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
95351 BAA10g04090 A10 1987097 G A upstream_gene_variant MODIFIER c.-2558G>A| S212
95352 BAA10g04090 A10 1987588 G A upstream_gene_variant MODIFIER c.-2067G>A| S217
S248
95353 BAA10g04090 A10 1987713 C T upstream_gene_variant MODIFIER c.-1942C>T| S54
95354 BAA10g04090 A10 1987744 C T upstream_gene_variant MODIFIER c.-1911C>T| S117
95355 BAA10g04090 A10 1987774 C T upstream_gene_variant MODIFIER c.-1881C>T| S149
95356 BAA10g04090 A10 1988261 G A upstream_gene_variant MODIFIER c.-1394G>A| S180
95357 BAA10g04090 A10 1988732 G A upstream_gene_variant MODIFIER c.-923G>A| S45
95358 BAA10g04080 A10 1988878 C T synonymous_variant LOW c.267G>A|p.Val89Val S204
95359 BAA10g04080 A10 1988949 C T missense_variant MODERATE c.196G>A|p.Ala66Thr S256
95360 BAA10g04080 A10 1989126 G A missense_variant MODERATE c.19C>T|p.Pro7Ser S60
95361 BAA10g04080 A10 1989151 C T upstream_gene_variant MODIFIER c.-7G>A| S41
95362 BAA10g04080 A10 1989167 G A upstream_gene_variant MODIFIER c.-23C>T| S153
S213
95363 BAA10g04080 A10 1989204 G A upstream_gene_variant MODIFIER c.-60C>T| S43
95364 BAA10g04080 A10 1989831 G A upstream_gene_variant MODIFIER c.-687C>T| S1
95365 BAA10g04090 A10 1990454 G A missense_variant MODERATE c.247G>A|p.Glu83Lys S13
95366 BAA10g04080 A10 1990916 C T upstream_gene_variant MODIFIER c.-1772G>A| S204
95367 BAA10g04080 A10 1991364 C T upstream_gene_variant MODIFIER c.-2220G>A| S14
S224
95368 BAA10g04080 A10 1992000 C T upstream_gene_variant MODIFIER c.-2856G>A| S143
95369 BAA10g04080 A10 1992420 G A upstream_gene_variant MODIFIER c.-3276C>T| S178
95370 BAA10g04080 A10 1992629 C T upstream_gene_variant MODIFIER c.-3485G>A| S269
95371 BAA10g04080 A10 1993870 G A upstream_gene_variant MODIFIER c.-4726C>T| S92
95372 BAA10g04080 A10 1993882 G A upstream_gene_variant MODIFIER c.-4738C>T| S198
95373 BAA10g04100 A10 1995229 T A missense_variant MODERATE c.1171A>T|p.Ile391Phe S16
S181
S217
S248
S56
95374 BAA10g04100 A10 1996955 G A splice_region_variant&intron_variant LOW c.269+5C>T| S231
95375 BAA10g04100 A10 1997110 G A missense_variant MODERATE c.119C>T|p.Pro40Leu S306