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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g15130 A07 22488716 G A upstream_gene_variant MODIFIER c.-3180G>A| S129
2 BAA07g15130 A07 22492094 C T missense_variant MODERATE c.199C>T|p.Pro67Ser S126
3 BAA07g15130 A07 22492384 C T synonymous_variant LOW c.489C>T|p.Phe163Phe S148
S30
4 BAA07g15130 A07 22492679 C T missense_variant MODERATE c.784C>T|p.Pro262Ser S162
5 BAA07g15130 A07 22492756 C T synonymous_variant LOW c.861C>T|p.Arg287Arg S132
S137
S215
6 BAA07g15130 A07 22492907 G A missense_variant MODERATE c.1012G>A|p.Val338Met S17
7 BAA07g15130 A07 22492957 C T synonymous_variant LOW c.1062C>T|p.Asn354Asn S165
8 BAA07g15130 A07 22493429 G A missense_variant MODERATE c.1534G>A|p.Ala512Thr S79
S91
9 BAA07g15130 A07 22494145 C T stop_gained HIGH c.2047C>T|p.Gln683* S67
10 BAA07g15130 A07 22494329 C T missense_variant MODERATE c.2231C>T|p.Thr744Ile S169
11 BAA07g15130 A07 22494919 C T missense_variant MODERATE c.2821C>T|p.Leu941Phe S216
12 BAA07g15130 A07 22495178 C T intron_variant MODIFIER c.2931+149C>T| S150
13 BAA07g15130 A07 22495603 C T intron_variant MODIFIER c.2931+574C>T| S275
14 BAA07g15130 A07 22499952 C T downstream_gene_variant MODIFIER c.*2511C>T| S187
15 BAA07g15130 A07 22500234 C T downstream_gene_variant MODIFIER c.*2793C>T| S197