Details for SCNN1A:c.1922G>T, p.Cys641Phe

CHROMOSOME 12
GENOMIC COORDINATES
hg19hg38
64571966348030
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed_and_verified
GENE SCNN1A
REFERENCE ALLELE C
ALTERNATE ALLELE A
TRANSCRIPT NM_001159575.1
CDNA CHANGE c.1922G>T
PROTEIN CHANGE p.Cys641Phe
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.03450.11040.01150.01590.00.0031

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.0070630.0890.0044930.00010460.0036580.00.00033720.0049160.003065

ESP
AAEA
0.08950.0005817
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedPossibly Damaging2.783486Polymorphism
DBSNP ID rs3741913
1 combination linked to SCNN1A:c.1922G>T, p.Cys641Phe OLI802
1 disease linked to SCNN1A:c.1922G>T, p.Cys641Phe Cystic fibrosis

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