NM_001289808.2(CRYAB):c.3G>A (p.Met1Ile) AND not provided

Germline classification:: Conflicting interpretations of pathogenicity (2 submissions)
Last evaluated:: Nov 24, 2021
Review status:: criteria provided, conflicting classifications

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:: RCV001787334.12

Allele description [Variation Report for NM_001289808.2(CRYAB):c.3G>A (p.Met1Ile)]

NM_001289808.2(CRYAB):c.3G>A (p.Met1Ile)

Gene:

CRYAB:crystallin alpha B [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q23.1

Genomic location:

Preferred name:

NM_001289808.2(CRYAB):c.3G>A (p.Met1Ile)

HGVS:

NC_000011.10:g.111911722C>T
NG_009824.3:g.17001G>A
NG_033080.2:g.3987C>T
NM_001289807.1:c.3G>A
NM_001289808.2:c.3G>AMANE SELECT
NM_001368245.1:c.3G>A
NM_001885.3:c.3G>A
NP_001276736.1:p.Met1Ile
NP_001276737.1:p.Met1Ile
NP_001355174.1:p.Met1Ile
NP_001876.1:p.Met1Ile
LRG_407t1:c.3G>A
LRG_407t2:c.3G>A
LRG_407:g.17001G>A
LRG_407p1:p.Met1Ile
LRG_407p2:p.Met1Ile
NC_000011.9:g.111782446C>T
NG_009824.2:g.17001G>A
NG_033080.1:g.3987C>T
NM_001885.1:c.3G>A
c.3G>A
p.Met1?

Protein change:

M1I

Links:

dbSNP: rs397516686

NCBI 1000 Genomes Browser:

rs397516686

Molecular consequence:

NM_001289807.1:c.3G>A - initiator_codon_variant - [Sequence Ontology: SO:0001582]
NM_001289808.2:c.3G>A - initiator_codon_variant - [Sequence Ontology: SO:0001582]
NM_001368245.1:c.3G>A - initiator_codon_variant - [Sequence Ontology: SO:0001582]
NM_001885.3:c.3G>A - initiator_codon_variant - [Sequence Ontology: SO:0001582]
NM_001289807.1:c.3G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001289808.2:c.3G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001368245.1:c.3G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001885.3:c.3G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000680849	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Pathogenic (Nov 24, 2021)	germline	clinical testing	Citation Link,
SCV003828666	Revvity Omics, Revvity	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Mar 24, 2021)	germline	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

SCV000680849

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Pathogenic
(Nov 24, 2021)

germline

clinical testing

Citation Link,

SCV003828666

Revvity Omics, Revvity

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Mar 24, 2021)

germline

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	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	yes	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 GeneDx, SCV000680849.4

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

Description

Initiation codon variant in a gene for which loss-of-function is a known mechanism of disease; This variant is associated with the following publications: (PMID: 31215171, 33834702)

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

From Revvity Omics, Revvity, SCV003828666.3

#	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	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Oct 13, 2024

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