U.S. flag

An official website of the United States government

NM_006580.4(CLDN16):c.392G>C (p.Gly131Ala) AND Inborn genetic diseases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 16, 2022
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
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:
RCV002564094.2

Allele description [Variation Report for NM_006580.4(CLDN16):c.392G>C (p.Gly131Ala)]

NM_006580.4(CLDN16):c.392G>C (p.Gly131Ala)

Gene:
CLDN16:claudin 16 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
3q28
Genomic location:
Preferred name:
NM_006580.4(CLDN16):c.392G>C (p.Gly131Ala)
HGVS:
  • NC_000003.12:g.190408323G>C
  • NG_008149.1:g.25272G>C
  • NM_001378492.1:c.392G>C
  • NM_001378493.1:c.392G>C
  • NM_006580.4:c.392G>CMANE SELECT
  • NP_001365421.1:p.Gly131Ala
  • NP_001365422.1:p.Gly131Ala
  • NP_006571.2:p.Gly131Ala
  • NC_000003.11:g.190126112G>C
  • NC_000003.11:g.190126112G>C
  • NM_006580.3:c.602G>C
Protein change:
G131A
Links:
dbSNP: rs138308105
NCBI 1000 Genomes Browser:
rs138308105
Molecular consequence:
  • NM_001378492.1:c.392G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001378493.1:c.392G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_006580.4:c.392G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Inborn genetic diseases
Identifiers:
MeSH: D030342; MedGen: C0950123

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003758804Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Aug 16, 2022) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV003758804.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The c.602G>C (p.G201A) alteration is located in exon 4 (coding exon 4) of the CLDN16 gene. This alteration results from a G to C substitution at nucleotide position 602, causing the glycine (G) at amino acid position 201 to be replaced by an alanine (A). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024