Details for KCNQ3:c.1360C>T, p.Pro454Ser

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
133146616132134369
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed_and_verified
GENE KCNQ3
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_001204824.2
CDNA CHANGE c.1360C>T
PROTEIN CHANGE p.Pro454Ser
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00160.00.00290.00.0060.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.0021240.00079970.0026310.00099250.00.00032340.0034550.0032570.0

ESP
AAEA
0.0002270.003721
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging3.663527Disease causing
DBSNP ID rs74582884
1 combination linked to KCNQ3:c.1360C>T, p.Pro454Ser OLI560
1 disease linked to KCNQ3:c.1360C>T, p.Pro454Ser Generalized epilepsy with febrile seizures-plus

Found any issues with the data on this page? Report this entry.