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
135051 BAA10g21080 A10 18671513 C T upstream_gene_variant MODIFIER c.-577C>T| S297
135052 BAA10g21080 A10 18671883 G A upstream_gene_variant MODIFIER c.-207G>A| S65
135053 BAA10g21080 A10 18673297 G A missense_variant MODERATE c.1208G>A|p.Arg403His S74
135054 BAA10g21090 A10 18675011 C T missense_variant MODERATE c.2924G>A|p.Gly975Glu S48
135055 BAA10g21090 A10 18675398 G A missense_variant MODERATE c.2537C>T|p.Ser846Phe S243
S299
135056 BAA10g21090 A10 18676910 G A missense_variant MODERATE c.1025C>T|p.Thr342Ile S293
135057 BAA10g21090 A10 18677155 C T missense_variant MODERATE c.860G>A|p.Gly287Asp S11
135058 BAA10g21090 A10 18677419 C T synonymous_variant LOW c.708G>A|p.Glu236Glu S122
135059 BAA10g21090 A10 18678374 G A missense_variant MODERATE c.35C>T|p.Ser12Phe S79
S84
135060 BAA10g21090 A10 18678536 G A upstream_gene_variant MODIFIER c.-128C>T| S175
S293
135061 BAA10g21090 A10 18678809 C T upstream_gene_variant MODIFIER c.-401G>A| S244
135062 BAA10g21090 A10 18680684 G A upstream_gene_variant MODIFIER c.-2276C>T| S28
135063 BAA10g21090 A10 18681139 C T upstream_gene_variant MODIFIER c.-2731G>A| S41
135064 BAA10g21100 A10 18682934 C T missense_variant MODERATE c.1001G>A|p.Ser334Asn S255
135065 BAA10g21100 A10 18683012 G A missense_variant MODERATE c.923C>T|p.Ala308Val S303
135066 BAA10g21100 A10 18683468 G A synonymous_variant LOW c.757C>T|p.Leu253Leu S267
135067 BAA10g21110 A10 18683757 G A upstream_gene_variant MODIFIER c.-4564G>A| S190
135068 BAA10g21100 A10 18684178 G A missense_variant MODERATE c.490C>T|p.Pro164Ser S64
135069 BAA10g21100 A10 18684489 C T synonymous_variant LOW c.324G>A|p.Glu108Glu S121
135070 BAA10g21100 A10 18684566 G A splice_region_variant&intron_variant LOW c.318+4C>T| S82
S92
135071 BAA10g21110 A10 18684672 G A upstream_gene_variant MODIFIER c.-3649G>A| S284
135072 BAA10g21100 A10 18684913 G A missense_variant MODERATE c.143C>T|p.Ser48Phe S279
135073 BAA10g21100 A10 18685129 G A missense_variant MODERATE c.70C>T|p.Pro24Ser S287
135074 BAA10g21110 A10 18685281 G A upstream_gene_variant MODIFIER c.-3040G>A| S165
135075 BAA10g21100 A10 18686659 C T upstream_gene_variant MODIFIER c.-639G>A| S144