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


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g20350 A05 12470903 C T missense_variant MODERATE c.5867G>A|p.Arg1956Lys S207
2 BAA05g20350 A05 12471418 C T missense_variant MODERATE c.5515G>A|p.Glu1839Lys S207
3 BAA05g20350 A05 12472104 G A missense_variant MODERATE c.5095C>T|p.Leu1699Phe S288
4 BAA05g20350 A05 12472263 G A missense_variant MODERATE c.5023C>T|p.Pro1675Ser S15
5 BAA05g20350 A05 12472346 C T missense_variant MODERATE c.4940G>A|p.Gly1647Asp S305
6 BAA05g20350 A05 12474471 C T synonymous_variant LOW c.4236G>A|p.Glu1412Glu S255
7 BAA05g20350 A05 12475534 C T intron_variant MODIFIER c.3810+82G>A| S172
S217
8 BAA05g20350 A05 12475775 C T synonymous_variant LOW c.3651G>A|p.Lys1217Lys S174
9 BAA05g20350 A05 12475894 G A missense_variant MODERATE c.3532C>T|p.Pro1178Ser S127
10 BAA05g20350 A05 12476762 C T intron_variant MODIFIER c.2923-154G>A| S185
11 BAA05g20350 A05 12477245 C T splice_acceptor_variant&intron_variant HIGH c.2740-1G>A| S50
12 BAA05g20350 A05 12478092 G A missense_variant MODERATE c.2503C>T|p.Pro835Ser S66
13 BAA05g20350 A05 12478552 C T intron_variant MODIFIER c.2194-51G>A| S209
14 BAA05g20350 A05 12478697 G A missense_variant MODERATE c.2174C>T|p.Ser725Phe S240
15 BAA05g20350 A05 12479725 G A intron_variant MODIFIER c.1602+43C>T| S301
S304
16 BAA05g20350 A05 12480245 G A intron_variant MODIFIER c.1273-20C>T| S257
17 BAA05g20350 A05 12480930 C T missense_variant MODERATE c.919G>A|p.Ala307Thr S259
18 BAA05g20350 A05 12481810 C T synonymous_variant LOW c.39G>A|p.Glu13Glu S171
19 BAA05g20350 A05 12482295 G A upstream_gene_variant MODIFIER c.-447C>T| S62
20 BAA05g20350 A05 12483828 C T upstream_gene_variant MODIFIER c.-1980G>A| S18
21 BAA05g20350 A05 12484345 G A upstream_gene_variant MODIFIER c.-2497C>T| S279
22 BAA05g20350 A05 12484550 C T upstream_gene_variant MODIFIER c.-2702G>A| S17
23 BAA05g20350 A05 12485232 C T upstream_gene_variant MODIFIER c.-3384G>A| S152
24 BAA05g20350 A05 12485674 C T upstream_gene_variant MODIFIER c.-3826G>A| S247