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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g41290 A02 34644823 G A upstream_gene_variant MODIFIER c.-4786G>A| S66
2 BAA02g41290 A02 34645099 C T upstream_gene_variant MODIFIER c.-4510C>T| S19
3 BAA02g41290 A02 34645139 G A upstream_gene_variant MODIFIER c.-4470G>A| S2
4 BAA02g41290 A02 34646330 C T upstream_gene_variant MODIFIER c.-3279C>T| S122
5 BAA02g41290 A02 34648446 C T upstream_gene_variant MODIFIER c.-1163C>T| S122
6 BAA02g41290 A02 34649348 C T upstream_gene_variant MODIFIER c.-261C>T| S202
7 BAA02g41290 A02 34649357 C T upstream_gene_variant MODIFIER c.-252C>T| S33
8 BAA02g41290 A02 34649811 G A missense_variant MODERATE c.203G>A|p.Gly68Asp S175
9 BAA02g41290 A02 34650133 C T synonymous_variant LOW c.525C>T|p.Ile175Ile S260
10 BAA02g41290 A02 34652356 G A synonymous_variant LOW c.1476G>A|p.Glu492Glu S4
11 BAA02g41290 A02 34652491 G A stop_gained HIGH c.1611G>A|p.Trp537* S297
12 BAA02g41290 A02 34652842 G A splice_region_variant&intron_variant LOW c.1863+5G>A| S238
13 BAA02g41290 A02 34653166 G A missense_variant MODERATE c.1948G>A|p.Val650Met S230
14 BAA02g41290 A02 34653403 C T missense_variant MODERATE c.2185C>T|p.Pro729Ser S53
15 BAA02g41290 A02 34653651 G A synonymous_variant LOW c.2433G>A|p.Ser811Ser S251
16 BAA02g41290 A02 34654634 C T downstream_gene_variant MODIFIER c.*566C>T| S167
17 BAA02g41290 A02 34654667 G A downstream_gene_variant MODIFIER c.*599G>A| S302
18 BAA02g41290 A02 34655249 C T downstream_gene_variant MODIFIER c.*1181C>T| S128