NM_000275.3(OCA2):c.2207C>T (p.Ser736Leu) AND Tyrosinase-positive oculocutaneous albinism

Clinical significance:Likely pathogenic (Last evaluated: Jun 16, 2015)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000192656.1

Allele description [Variation Report for NM_000275.3(OCA2):c.2207C>T (p.Ser736Leu)]

NM_000275.3(OCA2):c.2207C>T (p.Ser736Leu)

Gene:
OCA2:OCA2 melanosomal transmembrane protein [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
15q13.1
Genomic location:
Preferred name:
NM_000275.3(OCA2):c.2207C>T (p.Ser736Leu)
HGVS:
  • NC_000015.10:g.27871191G>A
  • NG_009846.1:g.233122C>T
  • NM_000275.3:c.2207C>T
  • NM_001300984.2:c.2135C>T
  • NP_000266.2:p.Ser736Leu
  • NP_001287913.1:p.Ser712Leu
  • NC_000015.9:g.28116337G>A
  • NM_000275.2:c.2207C>T
  • Q04671:p.Ser736Leu
Protein change:
S712L
Links:
UniProtKB: Q04671#VAR_006144; dbSNP: rs780296175
NCBI 1000 Genomes Browser:
rs780296175
Molecular consequence:
  • NM_000275.3:c.2207C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001300984.2:c.2135C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Tyrosinase-positive oculocutaneous albinism (OCA2)
Synonyms:
ALBINISM II; Albinism, oculocutaneous, type II
Identifiers:
MedGen: C0268495; Orphanet: 79432; OMIM: 203200

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000248369Genetic Services Laboratory, University of Chicagocriteria provided, single submitter
Likely pathogenic
(Jun 16, 2015)
germlineclinical testing

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

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Genetic Services Laboratory, University of Chicago, SCV000248369.1

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

Last Updated: Aug 29, 2019

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