U.S. flag

An official website of the United States government

NM_153704.6(TMEM67):c.2374A>G (p.Arg792Gly) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Sep 22, 2021
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:
RCV002478013.1

Allele description [Variation Report for NM_153704.6(TMEM67):c.2374A>G (p.Arg792Gly)]

NM_153704.6(TMEM67):c.2374A>G (p.Arg792Gly)

Gene:
TMEM67:transmembrane protein 67 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
8q22.1
Genomic location:
Preferred name:
NM_153704.6(TMEM67):c.2374A>G (p.Arg792Gly)
HGVS:
  • NC_000008.11:g.93804813A>G
  • NG_009190.1:g.54970A>G
  • NM_001142301.1:c.2131A>G
  • NM_153704.6:c.2374A>GMANE SELECT
  • NP_001135773.1:p.Arg711Gly
  • NP_714915.3:p.Arg792Gly
  • LRG_688t2:c.2131A>G
  • LRG_688:g.54970A>G
  • LRG_688p2:p.Arg711Gly
  • NC_000008.10:g.94817041A>G
  • NR_024522.2:n.2395A>G
Protein change:
R711G
Links:
dbSNP: rs1815059174
NCBI 1000 Genomes Browser:
rs1815059174
Molecular consequence:
  • NM_001142301.1:c.2131A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_153704.6:c.2374A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NR_024522.2:n.2395A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Functional consequence:
variation affecting protein function [Variation Ontology: 0003]

Condition(s)

Name:
COACH syndrome 1
Identifiers:
MONDO: MONDO:0800103; MedGen: C5435651; Orphanet: 1454; OMIM: 216360
Name:
Joubert syndrome 6 (JBTS6)
Identifiers:
MONDO: MONDO:0012539; MedGen: C1853153; Orphanet: 475; OMIM: 610688
Name:
Meckel syndrome, type 3 (MKS3)
Synonyms:
MECKEL-GRUBER SYNDROME, TYPE 3
Identifiers:
MONDO: MONDO:0011821; MedGen: C1846357; Orphanet: 564; OMIM: 607361
Name:
RHYNS syndrome
Synonyms:
Retinitis pigmentosa, HYpopituitarism, Nephronophthisis, and mild Skeletal dysplasia; Retinitis pigmentosa syndrome
Identifiers:
MONDO: MONDO:0011202; MedGen: C1865794; Orphanet: 140976; OMIM: 602152
Name:
Bardet-Biedl syndrome 14 (BBS14)
Identifiers:
MONDO: MONDO:0014442; MedGen: C2673874; Orphanet: 110; OMIM: 615991
Name:
Nephronophthisis 11 (NPHP11)
Identifiers:
MONDO: MONDO:0013302; MedGen: C3150796; Orphanet: 84081; OMIM: 613550

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
SCV002783286Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Sep 22, 2021) 		unknownclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Fulgent Genetics, Fulgent Genetics, SCV002783286.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Mar 5, 2024