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NM_000311.5(PRNP):c.246A>G (p.Gly82=) AND Huntington disease-like 1

Germline classification:
Benign (1 submission)
Last evaluated:
Oct 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:
RCV000644591.7

Allele description [Variation Report for NM_000311.5(PRNP):c.246A>G (p.Gly82=)]

NM_000311.5(PRNP):c.246A>G (p.Gly82=)

Gene:
PRNP:prion protein (Kanno blood group) [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
20p13
Genomic location:
Preferred name:
NM_000311.5(PRNP):c.246A>G (p.Gly82=)
HGVS:
  • NC_000020.11:g.4699466A>G
  • NG_009087.1:g.18316A>G
  • NM_000311.5:c.246A>GMANE SELECT
  • NM_001080121.3:c.246A>G
  • NM_001080122.3:c.246A>G
  • NM_001080123.3:c.246A>G
  • NM_001271561.3:c.157A>G
  • NM_183079.4:c.246A>G
  • NP_000302.1:p.Gly82=
  • NP_001073590.1:p.Gly82=
  • NP_001073591.1:p.Gly82=
  • NP_001073592.1:p.Gly82=
  • NP_001258490.1:p.Thr53Ala
  • NP_898902.1:p.Gly82=
  • NC_000020.10:g.4680112A>G
  • NM_000311.3:c.246A>G
Protein change:
T53A
Links:
dbSNP: rs62643364
NCBI 1000 Genomes Browser:
rs62643364
Molecular consequence:
  • NM_001271561.3:c.157A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_000311.5:c.246A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001080121.3:c.246A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001080122.3:c.246A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001080123.3:c.246A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_183079.4:c.246A>G - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:
Huntington disease-like 1 (HDL1)
Synonyms:
HUNTINGTON-LIKE NEURODEGENERATIVE DISORDER 1; HUNTINGTON-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL DOMINANT; PRION DISEASE, EARLY-ONSET, WITH PROMINENT PSYCHIATRIC FEATURES
Identifiers:
MONDO: MONDO:0011299; MedGen: C1864112; Orphanet: 157941; OMIM: 603218

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000766291Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Benign
(Oct 21, 2020) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV000766291.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024