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
97551 BAA10g05450 A10 2790839 C A upstream_gene_variant MODIFIER c.-2971G>T| S179
97552 BAA10g05460 A10 2792953 C T missense_variant MODERATE c.1241C>T|p.Ser414Leu S287
97553 BAA10g05470 A10 2794281 G A missense_variant MODERATE c.1246C>T|p.Pro416Ser S251
97554 BAA10g05470 A10 2795001 C T missense_variant MODERATE c.526G>A|p.Asp176Asn S10
97555 BAA10g05470 A10 2795480 G A missense_variant MODERATE c.47C>T|p.Ser16Phe S262
97556 BAA10g05470 A10 2795613 G A upstream_gene_variant MODIFIER c.-87C>T| S219
S72
97557 BAA10g05470 A10 2796008 G A upstream_gene_variant MODIFIER c.-482C>T| S215
97558 BAA10g05470 A10 2796024 C T upstream_gene_variant MODIFIER c.-498G>A| S286
97559 BAA10g05470 A10 2796416 G A upstream_gene_variant MODIFIER c.-890C>T| S221
97560 BAA10g05470 A10 2796631 C T upstream_gene_variant MODIFIER c.-1105G>A| S200
97561 BAA10g05470 A10 2797184 G A upstream_gene_variant MODIFIER c.-1658C>T| S120
97562 BAA10g05470 A10 2799062 G A upstream_gene_variant MODIFIER c.-3536C>T| S50
97563 BAA10g05470 A10 2799411 C T upstream_gene_variant MODIFIER c.-3885G>A| S132
S137
S89
97564 BAA10g05470 A10 2799658 C T upstream_gene_variant MODIFIER c.-4132G>A| S235
97565 BAA10g05470 A10 2799813 C T upstream_gene_variant MODIFIER c.-4287G>A| S35
97566 BAA10g05470 A10 2799995 C T upstream_gene_variant MODIFIER c.-4469G>A| S282
97567 BAA10g05480 A10 2800285 G A missense_variant MODERATE c.19G>A|p.Ala7Thr S161
97568 BAA10g05480 A10 2800324 G A missense_variant MODERATE c.58G>A|p.Glu20Lys S103
97569 BAA10g05480 A10 2800394 C T missense_variant MODERATE c.128C>T|p.Ser43Leu S92
97570 BAA10g05480 A10 2801309 C T downstream_gene_variant MODIFIER c.*509C>T| S60
97571 BAA10g05480 A10 2801503 C T downstream_gene_variant MODIFIER c.*703C>T| S71
97572 BAA10g05480 A10 2801575 C T downstream_gene_variant MODIFIER c.*775C>T| S67
97573 BAA10g05490 A10 2801850 C T missense_variant MODERATE c.1282G>A|p.Asp428Asn S173
97574 BAA10g05490 A10 2802008 C T synonymous_variant LOW c.1209G>A|p.Glu403Glu S232
97575 BAA10g05490 A10 2802292 C T synonymous_variant LOW c.1014G>A|p.Arg338Arg S87