NM_020639.3(RIPK4):c.722G>A (p.Arg241His) AND Bartsocas-Papas syndrome 1

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Mar 26, 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:: RCV001706914.1

Allele description [Variation Report for NM_020639.3(RIPK4):c.722G>A (p.Arg241His)]

NM_020639.3(RIPK4):c.722G>A (p.Arg241His)

Gene:

RIPK4:receptor interacting serine/threonine kinase 4 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

21q22.3

Genomic location:

Preferred name:

NM_020639.3(RIPK4):c.722G>A (p.Arg241His)

HGVS:

NC_000021.9:g.41746723C>T
NG_032113.2:g.25367G>A
NM_020639.3:c.722G>AMANE SELECT
NP_065690.2:p.Arg241His
NC_000021.8:g.43166883C>T

Protein change:

R241H

Links:

dbSNP: rs891831110

NCBI 1000 Genomes Browser:

rs891831110

Molecular consequence:

NM_020639.3:c.722G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Bartsocas-Papas syndrome 1
Synonyms:: PTERYGIUM, POPLITEAL, LETHAL TYPE; Popliteal pterygium syndrome lethal type; MULTIPLE PTERYGIUM SYNDROME, ASLAN TYPE; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0009901; MedGen: C1849718; Orphanet: 1234; OMIM: 263650

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001934499	Institute of Human Genetics, University of Leipzig Medical Center	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic (Mar 26, 2021)	maternal	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

SCV001934499

Institute of Human Genetics, University of Leipzig Medical Center

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic
(Mar 26, 2021)

maternal

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	maternal	yes	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 Institute of Human Genetics, University of Leipzig Medical Center, SCV001934499.1

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

Description

This variant was identified as homozygous.

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

Last Updated: Dec 24, 2023

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