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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g16140 A10 16112037 C T upstream_gene_variant MODIFIER c.-64C>T| S45
2 BAA10g16140 A10 16112581 C T missense_variant MODERATE c.247C>T|p.Leu83Phe S5
3 BAA10g16140 A10 16112759 G A splice_acceptor_variant&intron_variant HIGH c.316-1G>A| S262
4 BAA10g16140 A10 16112812 C T missense_variant MODERATE c.368C>T|p.Ser123Phe S10
5 BAA10g16140 A10 16113540 G A missense_variant MODERATE c.583G>A|p.Glu195Lys S1
6 BAA10g16140 A10 16115208 G A missense_variant MODERATE c.2059G>A|p.Gly687Arg S219
7 BAA10g16140 A10 16115658 C T missense_variant MODERATE c.2341C>T|p.Leu781Phe S237
8 BAA10g16140 A10 16116189 G A missense_variant MODERATE c.2872G>A|p.Glu958Lys S262
9 BAA10g16140 A10 16116949 G A missense_variant MODERATE c.3632G>A|p.Ser1211Asn S198
10 BAA10g16140 A10 16117316 C T missense_variant MODERATE c.3782C>T|p.Pro1261Leu S53
11 BAA10g16140 A10 16118356 G A missense_variant MODERATE c.4736G>A|p.Gly1579Glu S289
12 BAA10g16140 A10 16118704 G A missense_variant MODERATE c.5084G>A|p.Arg1695Lys S67
13 BAA10g16140 A10 16118843 C T splice_region_variant&intron_variant LOW c.5128-3C>T| S281
14 BAA10g16140 A10 16119235 C T synonymous_variant LOW c.5400C>T|p.Asn1800Asn S162
15 BAA10g16140 A10 16119367 G A synonymous_variant LOW c.5532G>A|p.Lys1844Lys S198