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 BAA10g13710 A10 14675404 G A upstream_gene_variant MODIFIER c.-4123G>A| S290
2 BAA10g13710 A10 14676692 G A upstream_gene_variant MODIFIER c.-2835G>A| S293
3 BAA10g13710 A10 14676731 C T upstream_gene_variant MODIFIER c.-2796C>T| S116
4 BAA10g13710 A10 14677232 C T upstream_gene_variant MODIFIER c.-2295C>T| S301
S304
5 BAA10g13710 A10 14677328 C T upstream_gene_variant MODIFIER c.-2199C>T| S79
S91
6 BAA10g13710 A10 14677417 C T upstream_gene_variant MODIFIER c.-2110C>T| S131
7 BAA10g13710 A10 14677563 G A upstream_gene_variant MODIFIER c.-1964G>A| S138
8 BAA10g13710 A10 14678458 G C upstream_gene_variant MODIFIER c.-1069G>C| S286
9 BAA10g13710 A10 14678472 G A upstream_gene_variant MODIFIER c.-1055G>A| S64
10 BAA10g13710 A10 14678495 G A upstream_gene_variant MODIFIER c.-1032G>A| S59
11 BAA10g13710 A10 14679965 G A missense_variant MODERATE c.439G>A|p.Glu147Lys S125
12 BAA10g13710 A10 14680176 C G missense_variant MODERATE c.650C>G|p.Pro217Arg S129
13 BAA10g13710 A10 14680289 G A missense_variant MODERATE c.763G>A|p.Gly255Ser S9
14 BAA10g13710 A10 14680292 C T missense_variant MODERATE c.766C>T|p.Leu256Phe S135
15 BAA10g13710 A10 14680862 C T missense_variant MODERATE c.1336C>T|p.Leu446Phe S270
16 BAA10g13710 A10 14681661 G A missense_variant MODERATE c.2135G>A|p.Gly712Glu S4
17 BAA10g13710 A10 14682245 C T missense_variant MODERATE c.2719C>T|p.Pro907Ser S199
18 BAA10g13710 A10 14682921 C T stop_gained HIGH c.3313C>T|p.Arg1105* S121
19 BAA10g13710 A10 14684059 G A downstream_gene_variant MODIFIER c.*1091G>A| S291
20 BAA10g13710 A10 14684137 G A downstream_gene_variant MODIFIER c.*1169G>A| S158
21 BAA10g13710 A10 14684285 C T downstream_gene_variant MODIFIER c.*1317C>T| S162
22 BAA10g13710 A10 14687923 G A downstream_gene_variant MODIFIER c.*4955G>A| S239