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 BAA07g05870 A07 6716226 C T upstream_gene_variant MODIFIER c.-4873C>T| S98
2 BAA07g05870 A07 6716786 C T upstream_gene_variant MODIFIER c.-4313C>T| S58
3 BAA07g05870 A07 6719403 A T upstream_gene_variant MODIFIER c.-1696A>T| S138
4 BAA07g05870 A07 6720525 C T upstream_gene_variant MODIFIER c.-574C>T| S199
5 BAA07g05870 A07 6720542 G A upstream_gene_variant MODIFIER c.-557G>A| S187
6 BAA07g05870 A07 6720926 G A upstream_gene_variant MODIFIER c.-173G>A| S55
7 BAA07g05870 A07 6720933 C T upstream_gene_variant MODIFIER c.-166C>T| S283
8 BAA07g05870 A07 6721294 C T intron_variant MODIFIER c.25-49C>T| S240
9 BAA07g05870 A07 6721576 G A missense_variant MODERATE c.172G>A|p.Asp58Asn S256
10 BAA07g05870 A07 6721942 C T intron_variant MODIFIER c.330+108C>T| S44
11 BAA07g05870 A07 6722304 C T synonymous_variant LOW c.355C>T|p.Leu119Leu S257
12 BAA07g05870 A07 6722404 G A splice_region_variant&intron_variant LOW c.448+7G>A| S18
13 BAA07g05870 A07 6722461 G A intron_variant MODIFIER c.448+64G>A| S32
14 BAA07g05870 A07 6722486 G A intron_variant MODIFIER c.448+89G>A| S303
15 BAA07g05870 A07 6722567 G A intron_variant MODIFIER c.449-163G>A| S81
S85
16 BAA07g05870 A07 6722656 C T intron_variant MODIFIER c.449-74C>T| S177
17 BAA07g05870 A07 6722847 G A downstream_gene_variant MODIFIER c.*38G>A| S187
S188
S298
18 BAA07g05870 A07 6723252 G T downstream_gene_variant MODIFIER c.*443G>T| S50