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
130901 BAA10g18370 A10 17214495 G T synonymous_variant LOW c.1053G>T|p.Leu351Leu S222
S227
S75
130902 BAA10g18380 A10 17214724 G A upstream_gene_variant MODIFIER c.-1213G>A| S50
130903 BAA10g18370 A10 17214775 G A missense_variant MODERATE c.1163G>A|p.Arg388Lys S109
130904 BAA10g18380 A10 17214925 C T upstream_gene_variant MODIFIER c.-1012C>T| S55
130905 BAA10g18390 A10 17216118 G A upstream_gene_variant MODIFIER c.-2679G>A| S35
130906 BAA10g18380 A10 17216481 C T missense_variant MODERATE c.260C>T|p.Ser87Phe S156
130907 BAA10g18390 A10 17216614 C T upstream_gene_variant MODIFIER c.-2183C>T| S180
130908 BAA10g18390 A10 17216645 C T upstream_gene_variant MODIFIER c.-2152C>T| S156
130909 BAA10g18390 A10 17216806 G A upstream_gene_variant MODIFIER c.-1991G>A| S69
130910 BAA10g18390 A10 17217163 C T upstream_gene_variant MODIFIER c.-1634C>T| S256
130911 BAA10g18390 A10 17218572 G A upstream_gene_variant MODIFIER c.-225G>A| S176
130912 BAA10g18390 A10 17219344 G A missense_variant MODERATE c.372G>A|p.Met124Ile S38
130913 BAA10g18390 A10 17219365 G A synonymous_variant LOW c.393G>A|p.Ala131Ala S166
130914 BAA10g18370 A10 17219673 C T downstream_gene_variant MODIFIER c.*4526C>T| S61
130915 BAA10g18370 A10 17219863 C T downstream_gene_variant MODIFIER c.*4716C>T| S202
130916 BAA10g18390 A10 17220193 C T synonymous_variant LOW c.883C>T|p.Leu295Leu S163
130917 BAA10g18390 A10 17220448 G A missense_variant MODERATE c.1073G>A|p.Arg358Gln S279
130918 BAA10g18390 A10 17220937 C T synonymous_variant LOW c.1284C>T|p.Leu428Leu S144
130919 BAA10g18380 A10 17221015 G A downstream_gene_variant MODIFIER c.*3313G>A| S298
130920 BAA10g18390 A10 17221521 C T synonymous_variant LOW c.1638C>T|p.Pro546Pro S51
130921 BAA10g18390 A10 17221677 C T synonymous_variant LOW c.1693C>T|p.Leu565Leu S48
130922 BAA10g18390 A10 17221701 C T missense_variant MODERATE c.1717C>T|p.Pro573Ser S170
130923 BAA10g18380 A10 17222595 G A downstream_gene_variant MODIFIER c.*4893G>A| S65
130924 BAA10g18390 A10 17222757 G A downstream_gene_variant MODIFIER c.*200G>A| S15
S3
130925 BAA10g18390 A10 17223163 C T downstream_gene_variant MODIFIER c.*606C>T| S186