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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g01780 A07 1294985 C T upstream_gene_variant MODIFIER c.-4935C>T| S18
2 BAA07g01780 A07 1295449 C T upstream_gene_variant MODIFIER c.-4471C>T| S63
3 BAA07g01780 A07 1296144 G A upstream_gene_variant MODIFIER c.-3776G>A| S177
4 BAA07g01780 A07 1297590 C T upstream_gene_variant MODIFIER c.-2330C>T| S69
5 BAA07g01780 A07 1298889 C T upstream_gene_variant MODIFIER c.-1031C>T| S301
S304
6 BAA07g01780 A07 1299097 C T upstream_gene_variant MODIFIER c.-823C>T| S213
7 BAA07g01780 A07 1299800 C T upstream_gene_variant MODIFIER c.-120C>T| S249
8 BAA07g01780 A07 1300124 C T stop_gained HIGH c.205C>T|p.Gln69* S167
9 BAA07g01780 A07 1300126 G A synonymous_variant LOW c.207G>A|p.Gln69Gln S175
10 BAA07g01780 A07 1300135 C T synonymous_variant LOW c.216C>T|p.Phe72Phe S19
11 BAA07g01780 A07 1300481 C T missense_variant MODERATE c.562C>T|p.Pro188Ser S256
12 BAA07g01780 A07 1300549 C T synonymous_variant LOW c.630C>T|p.Phe210Phe S85
13 BAA07g01780 A07 1300703 G A missense_variant MODERATE c.784G>A|p.Asp262Asn S71
14 BAA07g01780 A07 1302388 G A missense_variant MODERATE c.2251G>A|p.Ala751Thr S219
S72