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
127601 BAA10g16030 A10 16080911 C T upstream_gene_variant MODIFIER c.-483C>T| S174
S27
S39
127602 BAA10g16030 A10 16080972 C T upstream_gene_variant MODIFIER c.-422C>T| S12
127603 BAA10g16030 A10 16081384 G A upstream_gene_variant MODIFIER c.-10G>A| S75
S81
127604 BAA10g16040 A10 16082453 G A upstream_gene_variant MODIFIER c.-3143G>A| S112
127605 BAA10g16040 A10 16082627 C T upstream_gene_variant MODIFIER c.-2969C>T| S229
127606 BAA10g16040 A10 16082911 C T upstream_gene_variant MODIFIER c.-2685C>T| S194
127607 BAA10g16040 A10 16083270 C T upstream_gene_variant MODIFIER c.-2326C>T| S259
127608 BAA10g16040 A10 16085373 G A upstream_gene_variant MODIFIER c.-223G>A| S4
127609 BAA10g16040 A10 16085530 C T upstream_gene_variant MODIFIER c.-66C>T| S187
127610 BAA10g16040 A10 16085630 C T missense_variant MODERATE c.35C>T|p.Ser12Phe S144
127611 BAA10g16040 A10 16086425 C T synonymous_variant LOW c.675C>T|p.Tyr225Tyr S170
127612 BAA10g16040 A10 16086871 C T splice_region_variant&intron_variant LOW c.844-8C>T| S152
127613 BAA10g16050 A10 16088262 C T upstream_gene_variant MODIFIER c.-1729C>T| S298
127614 BAA10g16050 A10 16088382 C T upstream_gene_variant MODIFIER c.-1609C>T| S33
127615 BAA10g16050 A10 16088588 C T upstream_gene_variant MODIFIER c.-1403C>T| S177
127616 BAA10g16050 A10 16088621 G A upstream_gene_variant MODIFIER c.-1370G>A| S16
127617 BAA10g16050 A10 16089657 C T upstream_gene_variant MODIFIER c.-334C>T| S70
127618 BAA10g16050 A10 16089659 G A upstream_gene_variant MODIFIER c.-332G>A| S157
S163
127619 BAA10g16070 A10 16090030 G A upstream_gene_variant MODIFIER c.-4702G>A| S251
127620 BAA10g16050 A10 16090194 G A synonymous_variant LOW c.108G>A|p.Lys36Lys S303
127621 BAA10g16050 A10 16091260 C T synonymous_variant LOW c.1098C>T|p.Val366Val S131
127622 BAA10g16070 A10 16092060 G A upstream_gene_variant MODIFIER c.-2672G>A| S157
S163
127623 BAA10g16060 A10 16092841 C T synonymous_variant LOW c.1035G>A|p.Lys345Lys S152
127624 BAA10g16060 A10 16093012 C T synonymous_variant LOW c.954G>A|p.Gln318Gln S299
127625 BAA10g16070 A10 16094786 C T missense_variant MODERATE c.55C>T|p.Pro19Ser S195