NM_006642.5(SDCCAG8):c.1409A>G (p.Glu470Gly) AND SDCCAG8-related disorder

Germline classification:: Benign (1 submission)
Last evaluated:: Jun 1, 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:: RCV004532738.2

Allele description [Variation Report for NM_006642.5(SDCCAG8):c.1409A>G (p.Glu470Gly)]

NM_006642.5(SDCCAG8):c.1409A>G (p.Glu470Gly)

Gene:

SDCCAG8:SHH signaling and ciliogenesis regulator SDCCAG8 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q43

Genomic location:

Preferred name:

NM_006642.5(SDCCAG8):c.1409A>G (p.Glu470Gly)

HGVS:

NC_000001.11:g.243344267A>G
NG_027811.1:g.93263A>G
NM_001350246.2:c.506A>G
NM_001350247.2:c.506A>G
NM_001350248.2:c.1505A>G
NM_001350249.2:c.1115A>G
NM_001350251.2:c.506A>G
NM_006642.5:c.1409A>GMANE SELECT
NP_001337175.1:p.Glu169Gly
NP_001337176.1:p.Glu169Gly
NP_001337177.1:p.Glu502Gly
NP_001337178.1:p.Glu372Gly
NP_001337180.1:p.Glu169Gly
NP_006633.1:p.Glu470Gly
NC_000001.10:g.243507569A>G
NM_006642.3:c.1409A>G

Protein change:

E169G

Links:

dbSNP: rs118064970

Molecular consequence:

NM_001350246.2:c.506A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350247.2:c.506A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350248.2:c.1505A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350249.2:c.1115A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001350251.2:c.506A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_006642.5:c.1409A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: SDCCAG8-related disorder
Synonyms:: SDCCAG8-Related Disorders; SDCCAG8-related condition
Identifiers:

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004729068	PreventionGenetics, part of Exact Sciences	no assertion criteria provided	Benign (Jun 1, 2020)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004729068

PreventionGenetics, part of Exact Sciences

no assertion criteria provided

Benign
(Jun 1, 2020)

germline

clinical testing

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 PreventionGenetics, part of Exact Sciences, SCV004729068.2

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

Description

This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

#	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: Jul 14, 2026

ClinVar

Relating variation to medicine