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
125901 BAA10g14880 A10 15455350 G A upstream_gene_variant MODIFIER c.-2183C>T| S241
125902 BAA10g14880 A10 15455569 G A upstream_gene_variant MODIFIER c.-2402C>T| S228
125903 BAA10g14880 A10 15455669 C T upstream_gene_variant MODIFIER c.-2502G>A| S249
125904 BAA10g14880 A10 15456432 G A upstream_gene_variant MODIFIER c.-3265C>T| S198
125905 BAA10g14900 A10 15460471 C T upstream_gene_variant MODIFIER c.-1370C>T| S44
125906 BAA10g14900 A10 15461478 G A upstream_gene_variant MODIFIER c.-363G>A| S128
125907 BAA10g14900 A10 15462376 G A missense_variant MODERATE c.536G>A|p.Gly179Glu S261
125908 BAA10g14900 A10 15462757 C T missense_variant MODERATE c.917C>T|p.Pro306Leu S194
125909 BAA10g14900 A10 15463395 G A missense_variant MODERATE c.1555G>A|p.Gly519Arg S166
125910 BAA10g14900 A10 15463422 G A missense_variant MODERATE c.1582G>A|p.Gly528Ser S15
S3
125911 BAA10g14900 A10 15463549 G A missense_variant MODERATE c.1709G>A|p.Gly570Asp S139
125912 BAA10g14910 A10 15465306 C T upstream_gene_variant MODIFIER c.-3234C>T| S87
125913 BAA10g14910 A10 15469272 G A splice_acceptor_variant&intron_variant HIGH c.241-1G>A| S65
125914 BAA10g14910 A10 15470084 C T synonymous_variant LOW c.774C>T|p.Gly258Gly S200
125915 BAA10g14910 A10 15470690 C T intron_variant MODIFIER c.1159+48C>T| S193
125916 BAA10g14910 A10 15472111 C T intron_variant MODIFIER c.1722-52C>T| S10
125917 BAA10g14910 A10 15472605 C T downstream_gene_variant MODIFIER c.*376C>T| S11
125918 BAA10g14910 A10 15472808 C T downstream_gene_variant MODIFIER c.*579C>T| S60
125919 BAA10g14910 A10 15474276 G A downstream_gene_variant MODIFIER c.*2047G>A| S66
125920 BAA10g14910 A10 15474389 G A downstream_gene_variant MODIFIER c.*2160G>A| S166
125921 BAA10g14910 A10 15474475 C T downstream_gene_variant MODIFIER c.*2246C>T| S103
125922 BAA10g14910 A10 15474799 G A downstream_gene_variant MODIFIER c.*2570G>A| S238
125923 BAA10g14910 A10 15476619 G A downstream_gene_variant MODIFIER c.*4390G>A| S71
125924 BAA10g14910-BAA10g14920 A10 15478107 C T intergenic_region MODIFIER n.15478107C>T| S202
125925 BAA10g14920 A10 15480580 G A downstream_gene_variant MODIFIER c.*2579C>T| S18