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 BAA01g39920 A01 26515141 C T missense_variant MODERATE c.1810G>A|p.Gly604Arg S120
2 BAA01g39920 A01 26515476 G A missense_variant MODERATE c.1475C>T|p.Ser492Phe S105
3 BAA01g39920 A01 26515532 C T synonymous_variant LOW c.1419G>A|p.Gln473Gln S303
4 BAA01g39920 A01 26515772 G A missense_variant MODERATE c.1271C>T|p.Ser424Phe S45
5 BAA01g39920 A01 26516088 G A missense_variant MODERATE c.1123C>T|p.His375Tyr S160
6 BAA01g39920 A01 26518011 C T missense_variant MODERATE c.364G>A|p.Gly122Ser S48
7 BAA01g39920 A01 26520016 C T intron_variant MODIFIER c.46-1349G>A| S134
8 BAA01g39920 A01 26520899 C T intron_variant MODIFIER c.46-2232G>A| S182
9 BAA01g39920 A01 26523066 G A intron_variant MODIFIER c.46-4399C>T| S281
10 BAA01g39920 A01 26523125 C T intron_variant MODIFIER c.46-4458G>A| S293
11 BAA01g39920 A01 26523775 G A intron_variant MODIFIER c.45+3942C>T| S71
12 BAA01g39920 A01 26524477 C T intron_variant MODIFIER c.45+3240G>A| S289
S290
13 BAA01g39920 A01 26528682 C T upstream_gene_variant MODIFIER c.-921G>A| S88