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
158051 BAA02g05710 A02 2444630 G A upstream_gene_variant MODIFIER c.-2779G>A| S51
158052 BAA02g05710 A02 2444787 C T upstream_gene_variant MODIFIER c.-2622C>T| S280
158053 BAA02g05710 A02 2447502 G A missense_variant MODERATE c.94G>A|p.Glu32Lys S302
158054 BAA02g05710 A02 2448183 C T missense_variant MODERATE c.458C>T|p.Ala153Val S216
158055 BAA02g05710 A02 2448554 C T missense_variant MODERATE c.619C>T|p.Pro207Ser S83
S88
158056 BAA02g05700 A02 2449221 C T upstream_gene_variant MODIFIER c.-2081G>A| S202
158057 BAA02g05720 A02 2450509 G A stop_gained HIGH c.75G>A|p.Trp25* S86
158058 BAA02g05720 A02 2451029 G A synonymous_variant LOW c.453G>A|p.Ala151Ala S247
158059 BAA02g05720 A02 2451102 C T missense_variant MODERATE c.526C>T|p.Leu176Phe S138
158060 BAA02g05720 A02 2451150 C T synonymous_variant LOW c.574C>T|p.Leu192Leu S241
158061 BAA02g05700 A02 2451254 C T upstream_gene_variant MODIFIER c.-4114G>A| S174
S265
S39
158062 BAA02g05720 A02 2452775 C T missense_variant MODERATE c.1454C>T|p.Thr485Ile S234
158063 BAA02g05730 A02 2453652 C T synonymous_variant LOW c.123G>A|p.Gln41Gln S257
158064 BAA02g05730 A02 2453693 G A missense_variant MODERATE c.82C>T|p.Leu28Phe S256
158065 BAA02g05730 A02 2455019 G A upstream_gene_variant MODIFIER c.-1245C>T| S303
158066 BAA02g05730 A02 2455098 G A upstream_gene_variant MODIFIER c.-1324C>T| S140
158067 BAA02g05730 A02 2455480 G A upstream_gene_variant MODIFIER c.-1706C>T| S20
158068 BAA02g05730 A02 2456046 G A upstream_gene_variant MODIFIER c.-2272C>T| S153
S213
158069 BAA02g05730 A02 2456940 G A upstream_gene_variant MODIFIER c.-3166C>T| S273
158070 BAA02g05730 A02 2457906 G A upstream_gene_variant MODIFIER c.-4132C>T| S128
158071 BAA02g05770 A02 2460611 G A synonymous_variant LOW c.885C>T|p.Ile295Ile S287
158072 BAA02g05770 A02 2462126 G A upstream_gene_variant MODIFIER c.-110C>T| S76
158073 BAA02g05770 A02 2462989 G A upstream_gene_variant MODIFIER c.-973C>T| S282
158074 BAA02g05770 A02 2464387 C T upstream_gene_variant MODIFIER c.-2371G>A| S67
158075 BAA02g05780 A02 2464750 G A missense_variant MODERATE c.517C>T|p.Leu173Phe S116