Details for MKKS:c.442C>T, p.Gln148Ter

CHROMOSOME 20
GENOMIC COORDINATES
hg19hg38
1039372110413073
VARIANT EFFECT nonsense
ANNOTATION FLAG manually_corrected
GENE MKKS
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_170784.3
CDNA CHANGE c.442C>T
PROTEIN CHANGE p.Gln148Ter
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone4.825142Disease causing
DBSNP ID rs137853154
1 combination linked to MKKS:c.442C>T, p.Gln148Ter OLI067
1 disease linked to MKKS:c.442C>T, p.Gln148Ter Bardet-Biedl syndrome

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