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Details for BBS10:p.Cys91Trp

CHROMOSOME

12

GENOMIC COORDINATES

hg19	hg38
76741492	76347712

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

C

TRANSCRIPT

N.A.

CDNA CHANGE

None

PROTEIN CHANGE

p.Cys91Trp

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
2.816e-05	0.0	0.0	0.0	0.0	0.0	5.308e-05	0.0001651	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Damaging	3.461183	Disease causing

DBSNP ID

1 combination linked to BBS10:p.Cys91Trp

2 diseases linked to BBS10:p.Cys91Trp

Alström syndrome; Bardet-Biedl syndrome

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