Details for NOBOX:c.1856C>T, p.Pro619Leu

CHROMOSOME 7
GENOMIC COORDINATES
hg19hg38
144094553144397460
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed_and_verified
GENE NOBOX
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_001080413.3
CDNA CHANGE c.1856C>T
PROTEIN CHANGE p.Pro619Leu
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00960.03480.00140.00.0010.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.0011060.015130.001180.00.00.00.00012540.00095240.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign0.484485Polymorphism
DBSNP ID rs146227301
1 combination linked to NOBOX:c.1856C>T, p.Pro619Leu OLI093
1 disease linked to NOBOX:c.1856C>T, p.Pro619Leu Primary ovarian failure

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