Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 21 of 21 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g27180 A05 31573517 C T downstream_gene_variant MODIFIER c.*2870G>A| S117
2 BAA05g27180 A05 31574840 G A downstream_gene_variant MODIFIER c.*1547C>T| S151
S263
3 BAA05g27180 A05 31574859 G A downstream_gene_variant MODIFIER c.*1528C>T| S245
4 BAA05g27180 A05 31575516 C T downstream_gene_variant MODIFIER c.*871G>A| S288
5 BAA05g27180 A05 31578154 C T missense_variant MODERATE c.2572G>A|p.Glu858Lys S143
6 BAA05g27180 A05 31578338 C T missense_variant MODERATE c.2473G>A|p.Glu825Lys S56
7 BAA05g27180 A05 31578488 G A missense_variant MODERATE c.2402C>T|p.Ala801Val S281
8 BAA05g27180 A05 31578563 C T missense_variant MODERATE c.2327G>A|p.Gly776Glu S208
S219
9 BAA05g27180 A05 31578573 G A splice_region_variant&intron_variant LOW c.2320-3C>T| S243
S299
10 BAA05g27180 A05 31579004 C T missense_variant MODERATE c.2023G>A|p.Asp675Asn S114
11 BAA05g27180 A05 31579273 G A missense_variant MODERATE c.1841C>T|p.Ser614Phe S283
12 BAA05g27180 A05 31581347 C T splice_donor_variant&intron_variant HIGH c.735+1G>A| S188
13 BAA05g27180 A05 31581357 G A synonymous_variant LOW c.726C>T|p.Arg242Arg S176
S282
14 BAA05g27180 A05 31581915 C T stop_gained HIGH c.255G>A|p.Trp85* S37
15 BAA05g27180 A05 31582334 C T upstream_gene_variant MODIFIER c.-165G>A| S45
16 BAA05g27180 A05 31582349 G A upstream_gene_variant MODIFIER c.-180C>T| S163
17 BAA05g27180 A05 31584594 C T upstream_gene_variant MODIFIER c.-2425G>A| S303
18 BAA05g27180 A05 31585298 C T upstream_gene_variant MODIFIER c.-3129G>A| S9
19 BAA05g27180 A05 31585730 C T upstream_gene_variant MODIFIER c.-3561G>A| S116
20 BAA05g27180 A05 31585754 C T upstream_gene_variant MODIFIER c.-3585G>A| S42
21 BAA05g27180 A05 31585776 C T upstream_gene_variant MODIFIER c.-3607G>A| S242