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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g45180 A02 37057010 G A missense_variant MODERATE c.587G>A|p.Ser196Asn S79
S91
2 BAA02g45180 A02 37057056 G A missense_variant MODERATE c.633G>A|p.Met211Ile S125
3 BAA02g45180 A02 37059126 C T synonymous_variant LOW c.1590C>T|p.Leu530Leu S17
4 BAA02g45180 A02 37061446 C T missense_variant MODERATE c.2666C>T|p.Pro889Leu S202
5 BAA02g45180 A02 37061710 C T intron_variant MODIFIER c.2695-51C>T| S122
6 BAA02g45180 A02 37062857 G A splice_region_variant&synonymous_variant LOW c.3393G>A|p.Leu1131Leu S168
7 BAA02g45180 A02 37063308 C T intron_variant MODIFIER c.3553-39C>T| S15
8 BAA02g45180 A02 37063548 G A missense_variant&splice_region_variant MODERATE c.3754G>A|p.Glu1252Lys S13
S246
9 BAA02g45180 A02 37064298 G A missense_variant MODERATE c.4102G>A|p.Asp1368Asn S261
10 BAA02g45180 A02 37065063 G A intron_variant MODIFIER c.4455+26G>A| S197
11 BAA02g45180 A02 37065093 A T intron_variant MODIFIER c.4456-33A>T| S11
12 BAA02g45180 A02 37065618 C T intron_variant MODIFIER c.4797+54C>T| S303
13 BAA02g45180 A02 37066132 G A missense_variant MODERATE c.5059G>A|p.Glu1687Lys S279
14 BAA02g45180 A02 37067598 C T synonymous_variant LOW c.5739C>T|p.Asp1913Asp S104
S52
15 BAA02g45180 A02 37067800 G A intron_variant MODIFIER c.5896-44G>A| S37
16 BAA02g45180 A02 37068229 C T intron_variant MODIFIER c.6168+29C>T| S115
17 BAA02g45180 A02 37068887 C T downstream_gene_variant MODIFIER c.*519C>T| S112
18 BAA02g45180 A02 37070300 G A downstream_gene_variant MODIFIER c.*1932G>A| S265
S39
19 BAA02g45180 A02 37070904 C T downstream_gene_variant MODIFIER c.*2536C>T| S15
20 BAA02g45180 A02 37073298 C T downstream_gene_variant MODIFIER c.*4930C>T| S64