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
18751 BAA01g13990 A01 6651493 A G upstream_gene_variant MODIFIER c.-4861A>G| S115
18752 BAA01g13980 A01 6652606 C T upstream_gene_variant MODIFIER c.-420G>A| S265
18753 BAA01g13980 A01 6653845 C T upstream_gene_variant MODIFIER c.-1659G>A| S249
18754 BAA01g13980 A01 6654294 C T upstream_gene_variant MODIFIER c.-2108G>A| S265
18755 BAA01g13980 A01 6654458 C T upstream_gene_variant MODIFIER c.-2272G>A| S211
S227
18756 BAA01g13980 A01 6654743 G A upstream_gene_variant MODIFIER c.-2557C>T| S13
18757 BAA01g13980 A01 6654810 C T upstream_gene_variant MODIFIER c.-2624G>A| S46
18758 BAA01g13980 A01 6655364 G A upstream_gene_variant MODIFIER c.-3178C>T| S165
18759 BAA01g13980 A01 6655446 C T upstream_gene_variant MODIFIER c.-3260G>A| S182
18760 BAA01g13990 A01 6656501 G A missense_variant MODERATE c.148G>A|p.Val50Met S129
18761 BAA01g13980 A01 6656545 G A upstream_gene_variant MODIFIER c.-4359C>T| S187
18762 BAA01g13990 A01 6656933 C T synonymous_variant LOW c.492C>T|p.Gly164Gly S80
18763 BAA01g13990 A01 6657702 G A missense_variant MODERATE c.1261G>A|p.Gly421Ser S105
S106
18764 BAA01g13990 A01 6658000 C T missense_variant MODERATE c.1492C>T|p.His498Tyr S249
18765 BAA01g13990 A01 6659019 G A synonymous_variant LOW c.2511G>A|p.Arg837Arg S122
18766 BAA01g13990 A01 6659224 G A missense_variant MODERATE c.2716G>A|p.Asp906Asn S8
18767 BAA01g13990 A01 6659341 G A missense_variant MODERATE c.2833G>A|p.Asp945Asn S110
18768 BAA01g13990 A01 6659367 C T synonymous_variant LOW c.2859C>T|p.Phe953Phe S226
18769 BAA01g13990 A01 6659630 C T missense_variant MODERATE c.3122C>T|p.Ser1041Phe S158
18770 BAA01g14000 A01 6660922 C T upstream_gene_variant MODIFIER c.-1729C>T| S148
S30
S31
18771 BAA01g14000 A01 6661255 C T upstream_gene_variant MODIFIER c.-1396C>T| S50
18772 BAA01g13990 A01 6661470 C T synonymous_variant LOW c.3579C>T|p.Arg1193Arg S2
18773 BAA01g13990 A01 6661509 T C synonymous_variant LOW c.3618T>C|p.Arg1206Arg S235
18774 BAA01g13990 A01 6661542 C T synonymous_variant LOW c.3651C>T|p.Leu1217Leu S132
S137
18775 BAA01g14000 A01 6661656 C T upstream_gene_variant MODIFIER c.-995C>T| S242