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
131501 BAA10g18730 A10 17431160 C T missense_variant MODERATE c.920G>A|p.Ser307Asn S267
S301
S304
131502 BAA10g18730 A10 17431688 G A missense_variant MODERATE c.506C>T|p.Pro169Leu S279
131503 BAA10g18730 A10 17432121 G A synonymous_variant LOW c.73C>T|p.Leu25Leu S113
131504 BAA10g18720 A10 17432276 C T upstream_gene_variant MODIFIER c.-3500G>A| S177
S277
131505 BAA10g18720 A10 17432851 G A upstream_gene_variant MODIFIER c.-4075C>T| S138
131506 BAA10g18720 A10 17432958 G A upstream_gene_variant MODIFIER c.-4182C>T| S240
131507 BAA10g18720 A10 17433390 C T upstream_gene_variant MODIFIER c.-4614G>A| S198
131508 BAA10g18730 A10 17437072 G A upstream_gene_variant MODIFIER c.-4879C>T| S71
131509 BAA10g18740 A10 17443433 C T upstream_gene_variant MODIFIER c.-635C>T| S210
131510 BAA10g18740 A10 17443795 G A upstream_gene_variant MODIFIER c.-273G>A| S111
131511 BAA10g18740 A10 17446138 G A missense_variant MODERATE c.778G>A|p.Ala260Thr S270
131512 BAA10g18750 A10 17447347 C T synonymous_variant LOW c.480G>A|p.Lys160Lys S45
131513 BAA10g18750 A10 17450082 C T upstream_gene_variant MODIFIER c.-1641G>A| S203
131514 BAA10g18750 A10 17450517 C T upstream_gene_variant MODIFIER c.-2076G>A| S115
131515 BAA10g18760 A10 17454559 G A upstream_gene_variant MODIFIER c.-2879G>A| S43
131516 BAA10g18760 A10 17455284 C T upstream_gene_variant MODIFIER c.-2154C>T| S18
131517 BAA10g18760 A10 17456589 C T upstream_gene_variant MODIFIER c.-849C>T| S206
131518 BAA10g18760 A10 17462058 C T downstream_gene_variant MODIFIER c.*4250C>T| S135
131519 BAA10g18760 A10 17462663 A G downstream_gene_variant MODIFIER c.*4855A>G| S255
131520 BAA10g18770 A10 17462983 G A upstream_gene_variant MODIFIER c.-4827G>A| S150
131521 BAA10g18770 A10 17468627 C A stop_gained&splice_region_variant HIGH c.726C>A|p.Tyr242* S133
131522 BAA10g18770 A10 17470199 G A missense_variant MODERATE c.1577G>A|p.Gly526Glu S62
131523 BAA10g18780 A10 17478360 G A upstream_gene_variant MODIFIER c.-1842G>A| S74
131524 BAA10g18780 A10 17478553 C T upstream_gene_variant MODIFIER c.-1649C>T| S70
131525 BAA10g18780 A10 17479047 G A upstream_gene_variant MODIFIER c.-1155G>A| S61