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NM_001048174.2(MUTYH):c.606+21C>A AND Hereditary cancer-predisposing syndrome

Germline classification:
Benign (1 submission)
Last evaluated:
Aug 21, 2020
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:
RCV002258082.4

Allele description [Variation Report for NM_001048174.2(MUTYH):c.606+21C>A]

NM_001048174.2(MUTYH):c.606+21C>A

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.606+21C>A
HGVS:
  • NC_000001.11:g.45332553G>T
  • NG_008189.1:g.12918C>A
  • NM_001048171.2:c.606+21C>A
  • NM_001048172.2:c.609+21C>A
  • NM_001048173.2:c.606+21C>A
  • NM_001048174.2:c.606+21C>AMANE SELECT
  • NM_001128425.2:c.690+21C>A
  • NM_001293190.2:c.651+21C>A
  • NM_001293191.2:c.639+21C>A
  • NM_001293192.2:c.330+21C>A
  • NM_001293195.2:c.606+21C>A
  • NM_001293196.2:c.330+21C>A
  • NM_001350650.2:c.261+21C>A
  • NM_001350651.2:c.261+21C>A
  • NM_012222.3:c.681+21C>A
  • LRG_220t1:c.690+21C>A
  • LRG_220:g.12918C>A
  • NC_000001.10:g.45798225G>T
  • NM_001128425.1:c.690+21C>A
Links:
dbSNP: rs148552450
NCBI 1000 Genomes Browser:
rs148552450
Molecular consequence:
  • NM_001048171.2:c.606+21C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001048172.2:c.609+21C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001048173.2:c.606+21C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001048174.2:c.606+21C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001128425.2:c.690+21C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001293190.2:c.651+21C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001293191.2:c.639+21C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001293192.2:c.330+21C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001293195.2:c.606+21C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001293196.2:c.330+21C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001350650.2:c.261+21C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001350651.2:c.261+21C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_012222.3:c.681+21C>A - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002532316Sema4, Sema4
criteria provided, single submitter

(Sema4 Curation Guidelines)		Benign
(Aug 21, 2020) 		germlinecuration

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedcuration

Details of each submission

From Sema4, Sema4, SCV002532316.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedcurationnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 20, 2024