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 BAA07g02180 A07 1639466 G A upstream_gene_variant MODIFIER c.-4920G>A| S142
2 BAA07g02180 A07 1640074 G A upstream_gene_variant MODIFIER c.-4312G>A| S225
S73
3 BAA07g02180 A07 1640201 C T upstream_gene_variant MODIFIER c.-4185C>T| S133
4 BAA07g02180 A07 1641051 C T upstream_gene_variant MODIFIER c.-3335C>T| S155
5 BAA07g02180 A07 1641373 G A upstream_gene_variant MODIFIER c.-3013G>A| S123
6 BAA07g02180 A07 1643650 C T upstream_gene_variant MODIFIER c.-736C>T| S140
S28
7 BAA07g02180 A07 1644282 G A upstream_gene_variant MODIFIER c.-104G>A| S131
8 BAA07g02180 A07 1645056 G A missense_variant MODERATE c.352G>A|p.Ala118Thr S76
9 BAA07g02180 A07 1645173 G A missense_variant MODERATE c.373G>A|p.Gly125Ser S74
10 BAA07g02180 A07 1645174 G A missense_variant MODERATE c.374G>A|p.Gly125Asp S112
11 BAA07g02180 A07 1645576 C T intron_variant MODIFIER c.416+360C>T| S155
S211
12 BAA07g02180 A07 1645805 C T intron_variant MODIFIER c.416+589C>T| S128
13 BAA07g02180 A07 1646290 C T intron_variant MODIFIER c.417-137C>T| S246
14 BAA07g02180 A07 1646304 G A intron_variant MODIFIER c.417-123G>A| S119
15 BAA07g02180 A07 1646474 C T missense_variant MODERATE c.464C>T|p.Thr155Ile S104
S52
16 BAA07g02180 A07 1646545 G A missense_variant MODERATE c.535G>A|p.Asp179Asn S15
S3
17 BAA07g02180 A07 1646786 C T downstream_gene_variant MODIFIER c.*14C>T| S23
18 BAA07g02180 A07 1649831 G A downstream_gene_variant MODIFIER c.*3059G>A| S237
19 BAA07g02180 A07 1650164 G A downstream_gene_variant MODIFIER c.*3392G>A| S16
20 BAA07g02180 A07 1651640 C T downstream_gene_variant MODIFIER c.*4868C>T| S69