NM_014425.5(INVS):c.815A>C (p.His272Pro) AND Infantile nephronophthisis

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Feb 15, 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:: RCV002476286.1

Allele description [Variation Report for NM_014425.5(INVS):c.815A>C (p.His272Pro)]

NM_014425.5(INVS):c.815A>C (p.His272Pro)

Gene:

INVS:inversin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9q31.1

Genomic location:

Preferred name:

NM_014425.5(INVS):c.815A>C (p.His272Pro)

HGVS:

NC_000009.12:g.100242588A>C
NG_008316.1:g.148360A>C
NM_001318381.2:c.527A>C
NM_001318382.2:c.-175A>C
NM_014425.5:c.815A>CMANE SELECT
NP_001305310.1:p.His176Pro
NP_055240.2:p.His272Pro
NC_000009.11:g.103004870A>C
NR_134606.2:n.1013A>C

Protein change:

H176P

Links:

dbSNP: rs151080341

NCBI 1000 Genomes Browser:

rs151080341

Molecular consequence:

NM_001318382.2:c.-175A>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001318381.2:c.527A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_014425.5:c.815A>C - missense variant - [Sequence Ontology: SO:0001583]
NR_134606.2:n.1013A>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Infantile nephronophthisis (NPHP2)
Synonyms:: Nephronophthisis 2; Nephronophthisis 2, infantile
Identifiers:: MONDO: MONDO:0011190; MedGen: C1865872; Orphanet: 655; OMIM: 602088

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
SCV002787550	Fulgent Genetics, Fulgent Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Feb 15, 2022)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002787550

Fulgent Genetics, Fulgent Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Feb 15, 2022)

unknown

clinical testing

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

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	clinical 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, SCV002787550.1

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

#	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: Sep 29, 2024

ClinVar

Relating variation to medicine