This site uses cookies!

We use cookies for security, analytics and session persistence reasons. Please refer to our Cookie Policy for more information.

Select Cookie Preferences (Hover for info)

Details for PINK1:c.1444G>A, p.Val482Met

CHROMOSOME

1

GENOMIC COORDINATES

hg19	hg38
20975680	20649187

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

CDNA CHANGE

c.1444G>A

PROTEIN CHANGE

p.Val482Met

ALLELE FREQUENCY

1KGP
Global	AFR	AMR	EAS	EUR	SAS
None	None	None	None	None	None

Gnomad
Global	AFR	AMR	ASJ	EAS	FIN	NFE	OTH	SAS
2.789e-05	0.0	0.0	0.0	0.0001632	0.0	1.765e-05	0.0001633	3.266e-05

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Tolerated	Benign	0.2159	Disease causing

DBSNP ID

1 combination linked to PINK1:c.1444G>A, p.Val482Met

1 disease linked to PINK1:c.1444G>A, p.Val482Met

Parkinson disease

Found any issues with the data on this page? Report this entry.