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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAS13g00060 Scaffold13 3581266 G A upstream_gene_variant MODIFIER c.-4908G>A| S68
2 BAS13g00060 Scaffold13 3581632 G A upstream_gene_variant MODIFIER c.-4542G>A| S67
3 BAS13g00060 Scaffold13 3581655 A T upstream_gene_variant MODIFIER c.-4519A>T| S134
4 BAS13g00060 Scaffold13 3581762 G A upstream_gene_variant MODIFIER c.-4412G>A| S187
5 BAS13g00060 Scaffold13 3584992 G A upstream_gene_variant MODIFIER c.-1182G>A| S57
6 BAS13g00060 Scaffold13 3585174 G C upstream_gene_variant MODIFIER c.-1000G>C| S212
7 BAS13g00060 Scaffold13 3586291 G A missense_variant MODERATE c.118G>A|p.Ala40Thr S278
8 BAS13g00060 Scaffold13 3587095 G A synonymous_variant LOW c.849G>A|p.Arg283Arg S281
9 BAS13g00060 Scaffold13 3587405 C T missense_variant MODERATE c.1159C>T|p.His387Tyr S63
10 BAS13g00060 Scaffold13 3587513 C T missense_variant MODERATE c.1267C>T|p.Leu423Phe S194
11 BAS13g00060 Scaffold13 3587919 G A missense_variant MODERATE c.1589G>A|p.Gly530Glu S150
12 BAS13g00060 Scaffold13 3588090 C T missense_variant MODERATE c.1760C>T|p.Pro587Leu
13 BAS13g00060 Scaffold13 3588731 C T downstream_gene_variant MODIFIER c.*592C>T| S219
14 BAS13g00060 Scaffold13 3588740 G A downstream_gene_variant MODIFIER c.*601G>A| S182