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NM_001330074.2(WASHC2C):c.1579C>G (p.Pro527Ala) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 12, 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:
RCV004683515.1

Allele description [Variation Report for NM_001330074.2(WASHC2C):c.1579C>G (p.Pro527Ala)]

NM_001330074.2(WASHC2C):c.1579C>G (p.Pro527Ala)

Gene:
WASHC2C:WASH complex subunit 2C [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
10q11.22
Genomic location:
Preferred name:
NM_001330074.2(WASHC2C):c.1579C>G (p.Pro527Ala)
HGVS:
  • NC_000010.11:g.45759345C>G
  • NM_001169106.2:c.1579C>G
  • NM_001169107.2:c.1507C>G
  • NM_001330074.2:c.1579C>GMANE SELECT
  • NM_001367393.1:c.1573C>G
  • NM_001367394.1:c.1507C>G
  • NM_001367395.1:c.1507C>G
  • NM_001367396.1:c.1507C>G
  • NM_001367397.1:c.1579C>G
  • NM_001367398.1:c.928C>G
  • NM_001367399.1:c.1315C>G
  • NM_001367400.1:c.1507C>G
  • NM_001367401.1:c.1548+2206C>G
  • NM_001367402.1:c.1000C>G
  • NM_001367403.1:c.1507C>G
  • NM_001367404.1:c.1420C>G
  • NM_001367405.1:c.1000C>G
  • NM_001367406.1:c.-142C>G
  • NM_001367407.1:c.1000C>G
  • NM_001367408.1:c.1579C>G
  • NM_001367409.1:c.1318C>G
  • NM_001367410.1:c.1315C>G
  • NM_001367411.1:c.1318C>G
  • NM_001367412.1:c.1000C>G
  • NM_001367413.1:c.1246C>G
  • NM_001367414.1:c.1000C>G
  • NM_001367415.1:c.1507C>G
  • NM_001367416.1:c.1579C>G
  • NM_015262.3:c.1579C>G
  • NP_001162577.1:p.Pro527Ala
  • NP_001162578.1:p.Pro503Ala
  • NP_001317003.1:p.Pro527Ala
  • NP_001354322.1:p.Pro525Ala
  • NP_001354323.1:p.Pro503Ala
  • NP_001354324.1:p.Pro503Ala
  • NP_001354325.1:p.Pro503Ala
  • NP_001354326.1:p.Pro527Ala
  • NP_001354327.1:p.Pro310Ala
  • NP_001354328.1:p.Pro439Ala
  • NP_001354329.1:p.Pro503Ala
  • NP_001354331.1:p.Pro334Ala
  • NP_001354332.1:p.Pro503Ala
  • NP_001354333.1:p.Pro474Ala
  • NP_001354334.1:p.Pro334Ala
  • NP_001354336.1:p.Pro334Ala
  • NP_001354337.1:p.Pro527Ala
  • NP_001354338.1:p.Pro440Ala
  • NP_001354339.1:p.Pro439Ala
  • NP_001354340.1:p.Pro440Ala
  • NP_001354341.1:p.Pro334Ala
  • NP_001354342.1:p.Pro416Ala
  • NP_001354343.1:p.Pro334Ala
  • NP_001354344.1:p.Pro503Ala
  • NP_001354345.1:p.Pro527Ala
  • NP_056077.2:p.Pro527Ala
  • NC_000010.10:g.46254793C>G
  • NM_015262.2:c.1579C>G
  • NR_159966.1:n.1841C>G
Protein change:
P310A
Molecular consequence:
  • NM_001367406.1:c.-142C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001367401.1:c.1548+2206C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001169106.2:c.1579C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001169107.2:c.1507C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001330074.2:c.1579C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367393.1:c.1573C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367394.1:c.1507C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367395.1:c.1507C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367396.1:c.1507C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367397.1:c.1579C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367398.1:c.928C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367399.1:c.1315C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367400.1:c.1507C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367402.1:c.1000C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367403.1:c.1507C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367404.1:c.1420C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367405.1:c.1000C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367407.1:c.1000C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367408.1:c.1579C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367409.1:c.1318C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367410.1:c.1315C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367411.1:c.1318C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367412.1:c.1000C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367413.1:c.1246C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367414.1:c.1000C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367415.1:c.1507C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001367416.1:c.1579C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_015262.3:c.1579C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NR_159966.1:n.1841C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005179079Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Apr 12, 2024) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV005179079.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The c.1579C>G (p.P527A) alteration is located in exon 17 (coding exon 17) of the FAM21C gene. This alteration results from a C to G substitution at nucleotide position 1579, causing the proline (P) at amino acid position 527 to be replaced by an alanine (A). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Aug 11, 2024