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
91701 BAA10g01640 A10 793916 C T downstream_gene_variant MODIFIER c.*1698G>A| S35
91702 BAA10g01640 A10 794102 C T downstream_gene_variant MODIFIER c.*1512G>A| S276
91703 BAA10g01630 A10 794592 C T missense_variant&splice_region_variant MODERATE c.139G>A|p.Ala47Thr S110
91704 BAA10g01630 A10 794847 C T upstream_gene_variant MODIFIER c.-117G>A| S150
91705 BAA10g01630 A10 795200 G A upstream_gene_variant MODIFIER c.-470C>T| S80
91706 BAA10g01640 A10 796932 C T missense_variant MODERATE c.2942G>A|p.Gly981Glu S162
91707 BAA10g01640 A10 797172 G A missense_variant MODERATE c.2791C>T|p.Pro931Ser S230
91708 BAA10g01640 A10 797718 C T missense_variant MODERATE c.2510G>A|p.Arg837His S95
91709 BAA10g01640 A10 798440 G A missense_variant MODERATE c.2158C>T|p.Leu720Phe S133
91710 BAA10g01630 A10 798585 G A upstream_gene_variant MODIFIER c.-3855C>T| S216
91711 BAA10g01650 A10 799963 G A downstream_gene_variant MODIFIER c.*3868C>T| S136
91712 BAA10g01640 A10 801345 C T splice_region_variant&intron_variant LOW c.292+6G>A| S204
91713 BAA10g01640 A10 801435 C T missense_variant MODERATE c.208G>A|p.Asp70Asn S200
91714 BAA10g01640 A10 801667 G A missense_variant MODERATE c.67C>T|p.Arg23Cys S240
91715 BAA10g01640 A10 801740 C T upstream_gene_variant MODIFIER c.-7G>A| S294
91716 BAA10g01640 A10 801859 G A upstream_gene_variant MODIFIER c.-126C>T| S241
91717 BAA10g01650 A10 804057 C T missense_variant MODERATE c.143G>A|p.Gly48Asp S288
91718 BAA10g01640 A10 804257 T C upstream_gene_variant MODIFIER c.-2524A>G| S218
91719 BAA10g01640 A10 804916 G A upstream_gene_variant MODIFIER c.-3183C>T| S125
91720 BAA10g01640 A10 805355 G A upstream_gene_variant MODIFIER c.-3622C>T| S157
S163
91721 BAA10g01660 A10 805502 A G synonymous_variant LOW c.561T>C|p.Asp187Asp S147
S91
91722 BAA10g01660 A10 805523 A T synonymous_variant LOW c.540T>A|p.Thr180Thr S147
S91
91723 BAA10g01660 A10 805554 T G missense_variant MODERATE c.509A>C|p.His170Pro S147
S91
91724 BAA10g01660 A10 805555 G T missense_variant MODERATE c.508C>A|p.His170Asn S147
S91
91725 BAA10g01660 A10 805577 G T missense_variant MODERATE c.486C>A|p.His162Gln S147
S91