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
96251 BAA10g04540 A10 2320385 C T upstream_gene_variant MODIFIER c.-873G>A| S269
96252 BAA10g04540 A10 2320905 G A upstream_gene_variant MODIFIER c.-1393C>T| S16
96253 BAA10g04550 A10 2321334 C T missense_variant MODERATE c.509G>A|p.Arg170Gln S35
96254 BAA10g04550 A10 2321401 C T missense_variant MODERATE c.442G>A|p.Ala148Thr S281
96255 BAA10g04540 A10 2321831 G A upstream_gene_variant MODIFIER c.-2319C>T| S99
96256 BAA10g04540 A10 2322005 C T upstream_gene_variant MODIFIER c.-2493G>A| S162
96257 BAA10g04540 A10 2322266 G A upstream_gene_variant MODIFIER c.-2754C>T| S208
96258 BAA10g04540 A10 2322506 G A upstream_gene_variant MODIFIER c.-2994C>T| S43
96259 BAA10g04560 A10 2323514 G A missense_variant MODERATE c.4G>A|p.Asp2Asn S230
96260 BAA10g04560 A10 2323560 C T missense_variant MODERATE c.50C>T|p.Ser17Phe S143
96261 BAA10g04560 A10 2323869 G A missense_variant MODERATE c.359G>A|p.Gly120Asp S18
96262 BAA10g04560 A10 2325207 G A missense_variant MODERATE c.1352G>A|p.Gly451Glu S261
96263 BAA10g04560 A10 2326535 C T synonymous_variant LOW c.2286C>T|p.Cys762Cys S116
96264 BAA10g04560 A10 2327551 G A synonymous_variant LOW c.2886G>A|p.Arg962Arg S105
S106
96265 BAA10g04560 A10 2328171 C T missense_variant MODERATE c.3445C>T|p.Pro1149Ser S131
96266 BAA10g04570 A10 2329330 C T synonymous_variant LOW c.831G>A|p.Ser277Ser S40
S49
96267 BAA10g04560 A10 2330336 C T downstream_gene_variant MODIFIER c.*2133C>T| S88
96268 BAA10g04570 A10 2330736 C T missense_variant MODERATE c.116G>A|p.Gly39Glu S132
S137
S215
96269 BAA10g04570 A10 2330787 G A missense_variant MODERATE c.65C>T|p.Thr22Ile S65
96270 BAA10g04570 A10 2330937 G A upstream_gene_variant MODIFIER c.-86C>T| S257
96271 BAA10g04570 A10 2331355 C T upstream_gene_variant MODIFIER c.-504G>A| S275
96272 BAA10g04570 A10 2331643 C T upstream_gene_variant MODIFIER c.-792G>A| S132
S137
S215
S89
96273 BAA10g04570 A10 2331650 C T upstream_gene_variant MODIFIER c.-799G>A| S256
96274 BAA10g04570 A10 2332854 C T upstream_gene_variant MODIFIER c.-2003G>A| S88
96275 BAA10g04580 A10 2332936 C T missense_variant MODERATE c.2134G>A|p.Val712Ile S130