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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g10820 A05 5524778 G A missense_variant MODERATE c.232G>A|p.Glu78Lys S224
2 BAA05g10820 A05 5524959 C T missense_variant MODERATE c.413C>T|p.Ser138Phe S251
3 BAA05g10820 A05 5525144 G A missense_variant MODERATE c.598G>A|p.Asp200Asn S15
S3
4 BAA05g10820 A05 5525364 G A missense_variant MODERATE c.818G>A|p.Arg273Gln S178
5 BAA05g10820 A05 5525501 C T missense_variant MODERATE c.955C>T|p.Leu319Phe S13
6 BAA05g10820 A05 5525606 C T missense_variant MODERATE c.1060C>T|p.Leu354Phe S201
7 BAA05g10820 A05 5525612 C T stop_gained HIGH c.1066C>T|p.Gln356* S7
8 BAA05g10820 A05 5526010 G A synonymous_variant LOW c.1464G>A|p.Lys488Lys S280
9 BAA05g10820 A05 5526020 G A missense_variant MODERATE c.1474G>A|p.Ala492Thr S278
10 BAA05g10820 A05 5526386 G T stop_gained HIGH c.1840G>T|p.Glu614* S240
11 BAA05g10820 A05 5529391 C T missense_variant MODERATE c.2078C>T|p.Pro693Leu S9
12 BAA05g10820 A05 5529441 G A missense_variant MODERATE c.2128G>A|p.Gly710Ser S192
13 BAA05g10820 A05 5529879 C T missense_variant MODERATE c.2395C>T|p.Pro799Ser S167
14 BAA05g10820 A05 5530211 C T splice_region_variant&intron_variant LOW c.2722+5C>T| S163
15 BAA05g10820 A05 5530264 G A intron_variant MODIFIER c.2722+58G>A| S263
16 BAA05g10820 A05 5530284 C T intron_variant MODIFIER c.2722+78C>T| S181
17 BAA05g10820 A05 5530581 C T intron_variant MODIFIER c.2722+375C>T| S130