NM_201253.3(CRB1):c.3017C>A (p.Ser1006Tyr) AND Leber congenital amaurosis 8

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Sep 10, 2022
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:: RCV003475547.1

Allele description [Variation Report for NM_201253.3(CRB1):c.3017C>A (p.Ser1006Tyr)]

NM_201253.3(CRB1):c.3017C>A (p.Ser1006Tyr)

Gene:

CRB1:crumbs cell polarity complex component 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q31.3

Genomic location:

Preferred name:

NM_201253.3(CRB1):c.3017C>A (p.Ser1006Tyr)

HGVS:

NC_000001.11:g.197434880C>A
NG_008483.2:g.238419C>A
NG_008483.3:g.238378C>A
NM_001193640.2:c.2681C>A
NM_001257965.2:c.2945C>A
NM_001257966.2:c.2129-720C>A
NM_201253.3:c.3017C>AMANE SELECT
NP_001180569.1:p.Ser894Tyr
NP_001244894.1:p.Ser982Tyr
NP_957705.1:p.Ser1006Tyr
NC_000001.10:g.197404010C>A
NR_047563.2:n.2970C>A
NR_047564.2:n.3178C>A

Protein change:

S1006Y

Molecular consequence:

NM_001257966.2:c.2129-720C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001193640.2:c.2681C>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001257965.2:c.2945C>A - missense variant - [Sequence Ontology: SO:0001583]
NM_201253.3:c.3017C>A - missense variant - [Sequence Ontology: SO:0001583]
NR_047563.2:n.2970C>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_047564.2:n.3178C>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Leber congenital amaurosis 8 (LCA8)
Identifiers:: MONDO: MONDO:0013453; MedGen: C3151202; Orphanet: 65; OMIM: 613835

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004211237	Baylor Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Pathogenic (Sep 10, 2022)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004211237

Baylor Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Pathogenic
(Sep 10, 2022)

unknown

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical 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 Baylor Genetics, SCV004211237.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: May 7, 2024

ClinVar

Relating variation to medicine