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NM_032578.4(MYPN):c.3913A>G (p.Met1305Val) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jul 1, 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:
RCV001311707.22

Allele description [Variation Report for NM_032578.4(MYPN):c.3913A>G (p.Met1305Val)]

NM_032578.4(MYPN):c.3913A>G (p.Met1305Val)

Gene:
MYPN:myopalladin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
10q21.3
Genomic location:
Preferred name:
NM_032578.4(MYPN):c.3913A>G (p.Met1305Val)
HGVS:
  • NC_000010.11:g.68210405A>G
  • NG_032118.1:g.109289A>G
  • NM_001256267.2:c.3913A>G
  • NM_001256268.2:c.3031A>G
  • NM_032578.4:c.3913A>GMANE SELECT
  • NP_001243196.1:p.Met1305Val
  • NP_001243196.1:p.Met1305Val
  • NP_001243197.1:p.Met1011Val
  • NP_115967.2:p.Met1305Val
  • NP_115967.2:p.Met1305Val
  • LRG_410t1:c.3913A>G
  • LRG_410:g.109289A>G
  • LRG_410p1:p.Met1305Val
  • NC_000010.10:g.69970162A>G
  • NM_001256267.1:c.3913A>G
  • NM_032578.2:c.3913A>G
  • NM_032578.3:c.3913A>G
  • NM_032578.4:c.3913A>G
  • NR_045662.4:n.3450A>G
  • NR_045663.4:n.3987A>G
Protein change:
M1011V
Links:
dbSNP: rs730880170
NCBI 1000 Genomes Browser:
rs730880170
Molecular consequence:
  • NM_001256267.2:c.3913A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256268.2:c.3031A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_032578.4:c.3913A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NR_045662.4:n.3450A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_045663.4:n.3987A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Observations:
2

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001501990CeGaT Center for Human Genetics Tuebingen
criteria provided, single submitter

(CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)		Uncertain significance
(Jul 1, 2024) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes2not providednot providednot providednot providedclinical testing

Details of each submission

From CeGaT Center for Human Genetics Tuebingen, SCV001501990.23

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided2not providednot providedclinical testingnot provided

Description

MYPN: PM2:Supporting, BP4

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided2not providednot providednot provided

Last Updated: Oct 20, 2024