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


Gene ID

Results: 1 - 21 of 21 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g09590 A10 11526559 C T downstream_gene_variant MODIFIER c.*4093G>A| S155
S211
2 BAA10g09590 A10 11527052 C T downstream_gene_variant MODIFIER c.*3600G>A| S143
3 BAA10g09590 A10 11527170 C T downstream_gene_variant MODIFIER c.*3482G>A| S204
4 BAA10g09590 A10 11527210 C T downstream_gene_variant MODIFIER c.*3442G>A| S259
5 BAA10g09590 A10 11527231 G A downstream_gene_variant MODIFIER c.*3421C>T| S138
S288
6 BAA10g09590 A10 11527531 C T downstream_gene_variant MODIFIER c.*3121G>A| S224
7 BAA10g09590 A10 11530027 C T downstream_gene_variant MODIFIER c.*625G>A| S150
8 BAA10g09590 A10 11530352 T C downstream_gene_variant MODIFIER c.*300A>G| S111
9 BAA10g09590 A10 11530573 A T downstream_gene_variant MODIFIER c.*79T>A| S134
10 BAA10g09590 A10 11530822 C T missense_variant MODERATE c.910G>A|p.Val304Met S91
11 BAA10g09590 A10 11530969 C T missense_variant MODERATE c.763G>A|p.Glu255Lys S249
12 BAA10g09590 A10 11531386 G A missense_variant MODERATE c.553C>T|p.Pro185Ser S292
13 BAA10g09590 A10 11531573 C T intron_variant MODIFIER c.383-17G>A| S287
14 BAA10g09590 A10 11531718 G A intron_variant MODIFIER c.383-162C>T| S221
15 BAA10g09590 A10 11532913 C T missense_variant&splice_region_variant MODERATE c.205G>A|p.Gly69Arg S37
16 BAA10g09590 A10 11534327 G A upstream_gene_variant MODIFIER c.-928C>T| S1
S90
17 BAA10g09590 A10 11534334 G A upstream_gene_variant MODIFIER c.-935C>T| S303
18 BAA10g09590 A10 11534514 G T upstream_gene_variant MODIFIER c.-1115C>A| S256
19 BAA10g09590 A10 11535986 G A upstream_gene_variant MODIFIER c.-2587C>T| S172
20 BAA10g09590 A10 11537485 C T upstream_gene_variant MODIFIER c.-4086G>A| S255
21 BAA10g09590 A10 11537750 C T upstream_gene_variant MODIFIER c.-4351G>A| S150