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
182501 BAA02g21440 A02 11537259 A G upstream_gene_variant MODIFIER c.-1309A>G| S174
S216
S27
182502 BAA02g21440 A02 11538558 G A upstream_gene_variant MODIFIER c.-10G>A| S200
182503 BAA02g21450 A02 11539661 C T upstream_gene_variant MODIFIER c.-3666C>T| S301
S304
182504 BAA02g21450 A02 11539952 C T upstream_gene_variant MODIFIER c.-3375C>T| S174
182505 BAA02g21440 A02 11540405 C T missense_variant MODERATE c.397C>T|p.Arg133Trp S293
182506 BAA02g21450 A02 11542791 G A upstream_gene_variant MODIFIER c.-536G>A| S251
182507 BAA02g21450 A02 11543336 C T missense_variant MODERATE c.10C>T|p.Leu4Phe S286
182508 BAA02g21450 A02 11543346 C T missense_variant MODERATE c.20C>T|p.Pro7Leu S203
182509 BAA02g21450 A02 11543552 G A missense_variant MODERATE c.226G>A|p.Asp76Asn S116
182510 BAA02g21460 A02 11543806 C T upstream_gene_variant MODIFIER c.-4310C>T| S242
182511 BAA02g21460 A02 11544114 G A upstream_gene_variant MODIFIER c.-4002G>A| S146
182512 BAA02g21450 A02 11544527 G A synonymous_variant LOW c.549G>A|p.Arg183Arg S281
182513 BAA02g21450 A02 11545578 G A synonymous_variant LOW c.1251G>A|p.Val417Val S133
182514 BAA02g21460 A02 11546071 G A upstream_gene_variant MODIFIER c.-2045G>A| S293
182515 BAA02g21460 A02 11547237 C T upstream_gene_variant MODIFIER c.-879C>T| S226
182516 BAA02g21460 A02 11547285 G A upstream_gene_variant MODIFIER c.-831G>A| S148
S210
S30
S31
182517 BAA02g21460 A02 11547323 G A upstream_gene_variant MODIFIER c.-793G>A| S247
182518 BAA02g21460 A02 11548303 C T missense_variant MODERATE c.188C>T|p.Thr63Ile S281
182519 BAA02g21480 A02 11548840 C T upstream_gene_variant MODIFIER c.-1622C>T| S32
182520 BAA02g21480 A02 11549066 C T upstream_gene_variant MODIFIER c.-1396C>T| S292
182521 BAA02g21470 A02 11549447 G A missense_variant MODERATE c.116C>T|p.Ser39Phe S129
182522 BAA02g21480 A02 11550703 C T missense_variant MODERATE c.139C>T|p.Pro47Ser S302
182523 BAA02g21480 A02 11550715 G A missense_variant MODERATE c.151G>A|p.Asp51Asn S239
182524 BAA02g21470 A02 11552698 C T upstream_gene_variant MODIFIER c.-3136G>A| S268
182525 BAA02g21470 A02 11553792 C T upstream_gene_variant MODIFIER c.-4230G>A| S115