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 BAA10g05530 A10 2815712 C T missense_variant MODERATE c.3298G>A|p.Glu1100Lys S270
2 BAA10g05530 A10 2816179 C T missense_variant MODERATE c.2938G>A|p.Gly980Arg S298
3 BAA10g05530 A10 2817364 G A synonymous_variant LOW c.2424C>T|p.Phe808Phe S217
S248
4 BAA10g05530 A10 2817377 C T missense_variant MODERATE c.2411G>A|p.Gly804Glu S161
S228
S289
5 BAA10g05530 A10 2817463 C T synonymous_variant LOW c.2325G>A|p.Arg775Arg S210
S225
6 BAA10g05530 A10 2817642 G A synonymous_variant LOW c.2217C>T|p.Pro739Pro S42
7 BAA10g05530 A10 2817665 G A missense_variant MODERATE c.2194C>T|p.Arg732Cys S267
8 BAA10g05530 A10 2818031 C T missense_variant MODERATE c.2005G>A|p.Glu669Lys S281
9 BAA10g05530 A10 2818486 C T synonymous_variant LOW c.1647G>A|p.Lys549Lys S201
10 BAA10g05530 A10 2819849 G A missense_variant MODERATE c.764C>T|p.Pro255Leu S164
11 BAA10g05530 A10 2820358 G A synonymous_variant LOW c.448C>T|p.Leu150Leu S94
12 BAA10g05530 A10 2823669 C T upstream_gene_variant MODIFIER c.-2597G>A| S73
13 BAA10g05530 A10 2824884 C T upstream_gene_variant MODIFIER c.-3812G>A| S122