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
177451 BAA02g18830 A02 9695200 C T splice_region_variant&intron_variant LOW c.1776-4G>A| S218
177452 BAA02g18830 A02 9695282 C T intron_variant MODIFIER c.1776-86G>A| S177
177453 BAA02g18830 A02 9695975 C T synonymous_variant LOW c.1506G>A|p.Thr502Thr S209
177454 BAA02g18830 A02 9696322 G A missense_variant MODERATE c.1159C>T|p.Leu387Phe S166
177455 BAA02g18830 A02 9696338 G A synonymous_variant LOW c.1143C>T|p.Leu381Leu S173
177456 BAA02g18830 A02 9696494 G A synonymous_variant LOW c.987C>T|p.Gly329Gly S72
S78
177457 BAA02g18830 A02 9696917 G A synonymous_variant LOW c.564C>T|p.Asn188Asn S33
177458 BAA02g18830 A02 9698420 C T upstream_gene_variant MODIFIER c.-597G>A| S152
177459 BAA02g18830 A02 9698645 G A upstream_gene_variant MODIFIER c.-822C>T| S148
S210
S30
S31
177460 BAA02g18830 A02 9699248 G A upstream_gene_variant MODIFIER c.-1425C>T| S228
177461 BAA02g18830 A02 9699415 C T upstream_gene_variant MODIFIER c.-1592G>A| S302
177462 BAA02g18830 A02 9700837 C T upstream_gene_variant MODIFIER c.-3014G>A| S181
177463 BAA02g18830 A02 9701146 C T upstream_gene_variant MODIFIER c.-3323G>A| S2
177464 BAA02g18830 A02 9701291 G A upstream_gene_variant MODIFIER c.-3468C>T| S133
177465 BAA02g18840 A02 9701891 C T synonymous_variant LOW c.303C>T|p.Ser101Ser S135
177466 BAA02g18840 A02 9702032 C T synonymous_variant LOW c.444C>T|p.Leu148Leu S46
177467 BAA02g18850 A02 9703601 C T downstream_gene_variant MODIFIER c.*1532G>A| S167
177468 BAA02g18850 A02 9703667 C T downstream_gene_variant MODIFIER c.*1466G>A| S8
177469 BAA02g18850 A02 9705177 C T missense_variant MODERATE c.3004G>A|p.Asp1002Asn S121
177470 BAA02g18840 A02 9705291 C T downstream_gene_variant MODIFIER c.*777C>T| S175
177471 BAA02g18850 A02 9705609 C T missense_variant MODERATE c.2665G>A|p.Val889Ile S209
177472 BAA02g18850 A02 9705703 C T synonymous_variant LOW c.2637G>A|p.Lys879Lys S138
177473 BAA02g18850 A02 9705775 C T synonymous_variant LOW c.2565G>A|p.Leu855Leu S163
177474 BAA02g18850 A02 9705799 C T synonymous_variant LOW c.2541G>A|p.Val847Val S135
177475 BAA02g18850 A02 9706113 C T missense_variant MODERATE c.2227G>A|p.Ala743Thr S186