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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g16540 A05 9172620 G A upstream_gene_variant MODIFIER c.-3159G>A| S139
2 BAA05g16540 A05 9174535 C T upstream_gene_variant MODIFIER c.-1244C>T| S237
3 BAA05g16540 A05 9175581 G A upstream_gene_variant MODIFIER c.-198G>A| S192
4 BAA05g16540 A05 9175893 G A missense_variant MODERATE c.115G>A|p.Glu39Lys S260
5 BAA05g16540 A05 9175909 C T missense_variant MODERATE c.131C>T|p.Ser44Leu S268
6 BAA05g16540 A05 9176052 C T missense_variant MODERATE c.274C>T|p.Pro92Ser S143
7 BAA05g16540 A05 9176484 G A missense_variant MODERATE c.706G>A|p.Asp236Asn S13
S168
S219
S64
S72
8 BAA05g16540 A05 9176961 C T stop_gained HIGH c.1183C>T|p.Gln395* S292
9 BAA05g16540 A05 9177033 C T missense_variant MODERATE c.1255C>T|p.Pro419Ser S143
10 BAA05g16540 A05 9177179 C T synonymous_variant LOW c.1401C>T|p.His467His S164
11 BAA05g16540 A05 9177670 G A missense_variant MODERATE c.1892G>A|p.Gly631Asp S217
12 BAA05g16540 A05 9177966 G A missense_variant MODERATE c.2188G>A|p.Asp730Asn S32
13 BAA05g16540 A05 9178297 C T missense_variant MODERATE c.2353C>T|p.Pro785Ser S181
14 BAA05g16540 A05 9178578 G A intron_variant MODIFIER c.2360-96G>A| S172
15 BAA05g16540 A05 9179831 G A intron_variant MODIFIER c.3490+27G>A| S218
16 BAA05g16540 A05 9180301 C T stop_gained HIGH c.3796C>T|p.Gln1266* S286
17 BAA05g16540 A05 9180846 G A missense_variant MODERATE c.4262G>A|p.Arg1421Lys S4
18 BAA05g16540 A05 9183062 G A splice_acceptor_variant&intron_variant HIGH c.5710-1G>A| S7
19 BAA05g16540 A05 9184821 C T missense_variant MODERATE c.6422C>T|p.Thr2141Ile S69
20 BAA05g16540 A05 9184874 G A missense_variant MODERATE c.6475G>A|p.Glu2159Lys S174
S27
S39
21 BAA05g16540 A05 9186659 C T missense_variant MODERATE c.6958C>T|p.Pro2320Ser S27
22 BAA05g16540 A05 9187226 G A downstream_gene_variant MODIFIER c.*228G>A| S100