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
91551 BAA10g01470 A10 738431 G A missense_variant MODERATE c.229G>A|p.Asp77Asn S151
S263
91552 BAA10g01460 A10 740469 A T upstream_gene_variant MODIFIER c.-4801T>A| S62
91553 BAA10g01480 A10 743448 G A upstream_gene_variant MODIFIER c.-3442G>A| S133
91554 BAA10g01480 A10 744064 C T upstream_gene_variant MODIFIER c.-2826C>T| S206
S210
S26
91555 BAA10g01480 A10 744244 C T upstream_gene_variant MODIFIER c.-2646C>T| S113
91556 BAA10g01480 A10 744418 G A upstream_gene_variant MODIFIER c.-2472G>A| S264
91557 BAA10g01480 A10 744776 C T upstream_gene_variant MODIFIER c.-2114C>T| S31
91558 BAA10g01480 A10 745174 G A upstream_gene_variant MODIFIER c.-1716G>A| S69
91559 BAA10g01480 A10 745507 G A upstream_gene_variant MODIFIER c.-1383G>A| S17
91560 BAA10g01480 A10 745854 G A upstream_gene_variant MODIFIER c.-1036G>A| S48
91561 BAA10g01480 A10 746009 C T upstream_gene_variant MODIFIER c.-881C>T| S221
91562 BAA10g01480 A10 746450 C T upstream_gene_variant MODIFIER c.-440C>T| S31
91563 BAA10g01480 A10 746577 G A upstream_gene_variant MODIFIER c.-313G>A| S211
S227
91564 BAA10g01490 A10 747116 C T upstream_gene_variant MODIFIER c.-2837C>T| S169
91565 BAA10g01480 A10 747991 C T synonymous_variant LOW c.516C>T|p.Val172Val S31
91566 BAA10g01480 A10 748418 G A missense_variant MODERATE c.757G>A|p.Asp253Asn S219
S72
91567 BAA10g01480 A10 749462 C T synonymous_variant LOW c.1479C>T|p.Thr493Thr S286
91568 BAA10g01480 A10 749540 C T synonymous_variant LOW c.1557C>T|p.Asn519Asn S113
91569 BAA10g01490 A10 750006 C T synonymous_variant LOW c.54C>T|p.Arg18Arg S131
91570 BAA10g01490 A10 750841 G A synonymous_variant LOW c.354G>A|p.Arg118Arg S4
91571 BAA10g01490 A10 750849 G A missense_variant MODERATE c.362G>A|p.Ser121Asn S296
91572 BAA10g01490 A10 750919 G A synonymous_variant LOW c.432G>A|p.Glu144Glu S150
91573 BAA10g01500 A10 752606 C T missense_variant MODERATE c.2675G>A|p.Arg892Lys S182
91574 BAA10g01500 A10 753071 G A missense_variant MODERATE c.2210C>T|p.Ala737Val S178
91575 BAA10g01500 A10 754229 G A missense_variant MODERATE c.1132C>T|p.Leu378Phe S274