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NM_000531.6(OTC):c.794G>T (p.Trp265Leu) AND not provided

Germline classification:
Pathogenic (1 submission)
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
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:
RCV000083577.1

Allele description [Variation Report for NM_000531.6(OTC):c.794G>T (p.Trp265Leu)]

NM_000531.6(OTC):c.794G>T (p.Trp265Leu)

Gene:
OTC:ornithine transcarbamylase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Xp11.4
Genomic location:
Preferred name:
NM_000531.6(OTC):c.794G>T (p.Trp265Leu)
HGVS:
  • NC_000023.11:g.38408952G>T
  • NG_008471.1:g.61470G>T
  • NM_000531.6:c.794G>TMANE SELECT
  • NP_000522.3:p.Trp265Leu
  • LRG_846t1:c.794G>T
  • LRG_846:g.61470G>T
  • LRG_846p1:p.Trp265Leu
  • NC_000023.10:g.38268205G>T
  • NM_000531.5:c.794G>T
  • P00480:p.Trp265Leu
Protein change:
W265L
Links:
UniProtKB: P00480#VAR_010609; dbSNP: rs72558446
NCBI 1000 Genomes Browser:
rs72558446
Molecular consequence:
  • NM_000531.6:c.794G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000115663GenMed Metabolism Lab
no assertion criteria provided
pathogenicunknownnot provided

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

Description

p.Trp265Leu, Late, pH variant

SCV000115663

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownnot providednot providednot providednot provided1not providedliterature only

Citations

PubMed

Lymphocyte mRNA analysis of the ornithine transcarbamylase gene in Italian OTCD male patients and manifesting carriers: identification of novel mutations.

Giorgi M, Morrone A, Donati MA, Ciani F, Bardelli T, Biasucci G, Zammarchi E.

Hum Mutat. 2000 Apr;15(4):380-1.

PubMed [citation]
PMID:
10737985

Details of each submission

From GenMed Metabolism Lab, SCV000115663.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providednot provided PubMed (1)

Description

Converted during submission to Pathogenic.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownnot provided1not providednot providednot providednot providednot providednot provided

Last Updated: Mar 26, 2023