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
93301 BAA10g02770 A10 1326627 C T upstream_gene_variant MODIFIER c.-2320G>A| S183
93302 BAA10g02770 A10 1326952 G A upstream_gene_variant MODIFIER c.-2645C>T| S209
93303 BAA10g02770 A10 1327092 C T upstream_gene_variant MODIFIER c.-2785G>A| S8
93304 BAA10g02780 A10 1327354 T C synonymous_variant LOW c.598T>C|p.Leu200Leu S197
S210
S225
S229
S247
93305 BAA10g02780 A10 1327420 C T synonymous_variant LOW c.664C>T|p.Leu222Leu S246
93306 BAA10g02780 A10 1327738 G A missense_variant MODERATE c.766G>A|p.Gly256Arg S289
93307 BAA10g02770 A10 1328070 C T upstream_gene_variant MODIFIER c.-3763G>A| S162
93308 BAA10g02770 A10 1328564 C T upstream_gene_variant MODIFIER c.-4257G>A| S35
93309 BAA10g02770 A10 1329031 C T upstream_gene_variant MODIFIER c.-4724G>A| S245
93310 BAA10g02780 A10 1329596 G A downstream_gene_variant MODIFIER c.*1853G>A| S71
93311 BAA10g02780 A10 1329963 G A downstream_gene_variant MODIFIER c.*2220G>A| S156
93312 BAA10g02790 A10 1330539 C T missense_variant MODERATE c.4189G>A|p.Asp1397Asn S2
93313 BAA10g02780 A10 1330569 C T downstream_gene_variant MODIFIER c.*2826C>T| S139
93314 BAA10g02790 A10 1330759 C T missense_variant MODERATE c.4052G>A|p.Gly1351Glu S249
93315 BAA10g02790 A10 1331006 C T missense_variant&splice_region_variant MODERATE c.3805G>A|p.Val1269Ile S56
93316 BAA10g02790 A10 1331792 G A synonymous_variant LOW c.3177C>T|p.Leu1059Leu S129
93317 BAA10g02790 A10 1333161 C T synonymous_variant LOW c.2157G>A|p.Lys719Lys S170
93318 BAA10g02790 A10 1334007 C T missense_variant MODERATE c.1390G>A|p.Glu464Lys S23
93319 BAA10g02790 A10 1334444 G A missense_variant MODERATE c.953C>T|p.Pro318Leu S51
93320 BAA10g02790 A10 1334552 G A missense_variant MODERATE c.845C>T|p.Ser282Phe S164
93321 BAA10g02790 A10 1334561 C T missense_variant MODERATE c.836G>A|p.Arg279Lys S260
93322 BAA10g02790 A10 1334609 C T missense_variant MODERATE c.788G>A|p.Arg263Lys S177
93323 BAA10g02790 A10 1335287 G A missense_variant MODERATE c.110C>T|p.Ser37Phe S17
93324 BAA10g02790 A10 1335355 G A synonymous_variant LOW c.42C>T|p.Leu14Leu S71
93325 BAA10g02790 A10 1335652 G A upstream_gene_variant MODIFIER c.-256C>T| S149
S170