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 BAA03g00760 A03 279791 G A synonymous_variant LOW c.231G>A|p.Lys77Lys S274
2 BAA03g00760 A03 279928 C T missense_variant MODERATE c.368C>T|p.Ala123Val S17
3 BAA03g00760 A03 280054 G A missense_variant MODERATE c.494G>A|p.Gly165Glu S162
4 BAA03g00760 A03 280122 C T missense_variant MODERATE c.562C>T|p.Leu188Phe S96
5 BAA03g00760 A03 281150 G A missense_variant MODERATE c.1490G>A|p.Gly497Glu S35
6 BAA03g00760 A03 281312 G A missense_variant MODERATE c.1652G>A|p.Arg551His S143
7 BAA03g00760 A03 281729 G A missense_variant MODERATE c.2069G>A|p.Gly690Glu S262
8 BAA03g00760 A03 282470 G A synonymous_variant LOW c.2472G>A|p.Lys824Lys S261
9 BAA03g00760 A03 282949 C T missense_variant MODERATE c.2869C>T|p.Pro957Ser S219
S72
10 BAA03g00760 A03 283159 G A missense_variant MODERATE c.3079G>A|p.Asp1027Asn S206
S26
11 BAA03g00760 A03 283713 G A missense_variant MODERATE c.3418G>A|p.Glu1140Lys S119
12 BAA03g00760 A03 283768 C T missense_variant MODERATE c.3473C>T|p.Pro1158Leu S6
13 BAA03g00760 A03 283812 C T intron_variant MODIFIER c.3498+19C>T| S51
14 BAA03g00760 A03 283995 C T synonymous_variant LOW c.3591C>T|p.Arg1197Arg S127
15 BAA03g00760 A03 284457 G A synonymous_variant LOW c.4053G>A|p.Lys1351Lys S217
S248
16 BAA03g00760 A03 285179 C T missense_variant MODERATE c.4486C>T|p.Leu1496Phe S173
17 BAA03g00760 A03 285203 C T stop_gained HIGH c.4510C>T|p.Arg1504* S216
18 BAA03g00760 A03 285247 C T synonymous_variant LOW c.4554C>T|p.Ser1518Ser S280
19 BAA03g00760 A03 285630 C T missense_variant MODERATE c.4789C>T|p.Pro1597Ser S91
20 BAA03g00760 A03 285989 C T missense_variant MODERATE c.5069C>T|p.Pro1690Leu S242
21 BAA03g00760 A03 286327 C T synonymous_variant LOW c.5407C>T|p.Leu1803Leu S158
22 BAA03g00760 A03 287364 G A downstream_gene_variant MODIFIER c.*239G>A| S188