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
132251 BAA10g19220 A10 17705712 G A missense_variant MODERATE c.1415G>A|p.Arg472Lys S38
132252 BAA10g19220 A10 17706216 G A missense_variant MODERATE c.1919G>A|p.Gly640Asp S219
S72
132253 BAA10g19230 A10 17707120 G A upstream_gene_variant MODIFIER c.-4792G>A| S295
132254 BAA10g19230 A10 17707316 C T upstream_gene_variant MODIFIER c.-4596C>T| S187
132255 BAA10g19230 A10 17707498 G A upstream_gene_variant MODIFIER c.-4414G>A| S295
132256 BAA10g19230 A10 17708799 C T upstream_gene_variant MODIFIER c.-3113C>T| S45
132257 BAA10g19230 A10 17709251 G A upstream_gene_variant MODIFIER c.-2661G>A| S162
132258 BAA10g19230 A10 17710029 C T upstream_gene_variant MODIFIER c.-1883C>T| S281
132259 BAA10g19230 A10 17710788 C T upstream_gene_variant MODIFIER c.-1124C>T| S5
132260 BAA10g19230 A10 17711914 G A start_lost HIGH c.3G>A|p.Met1? S212
132261 BAA10g19230 A10 17712514 G A synonymous_variant LOW c.603G>A|p.Ala201Ala S155
S211
132262 BAA10g19240 A10 17714202 G A upstream_gene_variant MODIFIER c.-862C>T| S131
132263 BAA10g19240 A10 17714410 G A upstream_gene_variant MODIFIER c.-1070C>T| S278
132264 BAA10g19240 A10 17715385 C T upstream_gene_variant MODIFIER c.-2045G>A| S41
132265 BAA10g19250 A10 17716966 C T missense_variant&splice_region_variant MODERATE c.595G>A|p.Asp199Asn S37
132266 BAA10g19240 A10 17717274 G A upstream_gene_variant MODIFIER c.-3934C>T| S219
132267 BAA10g19250 A10 17718178 C T splice_region_variant&intron_variant LOW c.307+3G>A| S46
132268 BAA10g19250 A10 17718223 C T missense_variant MODERATE c.265G>A|p.Gly89Arg S25
132269 BAA10g19250 A10 17718230 C T synonymous_variant LOW c.258G>A|p.Ala86Ala S236
132270 BAA10g19260 A10 17718540 C T downstream_gene_variant MODIFIER c.*2081G>A| S115
132271 BAA10g19250 A10 17720337 C T upstream_gene_variant MODIFIER c.-1447G>A| S156
132272 BAA10g19250 A10 17720477 C T upstream_gene_variant MODIFIER c.-1587G>A| S11
132273 BAA10g19250 A10 17721039 G A upstream_gene_variant MODIFIER c.-2149C>T| S85
132274 BAA10g19270 A10 17722755 G A missense_variant MODERATE c.1117C>T|p.Pro373Ser S212
132275 BAA10g19250 A10 17723274 C T upstream_gene_variant MODIFIER c.-4384G>A| S262