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
136951 BAA10g22650 A10 19389390 G A missense_variant&splice_region_variant MODERATE c.380G>A|p.Gly127Asp S17
136952 BAA10g22650 A10 19389413 C T synonymous_variant LOW c.403C>T|p.Leu135Leu S162
136953 BAA10g22650 A10 19390126 G A missense_variant MODERATE c.721G>A|p.Val241Ile S176
136954 BAA10g22660 A10 19390486 G A upstream_gene_variant MODIFIER c.-578G>A| S103
136955 BAA10g22660 A10 19391066 G A start_lost HIGH c.3G>A|p.Met1? S240
136956 BAA10g22670 A10 19391410 G A upstream_gene_variant MODIFIER c.-4880G>A| S252
S276
136957 BAA10g22670 A10 19391427 G A upstream_gene_variant MODIFIER c.-4863G>A| S192
136958 BAA10g22670 A10 19392455 G A upstream_gene_variant MODIFIER c.-3835G>A| S150
136959 BAA10g22670 A10 19393602 G A upstream_gene_variant MODIFIER c.-2688G>A| S69
136960 BAA10g22670 A10 19394137 G A upstream_gene_variant MODIFIER c.-2153G>A| S192
136961 BAA10g22670 A10 19394273 C T upstream_gene_variant MODIFIER c.-2017C>T| S269
136962 BAA10g22670 A10 19394600 C T upstream_gene_variant MODIFIER c.-1690C>T| S98
136963 BAA10g22670 A10 19395928 C T upstream_gene_variant MODIFIER c.-362C>T| S41
136964 BAA10g22670 A10 19396633 C T missense_variant MODERATE c.344C>T|p.Ala115Val S189
136965 BAA10g22670 A10 19396898 G A splice_donor_variant&intron_variant HIGH c.608+1G>A| S164
136966 BAA10g22690 A10 19397781 G A upstream_gene_variant MODIFIER c.-1419G>A| S4
136967 BAA10g22680 A10 19398062 C T synonymous_variant LOW c.1095G>A|p.Arg365Arg S226
136968 BAA10g22680 A10 19398126 C T missense_variant MODERATE c.1031G>A|p.Gly344Glu S45
136969 BAA10g22680 A10 19398764 G A synonymous_variant LOW c.393C>T|p.Leu131Leu S202
136970 BAA10g22690 A10 19399216 C T missense_variant MODERATE c.17C>T|p.Thr6Ile S237
136971 BAA10g22680 A10 19400067 C T upstream_gene_variant MODIFIER c.-911G>A| S146
136972 BAA10g22680 A10 19400342 C T upstream_gene_variant MODIFIER c.-1186G>A| S229
136973 BAA10g22680 A10 19400741 C T upstream_gene_variant MODIFIER c.-1585G>A| S114
136974 BAA10g22690 A10 19401241 C T missense_variant MODERATE c.800C>T|p.Ala267Val S51
136975 BAA10g22690 A10 19401665 G A splice_acceptor_variant&intron_variant HIGH c.1019-1G>A| S67