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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g21680 A06 11673298 C T upstream_gene_variant MODIFIER c.-4163C>T| S207
2 BAA06g21680 A06 11673759 G A upstream_gene_variant MODIFIER c.-3702G>A| S129
3 BAA06g21680 A06 11674280 G A upstream_gene_variant MODIFIER c.-3181G>A| S169
4 BAA06g21680 A06 11674845 G A upstream_gene_variant MODIFIER c.-2616G>A| S123
5 BAA06g21680 A06 11674911 C T upstream_gene_variant MODIFIER c.-2550C>T| S291
6 BAA06g21680 A06 11675014 G A upstream_gene_variant MODIFIER c.-2447G>A| S32
7 BAA06g21680 A06 11675491 C T upstream_gene_variant MODIFIER c.-1970C>T| S15
S2
S3
8 BAA06g21680 A06 11676077 C T upstream_gene_variant MODIFIER c.-1384C>T| S191
9 BAA06g21680 A06 11676104 C T upstream_gene_variant MODIFIER c.-1357C>T| S164
10 BAA06g21680 A06 11676480 C T upstream_gene_variant MODIFIER c.-981C>T| S98
11 BAA06g21680 A06 11677794 G A missense_variant&splice_region_variant MODERATE c.271G>A|p.Val91Ile S117
12 BAA06g21680 A06 11678219 G A missense_variant MODERATE c.622G>A|p.Glu208Lys S158
13 BAA06g21680 A06 11678660 G A missense_variant MODERATE c.994G>A|p.Val332Ile S122
14 BAA06g21680 A06 11678794 C T synonymous_variant LOW c.1128C>T|p.Asn376Asn S163
15 BAA06g21680 A06 11679110 G A missense_variant MODERATE c.1444G>A|p.Gly482Ser S32
16 BAA06g21680 A06 11679303 C T missense_variant MODERATE c.1637C>T|p.Ser546Leu S155