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
124901 BAA10g14280 A10 15066009 C T upstream_gene_variant MODIFIER c.-1497C>T| S48
124902 BAA10g14280 A10 15066127 G A upstream_gene_variant MODIFIER c.-1379G>A| S284
124903 BAA10g14280 A10 15066675 G A upstream_gene_variant MODIFIER c.-831G>A| S237
124904 BAA10g14280 A10 15067194 C T upstream_gene_variant MODIFIER c.-312C>T| S237
124905 BAA10g14280 A10 15067566 G A missense_variant MODERATE c.61G>A|p.Ala21Thr S57
124906 BAA10g14290 A10 15069149 C T upstream_gene_variant MODIFIER c.-4958C>T| S115
124907 BAA10g14290 A10 15069700 C T upstream_gene_variant MODIFIER c.-4407C>T| S84
S93
124908 BAA10g14290 A10 15070820 C T upstream_gene_variant MODIFIER c.-3287C>T| S247
124909 BAA10g14290 A10 15071350 G A upstream_gene_variant MODIFIER c.-2757G>A| S18
124910 BAA10g14290 A10 15072885 G A upstream_gene_variant MODIFIER c.-1222G>A| S112
124911 BAA10g14290 A10 15073491 C T upstream_gene_variant MODIFIER c.-616C>T| S190
124912 BAA10g14290 A10 15073681 C T upstream_gene_variant MODIFIER c.-426C>T| S202
124913 BAA10g14290 A10 15074060 C T upstream_gene_variant MODIFIER c.-47C>T| S298
124914 BAA10g14300 A10 15074847 C T upstream_gene_variant MODIFIER c.-462C>T| S211
S227
124915 BAA10g14300 A10 15075114 C T upstream_gene_variant MODIFIER c.-195C>T| S47
124916 BAA10g14300 A10 15075429 C T missense_variant MODERATE c.121C>T|p.Pro41Ser S143
124917 BAA10g14300 A10 15075652 G A missense_variant MODERATE c.344G>A|p.Gly115Glu S262
124918 BAA10g14300 A10 15076255 C T missense_variant MODERATE c.947C>T|p.Pro316Leu S57
124919 BAA10g14300 A10 15076925 C T missense_variant MODERATE c.1523C>T|p.Ala508Val S177
124920 BAA10g14320 A10 15078188 G A upstream_gene_variant MODIFIER c.-3314G>A| S195
124921 BAA10g14310 A10 15078692 G A synonymous_variant LOW c.819C>T|p.Asp273Asp S112
124922 BAA10g14310 A10 15078984 C T synonymous_variant LOW c.672G>A|p.Gln224Gln S105
S106
124923 BAA10g14310 A10 15078994 G A missense_variant MODERATE c.662C>T|p.Ser221Phe S290
124924 BAA10g14310 A10 15079892 C T missense_variant MODERATE c.86G>A|p.Ser29Asn S190
124925 BAA10g14310 A10 15080054 G A missense_variant MODERATE c.71C>T|p.Ser24Phe S215