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NM_001048174.2(MUTYH):c.1321G>A (p.Val441Ile) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Sep 6, 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:
RCV000484811.4

Allele description [Variation Report for NM_001048174.2(MUTYH):c.1321G>A (p.Val441Ile)]

NM_001048174.2(MUTYH):c.1321G>A (p.Val441Ile)

Gene:
MUTYH:mutY DNA glycosylase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1p34.1
Genomic location:
Preferred name:
NM_001048174.2(MUTYH):c.1321G>A (p.Val441Ile)
HGVS:
  • NC_000001.11:g.45331253C>T
  • NG_008189.1:g.14218G>A
  • NM_001048171.2:c.1321G>A
  • NM_001048172.2:c.1324G>A
  • NM_001048173.2:c.1321G>A
  • NM_001048174.2:c.1321G>AMANE SELECT
  • NM_001128425.2:c.1405G>A
  • NM_001293190.2:c.1366G>A
  • NM_001293191.2:c.1354G>A
  • NM_001293192.2:c.1045G>A
  • NM_001293195.2:c.1321G>A
  • NM_001293196.2:c.1045G>A
  • NM_001350650.2:c.976G>A
  • NM_001350651.2:c.976G>A
  • NM_012222.3:c.1396G>A
  • NP_001041636.1:p.Val455Ile
  • NP_001041636.2:p.Val441Ile
  • NP_001041637.1:p.Val442Ile
  • NP_001041638.1:p.Val441Ile
  • NP_001041639.1:p.Val441Ile
  • NP_001121897.1:p.Val469Ile
  • NP_001121897.1:p.Val469Ile
  • NP_001280119.1:p.Val456Ile
  • NP_001280120.1:p.Val452Ile
  • NP_001280121.1:p.Val349Ile
  • NP_001280124.1:p.Val441Ile
  • NP_001280125.1:p.Val349Ile
  • NP_001337579.1:p.Val326Ile
  • NP_001337580.1:p.Val326Ile
  • NP_036354.1:p.Val466Ile
  • LRG_220t1:c.1405G>A
  • LRG_220:g.14218G>A
  • LRG_220p1:p.Val469Ile
  • NC_000001.10:g.45796925C>T
  • NM_001048171.1:c.1363G>A
  • NM_001128425.1:c.1405G>A
  • NR_146882.2:n.1549G>A
  • NR_146883.2:n.1398G>A
  • p.V469I
Protein change:
V326I
Links:
dbSNP: rs779701238
NCBI 1000 Genomes Browser:
rs779701238
Molecular consequence:
  • NM_001048171.2:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001048172.2:c.1324G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001048173.2:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001048174.2:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001128425.2:c.1405G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001293190.2:c.1366G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001293191.2:c.1354G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001293192.2:c.1045G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001293195.2:c.1321G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001293196.2:c.1045G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001350650.2:c.976G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001350651.2:c.976G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_012222.3:c.1396G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_146882.2:n.1549G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_146883.2:n.1398G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000567080GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Uncertain significance
(Sep 6, 2024)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From GeneDx, SCV000567080.7

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

Description

Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis indicates that this missense variant does not alter protein structure/function; Observed in cases and controls in a breast cancer case-control study (PMID: 33471991); This variant is associated with the following publications: (PMID: 23108399, 33471991)

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

Last Updated: Oct 13, 2024