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
134951 BAA10g20990 A10 18632977 C T missense_variant MODERATE c.419G>A|p.Ser140Asn S84
S93
134952 BAA10g20990 A10 18635032 C T upstream_gene_variant MODIFIER c.-1461G>A| S23
134953 BAA10g20990 A10 18635097 G A upstream_gene_variant MODIFIER c.-1526C>T| S105
S106
134954 BAA10g20990 A10 18638220 C T upstream_gene_variant MODIFIER c.-4649G>A| S132
S137
S215
134955 BAA10g21000 A10 18638895 G A upstream_gene_variant MODIFIER c.-2830C>T| S212
134956 BAA10g21020 A10 18639146 G A synonymous_variant LOW c.249G>A|p.Lys83Lys S219
S72
134957 BAA10g21020 A10 18639530 G A synonymous_variant LOW c.552G>A|p.Lys184Lys S112
134958 BAA10g21020 A10 18639764 G A synonymous_variant LOW c.696G>A|p.Arg232Arg S295
134959 BAA10g21020 A10 18640123 G A synonymous_variant LOW c.885G>A|p.Lys295Lys S7
134960 BAA10g21050 A10 18651730 C T upstream_gene_variant MODIFIER c.-1754C>T| S67
134961 BAA10g21040 A10 18651796 G A missense_variant MODERATE c.595C>T|p.Leu199Phe S303
134962 BAA10g21040 A10 18652133 G A missense_variant MODERATE c.383C>T|p.Thr128Ile S263
134963 BAA10g21040 A10 18652333 G A missense_variant MODERATE c.260C>T|p.Ala87Val S80
134964 BAA10g21040 A10 18652757 C T missense_variant MODERATE c.89G>A|p.Arg30His S104
134965 BAA10g21040 A10 18653175 G A upstream_gene_variant MODIFIER c.-330C>T| S103
134966 BAA10g21040 A10 18653419 G A upstream_gene_variant MODIFIER c.-574C>T| S33
134967 BAA10g21040 A10 18653543 C T upstream_gene_variant MODIFIER c.-698G>A| S5
134968 BAA10g21050 A10 18653688 C T synonymous_variant LOW c.129C>T|p.Leu43Leu S146
134969 BAA10g21050 A10 18653833 G A missense_variant MODERATE c.274G>A|p.Glu92Lys S71
134970 BAA10g21050 A10 18653966 C T missense_variant MODERATE c.407C>T|p.Pro136Leu S38
134971 BAA10g21050 A10 18654171 C T synonymous_variant LOW c.612C>T|p.Asn204Asn S107
134972 BAA10g21040 A10 18654522 C T upstream_gene_variant MODIFIER c.-1677G>A| S40
S49
134973 BAA10g21050 A10 18654570 C T missense_variant MODERATE c.935C>T|p.Ser312Leu S95
134974 BAA10g21050 A10 18654708 C T missense_variant MODERATE c.1073C>T|p.Pro358Leu S168
134975 BAA10g21050 A10 18654891 C T missense_variant MODERATE c.1256C>T|p.Ala419Val S305