NM_001267550.2(TTN):c.95884A>G (p.Asn31962Asp) AND not specified

Germline classification:: Likely benign (1 submission)
Last evaluated:: Mar 12, 2018
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:: RCV000605539.1

Allele description [Variation Report for NM_001267550.2(TTN):c.95884A>G (p.Asn31962Asp)]

NM_001267550.2(TTN):c.95884A>G (p.Asn31962Asp)

Genes:

TTN-AS1:TTN antisense RNA 1 [Gene - HGNC]
TTN:titin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q31.2

Genomic location:

Preferred name:

NM_001267550.2(TTN):c.95884A>G (p.Asn31962Asp)

Other names:

p.Asn29394Asp

HGVS:

NC_000002.12:g.178544345T>C
NG_011618.3:g.291458A>G
NG_051363.1:g.26519T>C
NM_001256850.1:c.90961A>G
NM_001267550.2:c.95884A>GMANE SELECT
NM_003319.4:c.68689A>G
NM_133378.4:c.88180A>G
NM_133432.3:c.69064A>G
NM_133437.4:c.69265A>G
NP_001243779.1:p.Asn30321Asp
NP_001254479.2:p.Asn31962Asp
NP_003310.4:p.Asn22897Asp
NP_596869.4:p.Asn29394Asp
NP_597676.3:p.Asn23022Asp
NP_597681.4:p.Asn23089Asp
LRG_391:g.291458A>G
NC_000002.11:g.179409072T>C
NM_001267550.2:c.95884A>G
NM_003319.4:c.68689A>G
NM_133378.4:c.88180A>G

Protein change:

N22897D

Links:

dbSNP: rs369087584

NCBI 1000 Genomes Browser:

rs369087584

Molecular consequence:

NM_001256850.1:c.90961A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001267550.2:c.95884A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_003319.4:c.68689A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_133378.4:c.88180A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_133432.3:c.69064A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_133437.4:c.69265A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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
SCV000728343	GeneDx	criteria provided, single submitter (GeneDx Variant Classification (06012015))	Likely benign (Mar 12, 2018)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000728343

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification (06012015))

Likely benign
(Mar 12, 2018)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneDx, SCV000728343.1

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

Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

#	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

Last Updated: Oct 13, 2024

ClinVar

Relating variation to medicine