Details for SCNN1A:c.609G>T, p.Leu203Leu

CHROMOSOME 12
GENOMIC COORDINATES
hg19hg38
64727536363587
VARIANT EFFECT silent
ANNOTATION FLAG automatically_attributed_and_verified
GENE SCNN1A
REFERENCE ALLELE C
ALTERNATE ALLELE A
TRANSCRIPT NM_001159575.1
CDNA CHANGE c.609G>T
PROTEIN CHANGE p.Leu203Leu
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00720.00.00720.00.02090.0102

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.018610.0046110.011780.034595.64e-050.014770.027160.02080.0106

ESP
AAEA
0.0038640.01745
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone-0.112424Polymorphism
DBSNP ID rs55859427
1 combination linked to SCNN1A:c.609G>T, p.Leu203Leu OLI803
1 disease linked to SCNN1A:c.609G>T, p.Leu203Leu Cystic fibrosis

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