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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g18770 A02 9649350 G A upstream_gene_variant MODIFIER c.-3981G>A| S107
2 BAA02g18770 A02 9650356 C T upstream_gene_variant MODIFIER c.-2975C>T| S308
3 BAA02g18770 A02 9651028 C T upstream_gene_variant MODIFIER c.-2303C>T| S32
4 BAA02g18770 A02 9651271 G A upstream_gene_variant MODIFIER c.-2060G>A| S28
5 BAA02g18770 A02 9651285 G A upstream_gene_variant MODIFIER c.-2046G>A| S197
6 BAA02g18770 A02 9651895 A G upstream_gene_variant MODIFIER c.-1436A>G| S178
7 BAA02g18770 A02 9651934 G A upstream_gene_variant MODIFIER c.-1397G>A| S126
8 BAA02g18770 A02 9652142 G A upstream_gene_variant MODIFIER c.-1189G>A| S41
9 BAA02g18770 A02 9653286 G A upstream_gene_variant MODIFIER c.-45G>A| S149
10 BAA02g18770 A02 9653341 C T missense_variant MODERATE c.11C>T|p.Ser4Phe S105
S106
11 BAA02g18770 A02 9653433 C T synonymous_variant LOW c.103C>T|p.Leu35Leu S283
12 BAA02g18770 A02 9654306 G A missense_variant MODERATE c.907G>A|p.Glu303Lys S206
S26
13 BAA02g18770 A02 9654323 G A synonymous_variant LOW c.924G>A|p.Ala308Ala S217
14 BAA02g18770 A02 9655132 C T missense_variant MODERATE c.1562C>T|p.Ser521Leu S299
15 BAA02g18770 A02 9655322 G A synonymous_variant LOW c.1668G>A|p.Arg556Arg S279
16 BAA02g18770 A02 9655608 G A missense_variant MODERATE c.1870G>A|p.Glu624Lys S13
17 BAA02g18770 A02 9655805 C T synonymous_variant LOW c.2067C>T|p.Asn689Asn S163
18 BAA02g18770 A02 9656969 C T missense_variant MODERATE c.2863C>T|p.Leu955Phe S194
19 BAA02g18770 A02 9657117 C T splice_region_variant&intron_variant LOW c.2931-5C>T| S58
20 BAA02g18770 A02 9657146 G A synonymous_variant LOW c.2955G>A|p.Arg985Arg S70