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
79201 BAA01g41630 A01 27692678 C T intron_variant MODIFIER c.581-95C>T| S233
79202 BAA01g41630 A01 27692848 G A missense_variant MODERATE c.656G>A|p.Cys219Tyr S129
79203 BAA01g41630 A01 27693520 G A intron_variant MODIFIER c.790+187G>A| S95
79204 BAA01g41630 A01 27694339 G A intron_variant MODIFIER c.790+1006G>A| S208
S219
79205 BAA01g41630 A01 27694760 G A intron_variant MODIFIER c.790+1427G>A| S265
79206 BAA01g41630 A01 27694945 C T intron_variant MODIFIER c.790+1612C>T| S48
79207 BAA01g41630 A01 27694974 G A intron_variant MODIFIER c.790+1641G>A| S245
79208 BAA01g41630 A01 27696575 C T intron_variant MODIFIER c.791-2150C>T| S275
79209 BAA01g41630 A01 27698992 C T missense_variant MODERATE c.1058C>T|p.Ser353Phe S133
S276
79210 BAA01g41630 A01 27699074 C T synonymous_variant LOW c.1140C>T|p.Thr380Thr S28
79211 BAA01g41640 A01 27701017 C T downstream_gene_variant MODIFIER c.*2352G>A| S275
79212 BAA01g41640 A01 27701243 G A downstream_gene_variant MODIFIER c.*2126C>T| S45
79213 BAA01g41630 A01 27702790 C T missense_variant MODERATE c.1991C>T|p.Thr664Ile S129
79214 BAA01g41640 A01 27704203 G A upstream_gene_variant MODIFIER c.-8C>T| S234
79215 BAA01g41640 A01 27704710 C T upstream_gene_variant MODIFIER c.-515G>A| S303
79216 BAA01g41640 A01 27706183 G A upstream_gene_variant MODIFIER c.-1988C>T| S70
79217 BAA01g41640 A01 27707076 C T upstream_gene_variant MODIFIER c.-2881G>A| S103
79218 BAA01g41640 A01 27707263 C T upstream_gene_variant MODIFIER c.-3068G>A| S237
79219 BAA01g41640 A01 27707433 C T upstream_gene_variant MODIFIER c.-3238G>A| S165
79220 BAA01g41640 A01 27708735 G A upstream_gene_variant MODIFIER c.-4540C>T| S86
79221 BAA01g41660 A01 27709692 G A missense_variant MODERATE c.83G>A|p.Gly28Glu S284
79222 BAA01g41660 A01 27709735 C T synonymous_variant LOW c.126C>T|p.Asn42Asn S146
79223 BAA01g41660 A01 27710387 C T missense_variant MODERATE c.548C>T|p.Ser183Phe S168
79224 BAA01g41660 A01 27710681 C T missense_variant MODERATE c.842C>T|p.Pro281Leu S211
S227
79225 BAA01g41660 A01 27710748 C T synonymous_variant LOW c.909C>T|p.Phe303Phe S239