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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g39920 A06 25992270 C T upstream_gene_variant MODIFIER c.-3890C>T| S15
S3
2 BAA06g39920 A06 25992475 C T upstream_gene_variant MODIFIER c.-3685C>T| S158
3 BAA06g39920 A06 25995152 C T upstream_gene_variant MODIFIER c.-1008C>T| S252
4 BAA06g39920 A06 25995319 C T upstream_gene_variant MODIFIER c.-841C>T| S192
5 BAA06g39920 A06 25996168 C T synonymous_variant LOW c.9C>T|p.Leu3Leu S210
6 BAA06g39920 A06 25996601 G A intron_variant MODIFIER c.137+305G>A| S192
7 BAA06g39920 A06 25996916 C T intron_variant MODIFIER c.137+620C>T| S279
8 BAA06g39920 A06 25997929 C T intron_variant MODIFIER c.137+1633C>T| S107
9 BAA06g39920 A06 25999065 G A intron_variant MODIFIER c.137+2769G>A| S9
10 BAA06g39920 A06 25999357 C T intron_variant MODIFIER c.138-2580C>T| S107
11 BAA06g39920 A06 25999642 G A intron_variant MODIFIER c.138-2295G>A| S67
12 BAA06g39920 A06 25999857 G A intron_variant MODIFIER c.138-2080G>A| S169
13 BAA06g39920 A06 26000680 C T intron_variant MODIFIER c.138-1257C>T| S230
14 BAA06g39920 A06 26002888 G A missense_variant MODERATE c.989G>A|p.Cys330Tyr S162
15 BAA06g39920 A06 26003057 C T synonymous_variant LOW c.1158C>T|p.Phe386Phe S252
16 BAA06g39920 A06 26003221 G A downstream_gene_variant MODIFIER c.*47G>A| S245
17 BAA06g39920 A06 26004025 G A downstream_gene_variant MODIFIER c.*851G>A| S164
18 BAA06g39920 A06 26005068 G A downstream_gene_variant MODIFIER c.*1894G>A| S76
19 BAA06g39920 A06 26005462 C T downstream_gene_variant MODIFIER c.*2288C>T| S109
20 BAA06g39920 A06 26005837 G A downstream_gene_variant MODIFIER c.*2663G>A| S218
21 BAA06g39920 A06 26005844 G A downstream_gene_variant MODIFIER c.*2670G>A| S12
22 BAA06g39920 A06 26007218 G A downstream_gene_variant MODIFIER c.*4044G>A| S231
23 BAA06g39920 A06 26007332 G A downstream_gene_variant MODIFIER c.*4158G>A| S276