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
94001 BAA10g03150 A10 1540602 G A missense_variant MODERATE c.469G>A|p.Asp157Asn S33
94002 BAA10g03150 A10 1541904 G A missense_variant MODERATE c.949G>A|p.Val317Ile S17
94003 BAA10g03160 A10 1543345 G A upstream_gene_variant MODIFIER c.-1049G>A| S240
94004 BAA10g03160 A10 1543389 C T upstream_gene_variant MODIFIER c.-1005C>T| S28
94005 BAA10g03160 A10 1543566 C T upstream_gene_variant MODIFIER c.-828C>T| S226
94006 BAA10g03160 A10 1544318 C T upstream_gene_variant MODIFIER c.-76C>T| S37
94007 BAA10g03160 A10 1544408 C T synonymous_variant LOW c.15C>T|p.Ile5Ile S180
94008 BAA10g03160 A10 1545283 C T missense_variant MODERATE c.533C>T|p.Ala178Val S202
94009 BAA10g03160 A10 1545349 G A missense_variant MODERATE c.599G>A|p.Ser200Asn S18
94010 BAA10g03150 A10 1546759 C T downstream_gene_variant MODIFIER c.*3565C>T| S165
94011 BAA10g03170 A10 1547511 C T missense_variant MODERATE c.940G>A|p.Ala314Thr S139
94012 BAA10g03160 A10 1548394 T A downstream_gene_variant MODIFIER c.*2191T>A| S152
94013 BAA10g03170 A10 1548499 C T splice_donor_variant&intron_variant HIGH c.505+1G>A| S2
94014 BAA10g03160 A10 1548681 C T downstream_gene_variant MODIFIER c.*2478C>T| S104
S52
94015 BAA10g03160 A10 1548967 G A downstream_gene_variant MODIFIER c.*2764G>A| S128
94016 BAA10g03160 A10 1549211 G A downstream_gene_variant MODIFIER c.*3008G>A| S186
94017 BAA10g03170 A10 1549703 C T missense_variant MODERATE c.247G>A|p.Glu83Lys S131
94018 BAA10g03170 A10 1549970 C T upstream_gene_variant MODIFIER c.-21G>A| S189
94019 BAA10g03170 A10 1550676 G A upstream_gene_variant MODIFIER c.-727C>T| S211
S227
94020 BAA10g03170 A10 1551143 G A upstream_gene_variant MODIFIER c.-1194C>T| S179
94021 BAA10g03170 A10 1551961 G A upstream_gene_variant MODIFIER c.-2012C>T| S17
94022 BAA10g03170 A10 1552348 C T upstream_gene_variant MODIFIER c.-2399G>A| S152
94023 BAA10g03180 A10 1552885 G A missense_variant MODERATE c.1097C>T|p.Ser366Phe S53
94024 BAA10g03180 A10 1553227 C T missense_variant MODERATE c.755G>A|p.Gly252Glu S107
94025 BAA10g03180 A10 1553725 G A missense_variant MODERATE c.328C>T|p.Pro110Ser S66