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
89951 BAA10g00120 A10 47538 G A missense_variant MODERATE c.38C>T|p.Thr13Ile S176
89952 BAA10g00130 A10 52147 G A stop_gained HIGH c.1497G>A|p.Trp499* S234
89953 BAA10g00130 A10 52566 C T splice_region_variant&intron_variant LOW c.1708-3C>T| S286
89954 BAA10g00130 A10 52595 G A synonymous_variant LOW c.1734G>A|p.Val578Val S67
89955 BAA10g00130 A10 52700 G A intron_variant MODIFIER c.1830+9G>A| S57
89956 BAA10g00130 A10 54058 C T intron_variant MODIFIER c.2506-135C>T| S56
89957 BAA10g00130 A10 54307 G A missense_variant MODERATE c.2620G>A|p.Val874Ile S107
89958 BAA10g00130 A10 55713 G A synonymous_variant LOW c.3393G>A|p.Lys1131Lys S60
89959 BAA10g00130 A10 55901 G A missense_variant MODERATE c.3478G>A|p.Glu1160Lys S192
89960 BAA10g00130 A10 56030 G A missense_variant MODERATE c.3607G>A|p.Asp1203Asn S215
89961 BAA10g00130 A10 56956 G A missense_variant MODERATE c.4018G>A|p.Ala1340Thr S290
89962 BAA10g00130 A10 57914 C T synonymous_variant LOW c.4599C>T|p.Ile1533Ile S202
89963 BAA10g00130 A10 58471 G A missense_variant MODERATE c.4885G>A|p.Val1629Met S76
89964 BAA10g00130 A10 58602 G A intron_variant MODIFIER c.4917+99G>A| S256
89965 BAA10g00130 A10 58783 C T stop_gained HIGH c.4990C>T|p.Gln1664* S104
S52
89966 BAA10g00130 A10 59078 C T intron_variant MODIFIER c.5113-45C>T| S87
89967 BAA10g00130 A10 60469 G A missense_variant&splice_region_variant MODERATE c.5710G>A|p.Glu1904Lys S184
89968 BAA10g00130 A10 60755 G A splice_region_variant&intron_variant LOW c.5889+5G>A| S153
S213
89969 BAA10g00150 A10 63742 C T upstream_gene_variant MODIFIER c.-3700C>T| S165
89970 BAA10g00140 A10 65203 C T synonymous_variant LOW c.255G>A|p.Arg85Arg S139
89971 BAA10g00140 A10 66207 G A upstream_gene_variant MODIFIER c.-668C>T| S25
89972 BAA10g00140 A10 66975 C T upstream_gene_variant MODIFIER c.-1436G>A| S201
89973 BAA10g00150 A10 67444 G A start_lost HIGH c.3G>A|p.Met1? S293
89974 BAA10g00150 A10 67778 A T stop_gained HIGH c.337A>T|p.Lys113* S174
S27
89975 BAA10g00150 A10 67947 G A missense_variant MODERATE c.506G>A|p.Arg169Lys S228