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NM_001166108.2(PALLD):c.1965-12573C>G AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Nov 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:
RCV004837776.1

Allele description [Variation Report for NM_001166108.2(PALLD):c.1965-12573C>G]

NM_001166108.2(PALLD):c.1965-12573C>G

Gene:
PALLD:palladin, cytoskeletal associated protein [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
4q32.3
Genomic location:
Preferred name:
NM_001166108.2(PALLD):c.1965-12573C>G
HGVS:
  • NC_000004.12:g.168878349C>G
  • NG_013376.1:g.386284C>G
  • NM_001166108.2:c.1965-12573C>GMANE SELECT
  • NM_001166109.2:c.819-12573C>G
  • NM_001166110.2:c.458C>G
  • NM_001367567.1:c.-157-12573C>G
  • NM_001367568.1:c.-157-12573C>G
  • NM_001367569.1:c.-157-12573C>G
  • NM_001367570.1:c.-157-12573C>G
  • NM_016081.4:c.1965-12573C>G
  • NP_001159582.1:p.Pro153Arg
  • NC_000004.11:g.169799500C>G
  • NM_001166110.1:c.458C>G
Protein change:
P153R
Links:
dbSNP: rs1220928329
NCBI 1000 Genomes Browser:
rs1220928329
Molecular consequence:
  • NM_001166108.2:c.1965-12573C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001166109.2:c.819-12573C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001367567.1:c.-157-12573C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001367568.1:c.-157-12573C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001367569.1:c.-157-12573C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001367570.1:c.-157-12573C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_016081.4:c.1965-12573C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001166110.2:c.458C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005463845Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Nov 23, 2024) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV005463845.1

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

Description

The p.P153R variant (also known as c.458C>G), located in coding exon 1 of the PALLD gene, results from a C to G substitution at nucleotide position 458. The proline at codon 153 is replaced by arginine, an amino acid with dissimilar properties. This amino acid position is conserved. In addition, the in silico prediction for this alteration is inconclusive. Based on the available evidence, the clinical significance of this variant remains unclear.

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

Last Updated: Feb 25, 2025