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
96001 BAA10g04460 A10 2246991 G A upstream_gene_variant MODIFIER c.-596G>A| S242
96002 BAA10g04460 A10 2247261 G A upstream_gene_variant MODIFIER c.-326G>A| S295
96003 BAA10g04450 A10 2247826 C T downstream_gene_variant MODIFIER c.*4555C>T| S125
96004 BAA10g04450 A10 2248208 G A downstream_gene_variant MODIFIER c.*4937G>A| S263
96005 BAA10g04470 A10 2249755 A T downstream_gene_variant MODIFIER c.*3177T>A| S153
S213
96006 BAA10g04470 A10 2251943 C T downstream_gene_variant MODIFIER c.*989G>A| S108
96007 BAA10g04460 A10 2252632 G A downstream_gene_variant MODIFIER c.*207G>A| S120
96008 BAA10g04470 A10 2253198 C T missense_variant MODERATE c.1153G>A|p.Glu385Lys S177
96009 BAA10g04470 A10 2253290 C T missense_variant MODERATE c.1061G>A|p.Gly354Glu S225
S73
96010 BAA10g04470 A10 2253720 G A synonymous_variant LOW c.631C>T|p.Leu211Leu S219
S72
96011 BAA10g04470 A10 2253995 C T stop_gained HIGH c.356G>A|p.Trp119* S12
96012 BAA10g04470 A10 2254508 C T upstream_gene_variant MODIFIER c.-158G>A| S143
96013 BAA10g04470 A10 2254534 C T upstream_gene_variant MODIFIER c.-184G>A| S149
96014 BAA10g04470 A10 2255984 G A upstream_gene_variant MODIFIER c.-1634C>T| S95
96015 BAA10g04480 A10 2256515 C T synonymous_variant LOW c.4971G>A|p.Lys1657Lys S271
96016 BAA10g04470 A10 2257205 C T upstream_gene_variant MODIFIER c.-2855G>A| S37
96017 BAA10g04480 A10 2258281 C T missense_variant MODERATE c.4303G>A|p.Val1435Ile S155
S211
96018 BAA10g04470 A10 2258544 G A upstream_gene_variant MODIFIER c.-4194C>T| S25
96019 BAA10g04480 A10 2259220 C T missense_variant MODERATE c.3794G>A|p.Ser1265Asn S108
96020 BAA10g04480 A10 2260797 C T missense_variant MODERATE c.2875G>A|p.Glu959Lys S73
S91
96021 BAA10g04480 A10 2261944 G A intron_variant MODIFIER c.2259+16C>T| S208
S219
96022 BAA10g04480 A10 2261974 G A missense_variant MODERATE c.2245C>T|p.Arg749Cys S105
S106
96023 BAA10g04480 A10 2262160 C T missense_variant MODERATE c.2143G>A|p.Val715Ile S23
96024 BAA10g04480 A10 2262917 G A missense_variant MODERATE c.1748C>T|p.Thr583Ile S60
96025 BAA10g04480 A10 2262992 G A missense_variant MODERATE c.1673C>T|p.Ala558Val S292