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 BAA05g27440 A05 31690474 C T missense_variant MODERATE c.967G>A|p.Asp323Asn S152
2 BAA05g27440 A05 31690933 G A synonymous_variant LOW c.771C>T|p.Thr257Thr S263
S51
3 BAA05g27440 A05 31692581 G A intron_variant MODIFIER c.490-1212C>T| S200
4 BAA05g27440 A05 31692617 C T intron_variant MODIFIER c.490-1248G>A| S100
S188
5 BAA05g27440 A05 31693094 C T intron_variant MODIFIER c.490-1725G>A| S207
6 BAA05g27440 A05 31693270 G A intron_variant MODIFIER c.490-1901C>T| S85
7 BAA05g27440 A05 31693392 C T intron_variant MODIFIER c.490-2023G>A| S33
8 BAA05g27440 A05 31693529 G A intron_variant MODIFIER c.490-2160C>T| S218
9 BAA05g27440 A05 31693554 G A intron_variant MODIFIER c.489+2154C>T| S107
10 BAA05g27440 A05 31693978 G A intron_variant MODIFIER c.489+1730C>T| S262
11 BAA05g27440 A05 31694454 G A intron_variant MODIFIER c.489+1254C>T| S279
12 BAA05g27440 A05 31694613 G A intron_variant MODIFIER c.489+1095C>T| S18
13 BAA05g27440 A05 31694946 C T intron_variant MODIFIER c.489+762G>A| S202
14 BAA05g27440 A05 31696094 C T intron_variant MODIFIER c.399+199G>A| S63
15 BAA05g27440 A05 31696449 C T synonymous_variant LOW c.243G>A|p.Lys81Lys S226
16 BAA05g27440 A05 31697257 G A upstream_gene_variant MODIFIER c.-495C>T| S104
S52
17 BAA05g27440 A05 31697416 G A upstream_gene_variant MODIFIER c.-654C>T| S296