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 BAA02g01900 A02 831997 C T missense_variant MODERATE c.1169C>T|p.Ser390Phe S174
2 BAA02g01900 A02 832240 G A splice_acceptor_variant&intron_variant HIGH c.1216-1G>A| S302
3 BAA02g01900 A02 832289 G A missense_variant MODERATE c.1264G>A|p.Asp422Asn S136
S305
4 BAA02g01900 A02 833228 C T missense_variant MODERATE c.2131C>T|p.Leu711Phe S120
5 BAA02g01900 A02 833340 C T missense_variant&splice_region_variant MODERATE c.2147C>T|p.Ala716Val S33
6 BAA02g01900 A02 834708 C T synonymous_variant LOW c.2643C>T|p.Ile881Ile S255
7 BAA02g01900 A02 836169 C T intron_variant MODIFIER c.3042+110C>T| S144
8 BAA02g01900 A02 836900 G A intron_variant MODIFIER c.3186+37G>A| S59
9 BAA02g01900 A02 837346 C T missense_variant MODERATE c.3314C>T|p.Ser1105Phe S218
10 BAA02g01900 A02 837546 C T missense_variant MODERATE c.3377C>T|p.Ser1126Leu S81
S85
11 BAA02g01900 A02 838163 G A missense_variant MODERATE c.3682G>A|p.Asp1228Asn S158
12 BAA02g01900 A02 838463 C T intron_variant MODIFIER c.3844-56C>T| S16
13 BAA02g01900 A02 839600 C T synonymous_variant LOW c.4413C>T|p.Pro1471Pro S179
14 BAA02g01900 A02 844617 G A downstream_gene_variant MODIFIER c.*3693G>A| S25