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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g01120 A06 766361 G A upstream_gene_variant MODIFIER c.-3987G>A| S40
S49
2 BAA06g01120 A06 766496 G A upstream_gene_variant MODIFIER c.-3852G>A| S252
3 BAA06g01120 A06 767793 C T upstream_gene_variant MODIFIER c.-2555C>T| S181
4 BAA06g01120 A06 767807 C T upstream_gene_variant MODIFIER c.-2541C>T| S190
5 BAA06g01120 A06 767975 G A upstream_gene_variant MODIFIER c.-2373G>A| S170
6 BAA06g01120 A06 770460 G A missense_variant MODERATE c.113G>A|p.Arg38Lys S260
7 BAA06g01120 A06 770518 G A stop_gained HIGH c.171G>A|p.Trp57* S15
S156
S2
S213
S3
S34
S4
S6
8 BAA06g01120 A06 770808 C T missense_variant MODERATE c.461C>T|p.Ser154Phe S153
9 BAA06g01120 A06 770882 G A missense_variant MODERATE c.535G>A|p.Asp179Asn S239
10 BAA06g01120 A06 771516 C T missense_variant MODERATE c.1169C>T|p.Ser390Phe S265
11 BAA06g01120 A06 771588 C T missense_variant MODERATE c.1241C>T|p.Ser414Leu S244
12 BAA06g01120 A06 772349 C T missense_variant MODERATE c.2002C>T|p.Leu668Phe S283
13 BAA06g01120 A06 772415 C T missense_variant MODERATE c.2068C>T|p.Pro690Ser S117
14 BAA06g01120 A06 772607 C T missense_variant MODERATE c.2260C>T|p.His754Tyr S110
15 BAA06g01120 A06 773243 G A missense_variant MODERATE c.2896G>A|p.Glu966Lys S162
16 BAA06g01120 A06 773728 C T synonymous_variant LOW c.3381C>T|p.Leu1127Leu S51
17 BAA06g01120 A06 773895 C T missense_variant MODERATE c.3548C>T|p.Ala1183Val S139