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 BAA08g29290 A08 20156217 C T missense_variant MODERATE c.140C>T|p.Ala47Val S192
2 BAA08g29290 A08 20157729 C T synonymous_variant LOW c.633C>T|p.Arg211Arg S112
3 BAA08g29290 A08 20158324 G A missense_variant MODERATE c.1070G>A|p.Arg357Gln S62
4 BAA08g29290 A08 20158674 C T synonymous_variant LOW c.1237C>T|p.Leu413Leu S268
5 BAA08g29290 A08 20159095 G A splice_acceptor_variant&intron_variant HIGH c.1326-1G>A| S118
6 BAA08g29290 A08 20159106 G A missense_variant MODERATE c.1336G>A|p.Asp446Asn S297
7 BAA08g29290 A08 20159309 G A downstream_gene_variant MODIFIER c.*135G>A| S246
8 BAA08g29290 A08 20159432 G A downstream_gene_variant MODIFIER c.*258G>A| S267
9 BAA08g29290 A08 20159440 C T downstream_gene_variant MODIFIER c.*266C>T| S268
10 BAA08g29290 A08 20160323 C T downstream_gene_variant MODIFIER c.*1149C>T| S162
11 BAA08g29290 A08 20161484 C T downstream_gene_variant MODIFIER c.*2310C>T| S13
12 BAA08g29290 A08 20162136 G A downstream_gene_variant MODIFIER c.*2962G>A| S183
13 BAA08g29290 A08 20162160 C T downstream_gene_variant MODIFIER c.*2986C>T| S151
S157
S167
S236
S262
S263