NM_001379270.1(CNGA1):c.1570G>C (p.Ala524Pro) AND Retinitis pigmentosa

Germline classification:: not provided (1 submission)
Review status:: no classification 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:: RCV000844915.1

Allele description [Variation Report for NM_001379270.1(CNGA1):c.1570G>C (p.Ala524Pro)]

NM_001379270.1(CNGA1):c.1570G>C (p.Ala524Pro)

Genes:

CNGA1:cyclic nucleotide gated channel subunit alpha 1 [Gene - OMIM - HGNC]
LOC101927157:uncharacterized LOC101927157 [Gene]

Variant type:

single nucleotide variant

Cytogenetic location:

4p12

Genomic location:

Preferred name:

NM_001379270.1(CNGA1):c.1570G>C (p.Ala524Pro)

HGVS:

NC_000004.12:g.47936912C>G
NG_009193.1:g.81033G>C
NM_000087.5:c.1570G>C
NM_001142564.2:c.1570G>C
NM_001379270.1:c.1570G>CMANE SELECT
NP_000078.3:p.Ala524Pro
NP_001136036.2:p.Ala524Pro
NP_001366199.1:p.Ala524Pro
NC_000004.11:g.47938929C>G
NM_000087.3:c.1582G>C

Protein change:

A524P

Links:

dbSNP: rs373946784

NCBI 1000 Genomes Browser:

rs373946784

Molecular consequence:

NM_000087.5:c.1570G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001142564.2:c.1570G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001379270.1:c.1570G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Retinitis pigmentosa (RP)
Synonyms:: Tapetoretinal degeneration
Identifiers:: MONDO: MONDO:0019200; MeSH: D012174; MedGen: C0035334; Orphanet: 791; OMIM: 268000; OMIM: PS268000

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000986722	GenomeConnect, ClinGen	no classification provided	not provided	unknown	phenotyping only

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000986722

GenomeConnect, ClinGen

no classification provided

not provided

unknown

phenotyping only

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	phenotyping only

Details of each submission

From GenomeConnect, ClinGen, SCV000986722.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	phenotyping only	not provided

Description

Variant interpretted as Uncertain significance and reported on 01/15/2018 by GTR ID Blueprint Genetics. GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant.

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

Last Updated: Apr 23, 2022

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