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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g04380 A07 3581887 G A downstream_gene_variant MODIFIER c.*4414C>T| S271
2 BAA07g04380 A07 3582464 C T downstream_gene_variant MODIFIER c.*3837G>A| S128
3 BAA07g04380 A07 3582842 G A downstream_gene_variant MODIFIER c.*3459C>T| S273
4 BAA07g04380 A07 3583078 G A downstream_gene_variant MODIFIER c.*3223C>T| S259
5 BAA07g04380 A07 3583240 C T downstream_gene_variant MODIFIER c.*3061G>A| S178
6 BAA07g04380 A07 3583297 A T downstream_gene_variant MODIFIER c.*3004T>A| S190
7 BAA07g04380 A07 3583691 G A downstream_gene_variant MODIFIER c.*2610C>T| S193
8 BAA07g04380 A07 3583900 G A downstream_gene_variant MODIFIER c.*2401C>T| S208
9 BAA07g04380 A07 3584132 G A downstream_gene_variant MODIFIER c.*2169C>T| S190
10 BAA07g04380 A07 3585019 C T downstream_gene_variant MODIFIER c.*1282G>A| S277
S287
11 BAA07g04380 A07 3585140 G A downstream_gene_variant MODIFIER c.*1161C>T| S187
12 BAA07g04380 A07 3585186 C T downstream_gene_variant MODIFIER c.*1115G>A| S152
13 BAA07g04380 A07 3585403 C T downstream_gene_variant MODIFIER c.*898G>A| S252
14 BAA07g04380 A07 3586701 G A intron_variant MODIFIER c.447-118C>T| S164
S224
15 BAA07g04380 A07 3589032 C T missense_variant MODERATE c.145G>A|p.Asp49Asn S212
16 BAA07g04380 A07 3589070 C T missense_variant MODERATE c.107G>A|p.Gly36Asp S298
17 BAA07g04380 A07 3589793 C T upstream_gene_variant MODIFIER c.-617G>A| S23
18 BAA07g04380 A07 3589990 C T upstream_gene_variant MODIFIER c.-814G>A| S173
19 BAA07g04380 A07 3593231 C T upstream_gene_variant MODIFIER c.-4055G>A| S126