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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g07500 A10 4368192 C T downstream_gene_variant MODIFIER c.*4169G>A| S160
2 BAA10g07500 A10 4368264 G A downstream_gene_variant MODIFIER c.*4097C>T| S17
3 BAA10g07500 A10 4368400 G A downstream_gene_variant MODIFIER c.*3961C>T| S274
4 BAA10g07500 A10 4369081 C T downstream_gene_variant MODIFIER c.*3280G>A| S174
S27
5 BAA10g07500 A10 4369103 C T downstream_gene_variant MODIFIER c.*3258G>A| S36
6 BAA10g07500 A10 4369167 C T downstream_gene_variant MODIFIER c.*3194G>A| S17
7 BAA10g07500 A10 4369476 C T downstream_gene_variant MODIFIER c.*2885G>A| S294
8 BAA10g07500 A10 4369496 C T downstream_gene_variant MODIFIER c.*2865G>A| S126
9 BAA10g07500 A10 4370292 C T downstream_gene_variant MODIFIER c.*2069G>A| S298
10 BAA10g07500 A10 4370772 G A downstream_gene_variant MODIFIER c.*1589C>T| S125
11 BAA10g07500 A10 4370922 G A downstream_gene_variant MODIFIER c.*1439C>T| S95
12 BAA10g07500 A10 4372403 G A synonymous_variant LOW c.870C>T|p.Val290Val S212
13 BAA10g07500 A10 4372779 C T splice_region_variant&synonymous_variant LOW c.612G>A|p.Lys204Lys S67
14 BAA10g07500 A10 4372993 C T missense_variant MODERATE c.517G>A|p.Val173Ile S225
15 BAA10g07500 A10 4373118 C T intron_variant MODIFIER c.513+39G>A| S249
16 BAA10g07500 A10 4373491 G A missense_variant MODERATE c.298C>T|p.Leu100Phe S107
17 BAA10g07500 A10 4375549 C T upstream_gene_variant MODIFIER c.-1761G>A| S10
18 BAA10g07500 A10 4375735 G A upstream_gene_variant MODIFIER c.-1947C>T| S33
19 BAA10g07500 A10 4375826 G A upstream_gene_variant MODIFIER c.-2038C>T| S180
20 BAA10g07500 A10 4377783 C T upstream_gene_variant MODIFIER c.-3995G>A| S183
21 BAA10g07500 A10 4378237 G A upstream_gene_variant MODIFIER c.-4449C>T| S151
S263
22 BAA10g07500 A10 4378503 C T upstream_gene_variant MODIFIER c.-4715G>A| S150