NM_021634.4(RXFP1):c.698T>A (p.Val233Asp) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jan 23, 2024
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:: RCV004447118.1

Allele description [Variation Report for NM_021634.4(RXFP1):c.698T>A (p.Val233Asp)]

NM_021634.4(RXFP1):c.698T>A (p.Val233Asp)

Gene:

RXFP1:relaxin family peptide receptor 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

4q32.1

Genomic location:

Preferred name:

NM_021634.4(RXFP1):c.698T>A (p.Val233Asp)

HGVS:

NC_000004.12:g.158617148T>A
NG_031835.2:g.100435T>A
NM_001253727.2:c.779T>A
NM_001253728.2:c.599T>A
NM_001253729.2:c.698T>A
NM_001253730.2:c.308T>A
NM_001253732.2:c.302T>A
NM_001253733.2:c.302T>A
NM_001363776.1:c.455T>A
NM_021634.4:c.698T>AMANE SELECT
NP_001240656.1:p.Val260Asp
NP_001240657.1:p.Val200Asp
NP_001240658.1:p.Val233Asp
NP_001240659.1:p.Val103Asp
NP_001240661.1:p.Val101Asp
NP_001240662.1:p.Val101Asp
NP_001350705.1:p.Val152Asp
NP_067647.2:p.Val233Asp
NC_000004.11:g.159538300T>A
NM_021634.2:c.698T>A
NR_045579.2:n.1482T>A
NR_045580.2:n.846T>A
NR_045581.2:n.817T>A
NR_045582.2:n.898T>A
NR_045583.2:n.736T>A
NR_045584.2:n.846T>A

Protein change:

V101D

Molecular consequence:

NM_001253727.2:c.779T>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001253728.2:c.599T>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001253729.2:c.698T>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001253730.2:c.308T>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001253732.2:c.302T>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001253733.2:c.302T>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363776.1:c.455T>A - missense variant - [Sequence Ontology: SO:0001583]
NM_021634.4:c.698T>A - missense variant - [Sequence Ontology: SO:0001583]
NR_045579.2:n.1482T>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_045580.2:n.846T>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_045581.2:n.817T>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_045582.2:n.898T>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_045583.2:n.736T>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_045584.2:n.846T>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004943925	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jan 23, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004943925

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jan 23, 2024)

germline

clinical testing

Citation Link

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 Ambry Genetics, SCV004943925.1

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

Description

The c.698T>A (p.V233D) alteration is located in exon 9 (coding exon 9) of the RXFP1 gene. This alteration results from a T to A substitution at nucleotide position 698, causing the valine (V) at amino acid position 233 to be replaced by an aspartic acid (D). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	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: May 7, 2024

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