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
87701 BAA01g46720 A01 31149623 C T upstream_gene_variant MODIFIER c.-3773G>A| S239
87702 BAA01g46730 A01 31149955 G A missense_variant MODERATE c.520C>T|p.His174Tyr S218
87703 BAA01g46730 A01 31150092 C T missense_variant MODERATE c.383G>A|p.Ser128Asn S1
S90
87704 BAA01g46720 A01 31150663 C T upstream_gene_variant MODIFIER c.-4813G>A| S153
S213
87705 BAA01g46730 A01 31150789 G A splice_region_variant&intron_variant LOW c.289-5C>T| S306
87706 BAA01g46730 A01 31151511 G A upstream_gene_variant MODIFIER c.-125C>T| S265
87707 BAA01g46730 A01 31151780 C T upstream_gene_variant MODIFIER c.-394G>A| S98
87708 BAA01g46730 A01 31152148 G A upstream_gene_variant MODIFIER c.-762C>T| S176
87709 BAA01g46730 A01 31152188 C T upstream_gene_variant MODIFIER c.-802G>A| S146
87710 BAA01g46730 A01 31152363 C T upstream_gene_variant MODIFIER c.-977G>A| S256
87711 BAA01g46730 A01 31152842 C T upstream_gene_variant MODIFIER c.-1456G>A| S249
87712 BAA01g46740 A01 31153070 C T synonymous_variant LOW c.24C>T|p.Pro8Pro S201
87713 BAA01g46740 A01 31153093 C T missense_variant MODERATE c.47C>T|p.Ala16Val S230
87714 BAA01g46740 A01 31153148 C T synonymous_variant LOW c.102C>T|p.Ile34Ile S193
87715 BAA01g46740 A01 31153472 G A missense_variant&splice_region_variant MODERATE c.289G>A|p.Gly97Arg S175
87716 BAA01g46730 A01 31153988 C T upstream_gene_variant MODIFIER c.-2602G>A| S56
87717 BAA01g46730 A01 31154615 C T upstream_gene_variant MODIFIER c.-3229G>A| S37
87718 BAA01g46740 A01 31154940 C T missense_variant MODERATE c.716C>T|p.Thr239Ile S266
87719 BAA01g46730 A01 31155501 G A upstream_gene_variant MODIFIER c.-4115C>T| S86
87720 BAA01g46730 A01 31155736 C T upstream_gene_variant MODIFIER c.-4350G>A| S237
87721 BAA01g46740 A01 31155825 C T synonymous_variant LOW c.924C>T|p.His308His S200
87722 BAA01g46730 A01 31156140 C T upstream_gene_variant MODIFIER c.-4754G>A| S305
87723 BAA01g46750 A01 31156742 C T missense_variant MODERATE c.1001G>A|p.Gly334Glu S233
87724 BAA01g46750 A01 31156942 C T synonymous_variant LOW c.801G>A|p.Glu267Glu S37
87725 BAA01g46750 A01 31157415 C T missense_variant MODERATE c.328G>A|p.Val110Met S35