Details for SCNN1A:c.610C>T, p.Arg204Trp

CHROMOSOME 12
GENOMIC COORDINATES
hg19hg38
64727526363586
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed_and_verified
GENE SCNN1A
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_001159575.2
CDNA CHANGE c.610C>T
PROTEIN CHANGE p.Arg204Trp
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00720.00.00720.00.02090.0102

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.01860.0046260.011760.034555.643e-050.014780.027140.020820.01067

ESP
AAEA
0.0034090.01641
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging2.223628Polymorphism
DBSNP ID rs55797039
1 combination linked to SCNN1A:c.610C>T, p.Arg204Trp OLI803
1 disease linked to SCNN1A:c.610C>T, p.Arg204Trp Cystic fibrosis

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