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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g30490 A03 14292494 G A missense_variant MODERATE c.262G>A|p.Asp88Asn S305
2 BAA03g30490 A03 14292560 C T missense_variant MODERATE c.328C>T|p.Pro110Ser S43
3 BAA03g30490 A03 14293378 C T missense_variant MODERATE c.577C>T|p.Pro193Ser S140
4 BAA03g30490 A03 14294159 G A missense_variant MODERATE c.1168G>A|p.Gly390Arg S122
5 BAA03g30490 A03 14295577 G A intron_variant MODIFIER c.1875-9G>A| S5
6 BAA03g30490 A03 14295608 G A missense_variant MODERATE c.1897G>A|p.Gly633Arg S149
7 BAA03g30490 A03 14295940 C T intron_variant MODIFIER c.2095-10C>T| S191
8 BAA03g30490 A03 14296423 C T missense_variant MODERATE c.2414C>T|p.Pro805Leu S134
9 BAA03g30490 A03 14297253 C T missense_variant MODERATE c.2830C>T|p.Pro944Ser S170
10 BAA03g30490 A03 14297513 G A synonymous_variant LOW c.3003G>A|p.Thr1001Thr S296
11 BAA03g30490 A03 14297947 G A splice_acceptor_variant&intron_variant HIGH c.3079-1G>A| S180
12 BAA03g30490 A03 14298897 C T missense_variant MODERATE c.3560C>T|p.Ala1187Val S251
13 BAA03g30490 A03 14299175 C T synonymous_variant LOW c.3753C>T|p.Ser1251Ser S295