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NM_018941.4(CLN8):c.37A>G (p.Ile13Val) AND Neuronal ceroid lipofuscinosis 8

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 21, 2020
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV001279439.1

Allele description [Variation Report for NM_018941.4(CLN8):c.37A>G (p.Ile13Val)]

NM_018941.4(CLN8):c.37A>G (p.Ile13Val)

Gene:
CLN8:CLN8 transmembrane ER and ERGIC protein [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
8p23.3
Genomic location:
Preferred name:
NM_018941.4(CLN8):c.37A>G (p.Ile13Val)
HGVS:
  • NC_000008.11:g.1771091A>G
  • NG_008656.2:g.20314A>G
  • NM_018941.4:c.37A>GMANE SELECT
  • NP_061764.2:p.Ile13Val
  • LRG_691:g.20314A>G
  • NC_000008.10:g.1719257A>G
Protein change:
I13V
Links:
dbSNP: rs1563107126
NCBI 1000 Genomes Browser:
rs1563107126
Molecular consequence:
  • NM_018941.4:c.37A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Neuronal ceroid lipofuscinosis 8 (CLN8)
Synonyms:
CLN8-Related Neuronal Ceroid-Lipofuscinosis
Identifiers:
MONDO: MONDO:0010830; MedGen: C1838570; Orphanet: 168491; Orphanet: 228354; Orphanet: 79264; OMIM: 600143

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001466534Natera, Inc.
no assertion criteria provided
Uncertain significance
(Aug 21, 2020) 		germlineclinical testing

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Natera, Inc., SCV001466534.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Mar 26, 2023