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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g42980 A07 37044908 G A missense_variant MODERATE c.3554C>T|p.Ser1185Leu S84
S93
2 BAA07g42980 A07 37048014 C T synonymous_variant LOW c.2172G>A|p.Arg724Arg S284
3 BAA07g42980 A07 37048283 G A missense_variant MODERATE c.1978C>T|p.Pro660Ser S119
4 BAA07g42980 A07 37049596 G A intron_variant MODIFIER c.1639-899C>T| S107
5 BAA07g42980 A07 37049648 C T intron_variant MODIFIER c.1639-951G>A| S18
6 BAA07g42980 A07 37050069 G A intron_variant MODIFIER c.1639-1372C>T| S6
7 BAA07g42980 A07 37050247 C T intron_variant MODIFIER c.1639-1550G>A| S261
8 BAA07g42980 A07 37050330 G A intron_variant MODIFIER c.1639-1633C>T| S52
9 BAA07g42980 A07 37050341 G A intron_variant MODIFIER c.1639-1644C>T| S155
S211
10 BAA07g42980 A07 37050829 C T intron_variant MODIFIER c.1638+1821G>A| S203
11 BAA07g42980 A07 37051261 C T intron_variant MODIFIER c.1638+1389G>A| S133
12 BAA07g42980 A07 37052219 G A intron_variant MODIFIER c.1638+431C>T| S298
13 BAA07g42980 A07 37052332 C T intron_variant MODIFIER c.1638+318G>A| S213
14 BAA07g42980 A07 37053247 G A synonymous_variant LOW c.1041C>T|p.Pro347Pro S70
15 BAA07g42980 A07 37056798 C T missense_variant MODERATE c.311G>A|p.Ser104Asn S34
16 BAA07g42980 A07 37056846 G A missense_variant MODERATE c.263C>T|p.Thr88Ile S152
17 BAA07g42980 A07 37057171 C T missense_variant MODERATE c.173G>A|p.Gly58Glu S260
18 BAA07g42980 A07 37060149 C T upstream_gene_variant MODIFIER c.-2709G>A| S128