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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g13630 A09 7827708 C T downstream_gene_variant MODIFIER c.*3489G>A| S37
2 BAA09g13630 A09 7828657 C T downstream_gene_variant MODIFIER c.*2540G>A| S118
3 BAA09g13630 A09 7828770 G A downstream_gene_variant MODIFIER c.*2427C>T| S130
4 BAA09g13630 A09 7830228 C T downstream_gene_variant MODIFIER c.*969G>A| S177
5 BAA09g13630 A09 7830321 C T downstream_gene_variant MODIFIER c.*876G>A| S283
6 BAA09g13630 A09 7831080 G A downstream_gene_variant MODIFIER c.*117C>T| S267
7 BAA09g13630 A09 7831275 C T synonymous_variant LOW c.4305G>A|p.Glu1435Glu S257
8 BAA09g13630 A09 7831718 C T missense_variant MODERATE c.4025G>A|p.Arg1342Lys S149
9 BAA09g13630 A09 7831817 G A missense_variant MODERATE c.3926C>T|p.Ser1309Leu S233
10 BAA09g13630 A09 7832024 C T intron_variant MODIFIER c.3817-98G>A| S64
11 BAA09g13630 A09 7832352 G A intron_variant MODIFIER c.3678+21C>T| S219
S72
12 BAA09g13630 A09 7832835 G A missense_variant MODERATE c.3293C>T|p.Ala1098Val S273
13 BAA09g13630 A09 7833298 C T synonymous_variant LOW c.2994G>A|p.Gln998Gln S232
14 BAA09g13630 A09 7834503 G A synonymous_variant LOW c.2010C>T|p.Leu670Leu S235
15 BAA09g13630 A09 7835099 C T missense_variant MODERATE c.1414G>A|p.Glu472Lys S183
16 BAA09g13630 A09 7835379 G A synonymous_variant LOW c.1134C>T|p.His378His S225
17 BAA09g13630 A09 7835402 G A missense_variant MODERATE c.1111C>T|p.Leu371Phe S235
18 BAA09g13630 A09 7835629 G A missense_variant MODERATE c.884C>T|p.Pro295Leu S225
S73
19 BAA09g13630 A09 7835864 G A intron_variant MODIFIER c.745-25C>T| S277
20 BAA09g13630 A09 7838097 G A upstream_gene_variant MODIFIER c.-978C>T| S199
21 BAA09g13630 A09 7838406 C T upstream_gene_variant MODIFIER c.-1287G>A| S148
S210
22 BAA09g13630 A09 7840022 G A upstream_gene_variant MODIFIER c.-2903C>T| S240
23 BAA09g13630 A09 7841266 C T upstream_gene_variant MODIFIER c.-4147G>A| S272