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


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
138901 BAA10g24300 A10 20065585 G A synonymous_variant LOW c.558G>A|p.Lys186Lys S75
138902 BAA10g24310 A10 20066597 C T downstream_gene_variant MODIFIER c.*1625G>A| S206
S26
138903 BAA10g24300 A10 20066854 G A missense_variant MODERATE c.1507G>A|p.Asp503Asn S59
138904 BAA10g24310 A10 20069738 C T missense_variant MODERATE c.32G>A|p.Gly11Asp S45
138905 BAA10g24310 A10 20069949 C T upstream_gene_variant MODIFIER c.-180G>A| S169
138906 BAA10g24310 A10 20070014 C T upstream_gene_variant MODIFIER c.-245G>A| S36
138907 BAA10g24310 A10 20070039 C T upstream_gene_variant MODIFIER c.-270G>A| S221
138908 BAA10g24310 A10 20070428 G A upstream_gene_variant MODIFIER c.-659C>T| S39
138909 BAA10g24310 A10 20071002 C T upstream_gene_variant MODIFIER c.-1233G>A| S286
138910 BAA10g24310 A10 20072136 G A upstream_gene_variant MODIFIER c.-2367C>T| S90
138911 BAA10g24310 A10 20073023 C T upstream_gene_variant MODIFIER c.-3254G>A| S148
S30
S31
138912 BAA10g24320 A10 20074109 G A missense_variant MODERATE c.164G>A|p.Arg55Lys S71
138913 BAA10g24320 A10 20074328 G A missense_variant MODERATE c.383G>A|p.Arg128Lys S109
138914 BAA10g24310 A10 20074744 G A upstream_gene_variant MODIFIER c.-4975C>T| S208
138915 BAA10g24320 A10 20074995 G A intron_variant MODIFIER c.555+107G>A| S113
138916 BAA10g24320 A10 20074998 G A intron_variant MODIFIER c.555+110G>A| S286
138917 BAA10g24320 A10 20076792 C T downstream_gene_variant MODIFIER c.*878C>T| S165
138918 BAA10g24320 A10 20079792 C T downstream_gene_variant MODIFIER c.*3878C>T| S152
138919 BAA10g24330 A10 20083148 C T downstream_gene_variant MODIFIER c.*869G>A| S87
138920 BAA10g24330 A10 20083339 C T downstream_gene_variant MODIFIER c.*678G>A| S162
138921 BAA10g24330 A10 20083384 G A downstream_gene_variant MODIFIER c.*633C>T| S272
138922 BAA10g24330 A10 20084536 C T missense_variant MODERATE c.644G>A|p.Cys215Tyr S246
138923 BAA10g24330 A10 20084601 C T synonymous_variant LOW c.579G>A|p.Lys193Lys S11
138924 BAA10g24330 A10 20084678 C T missense_variant MODERATE c.502G>A|p.Val168Ile S33
138925 BAA10g24330 A10 20087918 C T upstream_gene_variant MODIFIER c.-2406G>A| S206
S26