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
141651 BAA10g26640 A10 21060869 C T synonymous_variant LOW c.294G>A|p.Leu98Leu S212
141652 BAA10g26650 A10 21061225 C T upstream_gene_variant MODIFIER c.-804C>T| S221
141653 BAA10g26640 A10 21061616 G A upstream_gene_variant MODIFIER c.-35C>T| S265
S273
141654 BAA10g26640 A10 21061777 G A upstream_gene_variant MODIFIER c.-196C>T| S112
S143
141655 BAA10g26640 A10 21061789 C T upstream_gene_variant MODIFIER c.-208G>A| S87
141656 BAA10g26640 A10 21061950 C T upstream_gene_variant MODIFIER c.-369G>A| S275
141657 BAA10g26640 A10 21062200 G A upstream_gene_variant MODIFIER c.-619C>T| S158
141658 BAA10g26650 A10 21063265 G A missense_variant MODERATE c.665G>A|p.Ser222Asn S257
141659 BAA10g26640 A10 21064171 C T upstream_gene_variant MODIFIER c.-2590G>A| S34
141660 BAA10g26660 A10 21064826 C T missense_variant MODERATE c.644C>T|p.Ser215Phe S203
141661 BAA10g26640 A10 21065322 C T upstream_gene_variant MODIFIER c.-3741G>A| S259
141662 BAA10g26640 A10 21065526 C T upstream_gene_variant MODIFIER c.-3945G>A| S201
141663 BAA10g26670 A10 21066237 G A missense_variant MODERATE c.1264C>T|p.Leu422Phe S64
141664 BAA10g26670 A10 21067568 C T missense_variant MODERATE c.241G>A|p.Ala81Thr S296
141665 BAA10g26670 A10 21067645 G A missense_variant MODERATE c.164C>T|p.Pro55Leu S189
141666 BAA10g26670 A10 21069534 C T upstream_gene_variant MODIFIER c.-1726G>A| S260
141667 BAA10g26670 A10 21070192 G A upstream_gene_variant MODIFIER c.-2384C>T| S118
141668 BAA10g26680 A10 21070893 G A missense_variant MODERATE c.29G>A|p.Gly10Asp S17
141669 BAA10g26680 A10 21071733 C T synonymous_variant LOW c.682C>T|p.Leu228Leu S79
S91
141670 BAA10g26680 A10 21073251 G A downstream_gene_variant MODIFIER c.*853G>A| S80
141671 BAA10g26690 A10 21074462 G A splice_region_variant&intron_variant LOW c.282+5G>A| S4
141672 BAA10g26710 A10 21078701 C T synonymous_variant LOW c.138C>T|p.His46His S301
S304
141673 BAA10g26710 A10 21078852 C T missense_variant MODERATE c.289C>T|p.Leu97Phe S25
141674 BAA10g26700 A10 21078911 G A upstream_gene_variant MODIFIER c.-2854C>T| S113
141675 BAA10g26700 A10 21080190 C T upstream_gene_variant MODIFIER c.-4133G>A| S79
S91