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 BAA10g06960 A10 3727071 G A upstream_gene_variant MODIFIER c.-4413G>A| S279
2 BAA10g06960 A10 3727077 G A upstream_gene_variant MODIFIER c.-4407G>A| S215
3 BAA10g06960 A10 3727202 C T upstream_gene_variant MODIFIER c.-4282C>T| S143
4 BAA10g06960 A10 3727824 G A upstream_gene_variant MODIFIER c.-3660G>A| S295
5 BAA10g06960 A10 3728003 C T upstream_gene_variant MODIFIER c.-3481C>T| S143
6 BAA10g06960 A10 3728604 G A upstream_gene_variant MODIFIER c.-2880G>A| S76
7 BAA10g06960 A10 3729022 C T upstream_gene_variant MODIFIER c.-2462C>T| S56
8 BAA10g06960 A10 3733072 G A intron_variant MODIFIER c.837+35G>A| S280
9 BAA10g06960 A10 3733134 G A missense_variant MODERATE c.851G>A|p.Gly284Glu S85
10 BAA10g06960 A10 3733262 G A missense_variant MODERATE c.979G>A|p.Glu327Lys S134
11 BAA10g06960 A10 3733702 G A stop_gained HIGH c.1347G>A|p.Trp449* S7
12 BAA10g06960 A10 3734585 C T downstream_gene_variant MODIFIER c.*856C>T| S44
13 BAA10g06960 A10 3737539 G A downstream_gene_variant MODIFIER c.*3810G>A| S282
14 BAA10g06960 A10 3737618 G A downstream_gene_variant MODIFIER c.*3889G>A| S263
15 BAA10g06960 A10 3737829 C T downstream_gene_variant MODIFIER c.*4100C>T| S294
16 BAA10g06960 A10 3738010 G A downstream_gene_variant MODIFIER c.*4281G>A| S1
S90
17 BAA10g06960 A10 3738192 C T downstream_gene_variant MODIFIER c.*4463C>T| S308
18 BAA10g06960 A10 3738341 C T downstream_gene_variant MODIFIER c.*4612C>T| S65
19 BAA10g06960 A10 3738681 C T downstream_gene_variant MODIFIER c.*4952C>T| S42