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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g05740 A01 2557364 G A synonymous_variant LOW c.5538C>T|p.Leu1846Leu S6
2 BAA01g05740 A01 2557485 G A missense_variant MODERATE c.5417C>T|p.Thr1806Ile S23
3 BAA01g05740 A01 2557540 G A missense_variant MODERATE c.5362C>T|p.Pro1788Ser S13
4 BAA01g05740 A01 2558171 C T stop_gained HIGH c.4952G>A|p.Trp1651* S18
5 BAA01g05740 A01 2559109 G A missense_variant MODERATE c.4160C>T|p.Pro1387Leu S146
6 BAA01g05740 A01 2559906 G A synonymous_variant LOW c.3600C>T|p.Asn1200Asn S201
7 BAA01g05740 A01 2560007 C T missense_variant MODERATE c.3499G>A|p.Ala1167Thr S171
8 BAA01g05740 A01 2560065 C T splice_acceptor_variant&intron_variant HIGH c.3442-1G>A| S206
S26
9 BAA01g05740 A01 2560092 G A intron_variant MODIFIER c.3442-28C>T| S279
10 BAA01g05740 A01 2560808 C T missense_variant MODERATE c.3058G>A|p.Glu1020Lys S267
11 BAA01g05740 A01 2560858 G A missense_variant MODERATE c.3008C>T|p.Thr1003Ile S183
S198
12 BAA01g05740 A01 2561806 C T missense_variant MODERATE c.2371G>A|p.Asp791Asn S112
13 BAA01g05740 A01 2563477 G A synonymous_variant LOW c.1578C>T|p.Tyr526Tyr S144
14 BAA01g05740 A01 2565573 C T missense_variant MODERATE c.194G>A|p.Ser65Asn S51
15 BAA01g05740 A01 2565649 C T missense_variant MODERATE c.118G>A|p.Glu40Lys S130
16 BAA01g05740 A01 2566194 G A missense_variant MODERATE c.17C>T|p.Ser6Phe S142