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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g19050 A10 17615940 G A missense_variant MODERATE c.185G>A|p.Gly62Glu S262
2 BAA10g19050 A10 17616480 C T intron_variant MODIFIER c.516+95C>T| S174
S216
S265
3 BAA10g19050 A10 17616590 G A missense_variant MODERATE c.520G>A|p.Asp174Asn S264
4 BAA10g19050 A10 17616597 G A missense_variant MODERATE c.527G>A|p.Arg176Lys S250
5 BAA10g19050 A10 17616683 G A missense_variant MODERATE c.613G>A|p.Glu205Lys S4
6 BAA10g19050 A10 17617333 C T missense_variant MODERATE c.827C>T|p.Ser276Phe S269
7 BAA10g19050 A10 17617646 G A missense_variant MODERATE c.1036G>A|p.Val346Ile S155
8 BAA10g19050 A10 17618403 C T splice_region_variant&intron_variant LOW c.1605-8C>T| S190
9 BAA10g19050 A10 17618787 G A missense_variant MODERATE c.1720G>A|p.Asp574Asn S181
10 BAA10g19050 A10 17619261 C T missense_variant MODERATE c.1936C>T|p.Pro646Ser S46
11 BAA10g19050 A10 17619735 C T synonymous_variant LOW c.2410C>T|p.Leu804Leu S135
12 BAA10g19050 A10 17619777 C T missense_variant MODERATE c.2452C>T|p.Pro818Ser S260
13 BAA10g19050 A10 17624812 C T downstream_gene_variant MODIFIER c.*3341C>T| S204
14 BAA10g19050 A10 17625017 G A downstream_gene_variant MODIFIER c.*3546G>A| S162
15 BAA10g19050 A10 17625519 C T downstream_gene_variant MODIFIER c.*4048C>T| S194
16 BAA10g19050 A10 17625743 G A downstream_gene_variant MODIFIER c.*4272G>A| S262
17 BAA10g19050 A10 17626369 G A downstream_gene_variant MODIFIER c.*4898G>A| S245
18 BAA10g19050 A10 17626371 G A downstream_gene_variant MODIFIER c.*4900G>A| S262
19 BAA10g19050 A10 17626456 G A downstream_gene_variant MODIFIER c.*4985G>A| S63