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 RYR1:c.4213C>A, p.Pro1405Thr

CHROMOSOME

19

GENOMIC COORDINATES

hg19	hg38
38966010	38475370

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

A

TRANSCRIPT

CDNA CHANGE

c.4213C>A

PROTEIN CHANGE

p.Pro1405Thr

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
1.61e-05	0.0	0.0	0.0	0.0	0.0	3.562e-05	0.0	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Benign	1.905579	Disease causing

DBSNP ID

1 combination linked to RYR1:c.4213C>A, p.Pro1405Thr

1 disease linked to RYR1:c.4213C>A, p.Pro1405Thr

Rare pervasive developmental disorder

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