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 BAA05g03920 A05 1944721 C T missense_variant MODERATE c.202C>T|p.Pro68Ser S180
2 BAA05g03920 A05 1944975 C T synonymous_variant LOW c.456C>T|p.Ile152Ile S128
3 BAA05g03920 A05 1945201 G A missense_variant MODERATE c.682G>A|p.Glu228Lys S169
4 BAA05g03920 A05 1945481 G A missense_variant MODERATE c.962G>A|p.Arg321Lys S200
5 BAA05g03920 A05 1946147 G A missense_variant MODERATE c.1628G>A|p.Gly543Asp S211
6 BAA05g03920 A05 1946748 G A missense_variant MODERATE c.2084G>A|p.Arg695Gln S144
7 BAA05g03920 A05 1946811 C T missense_variant MODERATE c.2147C>T|p.Ser716Phe S255
8 BAA05g03920 A05 1946836 C T synonymous_variant LOW c.2172C>T|p.Asp724Asp S94
9 BAA05g03920 A05 1947279 C T missense_variant MODERATE c.2615C>T|p.Ala872Val S171
10 BAA05g03920 A05 1948054 C T downstream_gene_variant MODIFIER c.*391C>T| S298
11 BAA05g03920 A05 1948758 C T downstream_gene_variant MODIFIER c.*1095C>T| S135
12 BAA05g03920 A05 1949049 C T downstream_gene_variant MODIFIER c.*1386C>T| S176
13 BAA05g03920 A05 1949059 C T downstream_gene_variant MODIFIER c.*1396C>T| S189