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Details for BBS12:c.476C>T, p.Pro159Leu

CHROMOSOME

4

GENOMIC COORDINATES

hg19	hg38
123663523	122742368

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

T

TRANSCRIPT

CDNA CHANGE

c.476C>T

PROTEIN CHANGE

p.Pro159Leu

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
7.957e-06	0.0	0.0	0.0	0.0	0.0	1.76e-05	0.0	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Benign	1.415137	Disease causing

DBSNP ID

1 combination linked to BBS12:c.476C>T, p.Pro159Leu

1 disease linked to BBS12:c.476C>T, p.Pro159Leu

Bardet-Biedl syndrome

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