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
74601 BAA01g39320 A01 26109155 C T missense_variant MODERATE c.772C>T|p.Arg258Trp S213
74602 BAA01g39320 A01 26109164 G A missense_variant MODERATE c.781G>A|p.Glu261Lys S60
74603 BAA01g39320 A01 26109248 G A missense_variant MODERATE c.865G>A|p.Ala289Thr S223
74604 BAA01g39330 A01 26110792 G A upstream_gene_variant MODIFIER c.-4394G>A| S121
74605 BAA01g39330 A01 26110894 G A upstream_gene_variant MODIFIER c.-4292G>A| S116
74606 BAA01g39330 A01 26111285 G A upstream_gene_variant MODIFIER c.-3901G>A| S163
74607 BAA01g39330 A01 26111883 G A upstream_gene_variant MODIFIER c.-3303G>A| S123
74608 BAA01g39330 A01 26112223 G A upstream_gene_variant MODIFIER c.-2963G>A| S110
74609 BAA01g39330 A01 26112855 G A upstream_gene_variant MODIFIER c.-2331G>A| S51
74610 BAA01g39340 A01 26115733 C T downstream_gene_variant MODIFIER c.*2424G>A| S18
74611 BAA01g39340 A01 26115835 C T downstream_gene_variant MODIFIER c.*2322G>A| S303
74612 BAA01g39330 A01 26116606 G A missense_variant MODERATE c.610G>A|p.Glu204Lys S284
74613 BAA01g39330 A01 26116689 C T synonymous_variant LOW c.693C>T|p.Ser231Ser S107
74614 BAA01g39330 A01 26116740 C T synonymous_variant LOW c.744C>T|p.Ile248Ile S213
74615 BAA01g39330 A01 26117585 C T missense_variant MODERATE c.991C>T|p.Leu331Phe S77
S82
74616 BAA01g39330 A01 26117730 G A downstream_gene_variant MODIFIER c.*11G>A| S6
74617 BAA01g39340 A01 26118168 C T missense_variant MODERATE c.841G>A|p.Ala281Thr S294
74618 BAA01g39340 A01 26118333 G A missense_variant MODERATE c.676C>T|p.Leu226Phe S84
S93
74619 BAA01g39340 A01 26118389 C T missense_variant MODERATE c.620G>A|p.Arg207Lys S233
74620 BAA01g39330 A01 26118567 G A downstream_gene_variant MODIFIER c.*848G>A| S95
74621 BAA01g39330 A01 26118741 C T downstream_gene_variant MODIFIER c.*1022C>T| S264
74622 BAA01g39330 A01 26119624 C T downstream_gene_variant MODIFIER c.*1905C>T| S292
74623 BAA01g39340 A01 26120400 G A synonymous_variant LOW c.457C>T|p.Leu153Leu S125
74624 BAA01g39330 A01 26121727 G A downstream_gene_variant MODIFIER c.*4008G>A| S189
74625 BAA01g39340 A01 26122986 G A intron_variant MODIFIER c.263-2392C>T| S15