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


Gene ID

Results: 1 - 27 of 27 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g39140 A06 25613309 G A upstream_gene_variant MODIFIER c.-4025G>A| S213
2 BAA06g39140 A06 25613318 C G upstream_gene_variant MODIFIER c.-4016C>G| S223
3 BAA06g39140 A06 25613319 A T upstream_gene_variant MODIFIER c.-4015A>T| S223
4 BAA06g39140 A06 25616223 G A upstream_gene_variant MODIFIER c.-1111G>A| S23
5 BAA06g39140 A06 25616409 G A upstream_gene_variant MODIFIER c.-925G>A| S193
6 BAA06g39140 A06 25616454 G A upstream_gene_variant MODIFIER c.-880G>A| S1
S90
7 BAA06g39140 A06 25616732 C T upstream_gene_variant MODIFIER c.-602C>T| S142
8 BAA06g39140 A06 25616764 C T upstream_gene_variant MODIFIER c.-570C>T| S155
S211
S47
9 BAA06g39140 A06 25616919 C T upstream_gene_variant MODIFIER c.-415C>T| S15
S3
10 BAA06g39140 A06 25617119 G A upstream_gene_variant MODIFIER c.-215G>A| S190
11 BAA06g39140 A06 25617151 C T upstream_gene_variant MODIFIER c.-183C>T| S107
12 BAA06g39140 A06 25618152 C T splice_region_variant&intron_variant LOW c.300-4C>T| S263
13 BAA06g39140 A06 25618743 G A missense_variant&splice_region_variant MODERATE c.373G>A|p.Asp125Asn S119
14 BAA06g39140 A06 25618814 C T intron_variant MODIFIER c.431+13C>T| S43
15 BAA06g39140 A06 25619602 C T synonymous_variant LOW c.579C>T|p.Asn193Asn S171
16 BAA06g39140 A06 25619610 G A missense_variant MODERATE c.587G>A|p.Gly196Glu S75
S81
17 BAA06g39140 A06 25619861 G A missense_variant MODERATE c.838G>A|p.Val280Ile S185
18 BAA06g39140 A06 25620451 G A intron_variant MODIFIER c.1184-44G>A| S1
S90
19 BAA06g39140 A06 25620983 C T missense_variant MODERATE c.1484C>T|p.Ser495Phe S212
20 BAA06g39140 A06 25621428 G A missense_variant MODERATE c.1837G>A|p.Glu613Lys S13
21 BAA06g39140 A06 25621497 C T intron_variant MODIFIER c.1880+26C>T| S298
22 BAA06g39140 A06 25622318 G A downstream_gene_variant MODIFIER c.*133G>A| S152
23 BAA06g39140 A06 25622351 G A downstream_gene_variant MODIFIER c.*166G>A| S208
24 BAA06g39140 A06 25622554 G A downstream_gene_variant MODIFIER c.*369G>A| S125
25 BAA06g39140 A06 25624862 G A downstream_gene_variant MODIFIER c.*2677G>A| S89