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 BBS1:c.1016A>T, p.His339Leu

CHROMOSOME

11

GENOMIC COORDINATES

hg19	hg38
66291259	66523788

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

A

ALTERNATE ALLELE

T

TRANSCRIPT

CDNA CHANGE

c.1016A>T

PROTEIN CHANGE

p.His339Leu

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
3.99e-06	0.0	0.0	0.0	0.0	0.0	8.805e-06	0.0	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Tolerated	Benign	0.683993	Polymorphism

DBSNP ID

1 combination linked to BBS1:c.1016A>T, p.His339Leu

1 disease linked to BBS1:c.1016A>T, p.His339Leu

Bardet-Biedl syndrome

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