884 | |||||||
chr12:25998897 | A | G | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-109+3767A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998897 | |||||||
chr12:25998958 | G | A | 7 | a0001c0001t0002g0233 a0001c0001t0012g0005 a0001c0001t0012g0024 others(4): Show |
8 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-109+3828G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25998958 | |||||||
chr12:25999078 | A | T | 1 | a0001c0002t0001g0047 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-109+3948A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25999078 | |||||||
chr12:25999189 | T | TC | 14 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-109+4060dupC | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 25999189 | ||||||
chr12:25999264 | C | T | 1 | a0001c0001t0023g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-109+4134C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25999264 | |||||||
chr12:25999409 | T | C | 1 | a0001c0001t0004g0343 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-109+4279T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25999409 | |||||||
chr12:25999451 | A | G | 51 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(48): Show |
51 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-109+4321A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25999451 | |||||||
chr12:25999773 | T | C | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-109+4643T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25999773 | |||||||
chr12:25999892 | A | G | 39 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(36): Show |
41 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.-109+4762A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 25999892 | |||||||
chr12:26000147 | C | G | 1 | a0001c0001t0020g0250 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-109+5017C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000147 | |||||||
chr12:26000271 | A | G | 1 | a0001c0003t0020g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-109+5141A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000271 | |||||||
chr12:26000300 | A | G | 1 | a0001c0002t0006g0098 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-109+5170A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000300 | |||||||
chr12:26000312 | C | T | 5 | a0001c0001t0031g0020 a0001c0005t0006g0255 a0001c0005t0006g0256 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+5182C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000312 | |||||||
chr12:26000388 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-109+5258T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000388 | |||||||
chr12:26000436 | G | A | 1 | a0001c0001t0006g0261 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-109+5306G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000436 | |||||||
chr12:26000597 | G | A | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-109+5467G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000597 | |||||||
chr12:26000611 | G | A | 5 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+5481G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000611 | |||||||
chr12:26000615 | T | C | 1 | a0001c0001t0003g0248 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-109+5485T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000615 | |||||||
chr12:26000717 | G | T | 269 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(266): Show |
288 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-109+5587G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000717 | |||||||
chr12:26000728 | G | A | 1 | a0001c0002t0002g0045 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-109+5598G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000728 | |||||||
chr12:26000908 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-109+5778G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000908 | |||||||
chr12:26000948 | G | C | 96 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(93): Show |
102 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-109+5818G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000948 | |||||||
chr12:26000958 | G | A | 61 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0015g0059 others(58): Show |
68 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-109+5828G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26000958 | |||||||
chr12:26000982 | C | CT | 125 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(122): Show |
132 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.-109+5875dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26000982 | ||||||
chr12:26000982 | C | CTT | 14 | a0001c0001t0002g0165 a0001c0001t0005g0132 a0001c0001t0005g0156 others(11): Show |
15 | HG00597.hp2 HG01884.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-109+5874_-109+587 others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26000982 | ||||||
chr12:26000982 | CT | C | 78 | a0001c0001t0003g0017 a0001c0001t0004g0329 a0001c0001t0004g0330 others(75): Show |
79 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-109+5875delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26000982 | ||||||
chr12:26000982 | CTT | C | 6 | a0001c0001t0008g0031 a0001c0001t0009g0296 a0001c0001t0009g0315 others(3): Show |
6 | HG00323.hp2 HG02895.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+5874_-109+587 others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26000982 | ||||||
chr12:26000982 | CTTT | C | 13 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(10): Show |
14 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-109+5873_-109+587 others(7): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26000982 | ||||||
chr12:26001038 | G | A | 3 | a0001c0001t0008g0006 a0001c0001t0008g0033 a0001c0001t0023g0032 |
4 | HG02145.hp1 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+5908G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001038 | |||||||
chr12:26001110 | G | C | 1 | a0004c0010t0061g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-109+5980G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001110 | |||||||
chr12:26001186 | C | T | 2 | a0001c0001t0009g0306 a0001c0001t0024g0222 |
2 | HG00408.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-109+6056C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001186 | |||||||
chr12:26001199 | A | AT | 106 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(103): Show |
112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.-109+6085dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26001199 | ||||||
chr12:26001199 | AT | A | 9 | a0001c0001t0008g0006 a0001c0001t0008g0030 a0001c0001t0008g0031 others(6): Show |
10 | HG00741.hp1 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-109+6085delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26001199 | ||||||
chr12:26001313 | G | T | 1 | a0001c0001t0010g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-109+6183G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001313 | |||||||
chr12:26001342 | T | A | 1 | a0001c0001t0002g0012 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-109+6212T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001342 | |||||||
chr12:26001389 | T | A | 3 | a0001c0001t0023g0028 a0001c0006t0007g0325 a0001c0006t0057g0295 |
3 | HG02257.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-109+6259T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001389 | |||||||
chr12:26001495 | G | A | 1 | a0001c0001t0040g0300 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-109+6365G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001495 | |||||||
chr12:26001503 | G | A | 1 | a0001c0002t0002g0045 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-109+6373G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001503 | |||||||
chr12:26001505 | G | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0100 |
2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-109+6375G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001505 | |||||||
chr12:26001550 | T | A | 89 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(86): Show |
94 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-109+6420T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001550 | |||||||
chr12:26001586 | A | C | 5 | a0001c0001t0031g0020 a0001c0005t0006g0255 a0001c0005t0006g0256 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+6456A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001586 | |||||||
chr12:26001672 | A | G | 96 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(93): Show |
102 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-109+6542A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001672 | |||||||
chr12:26001835 | A | G | 3 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0005c0009t0054g0236 |
3 | HG01192.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-109+6705A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001835 | |||||||
chr12:26001909 | G | C | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-109+6779G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26001909 | |||||||
chr12:26002062 | A | G | 1 | a0001c0001t0010g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-109+6932A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002062 | |||||||
chr12:26002076 | G | A | 3 | a0001c0001t0006g0261 a0001c0001t0007g0259 a0001c0001t0046g0260 |
3 | HG02258.hp2 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-109+6946G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002076 | |||||||
chr12:26002077 | T | C | 1 | a0001c0001t0010g0223 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-109+6947T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002077 | |||||||
chr12:26002130 | C | T | 94 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(91): Show |
100 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-109+7000C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002130 | |||||||
chr12:26002160 | C | G | 14 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-109+7030C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002160 | |||||||
chr12:26002254 | A | T | 1 | a0001c0001t0002g0037 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-109+7124A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002254 | |||||||
chr12:26002390 | G | A | 61 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0015g0059 others(58): Show |
68 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-109+7260G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002390 | |||||||
chr12:26002395 | T | C | 1 | a0001c0001t0005g0118 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-109+7265T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002395 | |||||||
chr12:26002417 | A | C | 5 | a0001c0002t0001g0008 a0001c0002t0001g0069 a0001c0002t0001g0080 others(2): Show |
6 | HG02040.hp1 HG02132.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+7287A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002417 | |||||||
chr12:26002418 | G | A | 1 | a0001c0001t0002g0013 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-109+7288G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002418 | |||||||
chr12:26002436 | A | G | 1 | a0001c0006t0057g0295 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-109+7306A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002436 | |||||||
chr12:26002557 | C | T | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-109+7427C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002557 | |||||||
chr12:26002558 | G | A | 51 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(48): Show |
51 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-109+7428G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002558 | |||||||
chr12:26002643 | C | T | 1 | a0001c0001t0008g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-109+7513C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002643 | |||||||
chr12:26002809 | C | T | 1 | a0001c0001t0025g0320 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-109+7679C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002809 | |||||||
chr12:26002867 | A | G | 95 | a0001c0001t0002g0012 a0001c0001t0002g0079 a0001c0001t0003g0083 others(92): Show |
104 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.-109+7737A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002867 | |||||||
chr12:26002991 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-109+7861A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26002991 | |||||||
chr12:26003075 | T | A | 80 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0003g0265 others(77): Show |
88 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-109+7945T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003075 | |||||||
chr12:26003298 | T | C | 4 | a0001c0001t0027g0102 a0001c0001t0027g0163 a0001c0001t0030g0152 others(1): Show |
4 | HG00099.hp1 HG01123.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+8168T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003298 | |||||||
chr12:26003306 | A | G | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-109+8176A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003306 | |||||||
chr12:26003315 | T | C | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-109+8185T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003315 | |||||||
chr12:26003358 | G | A | 12 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0008g0006 others(9): Show |
13 | HG00741.hp1 HG01192.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-109+8228G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003358 | |||||||
chr12:26003378 | G | A | 21 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(18): Show |
21 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.-109+8248G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003378 | |||||||
chr12:26003439 | G | T | 5 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+8309G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003439 | |||||||
chr12:26003443 | G | GAAGT | 96 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(93): Show |
102 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-109+8317_-109+832 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26003443 | ||||||
chr12:26003494 | C | G | 81 | a0001c0001t0003g0017 a0001c0001t0004g0329 a0001c0001t0004g0330 others(78): Show |
81 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-109+8364C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003494 | |||||||
chr12:26003651 | A | G | 39 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(36): Show |
41 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.-109+8521A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003651 | |||||||
chr12:26003784 | A | T | 14 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-109+8654A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003784 | |||||||
chr12:26003890 | C | T | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-109+8760C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003890 | |||||||
chr12:26003904 | C | T | 1 | a0001c0001t0005g0114 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-109+8774C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003904 | |||||||
chr12:26003928 | G | T | 160 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(157): Show |
169 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.-109+8798G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003928 | |||||||
chr12:26003972 | T | C | 2 | a0001c0003t0004g0293 a0001c0003t0011g0292 |
2 | HG02165.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-109+8842T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003972 | |||||||
chr12:26003988 | G | A | 51 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(48): Show |
51 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-109+8858G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26003988 | |||||||
chr12:26004101 | T | C | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-109+8971T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004101 | |||||||
chr12:26004159 | AG | A | 3 | a0001c0001t0006g0261 a0001c0001t0007g0259 a0001c0001t0046g0260 |
3 | HG02258.hp2 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-109+9030delG | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004159 | |||||||
chr12:26004161 | A | C | 3 | a0001c0001t0006g0261 a0001c0001t0007g0259 a0001c0001t0046g0260 |
3 | HG02258.hp2 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-109+9031A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004161 | |||||||
chr12:26004189 | C | A | 80 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0003g0265 others(77): Show |
88 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-109+9059C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004189 | |||||||
chr12:26004243 | C | G | 2 | a0001c0001t0003g0279 a0001c0001t0006g0280 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-109+9113C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004243 | |||||||
chr12:26004312 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-109+9182A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004312 | |||||||
chr12:26004344 | G | A | 51 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(48): Show |
51 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-109+9214G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004344 | |||||||
chr12:26004564 | G | A | 6 | a0001c0001t0010g0014 a0001c0001t0010g0266 a0001c0001t0010g0269 others(3): Show |
7 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+9434G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004564 | |||||||
chr12:26004619 | T | G | 1 | a0001c0001t0015g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-109+9489T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004619 | |||||||
chr12:26004716 | A | AGAG | 61 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0015g0059 others(58): Show |
68 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-109+9598_-109+960 others(7): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26004716 | ||||||
chr12:26004736 | A | G | 1 | a0001c0001t0009g0306 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-109+9606A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004736 | |||||||
chr12:26004820 | C | T | 1 | a0001c0001t0003g0044 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-109+9690C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004820 | |||||||
chr12:26004826 | A | T | 3 | a0001c0003t0004g0291 a0001c0003t0004g0293 a0001c0003t0011g0292 |
3 | HG02165.hp1 HG02523.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-109+9696A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004826 | |||||||
chr12:26004827 | C | T | 269 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(266): Show |
288 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-109+9697C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004827 | |||||||
chr12:26004872 | T | C | 1 | a0001c0001t0002g0012 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-109+9742T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26004872 | |||||||
chr12:26004908 | C | CT | 12 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(9): Show |
13 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-109+9781dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26004908 | ||||||
chr12:26004998 | T | TA | 61 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0015g0059 others(58): Show |
68 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-109+9877dupA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26004998 | ||||||
chr12:26005022 | T | C | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-109+9892T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26005022 | |||||||
chr12:26005125 | A | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-109+9995A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26005125 | |||||||
chr12:26005130 | G | A | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-109+10000G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26005130 | |||||||
chr12:26005164 | G | GGT | 59 | a0001c0001t0003g0017 a0001c0001t0003g0265 a0001c0001t0003g0271 others(56): Show |
64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-109+10057_-109+10 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26005164 | ||||||
chr12:26005164 | G | GGTGT | 96 | a0001c0001t0002g0012 a0001c0001t0002g0079 a0001c0001t0003g0279 others(93): Show |
105 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.-109+10055_-109+10 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26005164 | ||||||
chr12:26005164 | G | GGTGTGT | 4 | a0001c0001t0003g0083 a0001c0001t0008g0237 a0001c0002t0001g0053 others(1): Show |
4 | HG03516.hp2 NA19084.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+10053_-109+10 others(12): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26005164 | ||||||
chr12:26005164 | GGT | G | 46 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(43): Show |
46 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.-109+10057_-109+10 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26005164 | ||||||
chr12:26005164 | GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-109+10049_-109+10 others(16): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26005164 | ||||||
chr12:26005166 | T | G | 2 | a0001c0001t0003g0248 a0001c0001t0020g0250 |
2 | HG00733.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.-109+10036T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26005166 | |||||||
chr12:26005379 | G | A | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-109+10249G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26005379 | |||||||
chr12:26005455 | A | G | 350 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(347): Show |
369 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.-109+10325A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26005455 | |||||||
chr12:26005547 | T | A | 2 | a0001c0001t0004g0372 a0001c0001t0004g0373 |
2 | NA19005.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-109+10417T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26005547 | |||||||
chr12:26005722 | A | G | 3 | a0001c0001t0006g0261 a0001c0001t0007g0259 a0001c0001t0046g0260 |
3 | HG02258.hp2 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-109+10592A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26005722 | |||||||
chr12:26005892 | G | A | 21 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(18): Show |
21 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.-109+10762G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26005892 | |||||||
chr12:26005925 | T | G | 5 | a0001c0001t0031g0020 a0001c0005t0006g0255 a0001c0005t0006g0256 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+10795T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26005925 | |||||||
chr12:26006017 | G | A | 350 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(347): Show |
369 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.-109+10887G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26006017 | |||||||
chr12:26006026 | T | C | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-109+10896T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26006026 | |||||||
chr12:26006060 | G | GAC | 4 | a0001c0001t0002g0116 a0001c0001t0002g0142 a0001c0001t0002g0144 others(1): Show |
4 | HG00639.hp1 HG01099.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+10947_-109+10 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26006060 | ||||||
chr12:26006093 | C | G | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-109+10963C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26006093 | |||||||
chr12:26006130 | A | C | 95 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(92): Show |
101 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.-109+11000A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26006130 | |||||||
chr12:26006165 | T | C | 268 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(265): Show |
287 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-109+11035T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26006165 | |||||||
chr12:26006224 | G | A | 1 | a0001c0001t0005g0118 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-109+11094G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26006224 | |||||||
chr12:26006341 | T | C | 189 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(186): Show |
200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.-109+11211T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26006341 | |||||||
chr12:26006346 | G | A | 8 | a0001c0002t0001g0050 a0001c0002t0001g0057 a0001c0002t0001g0066 others(5): Show |
8 | NA18940.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.-109+11216G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26006346 | |||||||
chr12:26006505 | G | A | 5 | a0001c0001t0031g0020 a0001c0005t0006g0255 a0001c0005t0006g0256 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+11375G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26006505 | |||||||
chr12:26006624 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-109+11494G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26006624 | |||||||
chr12:26006682 | A | G | 2 | a0001c0002t0001g0096 a0001c0002t0001g0097 |
2 | HG00642.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.-109+11552A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26006682 | |||||||
chr12:26006809 | C | T | 2 | a0001c0001t0002g0161 a0001c0001t0002g0169 |
2 | HG03239.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-109+11679C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26006809 | |||||||
chr12:26007125 | T | C | 1 | a0001c0001t0002g0012 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-109+11995T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26007125 | |||||||
chr12:26007131 | A | G | 45 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-109+12001A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26007131 | |||||||
chr12:26007241 | C | T | 12 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(9): Show |
13 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-109+12111C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26007241 | |||||||
chr12:26007370 | C | T | 66 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0010g0274 others(63): Show |
73 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-109+12240C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26007370 | |||||||
chr12:26007440 | A | G | 4 | a0001c0001t0005g0135 a0001c0001t0005g0140 a0001c0001t0005g0154 others(1): Show |
4 | HG02080.hp2 HG02129.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+12310A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26007440 | |||||||
chr12:26007691 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-109+12561G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26007691 | |||||||
chr12:26007805 | A | G | 1 | a0001c0002t0047g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-109+12675A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26007805 | |||||||
chr12:26007878 | G | C | 66 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0010g0274 others(63): Show |
73 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-109+12748G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26007878 | |||||||
chr12:26007886 | A | G | 189 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(186): Show |
200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.-109+12756A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26007886 | |||||||
chr12:26008016 | G | A | 161 | a0001c0001t0002g0079 a0001c0001t0003g0017 a0001c0001t0003g0083 others(158): Show |
169 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.-109+12886G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008016 | |||||||
chr12:26008039 | C | T | 1 | a0001c0001t0003g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-109+12909C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008039 | |||||||
chr12:26008040 | G | A | 3 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0049 |
3 | HG02080.hp1 HG02129.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-109+12910G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008040 | |||||||
chr12:26008045 | G | A | 3 | a0001c0001t0003g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | HG03710.hp1 HG03927.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-109+12915G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008045 | |||||||
chr12:26008142 | G | A | 48 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(45): Show |
48 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-109+13012G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008142 | |||||||
chr12:26008205 | G | A | 28 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0180 others(25): Show |
29 | HG00099.hp2 HG00621.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.-109+13075G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008205 | |||||||
chr12:26008224 | G | C | 1 | a0001c0001t0051g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-109+13094G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008224 | |||||||
chr12:26008269 | T | TA | 47 | a0001c0001t0002g0012 a0001c0001t0003g0227 a0001c0001t0003g0279 others(44): Show |
51 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-109+13151dupA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26008269 | ||||||
chr12:26008288 | C | G | 61 | a0001c0001t0002g0079 a0001c0001t0003g0083 a0001c0001t0015g0059 others(58): Show |
68 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-109+13158C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008288 | |||||||
chr12:26008322 | G | A | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-109+13192G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008322 | |||||||
chr12:26008474 | T | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-109+13344T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008474 | |||||||
chr12:26008513 | C | T | 89 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(86): Show |
94 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-109+13383C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008513 | |||||||
chr12:26008518 | A | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-109+13388A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008518 | |||||||
chr12:26008576 | A | C | 1 | a0001c0001t0008g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-109+13446A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008576 | |||||||
chr12:26008593 | T | C | 1 | a0001c0001t0003g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-109+13463T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008593 | |||||||
chr12:26008735 | G | A | 1 | a0001c0001t0006g0180 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-109+13605G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008735 | |||||||
chr12:26008748 | G | A | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-109+13618G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008748 | |||||||
chr12:26008913 | G | T | 5 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+13783G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008913 | |||||||
chr12:26008946 | A | G | 1 | a0001c0002t0001g0078 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-109+13816A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008946 | |||||||
chr12:26008998 | G | A | 2 | a0001c0001t0004g0330 a0001c0001t0004g0344 |
2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-109+13868G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26008998 | |||||||
chr12:26009037 | T | C | 354 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(351): Show |
373 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.-109+13907T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009037 | |||||||
chr12:26009043 | C | T | 21 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(18): Show |
21 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.-109+13913C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009043 | |||||||
chr12:26009088 | A | G | 1 | a0001c0002t0001g0084 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-109+13958A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009088 | |||||||
chr12:26009149 | C | T | 1 | a0001c0001t0006g0186 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-109+14019C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009149 | |||||||
chr12:26009152 | C | T | 1 | a0001c0001t0041g0309 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-109+14022C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009152 | |||||||
chr12:26009170 | T | C | 48 | a0001c0001t0002g0012 a0001c0001t0003g0279 a0001c0001t0006g0015 others(45): Show |
51 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-109+14040T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009170 | |||||||
chr12:26009202 | A | C | 1 | a0001c0002t0001g0066 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-109+14072A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009202 | |||||||
chr12:26009239 | G | C | 1 | a0001c0005t0006g0257 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-109+14109G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009239 | |||||||
chr12:26009278 | G | A | 45 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-109+14148G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009278 | |||||||
chr12:26009337 | T | C | 1 | a0001c0001t0044g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-109+14207T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009337 | |||||||
chr12:26009496 | A | G | 351 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(348): Show |
370 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(367): Show |
intron_variant | MODIFIER | c.-109+14366A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009496 | |||||||
chr12:26009513 | C | T | 51 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(48): Show |
51 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-109+14383C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009513 | |||||||
chr12:26009648 | G | T | 21 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(18): Show |
21 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.-109+14518G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009648 | |||||||
chr12:26009775 | C | A | 51 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(48): Show |
51 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-109+14645C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009775 | |||||||
chr12:26009842 | T | G | 5 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+14712T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009842 | |||||||
chr12:26009893 | G | T | 28 | a0001c0001t0003g0279 a0001c0001t0006g0015 a0001c0001t0006g0180 others(25): Show |
29 | HG00099.hp2 HG00621.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.-109+14763G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009893 | |||||||
chr12:26009942 | G | A | 1 | a0001c0001t0031g0020 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-109+14812G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009942 | |||||||
chr12:26009979 | T | C | 10 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(7): Show |
11 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-109+14849T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26009979 | |||||||
chr12:26010032 | G | A | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-109+14902G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26010032 | |||||||
chr12:26010089 | C | T | 1 | a0001c0005t0006g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-109+14959C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26010089 | |||||||
chr12:26010096 | C | A | 62 | a0001c0001t0002g0079 a0001c0001t0002g0161 a0001c0001t0002g0169 others(59): Show |
66 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-109+14966C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26010096 | |||||||
chr12:26010204 | TAGTC | T | 69 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 others(66): Show |
74 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-109+15077_-109+15 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26010204 | ||||||
chr12:26010223 | G | A | 68 | a0001c0001t0002g0079 a0001c0001t0002g0161 a0001c0001t0002g0169 others(65): Show |
75 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-109+15093G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26010223 | |||||||
chr12:26010245 | TAAATTAG | T | 10 | a0001c0001t0008g0006 a0001c0001t0008g0030 a0001c0001t0008g0031 others(7): Show |
11 | HG00741.hp1 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-109+15132_-109+15 others(13): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26010245 | ||||||
chr12:26010270 | G | A | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-109+15140G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26010270 | |||||||
chr12:26010436 | A | G | 2 | a0001c0002t0001g0002 a0001c0002t0001g0061 |
4 | NA19058.hp1 NA19077.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+15306A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26010436 | |||||||
chr12:26010437 | G | T | 12 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(9): Show |
13 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-109+15307G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26010437 | |||||||
chr12:26010510 | CCCTCCTG others(4): Show |
C | 1 | a0004c0010t0061g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-109+15383_-109+15 others(17): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26010510 | ||||||
chr12:26010603 | G | A | 269 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(266): Show |
288 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-109+15473G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26010603 | |||||||
chr12:26010729 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-109+15599G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26010729 | |||||||
chr12:26010830 | A | C | 1 | a0001c0001t0005g0130 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-109+15700A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26010830 | |||||||
chr12:26010840 | G | A | 12 | a0001c0001t0003g0265 a0001c0001t0003g0271 a0001c0001t0003g0272 others(9): Show |
13 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-109+15710G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26010840 | |||||||
chr12:26010939 | G | A | 1 | a0001c0001t0008g0035 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-109+15809G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26010939 | |||||||
chr12:26010957 | G | T | 1 | a0001c0002t0047g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-109+15827G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26010957 | |||||||
chr12:26011063 | T | G | 350 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(347): Show |
369 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.-109+15933T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011063 | |||||||
chr12:26011284 | ATAG | A | 87 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(84): Show |
92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-109+16158_-109+16 others(9): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26011284 | ||||||
chr12:26011366 | A | G | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-109+16236A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011366 | |||||||
chr12:26011525 | G | A | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-109+16395G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011525 | |||||||
chr12:26011542 | G | A | 1 | a0001c0002t0001g0063 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-109+16412G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011542 | |||||||
chr12:26011561 | C | T | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-109+16431C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011561 | |||||||
chr12:26011636 | G | A | 1 | a0001c0001t0005g0120 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-109+16506G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011636 | |||||||
chr12:26011731 | C | A | 1 | a0001c0001t0002g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-109+16601C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011731 | |||||||
chr12:26011785 | C | T | 2 | a0001c0001t0006g0277 a0001c0002t0014g0305 |
2 | HG02056.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-109+16655C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011785 | |||||||
chr12:26011803 | C | A | 1 | a0001c0001t0039g0302 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-109+16673C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011803 | |||||||
chr12:26011840 | T | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-109+16710T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011840 | |||||||
chr12:26011890 | A | G | 1 | a0001c0001t0006g0283 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-109+16760A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011890 | |||||||
chr12:26011929 | G | A | 62 | a0001c0001t0003g0083 a0001c0001t0015g0059 a0001c0001t0015g0068 others(59): Show |
69 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-109+16799G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011929 | |||||||
chr12:26011952 | T | G | 48 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(45): Show |
50 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.-109+16822T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011952 | |||||||
chr12:26011955 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-109+16825G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011955 | |||||||
chr12:26011974 | T | G | 45 | a0001c0001t0002g0012 a0001c0001t0003g0265 a0001c0001t0003g0271 others(42): Show |
48 | HG00099.hp2 HG00621.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-109+16844T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26011974 | |||||||
chr12:26012048 | A | G | 3 | a0001c0001t0006g0261 a0001c0001t0007g0259 a0001c0001t0046g0260 |
3 | HG02258.hp2 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-109+16918A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012048 | |||||||
chr12:26012243 | G | C | 2 | a0001c0001t0004g0330 a0001c0001t0004g0344 |
2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-109+17113G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012243 | |||||||
chr12:26012340 | A | G | 97 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(94): Show |
103 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-109+17210A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012340 | |||||||
chr12:26012528 | G | A | 1 | a0001c0002t0001g0231 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-109+17398G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012528 | |||||||
chr12:26012549 | C | T | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-109+17419C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012549 | |||||||
chr12:26012652 | G | A | 107 | a0001c0001t0002g0012 a0001c0001t0003g0083 a0001c0001t0003g0265 others(104): Show |
117 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.-109+17522G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012652 | |||||||
chr12:26012682 | C | CT | 25 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0004g0355 others(22): Show |
26 | HG00544.hp1 HG00741.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.-109+17568dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26012682 | ||||||
chr12:26012682 | C | CTT | 57 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(54): Show |
60 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.-109+17567_-109+17 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26012682 | ||||||
chr12:26012682 | C | CTTT | 33 | a0001c0001t0002g0012 a0001c0001t0003g0279 a0001c0001t0006g0015 others(30): Show |
35 | HG00099.hp2 HG00621.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-109+17566_-109+17 others(9): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26012682 | ||||||
chr12:26012705 | G | C | 3 | a0001c0001t0024g0202 a0001c0001t0024g0222 a0001c0001t0033g0221 |
3 | HG03130.hp1 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-109+17575G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012705 | |||||||
chr12:26012721 | C | T | 1 | a0001c0001t0031g0020 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-109+17591C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012721 | |||||||
chr12:26012748 | A | G | 6 | a0001c0001t0003g0230 a0001c0001t0031g0020 a0001c0005t0006g0255 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+17618A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012748 | |||||||
chr12:26012752 | C | G | 117 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(114): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.-109+17622C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012752 | |||||||
chr12:26012787 | C | T | 1 | a0001c0006t0057g0295 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-109+17657C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012787 | |||||||
chr12:26012838 | G | C | 2 | a0001c0001t0007g0259 a0001c0001t0046g0260 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-109+17708G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012838 | |||||||
chr12:26012859 | A | G | 2 | a0001c0001t0002g0037 a0001c0001t0002g0264 |
2 | HG01243.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-109+17729A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012859 | |||||||
chr12:26012898 | A | G | 1 | a0004c0010t0061g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-109+17768A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012898 | |||||||
chr12:26012963 | A | G | 1 | a0001c0001t0038g0317 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-109+17833A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012963 | |||||||
chr12:26012979 | C | G | 2 | a0001c0001t0029g0267 a0001c0001t0029g0268 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-109+17849C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26012979 | |||||||
chr12:26012992 | A | AGCTGTGC others(6): Show |
1 | a0005c0009t0054g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-109+17866_-109+17 others(19): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26012992 | ||||||
chr12:26013150 | C | T | 351 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(348): Show |
370 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(367): Show |
intron_variant | MODIFIER | c.-109+18020C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26013150 | |||||||
chr12:26013208 | T | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0160 |
2 | HG01516.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-109+18078T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26013208 | |||||||
chr12:26013360 | G | A | 4 | a0001c0001t0031g0020 a0001c0005t0006g0255 a0001c0005t0006g0256 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+18230G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26013360 | |||||||
chr12:26013363 | A | G | 7 | a0001c0001t0002g0037 a0001c0001t0002g0079 a0001c0001t0002g0165 others(4): Show |
7 | HG01243.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+18233A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26013363 | |||||||
chr12:26013451 | C | T | 1 | a0001c0006t0057g0295 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-109+18321C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26013451 | |||||||
chr12:26013455 | G | T | 2 | a0003c0008t0019g0307 a0003c0008t0019g0308 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-109+18325G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26013455 | |||||||
chr12:26013526 | A | G | 1 | a0002c0007t0005g0107 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-109+18396A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26013526 | |||||||
chr12:26013601 | T | C | 351 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(348): Show |
370 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(367): Show |
intron_variant | MODIFIER | c.-109+18471T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26013601 | |||||||
chr12:26013631 | CT | C | 267 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(264): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-109+18512delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26013631 | ||||||
chr12:26013676 | G | A | 269 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(266): Show |
288 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-109+18546G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26013676 | |||||||
chr12:26013955 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-109+18825A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26013955 | |||||||
chr12:26014017 | G | A | 52 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(49): Show |
52 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-109+18887G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014017 | |||||||
chr12:26014025 | T | C | 6 | a0001c0001t0011g0310 a0001c0001t0018g0311 a0001c0001t0041g0309 others(3): Show |
6 | HG00558.hp2 HG03017.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+18895T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014025 | |||||||
chr12:26014215 | C | T | 3 | a0001c0001t0017g0340 a0001c0001t0017g0353 a0001c0001t0017g0354 |
3 | NA18964.hp1 NA19070.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-109+19085C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014215 | |||||||
chr12:26014327 | G | C | 207 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(204): Show |
219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-109+19197G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014327 | |||||||
chr12:26014394 | T | C | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-109+19264T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014394 | |||||||
chr12:26014414 | A | G | 11 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(8): Show |
11 | HG00597.hp1 HG00609.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-109+19284A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014414 | |||||||
chr12:26014474 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-109+19344C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014474 | |||||||
chr12:26014500 | A | G | 52 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(49): Show |
52 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-109+19370A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014500 | |||||||
chr12:26014572 | T | A | 1 | a0001c0001t0058g0294 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-109+19442T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014572 | |||||||
chr12:26014622 | AT | A | 8 | a0001c0001t0002g0233 a0001c0001t0012g0005 a0001c0001t0012g0024 others(5): Show |
9 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-109+19497delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26014622 | ||||||
chr12:26014791 | G | C | 4 | a0001c0001t0004g0355 a0001c0001t0004g0365 a0001c0001t0004g0369 others(1): Show |
4 | HG00544.hp1 HG02132.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+19661G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014791 | |||||||
chr12:26014828 | A | G | 2 | a0001c0001t0006g0234 a0001c0001t0006g0235 |
2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-109+19698A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014828 | |||||||
chr12:26014922 | C | T | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-109+19792C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014922 | |||||||
chr12:26014957 | G | A | 1 | a0001c0002t0001g0073 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-109+19827G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014957 | |||||||
chr12:26014985 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-109+19855C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26014985 | |||||||
chr12:26015030 | A | ACCCC | 43 | a0001c0001t0002g0012 a0001c0001t0003g0265 a0001c0001t0003g0271 others(40): Show |
46 | HG00099.hp2 HG00621.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.-109+19901_-109+19 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26015030 | ||||||
chr12:26015035 | G | A | 97 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(94): Show |
103 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-109+19905G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015035 | |||||||
chr12:26015042 | C | CAA | 45 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-109+19922_-109+19 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26015042 | ||||||
chr12:26015081 | C | T | 1 | a0001c0004t0015g0262 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-109+19951C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015081 | |||||||
chr12:26015206 | C | CA | 92 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(89): Show |
97 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-109+20091dupA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26015206 | ||||||
chr12:26015327 | G | T | 1 | a0001c0001t0005g0157 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-109+20197G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015327 | |||||||
chr12:26015372 | A | G | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-109+20242A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015372 | |||||||
chr12:26015378 | G | A | 6 | a0001c0002t0001g0008 a0001c0002t0001g0069 a0001c0002t0001g0074 others(3): Show |
7 | HG02040.hp1 HG02056.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+20248G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015378 | |||||||
chr12:26015406 | T | G | 1 | a0001c0001t0002g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-109+20276T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015406 | |||||||
chr12:26015469 | A | G | 1 | a0001c0001t0008g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-109+20339A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015469 | |||||||
chr12:26015522 | A | G | 1 | a0001c0002t0002g0045 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-109+20392A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015522 | |||||||
chr12:26015539 | C | A | 269 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(266): Show |
288 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-109+20409C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015539 | |||||||
chr12:26015562 | G | A | 1 | a0001c0001t0006g0281 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-109+20432G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015562 | |||||||
chr12:26015669 | T | TA | 367 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0037 others(364): Show |
387 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(384): Show |
intron_variant | MODIFIER | c.-109+20539_-109+20 others(7): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015669 | |||||||
chr12:26015711 | C | T | 21 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(18): Show |
21 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.-109+20581C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015711 | |||||||
chr12:26015850 | AT | A | 97 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(94): Show |
103 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-109+20722delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26015850 | ||||||
chr12:26015857 | A | G | 1 | a0001c0001t0031g0020 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-109+20727A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015857 | |||||||
chr12:26015859 | A | G | 1 | a0001c0002t0001g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-109+20729A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015859 | |||||||
chr12:26015860 | A | G | 2 | a0001c0001t0009g0298 a0001c0001t0009g0299 |
2 | HG01993.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-109+20730A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015860 | |||||||
chr12:26015933 | CACTA | C | 6 | a0001c0001t0031g0020 a0001c0001t0053g0022 a0001c0005t0006g0255 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+20813_-109+20 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26015933 | ||||||
chr12:26015950 | T | C | 20 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0008g0006 others(17): Show |
21 | HG00741.hp1 HG01192.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-109+20820T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26015950 | |||||||
chr12:26016056 | A | G | 3 | a0001c0002t0001g0067 a0001c0002t0001g0078 a0001c0002t0047g0058 |
3 | HG02602.hp2 HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-109+20926A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016056 | |||||||
chr12:26016058 | A | T | 97 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(94): Show |
103 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-109+20928A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016058 | |||||||
chr12:26016157 | G | C | 1 | a0001c0002t0001g0201 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-109+21027G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016157 | |||||||
chr12:26016198 | GT | G | 5 | a0001c0001t0003g0279 a0001c0001t0006g0280 a0001c0001t0010g0274 others(2): Show |
5 | HG02602.hp1 HG02735.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-109+21073delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26016198 | ||||||
chr12:26016203 | T | G | 40 | a0001c0001t0002g0012 a0001c0001t0003g0265 a0001c0001t0003g0271 others(37): Show |
43 | HG00099.hp2 HG00621.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.-109+21073T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016203 | |||||||
chr12:26016203 | T | TG | 45 | a0001c0001t0002g0106 a0001c0001t0003g0004 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-109+21076dupG | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26016203 | ||||||
chr12:26016206 | GT | G | 156 | a0001c0001t0002g0013 a0001c0001t0003g0017 a0001c0001t0003g0083 others(153): Show |
164 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.-109+21091delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26016206 | ||||||
chr12:26016207 | T | G | 120 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(117): Show |
127 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-109+21077T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016207 | |||||||
chr12:26016208 | T | G | 139 | a0001c0001t0003g0017 a0001c0001t0003g0083 a0001c0001t0004g0329 others(136): Show |
146 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-109+21078T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016208 | |||||||
chr12:26016210 | T | G | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-109+21080T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016210 | |||||||
chr12:26016261 | A | G | 5 | a0001c0001t0031g0020 a0001c0005t0006g0255 a0001c0005t0006g0256 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+21131A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016261 | |||||||
chr12:26016336 | T | C | 52 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(49): Show |
52 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-109+21206T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016336 | |||||||
chr12:26016371 | C | T | 60 | a0001c0001t0003g0083 a0001c0001t0015g0059 a0001c0001t0015g0068 others(57): Show |
67 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-109+21241C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016371 | |||||||
chr12:26016551 | T | C | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-109+21421T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016551 | |||||||
chr12:26016558 | G | A | 42 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-109+21428G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016558 | |||||||
chr12:26016574 | T | C | 1 | a0001c0001t0003g0271 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-109+21444T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016574 | |||||||
chr12:26016597 | C | A | 1 | a0001c0001t0003g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-109+21467C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016597 | |||||||
chr12:26016615 | TTC | T | 45 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-109+21487_-109+21 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26016615 | ||||||
chr12:26016649 | A | G | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-109+21519A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016649 | |||||||
chr12:26016658 | C | T | 2 | a0001c0001t0004g0331 a0001c0001t0004g0366 |
2 | NA18995.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-109+21528C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016658 | |||||||
chr12:26016729 | G | C | 7 | a0001c0001t0011g0310 a0001c0001t0018g0311 a0001c0001t0041g0309 others(4): Show |
7 | HG00558.hp2 HG02896.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+21599G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016729 | |||||||
chr12:26016797 | T | A | 270 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(267): Show |
289 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-109+21667T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016797 | |||||||
chr12:26016803 | A | G | 25 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(22): Show |
27 | HG00423.hp1 HG00438.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.-109+21673A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26016803 | |||||||
chr12:26017046 | A | G | 1 | a0001c0001t0004g0364 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-109+21916A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017046 | |||||||
chr12:26017122 | AT | A | 61 | a0001c0001t0003g0083 a0001c0001t0015g0059 a0001c0001t0015g0068 others(58): Show |
68 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-109+21999delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26017122 | ||||||
chr12:26017129 | T | A | 1 | a0001c0001t0008g0036 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-109+21999T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017129 | |||||||
chr12:26017130 | A | T | 1 | a0001c0001t0007g0247 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-109+22000A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017130 | |||||||
chr12:26017160 | A | G | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-109+22030A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017160 | |||||||
chr12:26017228 | C | G | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-109+22098C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017228 | |||||||
chr12:26017259 | G | T | 60 | a0001c0001t0003g0083 a0001c0001t0015g0059 a0001c0001t0015g0068 others(57): Show |
67 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-109+22129G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017259 | |||||||
chr12:26017368 | A | ATAAG | 270 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(267): Show |
289 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-109+22239_-109+22 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26017368 | ||||||
chr12:26017368 | A | G | 1 | a0001c0001t0004g0352 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-109+22238A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017368 | |||||||
chr12:26017425 | A | G | 1 | a0001c0001t0003g0204 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-109+22295A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017425 | |||||||
chr12:26017431 | T | C | 30 | a0001c0001t0003g0017 a0001c0001t0009g0296 a0001c0001t0009g0297 others(27): Show |
30 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.-109+22301T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017431 | |||||||
chr12:26017616 | A | C | 1 | a0001c0001t0002g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-109+22486A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017616 | |||||||
chr12:26017622 | G | T | 28 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-109+22492G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017622 | |||||||
chr12:26017648 | C | T | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-109+22518C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017648 | |||||||
chr12:26017650 | G | T | 62 | a0001c0001t0003g0083 a0001c0001t0015g0059 a0001c0001t0015g0068 others(59): Show |
69 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-109+22520G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017650 | |||||||
chr12:26017686 | G | A | 1 | a0001c0001t0043g0251 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-109+22556G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017686 | |||||||
chr12:26017772 | C | T | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-109+22642C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017772 | |||||||
chr12:26017863 | C | T | 45 | a0001c0001t0002g0012 a0001c0001t0003g0265 a0001c0001t0003g0271 others(42): Show |
48 | HG00099.hp2 HG00621.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-109+22733C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017863 | |||||||
chr12:26017884 | A | G | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-109+22754A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26017884 | |||||||
chr12:26018121 | AT | A | 89 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(86): Show |
94 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-109+22992delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26018121 | |||||||
chr12:26018233 | T | G | 1 | a0001c0001t0002g0100 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-109+23103T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26018233 | |||||||
chr12:26018421 | A | C | 1 | a0001c0001t0004g0351 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-109+23291A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26018421 | |||||||
chr12:26018518 | T | C | 1 | a0001c0002t0001g0085 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-109+23388T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26018518 | |||||||
chr12:26018631 | G | A | 1 | a0001c0002t0001g0066 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-109+23501G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26018631 | |||||||
chr12:26018643 | A | G | 163 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(160): Show |
172 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.-109+23513A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26018643 | |||||||
chr12:26018660 | C | A | 82 | a0001c0001t0003g0017 a0001c0001t0004g0329 a0001c0001t0004g0330 others(79): Show |
82 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.-109+23530C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26018660 | |||||||
chr12:26018715 | T | A | 1 | a0001c0001t0004g0344 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-109+23585T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26018715 | |||||||
chr12:26018739 | A | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-109+23609A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26018739 | |||||||
chr12:26018758 | G | A | 1 | a0001c0001t0016g0288 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-109+23628G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26018758 | |||||||
chr12:26018784 | G | A | 350 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(347): Show |
369 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.-109+23654G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26018784 | |||||||
chr12:26019118 | G | A | 352 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(349): Show |
371 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(368): Show |
intron_variant | MODIFIER | c.-109+23988G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019118 | |||||||
chr12:26019356 | A | G | 60 | a0001c0001t0003g0083 a0001c0001t0015g0059 a0001c0001t0015g0068 others(57): Show |
67 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-109+24226A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019356 | |||||||
chr12:26019369 | C | T | 1 | a0001c0001t0005g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-109+24239C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019369 | |||||||
chr12:26019370 | G | A | 7 | a0001c0001t0004g0352 a0001c0001t0004g0372 a0001c0001t0004g0373 others(4): Show |
7 | HG00621.hp2 NA18965.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+24240G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019370 | |||||||
chr12:26019384 | G | A | 1 | a0001c0001t0006g0286 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-109+24254G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019384 | |||||||
chr12:26019402 | C | T | 1 | a0001c0001t0005g0129 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-109+24272C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019402 | |||||||
chr12:26019403 | G | T | 1 | a0001c0001t0020g0250 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-109+24273G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019403 | |||||||
chr12:26019447 | C | T | 2 | a0001c0001t0006g0261 a0001c0001t0031g0020 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-109+24317C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019447 | |||||||
chr12:26019469 | G | T | 1 | a0001c0001t0034g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-109+24339G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019469 | |||||||
chr12:26019563 | C | CTG | 4 | a0001c0001t0002g0013 a0001c0001t0013g0238 a0001c0001t0013g0241 others(1): Show |
5 | HG01257.hp1 HG01258.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-109+24473_-109+24 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26019563 | ||||||
chr12:26019563 | C | CTGTG | 4 | a0001c0001t0003g0018 a0001c0001t0007g0243 a0001c0001t0007g0244 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+24471_-109+24 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26019563 | ||||||
chr12:26019563 | CTG | C | 10 | a0001c0001t0007g0040 a0001c0001t0007g0247 a0001c0001t0007g0249 others(7): Show |
10 | HG01168.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-109+24473_-109+24 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26019563 | ||||||
chr12:26019563 | CTGTG | C | 6 | a0001c0001t0007g0259 a0001c0001t0019g0322 a0001c0001t0027g0102 others(3): Show |
6 | HG01167.hp2 HG01496.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+24471_-109+24 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26019563 | ||||||
chr12:26019563 | CTGTGTG | C | 10 | a0001c0001t0002g0037 a0001c0001t0002g0043 a0001c0001t0002g0079 others(7): Show |
10 | HG01243.hp1 HG01258.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.-109+24469_-109+24 others(12): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26019563 | ||||||
chr12:26019563 | CTGTGTGT others(1): Show |
C | 117 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0099 others(114): Show |
124 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.-109+24467_-109+24 others(14): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26019563 | ||||||
chr12:26019563 | CTGTGTGT others(3): Show |
C | 65 | a0001c0001t0003g0279 a0001c0001t0004g0359 a0001c0001t0004g0362 others(62): Show |
67 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.-109+24465_-109+24 others(16): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26019563 | ||||||
chr12:26019563 | CTGTGTGT others(5): Show |
C | 65 | a0001c0001t0002g0012 a0001c0001t0002g0117 a0001c0001t0002g0143 others(62): Show |
67 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.-109+24463_-109+24 others(18): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26019563 | ||||||
chr12:26019563 | CTGTGTGT others(7): Show |
C | 82 | a0001c0001t0002g0165 a0001c0001t0006g0261 a0001c0001t0007g0164 others(79): Show |
90 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-109+24461_-109+24 others(20): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26019563 | ||||||
chr12:26019589 | GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-109+24469_-109+24 others(22): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26019589 | ||||||
chr12:26019593 | GTGTGTGT others(5): Show |
G | 4 | a0001c0001t0011g0310 a0001c0001t0018g0311 a0001c0001t0041g0309 others(1): Show |
4 | HG00558.hp2 HG02976.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+24473_-109+24 others(18): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26019593 | ||||||
chr12:26019595 | GTGTGTGT others(3): Show |
G | 4 | a0001c0004t0011g0312 a0001c0004t0011g0313 a0001c0004t0011g0314 others(1): Show |
4 | HG02896.hp2 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+24483_-109+24 others(16): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26019595 | ||||||
chr12:26019716 | T | A | 52 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(49): Show |
52 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-109+24586T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019716 | |||||||
chr12:26019717 | A | T | 1 | a0001c0001t0003g0133 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-109+24587A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019717 | |||||||
chr12:26019731 | T | G | 1 | a0001c0001t0015g0092 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-109+24601T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019731 | |||||||
chr12:26019842 | A | G | 3 | a0001c0002t0001g0067 a0001c0002t0001g0078 a0001c0002t0047g0058 |
3 | HG02602.hp2 HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-109+24712A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019842 | |||||||
chr12:26019845 | A | C | 1 | a0001c0001t0002g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-109+24715A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26019845 | |||||||
chr12:26020015 | G | A | 89 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(86): Show |
94 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-109+24885G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020015 | |||||||
chr12:26020151 | G | A | 1 | a0001c0001t0004g0365 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-109+25021G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020151 | |||||||
chr12:26020267 | T | A | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+25137T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020267 | |||||||
chr12:26020268 | T | G | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+25138T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020268 | |||||||
chr12:26020269 | C | A | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+25139C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020269 | |||||||
chr12:26020272 | T | G | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+25142T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020272 | |||||||
chr12:26020274 | C | G | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+25144C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020274 | |||||||
chr12:26020278 | A | T | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+25148A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020278 | |||||||
chr12:26020279 | A | T | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+25149A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020279 | |||||||
chr12:26020293 | C | T | 2 | a0001c0001t0027g0102 a0001c0001t0027g0163 |
2 | HG00099.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-109+25163C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020293 | |||||||
chr12:26020441 | T | A | 5 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+25311T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020441 | |||||||
chr12:26020508 | T | C | 1 | a0001c0001t0004g0368 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-109+25378T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020508 | |||||||
chr12:26020556 | G | A | 4 | a0001c0001t0002g0121 a0001c0001t0002g0128 a0001c0001t0003g0279 others(1): Show |
4 | HG01993.hp1 HG02602.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+25426G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020556 | |||||||
chr12:26020630 | A | G | 28 | a0001c0001t0003g0017 a0001c0001t0009g0296 a0001c0001t0009g0297 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-109+25500A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020630 | |||||||
chr12:26020672 | T | G | 273 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(270): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-109+25542T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020672 | |||||||
chr12:26020683 | G | A | 29 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(26): Show |
31 | HG00099.hp2 HG00621.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-109+25553G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020683 | |||||||
chr12:26020685 | C | G | 1 | a0004c0010t0061g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-109+25555C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020685 | |||||||
chr12:26020721 | A | C | 1 | a0001c0001t0004g0336 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-109+25591A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020721 | |||||||
chr12:26020752 | A | G | 1 | a0001c0001t0003g0133 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-109+25622A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020752 | |||||||
chr12:26020763 | T | G | 3 | a0001c0001t0003g0208 a0001c0001t0003g0211 a0001c0001t0003g0216 |
3 | HG00438.hp2 HG02015.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-109+25633T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020763 | |||||||
chr12:26020830 | G | C | 45 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-109+25700G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020830 | |||||||
chr12:26020903 | A | T | 14 | a0001c0001t0003g0133 a0001c0001t0003g0265 a0001c0001t0003g0271 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-109+25773A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020903 | |||||||
chr12:26020915 | C | T | 2 | a0001c0001t0022g0026 a0001c0001t0022g0027 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-109+25785C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26020915 | |||||||
chr12:26021249 | A | G | 1 | a0001c0001t0058g0294 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-109+26119A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26021249 | |||||||
chr12:26021300 | A | G | 1 | a0004c0010t0061g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-109+26170A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26021300 | |||||||
chr12:26021348 | A | G | 6 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0301 others(3): Show |
6 | HG00423.hp2 HG00544.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+26218A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26021348 | |||||||
chr12:26021483 | C | A | 1 | a0001c0006t0057g0295 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-109+26353C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26021483 | |||||||
chr12:26021571 | A | G | 1 | a0001c0001t0012g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-109+26441A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26021571 | |||||||
chr12:26021705 | A | G | 2 | a0001c0001t0006g0234 a0001c0001t0006g0235 |
2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-109+26575A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26021705 | |||||||
chr12:26021762 | C | T | 1 | a0001c0001t0005g0192 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-109+26632C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26021762 | |||||||
chr12:26021905 | C | T | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-109+26775C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26021905 | |||||||
chr12:26022680 | C | G | 64 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(61): Show |
71 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-109+27550C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26022680 | |||||||
chr12:26022701 | CA | C | 273 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(270): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-109+27579delA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26022701 | ||||||
chr12:26022984 | T | C | 309 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(306): Show |
326 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.-109+27854T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26022984 | |||||||
chr12:26023057 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-109+27927A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26023057 | |||||||
chr12:26023154 | T | C | 90 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(87): Show |
95 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-109+28024T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26023154 | |||||||
chr12:26023159 | G | A | 64 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(61): Show |
71 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-109+28029G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26023159 | |||||||
chr12:26023292 | C | G | 1 | a0001c0003t0004g0293 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-109+28162C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26023292 | |||||||
chr12:26023639 | C | T | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-109+28509C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26023639 | |||||||
chr12:26023646 | T | A | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-109+28516T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26023646 | |||||||
chr12:26023701 | ATTAG | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0278 |
3 | HG01070.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-109+28575_-109+28 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26023701 | ||||||
chr12:26023718 | G | C | 1 | a0001c0001t0003g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-109+28588G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26023718 | |||||||
chr12:26023819 | G | T | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-109+28689G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26023819 | |||||||
chr12:26023830 | T | C | 14 | a0001c0001t0003g0133 a0001c0001t0003g0265 a0001c0001t0003g0271 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-109+28700T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26023830 | |||||||
chr12:26023888 | G | C | 1 | a0001c0001t0005g0140 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-109+28758G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26023888 | |||||||
chr12:26023957 | A | G | 7 | a0001c0001t0010g0014 a0001c0001t0010g0223 a0001c0001t0010g0266 others(4): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-109+28827A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26023957 | |||||||
chr12:26024364 | A | G | 64 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(61): Show |
71 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-109+29234A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024364 | |||||||
chr12:26024415 | A | G | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-109+29285A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024415 | |||||||
chr12:26024452 | G | C | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+29322G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024452 | |||||||
chr12:26024453 | T | A | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+29323T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024453 | |||||||
chr12:26024459 | C | A | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+29329C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024459 | |||||||
chr12:26024462 | A | C | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+29332A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024462 | |||||||
chr12:26024463 | T | G | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+29333T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024463 | |||||||
chr12:26024465 | C | G | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+29335C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024465 | |||||||
chr12:26024467 | G | T | 1 | a0001c0001t0018g0367 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-109+29337G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024467 | |||||||
chr12:26024658 | T | C | 7 | a0001c0001t0006g0261 a0001c0001t0031g0020 a0001c0005t0002g0245 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+29528T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024658 | |||||||
chr12:26024683 | G | A | 1 | a0001c0001t0006g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-109+29553G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024683 | |||||||
chr12:26024808 | T | G | 18 | a0001c0001t0003g0133 a0001c0001t0003g0265 a0001c0001t0003g0271 others(15): Show |
19 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-109+29678T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024808 | |||||||
chr12:26024814 | G | A | 62 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(59): Show |
69 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-109+29684G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024814 | |||||||
chr12:26024818 | G | A | 1 | a0001c0001t0053g0022 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-109+29688G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024818 | |||||||
chr12:26024826 | G | A | 6 | a0001c0001t0006g0181 a0001c0001t0006g0182 a0001c0001t0006g0183 others(3): Show |
6 | NA18945.hp1 NA18963.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+29696G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26024826 | |||||||
chr12:26025075 | T | C | 273 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(270): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-109+29945T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26025075 | |||||||
chr12:26025191 | T | G | 1 | a0001c0001t0020g0250 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-108-30045T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26025191 | |||||||
chr12:26025295 | C | T | 1 | a0001c0002t0001g0060 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-108-29941C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26025295 | |||||||
chr12:26025333 | A | G | 273 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(270): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-108-29903A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26025333 | |||||||
chr12:26025384 | C | T | 1 | a0001c0001t0051g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-108-29852C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26025384 | |||||||
chr12:26025393 | T | C | 89 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(86): Show |
94 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-108-29843T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26025393 | |||||||
chr12:26025450 | G | A | 5 | a0001c0001t0006g0261 a0001c0001t0031g0020 a0001c0005t0006g0255 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-108-29786G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26025450 | |||||||
chr12:26025468 | A | C | 2 | a0001c0001t0006g0285 a0001c0001t0006g0286 |
2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-108-29768A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26025468 | |||||||
chr12:26025486 | C | T | 1 | a0001c0001t0002g0042 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-108-29750C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26025486 | |||||||
chr12:26025521 | C | T | 78 | a0001c0001t0003g0017 a0001c0001t0004g0329 a0001c0001t0004g0330 others(75): Show |
78 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-108-29715C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26025521 | |||||||
chr12:26025562 | C | CA | 17 | a0001c0001t0003g0017 a0001c0001t0003g0230 a0001c0001t0004g0344 others(14): Show |
18 | HG00544.hp2 HG00738.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-108-29656dupA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26025562 | ||||||
chr12:26025562 | C | CAA | 19 | a0001c0001t0003g0083 a0001c0001t0003g0213 a0001c0001t0003g0214 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.-108-29657_-108-29 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26025562 | ||||||
chr12:26025562 | C | CAAA | 25 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(22): Show |
27 | HG00423.hp1 HG00438.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.-108-29658_-108-29 others(9): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26025562 | ||||||
chr12:26025562 | CA | C | 198 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(195): Show |
213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-108-29656delA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26025562 | ||||||
chr12:26025595 | A | G | 1 | a0001c0001t0025g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-108-29641A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26025595 | |||||||
chr12:26025631 | A | G | 45 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-108-29605A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26025631 | |||||||
chr12:26025913 | T | C | 7 | a0001c0001t0006g0261 a0001c0001t0031g0020 a0001c0005t0002g0245 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-108-29323T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26025913 | |||||||
chr12:26026000 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-108-29236C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026000 | |||||||
chr12:26026117 | A | G | 1 | a0001c0001t0005g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-108-29119A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026117 | |||||||
chr12:26026172 | AC | A | 13 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0008g0006 others(10): Show |
14 | HG00741.hp1 HG01192.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-108-29062delC | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26026172 | ||||||
chr12:26026323 | A | G | 3 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0101 |
3 | NA19007.hp2 NA19060.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-108-28913A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026323 | |||||||
chr12:26026329 | A | C | 1 | a0001c0001t0006g0283 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-108-28907A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026329 | |||||||
chr12:26026335 | C | A | 1 | a0001c0001t0005g0192 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-108-28901C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026335 | |||||||
chr12:26026341 | A | G | 10 | a0001c0001t0002g0013 a0001c0001t0003g0248 a0001c0001t0007g0040 others(7): Show |
11 | HG01069.hp2 HG01074.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-28895A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026341 | |||||||
chr12:26026376 | A | G | 2 | a0001c0001t0024g0202 a0001c0001t0024g0222 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-108-28860A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026376 | |||||||
chr12:26026464 | C | T | 14 | a0001c0001t0003g0133 a0001c0001t0003g0265 a0001c0001t0003g0271 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-108-28772C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026464 | |||||||
chr12:26026476 | C | T | 2 | a0001c0001t0002g0099 a0001c0001t0002g0100 |
2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-108-28760C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026476 | |||||||
chr12:26026482 | T | C | 3 | a0001c0001t0009g0306 a0001c0001t0039g0302 a0001c0001t0040g0300 |
3 | HG00408.hp1 NA19012.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-108-28754T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026482 | |||||||
chr12:26026497 | G | A | 47 | a0001c0001t0002g0012 a0001c0001t0003g0133 a0001c0001t0003g0265 others(44): Show |
50 | HG00099.hp2 HG00621.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.-108-28739G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026497 | |||||||
chr12:26026596 | C | T | 1 | a0001c0006t0057g0295 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-108-28640C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026596 | |||||||
chr12:26026688 | G | A | 1 | a0001c0002t0001g0093 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-108-28548G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026688 | |||||||
chr12:26026857 | A | G | 47 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(44): Show |
47 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-108-28379A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026857 | |||||||
chr12:26026867 | C | T | 50 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(47): Show |
50 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-108-28369C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026867 | |||||||
chr12:26026940 | T | A | 11 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(8): Show |
11 | HG00597.hp1 HG00609.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-108-28296T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026940 | |||||||
chr12:26026975 | C | T | 5 | a0001c0001t0006g0261 a0001c0001t0031g0020 a0001c0005t0006g0255 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-108-28261C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26026975 | |||||||
chr12:26027050 | TAA | T | 3 | a0001c0001t0005g0003 a0001c0001t0005g0173 a0001c0001t0005g0174 |
5 | NA18955.hp1 NA18988.hp1 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108-28180_-108-28 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26027050 | ||||||
chr12:26027111 | T | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-108-28125T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26027111 | |||||||
chr12:26027227 | G | A | 28 | a0001c0001t0003g0017 a0001c0001t0009g0296 a0001c0001t0009g0297 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-108-28009G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26027227 | |||||||
chr12:26027248 | A | G | 97 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(94): Show |
103 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-108-27988A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26027248 | |||||||
chr12:26027273 | T | C | 64 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(61): Show |
71 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-108-27963T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26027273 | |||||||
chr12:26027396 | C | T | 2 | a0001c0001t0006g0280 a0001c0001t0011g0358 |
2 | HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-108-27840C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26027396 | |||||||
chr12:26027502 | A | G | 27 | a0001c0001t0006g0015 a0001c0001t0006g0180 a0001c0001t0006g0181 others(24): Show |
28 | HG00099.hp2 HG00621.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.-108-27734A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26027502 | |||||||
chr12:26027636 | C | T | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-108-27600C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26027636 | |||||||
chr12:26027689 | C | G | 1 | a0001c0001t0006g0015 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-108-27547C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26027689 | |||||||
chr12:26027825 | T | C | 3 | a0001c0001t0002g0165 a0001c0001t0007g0164 a0001c0001t0034g0104 |
3 | HG01884.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-108-27411T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26027825 | |||||||
chr12:26027825 | T | G | 4 | a0001c0001t0004g0355 a0001c0001t0004g0365 a0001c0001t0004g0369 others(1): Show |
4 | HG00544.hp1 HG02132.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-27411T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26027825 | |||||||
chr12:26027838 | C | T | 10 | a0001c0001t0008g0006 a0001c0001t0008g0030 a0001c0001t0008g0031 others(7): Show |
11 | HG00741.hp1 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-27398C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26027838 | |||||||
chr12:26027938 | A | G | 2 | a0001c0001t0002g0171 a0001c0001t0002g0172 |
2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-108-27298A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26027938 | |||||||
chr12:26027962 | A | G | 45 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-108-27274A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26027962 | |||||||
chr12:26028116 | G | A | 273 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(270): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-108-27120G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028116 | |||||||
chr12:26028194 | ATTTTCT | A | 97 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(94): Show |
103 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-108-27039_-108-27 others(12): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26028194 | ||||||
chr12:26028205 | C | G | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-108-27031C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028205 | |||||||
chr12:26028277 | G | A | 45 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-108-26959G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028277 | |||||||
chr12:26028328 | A | G | 29 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(26): Show |
31 | HG00099.hp2 HG00621.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-108-26908A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028328 | |||||||
chr12:26028413 | A | G | 8 | a0001c0001t0011g0310 a0001c0001t0018g0311 a0001c0001t0041g0309 others(5): Show |
8 | HG00558.hp2 HG02257.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.-108-26823A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028413 | |||||||
chr12:26028496 | T | C | 45 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-108-26740T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028496 | |||||||
chr12:26028520 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-108-26716T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028520 | |||||||
chr12:26028541 | C | T | 1 | a0001c0002t0006g0185 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-108-26695C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028541 | |||||||
chr12:26028717 | G | A | 45 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-108-26519G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028717 | |||||||
chr12:26028727 | G | A | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-108-26509G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028727 | |||||||
chr12:26028752 | A | G | 97 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(94): Show |
103 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-108-26484A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028752 | |||||||
chr12:26028831 | A | G | 45 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-108-26405A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028831 | |||||||
chr12:26028943 | C | A | 3 | a0001c0005t0006g0255 a0001c0005t0006g0256 a0001c0005t0006g0257 |
3 | HG01884.hp1 HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-108-26293C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028943 | |||||||
chr12:26028961 | T | C | 1 | a0001c0001t0004g0342 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-108-26275T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028961 | |||||||
chr12:26028963 | C | G | 4 | a0001c0001t0005g0126 a0001c0001t0005g0127 a0001c0001t0005g0129 others(1): Show |
4 | HG02083.hp2 NA18939.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-26273C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028963 | |||||||
chr12:26028983 | C | T | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-108-26253C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26028983 | |||||||
chr12:26029195 | C | T | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-108-26041C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26029195 | |||||||
chr12:26029711 | A | G | 45 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-108-25525A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26029711 | |||||||
chr12:26029854 | T | A | 45 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-108-25382T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26029854 | |||||||
chr12:26030131 | C | A | 18 | a0001c0001t0003g0133 a0001c0001t0003g0265 a0001c0001t0003g0271 others(15): Show |
19 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-108-25105C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26030131 | |||||||
chr12:26030149 | G | A | 366 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0037 others(363): Show |
386 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(383): Show |
intron_variant | MODIFIER | c.-108-25087G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26030149 | |||||||
chr12:26030153 | A | G | 146 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(143): Show |
155 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.-108-25083A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26030153 | |||||||
chr12:26030217 | GT | G | 9 | a0001c0001t0008g0006 a0001c0001t0008g0030 a0001c0001t0008g0031 others(6): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-108-25012delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26030217 | ||||||
chr12:26030237 | C | T | 3 | a0001c0003t0004g0291 a0001c0003t0004g0293 a0001c0003t0011g0292 |
3 | HG02165.hp1 HG02523.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-108-24999C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26030237 | |||||||
chr12:26030329 | CT | C | 45 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-108-24904delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26030329 | ||||||
chr12:26030396 | T | C | 62 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(59): Show |
69 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-108-24840T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26030396 | |||||||
chr12:26030647 | CTTCT | C | 4 | a0001c0001t0010g0274 a0001c0001t0028g0326 a0001c0001t0028g0327 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-24582_-108-24 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26030647 | ||||||
chr12:26030687 | C | CT | 6 | a0001c0001t0002g0149 a0001c0001t0027g0102 a0001c0001t0027g0163 others(3): Show |
6 | HG00099.hp1 HG01496.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-24537dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26030687 | ||||||
chr12:26030687 | CT | C | 62 | a0001c0001t0005g0151 a0001c0001t0015g0059 a0001c0001t0015g0068 others(59): Show |
69 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-108-24537delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26030687 | ||||||
chr12:26030748 | C | A | 1 | a0001c0002t0001g0081 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-108-24488C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26030748 | |||||||
chr12:26030782 | T | C | 1 | a0001c0003t0004g0293 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-108-24454T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26030782 | |||||||
chr12:26031052 | G | A | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-108-24184G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26031052 | |||||||
chr12:26031100 | C | T | 229 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(226): Show |
246 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.-108-24136C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26031100 | |||||||
chr12:26031237 | G | A | 26 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(23): Show |
26 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-108-23999G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26031237 | |||||||
chr12:26031481 | A | G | 1 | a0001c0001t0058g0294 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-108-23755A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26031481 | |||||||
chr12:26031510 | A | G | 3 | a0001c0001t0003g0214 a0001c0001t0003g0217 a0001c0001t0003g0218 |
3 | HG01070.hp1 HG01358.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-108-23726A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26031510 | |||||||
chr12:26031582 | A | T | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-108-23654A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26031582 | |||||||
chr12:26031722 | C | T | 1 | a0001c0001t0018g0374 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-108-23514C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26031722 | |||||||
chr12:26031735 | G | C | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-108-23501G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26031735 | |||||||
chr12:26031852 | A | G | 3 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0005c0009t0054g0236 |
3 | HG01192.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-108-23384A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26031852 | |||||||
chr12:26032297 | A | C | 1 | a0001c0001t0004g0339 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-108-22939A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26032297 | |||||||
chr12:26032564 | A | G | 355 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(352): Show |
374 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.-108-22672A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26032564 | |||||||
chr12:26032596 | G | GT | 42 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(39): Show |
45 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.-108-22633dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26032596 | ||||||
chr12:26032829 | A | G | 1 | a0001c0002t0001g0060 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-108-22407A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26032829 | |||||||
chr12:26032988 | G | A | 2 | a0001c0001t0011g0310 a0001c0001t0018g0311 |
2 | HG00558.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-108-22248G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26032988 | |||||||
chr12:26033028 | C | T | 1 | a0001c0002t0001g0060 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-108-22208C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26033028 | |||||||
chr12:26033234 | G | T | 3 | a0001c0002t0001g0067 a0001c0002t0001g0078 a0001c0002t0047g0058 |
3 | HG02602.hp2 HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-108-22002G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26033234 | |||||||
chr12:26033401 | A | G | 353 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(350): Show |
372 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(369): Show |
intron_variant | MODIFIER | c.-108-21835A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26033401 | |||||||
chr12:26033443 | T | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-108-21793T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26033443 | |||||||
chr12:26033445 | T | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-108-21791T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26033445 | |||||||
chr12:26033664 | G | A | 62 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(59): Show |
69 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-108-21572G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26033664 | |||||||
chr12:26033730 | A | G | 1 | a0001c0001t0008g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-108-21506A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26033730 | |||||||
chr12:26033946 | C | T | 10 | a0001c0001t0008g0006 a0001c0001t0008g0030 a0001c0001t0008g0031 others(7): Show |
11 | HG00741.hp1 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-21290C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26033946 | |||||||
chr12:26033951 | T | C | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-108-21285T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26033951 | |||||||
chr12:26033960 | A | G | 1 | a0001c0001t0051g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-108-21276A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26033960 | |||||||
chr12:26033998 | C | G | 3 | a0001c0001t0002g0165 a0001c0001t0007g0164 a0001c0001t0034g0104 |
3 | HG01884.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-108-21238C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26033998 | |||||||
chr12:26034169 | G | A | 1 | a0001c0001t0004g0338 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-108-21067G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034169 | |||||||
chr12:26034178 | G | A | 1 | a0001c0001t0050g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-108-21058G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034178 | |||||||
chr12:26034200 | T | A | 62 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0133 others(59): Show |
65 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.-108-21036T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034200 | |||||||
chr12:26034376 | C | T | 42 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(39): Show |
45 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.-108-20860C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034376 | |||||||
chr12:26034406 | T | TA | 69 | a0001c0001t0003g0133 a0001c0001t0003g0265 a0001c0001t0003g0271 others(66): Show |
77 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.-108-20814dupA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26034406 | ||||||
chr12:26034406 | TA | T | 167 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(164): Show |
174 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.-108-20814delA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26034406 | ||||||
chr12:26034406 | TAA | T | 35 | a0001c0001t0002g0012 a0001c0001t0005g0140 a0001c0001t0006g0015 others(32): Show |
37 | HG00099.hp2 HG00621.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.-108-20815_-108-20 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26034406 | ||||||
chr12:26034418 | A | G | 1 | a0001c0001t0038g0317 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-108-20818A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034418 | |||||||
chr12:26034435 | T | G | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-108-20801T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034435 | |||||||
chr12:26034462 | G | A | 44 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(41): Show |
46 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-108-20774G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034462 | |||||||
chr12:26034485 | C | T | 62 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(59): Show |
69 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-108-20751C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034485 | |||||||
chr12:26034491 | C | T | 161 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(158): Show |
171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-108-20745C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034491 | |||||||
chr12:26034564 | C | T | 1 | a0001c0006t0057g0295 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-108-20672C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034564 | |||||||
chr12:26034641 | G | C | 44 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(41): Show |
46 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-108-20595G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034641 | |||||||
chr12:26034775 | A | G | 1 | a0001c0001t0003g0018 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-108-20461A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034775 | |||||||
chr12:26034786 | C | T | 14 | a0001c0001t0003g0133 a0001c0001t0003g0265 a0001c0001t0003g0271 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-108-20450C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034786 | |||||||
chr12:26034846 | AC | A | 4 | a0001c0001t0003g0220 a0001c0001t0024g0202 a0001c0001t0024g0222 others(1): Show |
4 | HG03130.hp1 HG03139.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-20389delC | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034846 | |||||||
chr12:26034866 | A | G | 14 | a0001c0001t0003g0133 a0001c0001t0003g0265 a0001c0001t0003g0271 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-108-20370A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034866 | |||||||
chr12:26034899 | C | G | 10 | a0001c0001t0008g0006 a0001c0001t0008g0030 a0001c0001t0008g0031 others(7): Show |
11 | HG00741.hp1 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-20337C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034899 | |||||||
chr12:26034963 | A | G | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-108-20273A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26034963 | |||||||
chr12:26035044 | A | G | 2 | a0001c0001t0012g0005 a0001c0001t0012g0025 |
3 | HG02109.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-108-20192A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035044 | |||||||
chr12:26035075 | G | C | 44 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(41): Show |
46 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-108-20161G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035075 | |||||||
chr12:26035094 | T | C | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-108-20142T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035094 | |||||||
chr12:26035164 | T | C | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-108-20072T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035164 | |||||||
chr12:26035391 | T | TTATATGA others(19): Show |
48 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(45): Show |
48 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-108-19819_-108-19 others(32): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035391 | ||||||
chr12:26035404 | T | C | 28 | a0001c0001t0003g0017 a0001c0001t0009g0296 a0001c0001t0009g0297 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-108-19832T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035404 | |||||||
chr12:26035410 | T | TATATAAG others(50): Show |
1 | a0001c0001t0004g0333 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-108-19794_-108-19 others(63): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035410 | ||||||
chr12:26035410 | TATATAAG others(24): Show |
T | 158 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(155): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-108-19795_-108-19 others(37): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035410 | ||||||
chr12:26035417 | G | T | 4 | a0001c0001t0010g0274 a0001c0001t0028g0326 a0001c0001t0028g0327 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-19819G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035417 | |||||||
chr12:26035436 | TATATA | T | 33 | a0001c0001t0003g0017 a0001c0001t0004g0338 a0001c0001t0009g0296 others(30): Show |
33 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.-108-19793_-108-19 others(11): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035436 | ||||||
chr12:26035438 | T | TATTATAT others(1): Show |
3 | a0001c0001t0007g0324 a0001c0001t0058g0294 a0001c0004t0015g0262 |
3 | HG02559.hp2 HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-108-19796_-108-19 others(14): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035438 | ||||||
chr12:26035441 | A | T | 3 | a0001c0001t0007g0324 a0001c0001t0058g0294 a0001c0004t0015g0262 |
3 | HG02559.hp2 HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-108-19795A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035441 | |||||||
chr12:26035448 | G | GTATATGA others(32): Show |
2 | a0001c0001t0004g0349 a0001c0001t0024g0202 |
2 | NA18522.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-108-19764_-108-19 others(45): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035448 | ||||||
chr12:26035448 | G | T | 3 | a0001c0001t0007g0324 a0001c0001t0058g0294 a0001c0004t0015g0262 |
3 | HG02559.hp2 HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-108-19788G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035448 | |||||||
chr12:26035448 | GTATATGA others(32): Show |
G | 3 | a0001c0001t0004g0338 a0001c0001t0010g0274 a0001c0006t0035g0038 |
3 | HG02886.hp1 HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-108-19764_-108-19 others(45): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035448 | ||||||
chr12:26035469 | T | TATAATTA others(22): Show |
1 | a0001c0001t0058g0294 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-108-19765_-108-19 others(35): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035469 | ||||||
chr12:26035469 | T | TATTATAT others(19): Show |
1 | a0001c0001t0004g0366 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-108-19748_-108-19 others(32): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035469 | ||||||
chr12:26035472 | T | A | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-108-19764T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035472 | |||||||
chr12:26035480 | T | A | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-108-19756T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035480 | |||||||
chr12:26035480 | T | TATATAAT others(24): Show |
5 | a0001c0001t0003g0225 a0001c0001t0015g0092 a0001c0003t0004g0291 others(2): Show |
5 | HG00738.hp1 HG02165.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108-19732_-108-19 others(37): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035480 | ||||||
chr12:26035487 | T | G | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-108-19749T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035487 | |||||||
chr12:26035494 | AAATTATA others(1): Show |
A | 14 | a0001c0001t0003g0133 a0001c0001t0003g0265 a0001c0001t0003g0271 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-108-19730_-108-19 others(14): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035494 | ||||||
chr12:26035535 | TA | T | 8 | a0001c0001t0006g0261 a0001c0001t0031g0020 a0001c0005t0002g0245 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-108-19696delA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035535 | ||||||
chr12:26035569 | T | C | 8 | a0001c0001t0006g0261 a0001c0001t0031g0020 a0001c0005t0002g0245 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-108-19667T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035569 | |||||||
chr12:26035579 | A | G | 1 | a0001c0002t0001g0207 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-108-19657A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035579 | |||||||
chr12:26035629 | T | C | 1 | a0001c0001t0023g0032 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-108-19607T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035629 | |||||||
chr12:26035676 | T | C | 27 | a0001c0001t0006g0015 a0001c0001t0006g0180 a0001c0001t0006g0181 others(24): Show |
28 | HG00099.hp2 HG00621.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.-108-19560T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035676 | |||||||
chr12:26035708 | G | A | 1 | a0001c0002t0004g0346 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-108-19528G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035708 | |||||||
chr12:26035769 | A | T | 50 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(47): Show |
50 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-108-19467A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035769 | |||||||
chr12:26035858 | TATA | T | 64 | a0001c0001t0009g0298 a0001c0001t0009g0299 a0001c0001t0015g0059 others(61): Show |
71 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-108-19373_-108-19 others(9): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035858 | ||||||
chr12:26035859 | A | G | 10 | a0001c0001t0008g0006 a0001c0001t0008g0030 a0001c0001t0008g0031 others(7): Show |
11 | HG00741.hp1 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-19377A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035859 | |||||||
chr12:26035875 | TTA | T | 62 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(59): Show |
69 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-108-19355_-108-19 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26035875 | ||||||
chr12:26035906 | G | T | 2 | a0001c0001t0003g0204 a0001c0001t0003g0210 |
2 | HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-108-19330G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26035906 | |||||||
chr12:26036022 | A | G | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-108-19214A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26036022 | |||||||
chr12:26036155 | G | C | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-108-19081G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26036155 | |||||||
chr12:26036305 | G | T | 44 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(41): Show |
46 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-108-18931G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26036305 | |||||||
chr12:26036617 | T | C | 2 | a0001c0001t0004g0330 a0001c0001t0004g0344 |
2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-108-18619T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26036617 | |||||||
chr12:26036796 | C | T | 2 | a0001c0001t0008g0035 a0001c0001t0008g0036 |
2 | HG00741.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-108-18440C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26036796 | |||||||
chr12:26036823 | G | A | 62 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(59): Show |
69 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-108-18413G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26036823 | |||||||
chr12:26036915 | C | CA | 64 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(61): Show |
71 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-108-18314dupA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26036915 | ||||||
chr12:26036924 | A | T | 64 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(61): Show |
71 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-108-18312A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26036924 | |||||||
chr12:26036925 | A | T | 1 | a0001c0002t0001g0095 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-108-18311A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26036925 | |||||||
chr12:26036933 | A | C | 63 | a0001c0001t0002g0149 a0001c0001t0015g0059 a0001c0001t0015g0068 others(60): Show |
70 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-108-18303A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26036933 | |||||||
chr12:26037014 | A | T | 1 | a0001c0001t0005g0112 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-108-18222A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037014 | |||||||
chr12:26037120 | C | T | 1 | a0001c0002t0001g0052 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-108-18116C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037120 | |||||||
chr12:26037136 | G | A | 44 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(41): Show |
46 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-108-18100G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037136 | |||||||
chr12:26037173 | A | G | 8 | a0001c0001t0006g0261 a0001c0001t0031g0020 a0001c0005t0002g0245 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-108-18063A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037173 | |||||||
chr12:26037187 | G | A | 351 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(348): Show |
370 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(367): Show |
intron_variant | MODIFIER | c.-108-18049G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037187 | |||||||
chr12:26037209 | A | G | 2 | a0001c0001t0004g0372 a0001c0001t0004g0373 |
2 | NA19005.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-108-18027A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037209 | |||||||
chr12:26037220 | A | G | 3 | a0001c0001t0003g0213 a0001c0001t0003g0215 a0001c0001t0003g0224 |
3 | HG00639.hp2 HG01261.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-108-18016A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037220 | |||||||
chr12:26037248 | A | T | 1 | a0001c0002t0001g0046 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-108-17988A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037248 | |||||||
chr12:26037316 | C | T | 1 | a0001c0001t0018g0311 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-108-17920C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037316 | |||||||
chr12:26037328 | T | G | 1 | a0001c0001t0004g0352 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-108-17908T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037328 | |||||||
chr12:26037331 | C | A | 2 | a0001c0001t0004g0329 a0001c0001t0004g0341 |
2 | HG02071.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.-108-17905C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037331 | |||||||
chr12:26037338 | A | T | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-108-17898A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037338 | |||||||
chr12:26037380 | C | T | 47 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(44): Show |
47 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-108-17856C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037380 | |||||||
chr12:26037747 | G | A | 3 | a0001c0001t0002g0121 a0001c0001t0002g0128 a0001c0001t0003g0279 |
3 | HG02602.hp1 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-108-17489G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037747 | |||||||
chr12:26037917 | G | A | 64 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(61): Show |
71 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-108-17319G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26037917 | |||||||
chr12:26038118 | T | A | 351 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(348): Show |
370 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(367): Show |
intron_variant | MODIFIER | c.-108-17118T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26038118 | |||||||
chr12:26038285 | C | T | 4 | a0001c0001t0002g0037 a0001c0001t0002g0079 a0001c0001t0002g0263 others(1): Show |
4 | HG01243.hp1 HG01258.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-16951C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26038285 | |||||||
chr12:26038371 | A | G | 98 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(95): Show |
104 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.-108-16865A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26038371 | |||||||
chr12:26038423 | A | G | 1 | a0001c0001t0015g0092 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-108-16813A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26038423 | |||||||
chr12:26038476 | T | C | 1 | a0004c0010t0061g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-108-16760T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26038476 | |||||||
chr12:26038559 | G | T | 62 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(59): Show |
69 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-108-16677G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26038559 | |||||||
chr12:26038608 | A | AAC | 18 | a0001c0001t0003g0215 a0001c0001t0003g0218 a0001c0001t0003g0220 others(15): Show |
18 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.-108-16581_-108-16 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | A | AACAC | 18 | a0001c0001t0003g0214 a0001c0001t0003g0230 a0001c0001t0004g0333 others(15): Show |
18 | HG00642.hp2 HG01081.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-108-16583_-108-16 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | A | AACACAC | 15 | a0001c0001t0003g0083 a0001c0001t0003g0216 a0001c0001t0003g0219 others(12): Show |
15 | HG00438.hp2 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.-108-16585_-108-16 others(12): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | A | AACACACA others(1): Show |
20 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0194 others(17): Show |
22 | HG01070.hp1 HG01099.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.-108-16587_-108-16 others(14): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | A | AACACACA others(3): Show |
7 | a0001c0001t0003g0197 a0001c0001t0003g0206 a0001c0001t0003g0225 others(4): Show |
7 | HG00621.hp2 HG01069.hp1 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.-108-16589_-108-16 others(16): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | A | AACACACA others(5): Show |
6 | a0001c0001t0004g0339 a0001c0001t0004g0347 a0001c0001t0004g0373 others(3): Show |
6 | HG01106.hp2 HG02015.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-16591_-108-16 others(18): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | A | AACACACA others(7): Show |
3 | a0001c0001t0003g0210 a0001c0001t0004g0360 a0001c0001t0018g0367 |
3 | HG01981.hp1 HG02738.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.-108-16593_-108-16 others(20): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | A | AACACACA others(19): Show |
1 | a0001c0001t0004g0352 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-108-16605_-108-16 others(32): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | A | ACACACAC others(4): Show |
1 | a0001c0001t0003g0227 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-108-16628_-108-16 others(17): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26038608 | |||||||
chr12:26038608 | AAC | A | 30 | a0001c0001t0002g0013 a0001c0001t0002g0100 a0001c0001t0002g0144 others(27): Show |
31 | HG00639.hp1 HG01069.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-108-16581_-108-16 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | AACAC | A | 43 | a0001c0001t0002g0121 a0001c0001t0002g0149 a0001c0001t0002g0165 others(40): Show |
48 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.-108-16583_-108-16 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | AACACAC | A | 42 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0109 others(39): Show |
45 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-108-16585_-108-16 others(12): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | AACACACA others(1): Show |
A | 27 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0043 others(24): Show |
27 | HG00609.hp1 HG00738.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.-108-16587_-108-16 others(14): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | AACACACA others(3): Show |
A | 50 | a0001c0001t0002g0042 a0001c0001t0002g0128 a0001c0001t0003g0044 others(47): Show |
56 | HG00408.hp2 HG00642.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.-108-16589_-108-16 others(16): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | AACACACA others(5): Show |
A | 14 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0025g0320 others(11): Show |
14 | HG00597.hp1 HG00609.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.-108-16591_-108-16 others(18): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | AACACACA others(7): Show |
A | 6 | a0001c0001t0002g0079 a0001c0001t0006g0285 a0001c0001t0025g0321 others(3): Show |
6 | HG01074.hp1 HG01934.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-16593_-108-16 others(20): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | AACACACA others(9): Show |
A | 31 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(28): Show |
33 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.-108-16595_-108-16 others(22): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | AACACACA others(11): Show |
A | 5 | a0001c0001t0003g0017 a0001c0001t0007g0259 a0001c0001t0046g0260 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108-16597_-108-16 others(24): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038608 | AACACACA others(13): Show |
A | 23 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(20): Show |
23 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-108-16599_-108-16 others(26): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26038608 | ||||||
chr12:26038700 | A | G | 50 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(47): Show |
50 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-108-16536A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26038700 | |||||||
chr12:26038946 | T | C | 1 | a0001c0001t0023g0032 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-108-16290T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26038946 | |||||||
chr12:26039127 | C | G | 1 | a0001c0001t0006g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-108-16109C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26039127 | |||||||
chr12:26039223 | G | T | 1 | a0001c0001t0050g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-108-16013G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26039223 | |||||||
chr12:26039228 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-108-16008G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26039228 | |||||||
chr12:26039260 | G | A | 6 | a0001c0001t0006g0137 a0001c0001t0006g0138 a0001c0001t0006g0139 others(3): Show |
6 | HG02451.hp1 HG02886.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-15976G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26039260 | |||||||
chr12:26039270 | ATC | A | 4 | a0001c0001t0003g0017 a0001c0001t0051g0016 a0001c0006t0007g0325 others(1): Show |
4 | HG02257.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-15960_-108-15 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26039270 | ||||||
chr12:26039308 | G | C | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-108-15928G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26039308 | |||||||
chr12:26039391 | G | A | 2 | a0001c0001t0009g0315 a0001c0001t0009g0316 |
2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-108-15845G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26039391 | |||||||
chr12:26039422 | T | C | 1 | a0001c0001t0003g0133 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-108-15814T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26039422 | |||||||
chr12:26039615 | C | A | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-108-15621C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26039615 | |||||||
chr12:26039638 | G | A | 1 | a0001c0005t0006g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-108-15598G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26039638 | |||||||
chr12:26039662 | T | C | 98 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(95): Show |
104 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.-108-15574T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26039662 | |||||||
chr12:26039827 | A | C | 1 | a0001c0001t0030g0153 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-108-15409A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26039827 | |||||||
chr12:26039919 | T | A | 351 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(348): Show |
370 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(367): Show |
intron_variant | MODIFIER | c.-108-15317T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26039919 | |||||||
chr12:26039982 | T | C | 5 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-15254T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26039982 | |||||||
chr12:26040003 | T | C | 273 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(270): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-108-15233T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26040003 | |||||||
chr12:26040159 | TTAAA | T | 7 | a0001c0001t0011g0310 a0001c0001t0018g0311 a0001c0001t0041g0309 others(4): Show |
7 | HG00558.hp2 HG02896.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-108-15074_-108-15 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26040159 | ||||||
chr12:26040193 | A | G | 28 | a0001c0001t0003g0017 a0001c0001t0009g0296 a0001c0001t0009g0297 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-108-15043A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26040193 | |||||||
chr12:26040203 | A | C | 1 | a0001c0002t0001g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-108-15033A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26040203 | |||||||
chr12:26040226 | A | G | 1 | a0001c0001t0008g0229 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-108-15010A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26040226 | |||||||
chr12:26040361 | A | G | 106 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(103): Show |
112 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.-108-14875A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26040361 | |||||||
chr12:26040435 | C | T | 1 | a0001c0001t0003g0228 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-108-14801C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26040435 | |||||||
chr12:26040502 | T | A | 62 | a0001c0001t0015g0059 a0001c0001t0015g0068 a0001c0001t0015g0092 others(59): Show |
69 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-108-14734T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26040502 | |||||||
chr12:26040596 | C | A | 1 | a0001c0001t0004g0332 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-108-14640C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26040596 | |||||||
chr12:26040688 | T | G | 174 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 others(171): Show |
179 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.-108-14548T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26040688 | |||||||
chr12:26040765 | T | A | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-108-14471T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26040765 | |||||||
chr12:26040891 | GT | G | 177 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0003g0004 others(174): Show |
190 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.-108-14331delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26040891 | ||||||
chr12:26040971 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-108-14265G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26040971 | |||||||
chr12:26040992 | A | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-108-14244A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26040992 | |||||||
chr12:26041043 | G | A | 1 | a0001c0001t0051g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-108-14193G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26041043 | |||||||
chr12:26041054 | AT | A | 196 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(193): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-108-14171delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26041054 | ||||||
chr12:26041094 | T | G | 271 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(268): Show |
290 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.-108-14142T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26041094 | |||||||
chr12:26041477 | A | G | 355 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(352): Show |
374 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.-108-13759A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26041477 | |||||||
chr12:26041670 | TAAAC | T | 29 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(26): Show |
31 | HG00099.hp2 HG00621.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-108-13564_-108-13 others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26041670 | ||||||
chr12:26041674 | C | CAT | 4 | a0001c0001t0010g0274 a0001c0001t0028g0326 a0001c0001t0028g0327 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-13552_-108-13 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26041674 | ||||||
chr12:26041849 | A | G | 19 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(16): Show |
19 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-13387A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26041849 | |||||||
chr12:26041877 | G | A | 2 | a0001c0001t0011g0310 a0001c0001t0018g0311 |
2 | HG00558.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-108-13359G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26041877 | |||||||
chr12:26042027 | A | G | 1 | a0001c0001t0003g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-108-13209A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042027 | |||||||
chr12:26042068 | A | G | 14 | a0001c0001t0002g0177 a0001c0001t0005g0113 a0001c0001t0005g0115 others(11): Show |
14 | HG00597.hp2 HG00609.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.-108-13168A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042068 | |||||||
chr12:26042241 | G | C | 1 | a0001c0001t0044g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-108-12995G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042241 | |||||||
chr12:26042289 | A | G | 19 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(16): Show |
19 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-12947A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042289 | |||||||
chr12:26042372 | T | C | 10 | a0001c0001t0008g0006 a0001c0001t0008g0030 a0001c0001t0008g0031 others(7): Show |
11 | HG00741.hp1 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-108-12864T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042372 | |||||||
chr12:26042528 | ATTAAC | A | 29 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(26): Show |
31 | HG00099.hp2 HG00621.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-108-12705_-108-12 others(11): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26042528 | ||||||
chr12:26042594 | T | C | 59 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(56): Show |
66 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-108-12642T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042594 | |||||||
chr12:26042696 | G | C | 339 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(336): Show |
357 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.-108-12540G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042696 | |||||||
chr12:26042709 | A | G | 278 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(275): Show |
296 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.-108-12527A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042709 | |||||||
chr12:26042768 | G | T | 1 | a0001c0001t0004g0362 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-108-12468G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042768 | |||||||
chr12:26042781 | C | T | 17 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(14): Show |
17 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.-108-12455C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042781 | |||||||
chr12:26042798 | G | C | 61 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(58): Show |
68 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-108-12438G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042798 | |||||||
chr12:26042838 | A | G | 42 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-108-12398A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042838 | |||||||
chr12:26042870 | T | G | 5 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-12366T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042870 | |||||||
chr12:26042916 | T | C | 1 | a0001c0001t0002g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-108-12320T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042916 | |||||||
chr12:26042966 | A | G | 1 | a0001c0001t0050g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-108-12270A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26042966 | |||||||
chr12:26043026 | C | T | 1 | a0001c0001t0006g0184 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-108-12210C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26043026 | |||||||
chr12:26043162 | C | G | 2 | a0001c0001t0031g0021 a0001c0001t0041g0309 |
2 | HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-108-12074C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26043162 | |||||||
chr12:26043233 | C | T | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-108-12003C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26043233 | |||||||
chr12:26043335 | T | G | 61 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(58): Show |
68 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-108-11901T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26043335 | |||||||
chr12:26043422 | G | A | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-108-11814G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26043422 | |||||||
chr12:26043476 | C | T | 2 | a0001c0003t0004g0293 a0001c0003t0011g0292 |
2 | HG02165.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-108-11760C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26043476 | |||||||
chr12:26043493 | G | A | 339 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(336): Show |
357 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.-108-11743G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26043493 | |||||||
chr12:26043538 | G | C | 1 | a0001c0001t0002g0012 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-108-11698G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26043538 | |||||||
chr12:26043770 | G | A | 1 | a0001c0001t0003g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-108-11466G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26043770 | |||||||
chr12:26043795 | C | G | 19 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(16): Show |
19 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-11441C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26043795 | |||||||
chr12:26043998 | T | G | 1 | a0001c0001t0004g0365 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-108-11238T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26043998 | |||||||
chr12:26044076 | G | A | 9 | a0001c0001t0002g0233 a0001c0001t0012g0005 a0001c0001t0012g0024 others(6): Show |
10 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-11160G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26044076 | |||||||
chr12:26044092 | A | C | 2 | a0001c0001t0005g0110 a0001c0001t0005g0151 |
2 | NA18954.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-108-11144A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26044092 | |||||||
chr12:26044329 | G | A | 19 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(16): Show |
19 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-10907G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26044329 | |||||||
chr12:26044668 | A | C | 59 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(56): Show |
66 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-108-10568A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26044668 | |||||||
chr12:26044754 | G | A | 278 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(275): Show |
296 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.-108-10482G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26044754 | |||||||
chr12:26044861 | T | TAA | 4 | a0001c0001t0010g0274 a0001c0001t0028g0326 a0001c0001t0028g0327 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-10373_-108-10 others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26044861 | ||||||
chr12:26044897 | AAGTAT | A | 61 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(58): Show |
68 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-108-10336_-108-10 others(11): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26044897 | ||||||
chr12:26044913 | A | G | 1 | a0001c0001t0013g0242 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-108-10323A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26044913 | |||||||
chr12:26044934 | A | G | 19 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(16): Show |
19 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-10302A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26044934 | |||||||
chr12:26045015 | A | C | 4 | a0001c0001t0010g0274 a0001c0001t0028g0326 a0001c0001t0028g0327 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-10221A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26045015 | |||||||
chr12:26045175 | T | A | 1 | a0001c0002t0002g0045 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-108-10061T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26045175 | |||||||
chr12:26045240 | A | G | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-108-9996A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26045240 | |||||||
chr12:26045337 | G | A | 41 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(38): Show |
44 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.-108-9899G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26045337 | |||||||
chr12:26045385 | G | A | 339 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(336): Show |
357 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.-108-9851G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26045385 | |||||||
chr12:26045460 | G | A | 39 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(36): Show |
42 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-108-9776G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26045460 | |||||||
chr12:26045463 | T | G | 1 | a0001c0001t0006g0170 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-108-9773T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26045463 | |||||||
chr12:26045467 | C | T | 45 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-108-9769C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26045467 | |||||||
chr12:26045767 | G | A | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-108-9469G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26045767 | |||||||
chr12:26045794 | A | T | 10 | a0001c0001t0003g0017 a0001c0001t0011g0310 a0001c0001t0018g0311 others(7): Show |
10 | HG00558.hp2 HG02896.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-108-9442A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26045794 | |||||||
chr12:26045820 | G | A | 1 | a0001c0001t0007g0249 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-108-9416G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26045820 | |||||||
chr12:26045890 | G | A | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-108-9346G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26045890 | |||||||
chr12:26046008 | A | G | 1 | a0001c0001t0011g0358 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-108-9228A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26046008 | |||||||
chr12:26046022 | G | A | 2 | a0001c0001t0002g0165 a0001c0001t0007g0164 |
2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-108-9214G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26046022 | |||||||
chr12:26046024 | T | C | 92 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(89): Show |
97 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-108-9212T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26046024 | |||||||
chr12:26046060 | C | T | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-108-9176C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26046060 | |||||||
chr12:26046069 | T | G | 101 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(98): Show |
107 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-108-9167T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26046069 | |||||||
chr12:26046183 | G | A | 1 | a0001c0001t0006g0261 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-108-9053G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26046183 | |||||||
chr12:26046261 | C | T | 3 | a0001c0001t0003g0213 a0001c0001t0003g0215 a0001c0001t0003g0224 |
3 | HG00639.hp2 HG01261.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-108-8975C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26046261 | |||||||
chr12:26046480 | G | A | 1 | a0001c0006t0057g0295 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-108-8756G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26046480 | |||||||
chr12:26046602 | C | T | 1 | a0001c0001t0003g0228 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-108-8634C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26046602 | |||||||
chr12:26046623 | GA | G | 14 | a0001c0001t0003g0133 a0001c0001t0003g0265 a0001c0001t0003g0271 others(11): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-108-8612delA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26046623 | |||||||
chr12:26046672 | TA | T | 339 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(336): Show |
357 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.-108-8555delA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26046672 | ||||||
chr12:26046714 | T | C | 3 | a0001c0003t0004g0291 a0001c0003t0004g0293 a0001c0003t0011g0292 |
3 | HG02165.hp1 HG02523.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-108-8522T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26046714 | |||||||
chr12:26046823 | A | G | 51 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(48): Show |
53 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-108-8413A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26046823 | |||||||
chr12:26046833 | T | C | 1 | a0001c0001t0005g0168 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-108-8403T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26046833 | |||||||
chr12:26047039 | A | G | 19 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(16): Show |
19 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-8197A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26047039 | |||||||
chr12:26047056 | C | T | 2 | a0001c0001t0008g0006 a0001c0001t0008g0033 |
3 | HG02145.hp1 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-108-8180C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26047056 | |||||||
chr12:26047135 | A | C | 7 | a0001c0002t0001g0001 a0001c0002t0001g0053 a0001c0002t0001g0054 others(4): Show |
10 | NA18948.hp1 NA18950.hp1 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-8101A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26047135 | |||||||
chr12:26047162 | A | C | 59 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(56): Show |
66 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-108-8074A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26047162 | |||||||
chr12:26047272 | G | A | 9 | a0001c0001t0002g0233 a0001c0001t0012g0005 a0001c0001t0012g0024 others(6): Show |
10 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-7964G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26047272 | |||||||
chr12:26047499 | G | C | 1 | a0001c0001t0005g0124 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-108-7737G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26047499 | |||||||
chr12:26047572 | C | T | 2 | a0001c0001t0006g0234 a0001c0001t0006g0235 |
2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-108-7664C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26047572 | |||||||
chr12:26047632 | T | C | 101 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(98): Show |
107 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-108-7604T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26047632 | |||||||
chr12:26047647 | A | T | 1 | a0001c0001t0009g0299 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-108-7589A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26047647 | |||||||
chr12:26047668 | CTA | C | 10 | a0001c0001t0003g0017 a0001c0001t0011g0310 a0001c0001t0018g0311 others(7): Show |
10 | HG00558.hp2 HG02896.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-108-7566_-108-756 others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26047668 | ||||||
chr12:26047674 | C | T | 2 | a0001c0001t0006g0234 a0001c0001t0006g0235 |
2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-108-7562C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26047674 | |||||||
chr12:26047675 | G | A | 1 | a0001c0001t0018g0311 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-108-7561G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26047675 | |||||||
chr12:26047688 | A | G | 45 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-108-7548A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26047688 | |||||||
chr12:26048002 | C | T | 10 | a0001c0001t0003g0017 a0001c0001t0011g0310 a0001c0001t0018g0311 others(7): Show |
10 | HG00558.hp2 HG02896.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-108-7234C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048002 | |||||||
chr12:26048014 | A | G | 1 | a0001c0001t0003g0228 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-108-7222A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048014 | |||||||
chr12:26048140 | T | C | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-108-7096T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048140 | |||||||
chr12:26048140 | T | G | 7 | a0001c0001t0011g0310 a0001c0001t0018g0311 a0001c0001t0031g0021 others(4): Show |
7 | HG00558.hp2 HG03017.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-108-7096T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048140 | |||||||
chr12:26048230 | C | A | 339 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(336): Show |
357 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.-108-7006C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048230 | |||||||
chr12:26048390 | A | G | 102 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(99): Show |
108 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-108-6846A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048390 | |||||||
chr12:26048536 | T | G | 280 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(277): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.-108-6700T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048536 | |||||||
chr12:26048567 | G | A | 1 | a0001c0001t0032g0146 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-108-6669G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048567 | |||||||
chr12:26048618 | C | T | 51 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(48): Show |
53 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-108-6618C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048618 | |||||||
chr12:26048676 | T | C | 6 | a0001c0001t0006g0137 a0001c0001t0006g0138 a0001c0001t0006g0139 others(3): Show |
6 | HG02451.hp1 HG02886.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-6560T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048676 | |||||||
chr12:26048687 | A | C | 1 | a0001c0001t0004g0361 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-108-6549A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048687 | |||||||
chr12:26048714 | A | G | 281 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(278): Show |
299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.-108-6522A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048714 | |||||||
chr12:26048732 | T | C | 19 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(16): Show |
19 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-6504T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048732 | |||||||
chr12:26048763 | G | GT | 80 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(77): Show |
87 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-108-6466dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26048763 | ||||||
chr12:26048800 | C | T | 1 | a0001c0001t0006g0180 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-108-6436C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048800 | |||||||
chr12:26048830 | C | T | 1 | a0001c0001t0024g0222 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-108-6406C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048830 | |||||||
chr12:26048863 | C | T | 43 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(40): Show |
46 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.-108-6373C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048863 | |||||||
chr12:26048869 | T | G | 1 | a0001c0001t0002g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-108-6367T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048869 | |||||||
chr12:26048946 | C | A | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-108-6290C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048946 | |||||||
chr12:26048977 | C | T | 2 | a0001c0001t0010g0274 a0001c0006t0035g0038 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-108-6259C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048977 | |||||||
chr12:26048991 | C | T | 3 | a0001c0001t0004g0355 a0001c0001t0004g0369 a0001c0001t0004g0375 |
3 | HG00544.hp1 HG02523.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.-108-6245C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26048991 | |||||||
chr12:26049035 | G | A | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-108-6201G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049035 | |||||||
chr12:26049055 | G | A | 1 | a0001c0001t0023g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-108-6181G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049055 | |||||||
chr12:26049066 | T | C | 336 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(333): Show |
354 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(351): Show |
intron_variant | MODIFIER | c.-108-6170T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049066 | |||||||
chr12:26049076 | G | A | 6 | a0001c0001t0010g0274 a0001c0001t0025g0320 a0001c0001t0025g0321 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-6160G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049076 | |||||||
chr12:26049092 | C | A | 59 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(56): Show |
66 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-108-6144C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049092 | |||||||
chr12:26049271 | T | G | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-108-5965T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049271 | |||||||
chr12:26049339 | A | G | 8 | a0001c0002t0001g0050 a0001c0002t0001g0057 a0001c0002t0001g0066 others(5): Show |
8 | NA18940.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.-108-5897A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049339 | |||||||
chr12:26049435 | A | G | 3 | a0001c0005t0006g0255 a0001c0005t0006g0256 a0001c0005t0006g0257 |
3 | HG01884.hp1 HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-108-5801A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049435 | |||||||
chr12:26049489 | C | T | 59 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(56): Show |
66 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-108-5747C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049489 | |||||||
chr12:26049494 | T | C | 42 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(39): Show |
45 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.-108-5742T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049494 | |||||||
chr12:26049552 | C | T | 78 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 others(75): Show |
83 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-108-5684C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049552 | |||||||
chr12:26049553 | G | A | 1 | a0001c0002t0001g0070 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-108-5683G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049553 | |||||||
chr12:26049600 | T | C | 3 | a0001c0003t0004g0291 a0001c0003t0004g0293 a0001c0003t0011g0292 |
3 | HG02165.hp1 HG02523.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-108-5636T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049600 | |||||||
chr12:26049658 | C | A | 339 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(336): Show |
357 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.-108-5578C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049658 | |||||||
chr12:26049941 | C | T | 57 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(54): Show |
57 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-108-5295C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26049941 | |||||||
chr12:26050028 | C | T | 3 | a0001c0005t0006g0255 a0001c0005t0006g0256 a0001c0005t0006g0257 |
3 | HG01884.hp1 HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-108-5208C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26050028 | |||||||
chr12:26050053 | A | G | 339 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(336): Show |
357 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.-108-5183A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26050053 | |||||||
chr12:26050056 | T | C | 17 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(14): Show |
17 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.-108-5180T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26050056 | |||||||
chr12:26050073 | A | G | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-108-5163A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26050073 | |||||||
chr12:26050074 | C | A | 90 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(87): Show |
95 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-108-5162C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26050074 | |||||||
chr12:26050163 | T | A | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-108-5073T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26050163 | |||||||
chr12:26050421 | G | C | 1 | a0001c0002t0001g0071 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-108-4815G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26050421 | |||||||
chr12:26050511 | C | T | 2 | a0001c0001t0031g0021 a0001c0001t0041g0309 |
2 | HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-108-4725C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26050511 | |||||||
chr12:26050588 | A | G | 339 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(336): Show |
357 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.-108-4648A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26050588 | |||||||
chr12:26050589 | C | T | 3 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0005c0009t0054g0236 |
3 | HG01192.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-108-4647C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26050589 | |||||||
chr12:26050625 | A | T | 42 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(39): Show |
45 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.-108-4611A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26050625 | |||||||
chr12:26050869 | A | C | 5 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-4367A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26050869 | |||||||
chr12:26050971 | G | A | 3 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0005c0009t0054g0236 |
3 | HG01192.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-108-4265G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26050971 | |||||||
chr12:26051141 | C | T | 29 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(26): Show |
31 | HG00099.hp2 HG00621.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-108-4095C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26051141 | |||||||
chr12:26051210 | T | G | 1 | a0001c0001t0004g0338 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-108-4026T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26051210 | |||||||
chr12:26051270 | C | T | 6 | a0001c0001t0010g0274 a0001c0001t0025g0320 a0001c0001t0025g0321 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-3966C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26051270 | |||||||
chr12:26051272 | A | G | 1 | a0001c0001t0011g0310 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-108-3964A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26051272 | |||||||
chr12:26051294 | A | C | 1 | a0001c0001t0006g0261 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-108-3942A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26051294 | |||||||
chr12:26051336 | G | T | 2 | a0001c0001t0002g0037 a0001c0001t0002g0264 |
2 | HG01243.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-108-3900G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26051336 | |||||||
chr12:26051524 | A | G | 196 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(193): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-108-3712A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26051524 | |||||||
chr12:26051610 | T | G | 61 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(58): Show |
68 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-108-3626T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26051610 | |||||||
chr12:26051622 | T | G | 17 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(14): Show |
17 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.-108-3614T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26051622 | |||||||
chr12:26051763 | A | G | 45 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(42): Show |
47 | HG00423.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-108-3473A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26051763 | |||||||
chr12:26051876 | A | G | 1 | a0001c0001t0027g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-108-3360A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26051876 | |||||||
chr12:26051974 | C | T | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-108-3262C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26051974 | |||||||
chr12:26052091 | C | T | 1 | a0001c0001t0038g0317 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-108-3145C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052091 | |||||||
chr12:26052336 | T | G | 4 | a0001c0001t0025g0320 a0001c0001t0025g0321 a0001c0001t0028g0326 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-2900T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052336 | |||||||
chr12:26052446 | G | A | 322 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(319): Show |
340 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.-108-2790G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052446 | |||||||
chr12:26052462 | T | C | 5 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-2774T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052462 | |||||||
chr12:26052530 | C | G | 3 | a0001c0005t0006g0255 a0001c0005t0006g0256 a0001c0005t0006g0257 |
3 | HG01884.hp1 HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-108-2706C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052530 | |||||||
chr12:26052532 | A | C | 1 | a0001c0001t0051g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-108-2704A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052532 | |||||||
chr12:26052534 | T | C | 1 | a0001c0001t0004g0365 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-108-2702T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052534 | |||||||
chr12:26052554 | C | T | 1 | a0001c0001t0006g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-108-2682C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052554 | |||||||
chr12:26052555 | T | A | 1 | a0001c0001t0006g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-108-2681T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052555 | |||||||
chr12:26052556 | A | G | 1 | a0001c0001t0006g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-108-2680A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052556 | |||||||
chr12:26052578 | C | T | 1 | a0001c0002t0001g0089 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-108-2658C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052578 | |||||||
chr12:26052608 | T | A | 339 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(336): Show |
357 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.-108-2628T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052608 | |||||||
chr12:26052622 | C | T | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-108-2614C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052622 | |||||||
chr12:26052625 | T | C | 101 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(98): Show |
107 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-108-2611T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052625 | |||||||
chr12:26052684 | A | T | 2 | a0001c0001t0003g0017 a0001c0001t0051g0016 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-108-2552A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052684 | |||||||
chr12:26052920 | A | G | 1 | a0001c0006t0057g0295 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-108-2316A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26052920 | |||||||
chr12:26053000 | G | A | 341 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(338): Show |
359 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(356): Show |
intron_variant | MODIFIER | c.-108-2236G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26053000 | |||||||
chr12:26053015 | C | T | 108 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0003g0004 others(105): Show |
114 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-108-2221C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26053015 | |||||||
chr12:26053033 | C | A | 42 | a0001c0001t0002g0012 a0001c0001t0003g0017 a0001c0001t0006g0015 others(39): Show |
45 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.-108-2203C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26053033 | |||||||
chr12:26053049 | G | C | 60 | a0001c0001t0002g0161 a0001c0001t0002g0169 a0001c0002t0001g0001 others(57): Show |
67 | HG00597.hp1 HG00609.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.-108-2187G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26053049 | |||||||
chr12:26053066 | T | C | 4 | a0001c0001t0025g0320 a0001c0001t0025g0321 a0001c0001t0028g0326 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-2170T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26053066 | |||||||
chr12:26053155 | A | C | 1 | a0001c0001t0003g0265 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-108-2081A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26053155 | |||||||
chr12:26053187 | GA | G | 204 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(201): Show |
215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.-108-2037delA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26053187 | ||||||
chr12:26053272 | T | C | 19 | a0001c0001t0002g0108 a0001c0001t0002g0131 a0001c0001t0006g0234 others(16): Show |
19 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.-108-1964T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26053272 | |||||||
chr12:26053297 | T | C | 155 | a0001c0001t0002g0013 a0001c0001t0002g0037 a0001c0001t0002g0041 others(152): Show |
163 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.-108-1939T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26053297 | |||||||
chr12:26053556 | A | G | 74 | a0001c0001t0003g0204 a0001c0001t0003g0227 a0001c0002t0001g0001 others(71): Show |
81 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.-108-1680A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26053556 | |||||||
chr12:26053615 | TA | T | 280 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(277): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.-108-1619delA | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26053615 | ||||||
chr12:26053783 | A | G | 11 | a0001c0001t0002g0165 a0001c0001t0002g0233 a0001c0001t0012g0005 others(8): Show |
12 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-108-1453A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26053783 | |||||||
chr12:26053835 | A | G | 1 | a0001c0001t0006g0277 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-108-1401A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26053835 | |||||||
chr12:26053910 | A | T | 1 | a0001c0001t0006g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-108-1326A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26053910 | |||||||
chr12:26054158 | C | T | 57 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(54): Show |
57 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-108-1078C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26054158 | |||||||
chr12:26054414 | C | T | 1 | a0001c0001t0007g0258 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-108-822C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26054414 | |||||||
chr12:26054494 | A | C | 2 | a0001c0001t0022g0026 a0001c0001t0022g0027 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-108-742A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26054494 | |||||||
chr12:26054560 | C | T | 2 | a0001c0001t0012g0005 a0001c0001t0012g0025 |
3 | HG02109.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-108-676C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26054560 | |||||||
chr12:26054735 | TTTTG | T | 16 | a0001c0001t0003g0133 a0001c0001t0003g0248 a0001c0001t0003g0265 others(13): Show |
17 | HG00621.hp1 HG00738.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.-108-485_-108-482d others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 26054735 | ||||||
chr12:26054739 | G | T | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-108-497G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26054739 | |||||||
chr12:26054777 | T | C | 1 | a0001c0001t0008g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-108-459T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26054777 | |||||||
chr12:26054781 | A | G | 69 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(66): Show |
76 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.-108-455A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26054781 | |||||||
chr12:26054792 | A | G | 72 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(69): Show |
79 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-108-444A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26054792 | |||||||
chr12:26054800 | T | G | 1 | a0001c0001t0008g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-108-436T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26054800 | |||||||
chr12:26054850 | A | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-108-386A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26054850 | |||||||
chr12:26055084 | G | A | 6 | a0001c0001t0003g0133 a0001c0001t0003g0248 a0001c0001t0003g0265 others(3): Show |
6 | HG01069.hp2 HG01175.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-152G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 2/5 | chr12 | 26055084 | |||||||
chr12:26055495 | C | T | 1 | a0001c0001t0003g0220 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.103+49C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26055495 | |||||||
chr12:26055541 | C | A | 69 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(66): Show |
76 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.103+95C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26055541 | |||||||
chr12:26055555 | A | G | 69 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(66): Show |
76 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.103+109A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26055555 | |||||||
chr12:26055612 | G | A | 6 | a0001c0001t0006g0261 a0001c0005t0002g0245 a0001c0005t0006g0255 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.103+166G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26055612 | |||||||
chr12:26055742 | A | G | 8 | a0001c0001t0006g0261 a0001c0001t0028g0326 a0001c0001t0028g0327 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+296A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26055742 | |||||||
chr12:26055858 | C | T | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.103+412C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26055858 | |||||||
chr12:26055879 | T | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.103+433T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26055879 | |||||||
chr12:26055980 | G | A | 2 | a0001c0001t0022g0026 a0001c0001t0022g0027 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+534G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26055980 | |||||||
chr12:26056052 | G | A | 3 | a0001c0001t0006g0275 a0001c0001t0006g0276 a0001c0001t0006g0287 |
3 | NA18955.hp2 NA19003.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.103+606G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26056052 | |||||||
chr12:26056176 | C | T | 9 | a0001c0001t0002g0165 a0001c0001t0002g0233 a0001c0001t0012g0005 others(6): Show |
10 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.103+730C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26056176 | |||||||
chr12:26056228 | C | T | 8 | a0001c0001t0003g0083 a0001c0001t0003g0213 a0001c0001t0003g0215 others(5): Show |
8 | HG00639.hp2 HG01069.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+782C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26056228 | |||||||
chr12:26056277 | C | A | 2 | a0001c0001t0022g0026 a0001c0001t0022g0027 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+831C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26056277 | |||||||
chr12:26056365 | C | G | 93 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(90): Show |
98 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.103+919C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26056365 | |||||||
chr12:26056513 | C | T | 1 | a0001c0001t0008g0229 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.103+1067C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26056513 | |||||||
chr12:26056581 | T | C | 72 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(69): Show |
79 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.103+1135T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26056581 | |||||||
chr12:26057100 | T | TGTGTGTG others(6): Show |
1 | a0001c0001t0028g0326 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.103+1654_103+1655i others(15): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057100 | |||||||
chr12:26057100 | T | TTG | 10 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0004g0333 others(7): Show |
10 | HG01081.hp2 HG01123.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.103+1679_103+1680d others(4): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26057100 | ||||||
chr12:26057100 | T | TTGTG | 90 | a0001c0001t0002g0012 a0001c0001t0003g0004 a0001c0001t0003g0083 others(87): Show |
95 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.103+1677_103+1680d others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26057100 | ||||||
chr12:26057100 | T | TTGTGTG | 35 | a0001c0001t0002g0013 a0001c0001t0003g0133 a0001c0001t0003g0217 others(32): Show |
37 | HG01069.hp2 HG01070.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.103+1675_103+1680d others(8): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26057100 | ||||||
chr12:26057100 | T | TTGTGTGT others(1): Show |
48 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(45): Show |
48 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.103+1673_103+1680d others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26057100 | ||||||
chr12:26057100 | T | TTGTGTGT others(3): Show |
5 | a0001c0001t0004g0332 a0001c0001t0004g0351 a0001c0001t0007g0040 others(2): Show |
5 | HG01099.hp1 HG02723.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+1671_103+1680d others(12): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26057100 | ||||||
chr12:26057100 | T | TTGTGTGT others(5): Show |
9 | a0001c0001t0002g0165 a0001c0001t0002g0233 a0001c0001t0012g0005 others(6): Show |
10 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.103+1669_103+1680d others(14): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26057100 | ||||||
chr12:26057100 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0031g0020 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.103+1667_103+1680d others(16): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26057100 | ||||||
chr12:26057100 | TTG | T | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(65): Show |
75 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.103+1679_103+1680d others(4): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26057100 | ||||||
chr12:26057108 | G | GTGTGTGT others(3): Show |
93 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(90): Show |
98 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.103+1671_103+1672i others(12): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26057108 | ||||||
chr12:26057154 | T | C | 1 | a0001c0006t0035g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.103+1708T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057154 | |||||||
chr12:26057190 | G | C | 1 | a0001c0001t0004g0338 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.103+1744G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057190 | |||||||
chr12:26057192 | T | G | 69 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(66): Show |
76 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.103+1746T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057192 | |||||||
chr12:26057249 | G | C | 3 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0005c0009t0054g0236 |
3 | HG01192.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.103+1803G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057249 | |||||||
chr12:26057301 | C | T | 2 | a0001c0001t0023g0028 a0001c0001t0023g0032 |
2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.103+1855C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057301 | |||||||
chr12:26057537 | C | T | 1 | a0001c0001t0003g0271 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.103+2091C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057537 | |||||||
chr12:26057651 | G | A | 2 | a0001c0001t0022g0026 a0001c0001t0022g0027 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+2205G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057651 | |||||||
chr12:26057772 | C | T | 1 | a0001c0001t0005g0010 | 2 | NA18941.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.103+2326C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057772 | |||||||
chr12:26057826 | G | T | 1 | a0001c0001t0011g0358 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.103+2380G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057826 | |||||||
chr12:26057827 | G | C | 94 | a0001c0001t0002g0012 a0001c0001t0003g0004 a0001c0001t0003g0017 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.103+2381G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057827 | |||||||
chr12:26057884 | G | A | 7 | a0001c0001t0031g0021 a0001c0001t0041g0309 a0001c0004t0011g0312 others(4): Show |
7 | HG02559.hp2 HG02896.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+2438G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057884 | |||||||
chr12:26057906 | G | T | 35 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(32): Show |
37 | HG00438.hp2 HG00639.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.103+2460G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057906 | |||||||
chr12:26057945 | C | A | 2 | a0001c0001t0022g0026 a0001c0001t0022g0027 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+2499C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057945 | |||||||
chr12:26057973 | G | T | 56 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(53): Show |
56 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.103+2527G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26057973 | |||||||
chr12:26058285 | G | A | 1 | a0001c0004t0037g0323 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.103+2839G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058285 | |||||||
chr12:26058391 | C | T | 1 | a0001c0001t0004g0344 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.103+2945C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058391 | |||||||
chr12:26058432 | G | A | 1 | a0001c0001t0006g0261 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.103+2986G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058432 | |||||||
chr12:26058443 | A | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.103+2997A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058443 | |||||||
chr12:26058447 | T | C | 1 | a0001c0002t0001g0089 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.103+3001T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058447 | |||||||
chr12:26058471 | T | C | 1 | a0001c0001t0006g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.103+3025T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058471 | |||||||
chr12:26058491 | C | A | 2 | a0001c0001t0003g0272 a0001c0001t0003g0273 |
2 | HG03710.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.103+3045C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058491 | |||||||
chr12:26058528 | A | ACG | 3 | a0001c0001t0004g0341 a0001c0001t0006g0235 a0001c0006t0007g0325 |
3 | HG01192.hp2 HG02071.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103+3092_103+3093d others(4): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26058528 | ||||||
chr12:26058528 | ACG | A | 16 | a0001c0001t0003g0133 a0001c0001t0003g0248 a0001c0001t0003g0265 others(13): Show |
17 | HG00738.hp2 HG01069.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.103+3092_103+3093d others(4): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26058528 | ||||||
chr12:26058531 | C | A | 2 | a0001c0001t0006g0138 a0001c0001t0006g0186 |
2 | HG03516.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.103+3085C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058531 | |||||||
chr12:26058532 | G | A | 1 | a0001c0001t0006g0188 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.103+3086G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058532 | |||||||
chr12:26058534 | G | GCA | 7 | a0001c0001t0002g0165 a0001c0001t0002g0233 a0001c0001t0012g0005 others(4): Show |
8 | HG02109.hp2 HG02451.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.103+3089_103+3090i others(4): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26058534 | ||||||
chr12:26058536 | G | A | 3 | a0001c0001t0031g0020 a0001c0001t0058g0294 a0005c0009t0054g0236 |
3 | HG02486.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.103+3090G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058536 | |||||||
chr12:26058538 | G | A | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.103+3092G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058538 | |||||||
chr12:26058538 | G | GCA | 34 | a0001c0001t0004g0330 a0001c0001t0004g0331 a0001c0001t0004g0333 others(31): Show |
34 | HG00558.hp1 HG00733.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.103+3115_103+3116d others(4): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26058538 | ||||||
chr12:26058538 | G | GCACA | 9 | a0001c0001t0004g0339 a0001c0001t0004g0347 a0001c0001t0004g0365 others(6): Show |
9 | HG01106.hp2 HG02015.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.103+3113_103+3116d others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26058538 | ||||||
chr12:26058538 | G | GCGCACGC others(1): Show |
22 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0193 others(19): Show |
24 | HG00438.hp2 HG00639.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.103+3093_103+3094i others(10): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26058538 | ||||||
chr12:26058538 | G | GCGCACGC others(3): Show |
1 | a0001c0001t0003g0225 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.103+3093_103+3094i others(12): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26058538 | ||||||
chr12:26058538 | G | GCGCGCAC others(3): Show |
10 | a0001c0001t0003g0194 a0001c0001t0003g0195 a0001c0001t0003g0200 others(7): Show |
10 | HG00642.hp2 HG01261.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.103+3093_103+3094i others(12): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26058538 | ||||||
chr12:26058538 | GCA | G | 58 | a0001c0001t0002g0013 a0001c0001t0002g0100 a0001c0001t0002g0178 others(55): Show |
61 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.103+3115_103+3116d others(4): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26058538 | ||||||
chr12:26058538 | GCACA | G | 88 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(85): Show |
93 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.103+3113_103+3116d others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26058538 | ||||||
chr12:26058538 | GCACACAC others(3): Show |
G | 66 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(63): Show |
73 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.103+3107_103+3116d others(12): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26058538 | ||||||
chr12:26058538 | GCACACAC others(5): Show |
G | 1 | a0001c0002t0001g0080 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.103+3105_103+3116d others(14): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26058538 | ||||||
chr12:26058540 | A | G | 8 | a0001c0001t0006g0138 a0001c0001t0006g0139 a0001c0001t0006g0186 others(5): Show |
8 | HG00323.hp2 HG02486.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.103+3094A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058540 | |||||||
chr12:26058542 | A | G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0100 a0001c0001t0002g0178 others(1): Show |
5 | HG01257.hp1 HG01258.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+3096A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058542 | |||||||
chr12:26058548 | A | G | 2 | a0001c0002t0001g0051 a0001c0002t0001g0073 |
2 | NA18966.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.103+3102A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058548 | |||||||
chr12:26058587 | C | T | 1 | a0004c0010t0061g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.103+3141C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058587 | |||||||
chr12:26058739 | T | G | 102 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(99): Show |
108 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.103+3293T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058739 | |||||||
chr12:26058753 | G | A | 1 | a0001c0002t0016g0088 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.103+3307G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058753 | |||||||
chr12:26058952 | C | T | 3 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0005c0009t0054g0236 |
3 | HG01192.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.103+3506C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058952 | |||||||
chr12:26058955 | A | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.103+3509A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058955 | |||||||
chr12:26058997 | T | C | 2 | a0001c0006t0007g0325 a0001c0006t0057g0295 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.103+3551T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26058997 | |||||||
chr12:26059206 | C | T | 1 | a0005c0009t0054g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.103+3760C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26059206 | |||||||
chr12:26059296 | C | T | 1 | a0001c0006t0035g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.103+3850C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26059296 | |||||||
chr12:26059388 | T | C | 57 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(54): Show |
57 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.103+3942T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26059388 | |||||||
chr12:26059589 | A | G | 2 | a0001c0001t0022g0026 a0001c0001t0022g0027 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+4143A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26059589 | |||||||
chr12:26059649 | G | T | 1 | a0001c0001t0002g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.103+4203G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26059649 | |||||||
chr12:26059767 | C | A | 38 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0018 others(35): Show |
40 | HG00438.hp2 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.103+4321C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26059767 | |||||||
chr12:26059967 | C | T | 2 | a0001c0001t0027g0102 a0001c0001t0027g0163 |
2 | HG00099.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.103+4521C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26059967 | |||||||
chr12:26059984 | G | T | 2 | a0001c0001t0006g0234 a0001c0001t0006g0235 |
2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.104-4514G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26059984 | |||||||
chr12:26060052 | C | G | 7 | a0001c0001t0031g0021 a0001c0001t0041g0309 a0001c0004t0011g0312 others(4): Show |
7 | HG02559.hp2 HG02896.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-4446C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060052 | |||||||
chr12:26060133 | G | A | 28 | a0001c0001t0006g0015 a0001c0001t0006g0180 a0001c0001t0006g0181 others(25): Show |
29 | HG00099.hp2 HG01070.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.104-4365G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060133 | |||||||
chr12:26060289 | C | T | 280 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(277): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.104-4209C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060289 | |||||||
chr12:26060313 | T | C | 1 | a0005c0009t0054g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.104-4185T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060313 | |||||||
chr12:26060341 | T | TATTGAAT others(11): Show |
2 | a0001c0001t0002g0117 a0001c0001t0002g0143 |
2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.104-4157_104-4156i others(20): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060341 | |||||||
chr12:26060343 | C | G | 2 | a0001c0001t0002g0117 a0001c0001t0002g0143 |
2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.104-4155C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060343 | |||||||
chr12:26060345 | G | C | 2 | a0001c0001t0002g0117 a0001c0001t0002g0143 |
2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.104-4153G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060345 | |||||||
chr12:26060445 | T | C | 1 | a0001c0001t0053g0022 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.104-4053T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060445 | |||||||
chr12:26060516 | G | A | 56 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(53): Show |
56 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.104-3982G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060516 | |||||||
chr12:26060575 | A | G | 1 | a0001c0001t0005g0123 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.104-3923A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060575 | |||||||
chr12:26060591 | T | C | 8 | a0001c0001t0006g0261 a0001c0001t0028g0326 a0001c0001t0028g0327 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-3907T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060591 | |||||||
chr12:26060631 | G | A | 3 | a0001c0004t0011g0312 a0001c0004t0011g0313 a0001c0004t0011g0314 |
3 | HG03098.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.104-3867G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060631 | |||||||
chr12:26060658 | C | T | 360 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0037 others(357): Show |
380 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(377): Show |
intron_variant | MODIFIER | c.104-3840C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060658 | |||||||
chr12:26060705 | C | G | 72 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(69): Show |
79 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.104-3793C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060705 | |||||||
chr12:26060787 | C | T | 56 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(53): Show |
59 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.104-3711C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060787 | |||||||
chr12:26060807 | C | T | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.104-3691C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26060807 | |||||||
chr12:26061038 | A | C | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.104-3460A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26061038 | |||||||
chr12:26061333 | T | A | 1 | a0001c0001t0018g0311 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.104-3165T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26061333 | |||||||
chr12:26061344 | A | G | 2 | a0001c0001t0025g0320 a0001c0001t0025g0321 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.104-3154A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26061344 | |||||||
chr12:26061392 | A | G | 2 | a0001c0001t0003g0214 a0001c0001t0003g0217 |
2 | HG01070.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.104-3106A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26061392 | |||||||
chr12:26061511 | ACAC | A | 69 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(66): Show |
76 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.104-2986_104-2984d others(5): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26061511 | |||||||
chr12:26061549 | TG | T | 29 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(26): Show |
31 | HG00099.hp2 HG01070.hp2 HG01516.hp1 others(28): Show |
intron_variant | MODIFIER | c.104-2948delG | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26061549 | |||||||
chr12:26061570 | CAGAT | C | 56 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(53): Show |
59 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.104-2922_104-2919d others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26061570 | ||||||
chr12:26061630 | C | T | 72 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(69): Show |
79 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.104-2868C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26061630 | |||||||
chr12:26061655 | C | T | 38 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0018 others(35): Show |
40 | HG00438.hp2 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.104-2843C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26061655 | |||||||
chr12:26061945 | C | G | 1 | a0001c0002t0001g0008 | 2 | HG02132.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.104-2553C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26061945 | |||||||
chr12:26061952 | A | G | 1 | a0001c0001t0016g0289 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.104-2546A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26061952 | |||||||
chr12:26062064 | G | A | 69 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(66): Show |
76 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.104-2434G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26062064 | |||||||
chr12:26062174 | A | G | 50 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(47): Show |
50 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.104-2324A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26062174 | |||||||
chr12:26062240 | A | T | 18 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(15): Show |
18 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.104-2258A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26062240 | |||||||
chr12:26062322 | T | C | 72 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(69): Show |
79 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.104-2176T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26062322 | |||||||
chr12:26062387 | G | A | 2 | a0001c0001t0007g0259 a0001c0001t0046g0260 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.104-2111G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26062387 | |||||||
chr12:26062458 | C | T | 29 | a0001c0001t0002g0012 a0001c0001t0006g0015 a0001c0001t0006g0180 others(26): Show |
31 | HG00099.hp2 HG01070.hp2 HG01516.hp1 others(28): Show |
intron_variant | MODIFIER | c.104-2040C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26062458 | |||||||
chr12:26062696 | AAAAT | A | 72 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(69): Show |
79 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.104-1786_104-1783d others(6): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26062696 | ||||||
chr12:26062706 | A | G | 2 | a0001c0001t0007g0259 a0001c0001t0046g0260 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.104-1792A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26062706 | |||||||
chr12:26062774 | T | C | 2 | a0001c0001t0022g0026 a0001c0001t0022g0027 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.104-1724T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26062774 | |||||||
chr12:26062864 | G | A | 100 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(97): Show |
106 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.104-1634G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26062864 | |||||||
chr12:26063025 | A | T | 50 | a0001c0001t0004g0329 a0001c0001t0004g0330 a0001c0001t0004g0331 others(47): Show |
50 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.104-1473A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26063025 | |||||||
chr12:26063193 | G | A | 3 | a0001c0001t0012g0005 a0001c0001t0012g0024 a0001c0001t0012g0025 |
4 | HG02109.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-1305G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26063193 | |||||||
chr12:26063197 | GT | G | 9 | a0001c0001t0002g0165 a0001c0001t0002g0233 a0001c0001t0012g0005 others(6): Show |
10 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.104-1293delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26063197 | ||||||
chr12:26063301 | C | T | 69 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(66): Show |
76 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.104-1197C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26063301 | |||||||
chr12:26063308 | A | T | 279 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(276): Show |
297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.104-1190A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26063308 | |||||||
chr12:26063331 | C | T | 2 | a0001c0002t0001g0002 a0001c0002t0001g0061 |
4 | NA19058.hp1 NA19077.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-1167C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26063331 | |||||||
chr12:26063405 | G | GT | 6 | a0001c0001t0003g0248 a0001c0001t0006g0186 a0001c0001t0006g0235 others(3): Show |
6 | HG00597.hp1 HG01069.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-1083dupT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26063405 | ||||||
chr12:26063410 | T | G | 1 | a0001c0001t0004g0341 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.104-1088T>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26063410 | |||||||
chr12:26063422 | G | A | 72 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(69): Show |
79 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.104-1076G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26063422 | |||||||
chr12:26063474 | GC | G | 4 | a0001c0001t0002g0037 a0001c0001t0002g0079 a0001c0001t0002g0263 others(1): Show |
4 | HG01243.hp1 HG01258.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-1023delC | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26063474 | |||||||
chr12:26063538 | G | A | 91 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0042 others(88): Show |
96 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.104-960G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26063538 | |||||||
chr12:26063679 | T | C | 279 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(276): Show |
297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.104-819T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26063679 | |||||||
chr12:26063733 | GT | G | 34 | a0001c0001t0002g0013 a0001c0001t0003g0133 a0001c0001t0003g0248 others(31): Show |
36 | HG00738.hp2 HG01069.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.104-749delT | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 26063733 | ||||||
chr12:26064131 | T | A | 12 | a0001c0001t0009g0296 a0001c0001t0009g0297 a0001c0001t0009g0298 others(9): Show |
12 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.104-367T>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26064131 | |||||||
chr12:26064134 | C | T | 202 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(199): Show |
213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.104-364C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26064134 | |||||||
chr12:26064170 | C | T | 2 | a0001c0001t0022g0026 a0001c0001t0022g0027 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.104-328C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26064170 | |||||||
chr12:26064339 | G | A | 5 | a0001c0001t0002g0013 a0001c0001t0007g0040 a0001c0001t0007g0247 others(2): Show |
6 | HG01168.hp2 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-159G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26064339 | |||||||
chr12:26064368 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.104-130C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26064368 | |||||||
chr12:26064464 | A | G | 3 | a0001c0006t0007g0325 a0001c0006t0035g0038 a0001c0006t0057g0295 |
3 | HG02257.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.104-34A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 3/5 | chr12 | 26064464 | |||||||
chr12:26065613 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.993+226G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26065613 | |||||||
chr12:26065703 | T | C | 2 | a0001c0001t0029g0267 a0001c0001t0029g0268 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.993+316T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26065703 | |||||||
chr12:26066040 | G | A | 1 | a0001c0001t0003g0279 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.993+653G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26066040 | |||||||
chr12:26066106 | G | A | 335 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0041 others(332): Show |
353 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.993+719G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26066106 | |||||||
chr12:26066148 | A | G | 1 | a0001c0001t0007g0258 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.993+761A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26066148 | |||||||
chr12:26066312 | A | G | 3 | a0001c0006t0007g0325 a0001c0006t0035g0038 a0001c0006t0057g0295 |
3 | HG02257.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.993+925A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26066312 | |||||||
chr12:26066316 | A | G | 3 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0005c0009t0054g0236 |
3 | HG01192.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.993+929A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26066316 | |||||||
chr12:26066498 | T | C | 30 | a0001c0001t0002g0013 a0001c0001t0003g0133 a0001c0001t0003g0248 others(27): Show |
32 | HG00323.hp2 HG00738.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.994-1071T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26066498 | |||||||
chr12:26066537 | A | T | 2 | a0001c0001t0031g0021 a0001c0001t0041g0309 |
2 | HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.994-1032A>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26066537 | |||||||
chr12:26066670 | A | G | 3 | a0001c0006t0007g0325 a0001c0006t0035g0038 a0001c0006t0057g0295 |
3 | HG02257.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.994-899A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26066670 | |||||||
chr12:26066786 | C | T | 1 | a0001c0001t0002g0012 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.994-783C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26066786 | |||||||
chr12:26067037 | A | G | 1 | a0001c0001t0010g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.994-532A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26067037 | |||||||
chr12:26067085 | C | A | 1 | a0001c0005t0002g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.994-484C>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26067085 | |||||||
chr12:26067322 | G | A | 1 | a0001c0001t0005g0114 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.994-247G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26067322 | |||||||
chr12:26067358 | G | A | 3 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 |
3 | HG01433.hp1 HG02280.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.994-211G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26067358 | |||||||
chr12:26067447 | T | C | 1 | a0001c0006t0035g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.994-122T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 4/5 | chr12 | 26067447 | |||||||
chr12:26067856 | C | T | 2 | a0001c0001t0028g0326 a0001c0001t0028g0327 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1138+143C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 5/5 | chr12 | 26067856 | |||||||
chr12:26067896 | C | T | 3 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0051g0016 |
3 | HG01175.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1138+183C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 5/5 | chr12 | 26067896 | |||||||
chr12:26068118 | C | G | 1 | a0001c0001t0003g0150 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1138+405C>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 5/5 | chr12 | 26068118 | |||||||
chr12:26068140 | T | C | 1 | a0001c0001t0002g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1138+427T>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 5/5 | chr12 | 26068140 | |||||||
chr12:26068267 | G | T | 126 | a0001c0001t0004g0329 a0001c0001t0004g0331 a0001c0001t0004g0332 others(123): Show |
133 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1139-430G>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 5/5 | chr12 | 26068267 | |||||||
chr12:26068335 | G | A | 1 | a0001c0001t0003g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1139-362G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 5/5 | chr12 | 26068335 | |||||||
chr12:26068336 | G | A | 7 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0133 others(4): Show |
7 | HG01069.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.1139-361G>A | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 5/5 | chr12 | 26068336 | |||||||
chr12:26068458 | A | C | 3 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0005c0009t0054g0236 |
3 | HG01192.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1139-239A>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 5/5 | chr12 | 26068458 | |||||||
chr12:26068468 | A | G | 3 | a0001c0002t0001g0201 a0001c0002t0001g0205 a0001c0002t0001g0207 |
3 | NA18969.hp1 NA18987.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1139-229A>G | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 5/5 | chr12 | 26068468 | |||||||
chr12:26068548 | C | T | 1 | a0001c0002t0001g0073 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1139-149C>T | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 5/5 | chr12 | 26068548 | |||||||
chr12:26068628 | G | C | 1 | a0001c0001t0006g0281 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1139-69G>C | RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 5/5 | chr12 | 26068628 | |||||||
chr12:26068680 | CTT | C | 29 | a0001c0001t0002g0099 a0001c0001t0006g0015 a0001c0001t0006g0180 others(26): Show |
30 | HG00099.hp2 HG01070.hp2 HG01516.hp1 others(27): Show |
intron_variant | MODIFIER | c.1139-15_1139-14del others(2): Show |
RASSF8 | ENSG00000123094.16 | transcript | ENST00000689635.1 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 26068680 |