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 BAA10g12420 A10 13846768 C T splice_region_variant&intron_variant LOW c.2976+7G>A| S68
2 BAA10g12420 A10 13846835 G A synonymous_variant LOW c.2916C>T|p.Leu972Leu S251
3 BAA10g12420 A10 13847556 G A missense_variant MODERATE c.2456C>T|p.Pro819Leu S59
4 BAA10g12420 A10 13848858 G A missense_variant MODERATE c.1238C>T|p.Thr413Ile S262
5 BAA10g12420 A10 13848926 C T synonymous_variant LOW c.1170G>A|p.Lys390Lys S206
S26
6 BAA10g12420 A10 13849296 G A synonymous_variant LOW c.885C>T|p.Asn295Asn S15
S3
7 BAA10g12420 A10 13849332 C T synonymous_variant LOW c.849G>A|p.Gln283Gln S196
8 BAA10g12420 A10 13849947 G A synonymous_variant LOW c.234C>T|p.Ser78Ser S219
S72
9 BAA10g12420 A10 13850500 G A upstream_gene_variant MODIFIER c.-236C>T| S65
10 BAA10g12420 A10 13851025 C T upstream_gene_variant MODIFIER c.-761G>A| S63
11 BAA10g12420 A10 13851306 G A upstream_gene_variant MODIFIER c.-1042C>T| S139
12 BAA10g12420 A10 13851484 G A upstream_gene_variant MODIFIER c.-1220C>T| S273
13 BAA10g12420 A10 13853286 G A upstream_gene_variant MODIFIER c.-3022C>T| S221