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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g10990 A02 4943494 C T synonymous_variant LOW c.2526G>A|p.Gly842Gly S186
2 BAA02g10990 A02 4943529 G A synonymous_variant LOW c.2491C>T|p.Leu831Leu S296
3 BAA02g10990 A02 4943700 G A missense_variant MODERATE c.2320C>T|p.Pro774Ser S223
4 BAA02g10990 A02 4944696 C T synonymous_variant LOW c.1617G>A|p.Gln539Gln S277
5 BAA02g10990 A02 4945375 G A synonymous_variant LOW c.1245C>T|p.Phe415Phe S264
6 BAA02g10990 A02 4945504 C T missense_variant MODERATE c.1116G>A|p.Met372Ile S263
7 BAA02g10990 A02 4945984 C T missense_variant MODERATE c.728G>A|p.Ser243Asn S100
8 BAA02g10990 A02 4946450 C T missense_variant MODERATE c.262G>A|p.Gly88Arg S172
S217
S275
9 BAA02g10990 A02 4946505 G A synonymous_variant LOW c.207C>T|p.Phe69Phe S228
10 BAA02g10990 A02 4946610 C T missense_variant&splice_region_variant MODERATE c.199G>A|p.Ala67Thr S144
11 BAA02g10990 A02 4946728 G A synonymous_variant LOW c.81C>T|p.Ala27Ala S247
12 BAA02g10990 A02 4946810 T G upstream_gene_variant MODIFIER c.-2A>C| S298
13 BAA02g10990 A02 4946822 G A upstream_gene_variant MODIFIER c.-14C>T| S308
14 BAA02g10990 A02 4947541 G A upstream_gene_variant MODIFIER c.-733C>T| S155
15 BAA02g10990 A02 4948099 T A upstream_gene_variant MODIFIER c.-1291A>T| S213
16 BAA02g10990 A02 4948222 G A upstream_gene_variant MODIFIER c.-1414C>T| S149
17 BAA02g10990 A02 4948900 C T upstream_gene_variant MODIFIER c.-2092G>A| S130
18 BAA02g10990 A02 4949158 A G upstream_gene_variant MODIFIER c.-2350T>C| S148
S30
S31
19 BAA02g10990 A02 4949257 T A upstream_gene_variant MODIFIER c.-2449A>T| S200
20 BAA02g10990 A02 4949547 G A upstream_gene_variant MODIFIER c.-2739C>T| S96
21 BAA02g10990 A02 4950073 G A upstream_gene_variant MODIFIER c.-3265C>T| S48
22 BAA02g10990 A02 4951214 C T upstream_gene_variant MODIFIER c.-4406G>A| S231
S289
S290