NM_018899.6(PCDHAC2):c.2096G>A (p.Arg699Gln) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 1, 2023
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:: RCV004497887.1

Allele description [Variation Report for NM_018899.6(PCDHAC2):c.2096G>A (p.Arg699Gln)]

NM_018899.6(PCDHAC2):c.2096G>A (p.Arg699Gln)

Genes:

PCDHA10:protocadherin alpha 10 [Gene - OMIM - HGNC]
PCDHA11:protocadherin alpha 11 [Gene - OMIM - HGNC]
PCDHA12:protocadherin alpha 12 [Gene - OMIM - HGNC]
PCDHA13:protocadherin alpha 13 [Gene - OMIM - HGNC]
PCDHA1:protocadherin alpha 1 [Gene - OMIM - HGNC]
PCDHA2:protocadherin alpha 2 [Gene - OMIM - HGNC]
PCDHA3:protocadherin alpha 3 [Gene - OMIM - HGNC]
PCDHA4:protocadherin alpha 4 [Gene - OMIM - HGNC]
PCDHA5:protocadherin alpha 5 [Gene - OMIM - HGNC]
PCDHA6:protocadherin alpha 6 [Gene - OMIM - HGNC]
PCDHA7:protocadherin alpha 7 [Gene - OMIM - HGNC]
PCDHA8:protocadherin alpha 8 [Gene - OMIM - HGNC]
PCDHA9:protocadherin alpha 9 [Gene - OMIM - HGNC]
PCDHA@:protocadherin alpha cluster, complex locus [Gene - OMIM - HGNC]
PCDHAC1:protocadherin alpha subfamily C, 1 [Gene - OMIM - HGNC]
PCDHAC2:protocadherin alpha subfamily C, 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

5q31.3

Genomic location:

Preferred name:

NM_018899.6(PCDHAC2):c.2096G>A (p.Arg699Gln)

HGVS:

NC_000005.10:g.140968862G>A
NG_000016.2:g.234736G>A
NG_050672.1:g.47146G>A
NG_050674.1:g.117980G>A
NG_050675.1:g.172665G>A
NG_050677.1:g.179004G>A
NM_018898.5:c.2434-10087G>AMANE SELECT
NM_018899.6:c.2096G>AMANE SELECT
NM_018900.4:c.2395-10087G>AMANE SELECT
NM_018901.4:c.2389-10087G>AMANE SELECT
NM_018902.5:c.2392-10087G>AMANE SELECT
NM_018903.4:c.2368-10087G>AMANE SELECT
NM_018904.3:c.2395-10087G>AMANE SELECT
NM_018905.3:c.2389-10087G>AMANE SELECT
NM_018906.3:c.2395-10087G>AMANE SELECT
NM_018907.4:c.2386-10087G>AMANE SELECT
NM_018908.3:c.2353-10087G>AMANE SELECT
NM_018909.4:c.2395-10087G>AMANE SELECT
NM_018910.3:c.2356-10087G>AMANE SELECT
NM_018911.3:c.2395-10087G>AMANE SELECT
NM_031411.3:c.1603-10087G>A
NM_031849.3:c.1603-10087G>A
NM_031857.2:c.2395-10087G>AMANE SELECT
NM_031860.3:c.1600-10087G>A
NM_031883.2:c.2096G>A
NP_061722.1:p.Arg699Gln
NP_114089.1:p.Arg699Gln
NC_000005.9:g.140348447G>A
NM_018899.5:c.2096G>A

Protein change:

R699Q

Molecular consequence:

NM_018898.5:c.2434-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_018900.4:c.2395-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_018901.4:c.2389-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_018902.5:c.2392-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_018903.4:c.2368-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_018904.3:c.2395-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_018905.3:c.2389-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_018906.3:c.2395-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_018907.4:c.2386-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_018908.3:c.2353-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_018909.4:c.2395-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_018910.3:c.2356-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_018911.3:c.2395-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_031411.3:c.1603-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_031849.3:c.1603-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_031857.2:c.2395-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_031860.3:c.1600-10087G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_018899.6:c.2096G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_031883.2:c.2096G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004999510	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Dec 1, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004999510

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Dec 1, 2023)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV004999510.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The c.2096G>A (p.R699Q) alteration is located in exon 1 (coding exon 1) of the PCDHAC2 gene. This alteration results from a G to A substitution at nucleotide position 2096, causing the arginine (R) at amino acid position 699 to be replaced by a glutamine (Q). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 1, 2024

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