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
73651 BAA01g38650 A01 25761549 C T downstream_gene_variant MODIFIER c.*2190G>A| S170
73652 BAA01g38650 A01 25763939 C T missense_variant MODERATE c.133G>A|p.Glu45Lys S146
73653 BAA01g38650 A01 25764377 C T upstream_gene_variant MODIFIER c.-306G>A| S277
73654 BAA01g38650 A01 25764672 G A upstream_gene_variant MODIFIER c.-601C>T| S124
S99
73655 BAA01g38650 A01 25765439 C T upstream_gene_variant MODIFIER c.-1368G>A| S200
73656 BAA01g38650 A01 25766560 C T upstream_gene_variant MODIFIER c.-2489G>A| S16
73657 BAA01g38650 A01 25768307 C T upstream_gene_variant MODIFIER c.-4236G>A| S32
73658 BAA01g38650 A01 25768592 C T upstream_gene_variant MODIFIER c.-4521G>A| S98
73659 BAA01g38650 A01 25768912 G A upstream_gene_variant MODIFIER c.-4841C>T| S252
73660 BAA01g38650 A01 25768933 G A upstream_gene_variant MODIFIER c.-4862C>T| S2
73661 BAA01g38660 A01 25769061 C T synonymous_variant LOW c.108C>T|p.Ser36Ser S233
73662 BAA01g38660 A01 25769076 C T synonymous_variant LOW c.123C>T|p.Leu41Leu S146
73663 BAA01g38660 A01 25769370 C T synonymous_variant LOW c.417C>T|p.Ser139Ser S174
S27
73664 BAA01g38660 A01 25769807 C T synonymous_variant LOW c.732C>T|p.Leu244Leu S237
73665 BAA01g38660 A01 25770213 G A downstream_gene_variant MODIFIER c.*268G>A| S308
73666 BAA01g38660 A01 25770801 C T downstream_gene_variant MODIFIER c.*856C>T| S162
73667 BAA01g38670 A01 25771651 C T missense_variant MODERATE c.182G>A|p.Gly61Glu S134
73668 BAA01g38670 A01 25772026 G A upstream_gene_variant MODIFIER c.-194C>T| S297
73669 BAA01g38670 A01 25772857 G A upstream_gene_variant MODIFIER c.-1025C>T| S175
S276
73670 BAA01g38670 A01 25773026 C T upstream_gene_variant MODIFIER c.-1194G>A| S249
73671 BAA01g38670 A01 25774345 C T upstream_gene_variant MODIFIER c.-2513G>A| S88
73672 BAA01g38670 A01 25776403 G A upstream_gene_variant MODIFIER c.-4571C>T| S202
73673 BAA01g38680 A01 25776912 C T missense_variant MODERATE c.632G>A|p.Arg211Lys S94
73674 BAA01g38680 A01 25777272 G A synonymous_variant LOW c.408C>T|p.Asp136Asp S108
73675 BAA01g38680 A01 25777531 G A intron_variant MODIFIER c.191-42C>T| S62