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 TRIM32:c.896G>A, p.Arg299Gln

CHROMOSOME

9

GENOMIC COORDINATES

hg19	hg38
119460917	116698638

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

CDNA CHANGE

c.896G>A

PROTEIN CHANGE

p.Arg299Gln

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
3.584e-05	0.0	0.0	0.0	0.0	0.0	0.0	0.0	0.000294

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Tolerated	Benign	None	Polymorphism

DBSNP ID

1 combination linked to TRIM32:c.896G>A, p.Arg299Gln

1 disease linked to TRIM32:c.896G>A, p.Arg299Gln

Bardet-Biedl syndrome

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