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
146601 BAA10g31050 A10 22792363 C T upstream_gene_variant MODIFIER c.-3409C>T| S296
146602 BAA10g31050 A10 22794506 G A upstream_gene_variant MODIFIER c.-1266G>A| S231
146603 BAA10g31040 A10 22795285 G A upstream_gene_variant MODIFIER c.-84C>T| S289
S290
146604 BAA10g31050 A10 22795815 G A missense_variant MODERATE c.44G>A|p.Gly15Glu S66
146605 BAA10g31040 A10 22796123 G A upstream_gene_variant MODIFIER c.-922C>T| S125
146606 BAA10g31050 A10 22797118 G A missense_variant MODERATE c.898G>A|p.Gly300Arg S64
146607 BAA10g31050 A10 22797774 G A missense_variant MODERATE c.1292G>A|p.Arg431Gln S284
146608 BAA10g31040 A10 22798048 C T upstream_gene_variant MODIFIER c.-2847G>A| S51
146609 BAA10g31060 A10 22799410 C T missense_variant MODERATE c.173G>A|p.Gly58Glu S48
146610 BAA10g31040 A10 22799795 G A upstream_gene_variant MODIFIER c.-4594C>T| S197
146611 BAA10g31060 A10 22800895 C T upstream_gene_variant MODIFIER c.-1224G>A| S211
146612 BAA10g31060 A10 22801250 G A upstream_gene_variant MODIFIER c.-1579C>T| S106
146613 BAA10g31060 A10 22802764 C T upstream_gene_variant MODIFIER c.-3093G>A| S247
146614 BAA10g31060 A10 22804506 C T upstream_gene_variant MODIFIER c.-4835G>A| S2
146615 BAA10g31060 A10 22804616 C T upstream_gene_variant MODIFIER c.-4945G>A| S169
146616 BAA10g31070 A10 22805582 G A upstream_gene_variant MODIFIER c.-3526C>T| S84
S93
146617 BAA10g31070 A10 22806372 C T upstream_gene_variant MODIFIER c.-4316G>A| S114
146618 BAA10g31090 A10 22806597 C T synonymous_variant LOW c.172C>T|p.Leu58Leu S247
146619 BAA10g31080 A10 22807293 C T downstream_gene_variant MODIFIER c.*1761C>T| S153
S213
146620 BAA10g31100 A10 22807713 C T missense_variant MODERATE c.2839G>A|p.Val947Met S274
146621 BAA10g31100 A10 22808000 C T missense_variant MODERATE c.2616G>A|p.Met872Ile S2
146622 BAA10g31100 A10 22808006 G A synonymous_variant LOW c.2610C>T|p.Phe870Phe S138
146623 BAA10g31100 A10 22808301 C T missense_variant MODERATE c.2315G>A|p.Arg772His S11
146624 BAA10g31100 A10 22808501 C T stop_gained HIGH c.2193G>A|p.Trp731* S199
146625 BAA10g31100 A10 22808743 G A missense_variant MODERATE c.1951C>T|p.Pro651Ser S207