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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g17020 A10 16583621 G A missense_variant MODERATE c.1064C>T|p.Ser355Phe S148
S30
S31
2 BAA10g17020 A10 16583663 C T missense_variant MODERATE c.1022G>A|p.Arg341Lys S23
3 BAA10g17020 A10 16583727 G A missense_variant MODERATE c.958C>T|p.Pro320Ser S127
4 BAA10g17020 A10 16583814 G A missense_variant MODERATE c.871C>T|p.Pro291Ser S155
5 BAA10g17020 A10 16583864 C T missense_variant MODERATE c.821G>A|p.Ser274Asn S133
6 BAA10g17020 A10 16585827 G A intron_variant MODIFIER c.598-1660C>T| S16
7 BAA10g17020 A10 16586009 G C intron_variant MODIFIER c.598-1842C>G| S182
S292
S36
8 BAA10g17020 A10 16586360 T A intron_variant MODIFIER c.598-2193A>T| S153
S236
S257
9 BAA10g17020 A10 16586568 G A intron_variant MODIFIER c.598-2401C>T| S180
10 BAA10g17020 A10 16587162 G A intron_variant MODIFIER c.598-2995C>T| S166
11 BAA10g17020 A10 16587740 C T intron_variant MODIFIER c.597+2785G>A| S297
12 BAA10g17020 A10 16587743 C T intron_variant MODIFIER c.597+2782G>A| S48
13 BAA10g17020 A10 16588601 C T intron_variant MODIFIER c.597+1924G>A| S193
14 BAA10g17020 A10 16590660 G A synonymous_variant LOW c.462C>T|p.Asn154Asn S139
15 BAA10g17020 A10 16592997 G A synonymous_variant LOW c.105C>T|p.Tyr35Tyr S172
S217
16 BAA10g17020 A10 16593166 G A upstream_gene_variant MODIFIER c.-65C>T| S9
17 BAA10g17020 A10 16595493 G A upstream_gene_variant MODIFIER c.-2392C>T| S39
18 BAA10g17020 A10 16595517 G A upstream_gene_variant MODIFIER c.-2416C>T| S16
19 BAA10g17020 A10 16595775 C T upstream_gene_variant MODIFIER c.-2674G>A| S237
20 BAA10g17020 A10 16596610 G A upstream_gene_variant MODIFIER c.-3509C>T| S261