UNC13D: c.1240C>T p.Arg414Cys


Bibliography:

Biallelic:

Yes

Monoallelic:

-

Described >1 patient:

Yes

Functional Studies:

Yes

Disclaimer The information on this database is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. The authors are not responsible for neither its use nor misuse. The authors have worked with care in the development of this server, but assume no liability or responsibility for any error, weakness, incompleteness or temporariness of the resource and of the data provided.

Interpreting the variant


Learn more about the variant

Clinical Evidence ClinVar Uncertain significance
(criteria provided, single submitter)
UniProt -
Biological Relevance Functional residue Interaction with RAB27A
Variant Information dbSNP rs750811263
Ensembl variant
Population Allele Frequency ExAC 8e-06
gnomAD 1.1e-05

Explore the biomedical information

Disease Protein Gene
DECIPHER Reactome Ensembl
HPO STRING GeneCards
GeneReviews UniProt HGNC
MalaCards NCBI
MedGen OMIM
OMIM
Orphanet

Locate your variant in the protein