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
97801 BAA10g05600 A10 2880129 G A splice_acceptor_variant&intron_variant HIGH c.185-1G>A| S133
97802 BAA10g05600 A10 2880175 G A stop_gained HIGH c.230G>A|p.Trp77* S55
97803 BAA10g05600 A10 2880442 C T missense_variant MODERATE c.497C>T|p.Ser166Phe S199
97804 BAA10g05600 A10 2880447 C T missense_variant MODERATE c.502C>T|p.Pro168Ser S28
97805 BAA10g05600 A10 2880583 G A missense_variant&splice_region_variant MODERATE c.544G>A|p.Ala182Thr S95
97806 BAA10g05610 A10 2881489 G A upstream_gene_variant MODIFIER c.-2729G>A| S274
97807 BAA10g05610 A10 2881775 C T upstream_gene_variant MODIFIER c.-2443C>T| S84
S93
97808 BAA10g05610 A10 2883778 C T upstream_gene_variant MODIFIER c.-440C>T| S155
S211
97809 BAA10g05610 A10 2883922 C T upstream_gene_variant MODIFIER c.-296C>T| S175
S177
97810 BAA10g05610 A10 2884734 G A missense_variant MODERATE c.211G>A|p.Gly71Arg S142
S65
97811 BAA10g05610 A10 2885604 C T missense_variant MODERATE c.739C>T|p.Arg247Cys S51
97812 BAA10g05620 A10 2885968 G A upstream_gene_variant MODIFIER c.-1738G>A| S274
97813 BAA10g05620 A10 2885970 G A upstream_gene_variant MODIFIER c.-1736G>A| S264
97814 BAA10g05610 A10 2886209 C T missense_variant MODERATE c.1228C>T|p.Pro410Ser S35
97815 BAA10g05610 A10 2886455 C T missense_variant MODERATE c.1474C>T|p.Leu492Phe S87
97816 BAA10g05620 A10 2886721 C T upstream_gene_variant MODIFIER c.-985C>T| S135
97817 BAA10g05610 A10 2887105 C T missense_variant MODERATE c.1763C>T|p.Pro588Leu S292
97818 BAA10g05620 A10 2888001 G A missense_variant MODERATE c.215G>A|p.Ser72Asn S85
97819 BAA10g05610 A10 2888996 C T downstream_gene_variant MODIFIER c.*1848C>T| S229
97820 BAA10g05610 A10 2889656 G A downstream_gene_variant MODIFIER c.*2508G>A| S302
97821 BAA10g05630 A10 2890254 C T missense_variant MODERATE c.1276G>A|p.Glu426Lys S87
97822 BAA10g05630 A10 2890724 G A missense_variant MODERATE c.806C>T|p.Ser269Leu S228
97823 BAA10g05630 A10 2890916 C T missense_variant MODERATE c.614G>A|p.Arg205His S286
97824 BAA10g05630 A10 2891236 G A synonymous_variant LOW c.294C>T|p.Asp98Asp S53
97825 BAA10g05630 A10 2892144 C A upstream_gene_variant MODIFIER c.-615G>T| S35