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 RPGRIP1L:c.2156C>G, p.Thr719Arg

CHROMOSOME

16

GENOMIC COORDINATES

hg19	hg38
53683024	53649112

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

C

TRANSCRIPT

CDNA CHANGE

c.2156C>G

PROTEIN CHANGE

p.Thr719Arg

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
None	None	None	None	None	None	None	None	None

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Benign	2.198117	Polymorphism

DBSNP ID

1 combination linked to RPGRIP1L:c.2156C>G, p.Thr719Arg

1 disease linked to RPGRIP1L:c.2156C>G, p.Thr719Arg

Adolescent idiopathic scoliosis

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