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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g05600 A10 2875396 G A upstream_gene_variant MODIFIER c.-4495G>A| S16
2 BAA10g05600 A10 2875580 G A upstream_gene_variant MODIFIER c.-4311G>A| S15
S3
3 BAA10g05600 A10 2875655 C T upstream_gene_variant MODIFIER c.-4236C>T| S131
4 BAA10g05600 A10 2875692 G A upstream_gene_variant MODIFIER c.-4199G>A| S261
5 BAA10g05600 A10 2875812 G A upstream_gene_variant MODIFIER c.-4079G>A| S174
S216
S241
S265
S27
S39
6 BAA10g05600 A10 2876075 C T upstream_gene_variant MODIFIER c.-3816C>T| S287
7 BAA10g05600 A10 2877655 C T upstream_gene_variant MODIFIER c.-2236C>T| S229
8 BAA10g05600 A10 2878345 C T upstream_gene_variant MODIFIER c.-1546C>T| S204
9 BAA10g05600 A10 2879377 C T upstream_gene_variant MODIFIER c.-514C>T| S225
10 BAA10g05600 A10 2879471 G A upstream_gene_variant MODIFIER c.-420G>A| S32
11 BAA10g05600 A10 2879647 C T upstream_gene_variant MODIFIER c.-244C>T| S14
12 BAA10g05600 A10 2880129 G A splice_acceptor_variant&intron_variant HIGH c.185-1G>A| S133
13 BAA10g05600 A10 2880175 G A stop_gained HIGH c.230G>A|p.Trp77* S55
14 BAA10g05600 A10 2880442 C T missense_variant MODERATE c.497C>T|p.Ser166Phe S199
15 BAA10g05600 A10 2880447 C T missense_variant MODERATE c.502C>T|p.Pro168Ser S28
16 BAA10g05600 A10 2880583 G A missense_variant&splice_region_variant MODERATE c.544G>A|p.Ala182Thr S95