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 BAA07g08850 A07 17765974 C T downstream_gene_variant MODIFIER c.*4721G>A| S202
2 BAA07g08850 A07 17766130 G A downstream_gene_variant MODIFIER c.*4565C>T| S109
3 BAA07g08850 A07 17766763 C T downstream_gene_variant MODIFIER c.*3932G>A| S268
4 BAA07g08850 A07 17767164 C T downstream_gene_variant MODIFIER c.*3531G>A| S259
5 BAA07g08850 A07 17767170 C T downstream_gene_variant MODIFIER c.*3525G>A| S289
S290
6 BAA07g08850 A07 17767462 C T downstream_gene_variant MODIFIER c.*3233G>A| S179
7 BAA07g08850 A07 17767974 G A downstream_gene_variant MODIFIER c.*2721C>T| S245
8 BAA07g08850 A07 17769565 C T downstream_gene_variant MODIFIER c.*1130G>A| S40
S49
9 BAA07g08850 A07 17769646 C T downstream_gene_variant MODIFIER c.*1049G>A| S198
10 BAA07g08850 A07 17770377 G A downstream_gene_variant MODIFIER c.*318C>T| S2
11 BAA07g08850 A07 17770635 C T downstream_gene_variant MODIFIER c.*60G>A| S69
12 BAA07g08850 A07 17770636 C T downstream_gene_variant MODIFIER c.*59G>A| S34
13 BAA07g08850 A07 17770850 G A missense_variant MODERATE c.1084C>T|p.His362Tyr S275
14 BAA07g08850 A07 17770916 G A missense_variant MODERATE c.1018C>T|p.Leu340Phe S171
15 BAA07g08850 A07 17771711 C T missense_variant MODERATE c.223G>A|p.Gly75Arg S167
16 BAA07g08850 A07 17771848 C T missense_variant MODERATE c.86G>A|p.Ser29Asn S274
17 BAA07g08850 A07 17772445 G A upstream_gene_variant MODIFIER c.-512C>T| S124
18 BAA07g08850 A07 17773537 T A upstream_gene_variant MODIFIER c.-1604A>T| S249
19 BAA07g08850 A07 17773551 G A upstream_gene_variant MODIFIER c.-1618C>T| S182
20 BAA07g08850 A07 17774136 C T upstream_gene_variant MODIFIER c.-2203G>A| S136
21 BAA07g08850 A07 17775659 C T upstream_gene_variant MODIFIER c.-3726G>A| S162