Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g27110 A06 18614302 G A downstream_gene_variant MODIFIER c.*1653C>T| S11
2 BAA06g27110 A06 18616117 C T synonymous_variant LOW c.2106G>A|p.Ala702Ala S205
3 BAA06g27110 A06 18616159 C T synonymous_variant LOW c.2064G>A|p.Lys688Lys S267
4 BAA06g27110 A06 18616308 C T missense_variant MODERATE c.1915G>A|p.Glu639Lys S107
5 BAA06g27110 A06 18616406 C T missense_variant MODERATE c.1817G>A|p.Gly606Glu S293
6 BAA06g27110 A06 18616611 C G missense_variant MODERATE c.1612G>C|p.Gly538Arg S301
7 BAA06g27110 A06 18616645 C T synonymous_variant LOW c.1578G>A|p.Arg526Arg S238
8 BAA06g27110 A06 18616665 C T missense_variant MODERATE c.1558G>A|p.Glu520Lys S247
9 BAA06g27110 A06 18616704 C T missense_variant MODERATE c.1519G>A|p.Glu507Lys S280
10 BAA06g27110 A06 18616802 C T splice_acceptor_variant&intron_variant HIGH c.1422-1G>A| S96
11 BAA06g27110 A06 18616833 C T intron_variant MODIFIER c.1422-32G>A| S238
12 BAA06g27110 A06 18616881 G A missense_variant MODERATE c.1406C>T|p.Ser469Phe S51
13 BAA06g27110 A06 18617175 G A missense_variant MODERATE c.1112C>T|p.Ala371Val S166
14 BAA06g27110 A06 18617196 G A missense_variant MODERATE c.1091C>T|p.Ser364Phe S123
15 BAA06g27110 A06 18617761 C T missense_variant MODERATE c.526G>A|p.Asp176Asn S56
16 BAA06g27110 A06 18617863 C T missense_variant MODERATE c.424G>A|p.Ala142Thr S189
17 BAA06g27110 A06 18617907 C T stop_gained HIGH c.380G>A|p.Trp127* S267
18 BAA06g27110 A06 18618700 G A upstream_gene_variant MODIFIER c.-414C>T| S19
19 BAA06g27110 A06 18620134 G A upstream_gene_variant MODIFIER c.-1848C>T| S237
20 BAA06g27110 A06 18620360 G A upstream_gene_variant MODIFIER c.-2074C>T| S1
S90
21 BAA06g27110 A06 18621803 G A upstream_gene_variant MODIFIER c.-3517C>T| S237
22 BAA06g27110 A06 18621977 G A upstream_gene_variant MODIFIER c.-3691C>T| S166