NM_000363.5(TNNI3):c.575G>A (p.Arg192His) AND SUDDEN INFANT DEATH SYNDROME

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Aug 8, 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:: RCV003147282.1

Allele description [Variation Report for NM_000363.5(TNNI3):c.575G>A (p.Arg192His)]

NM_000363.5(TNNI3):c.575G>A (p.Arg192His)

Gene:

TNNI3:troponin I3, cardiac type [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.42

Genomic location:

Preferred name:

NM_000363.5(TNNI3):c.575G>A (p.Arg192His)

Other names:

p.R192H:CGC>CAC

HGVS:

NC_000019.10:g.55151892C>T
NG_007866.2:g.10841G>A
NG_011829.2:g.2347G>A
NM_000363.5:c.575G>AMANE SELECT
NP_000354.4:p.Arg192His
LRG_432t1:c.575G>A
LRG_432:g.10841G>A
LRG_679:g.2347G>A
NC_000019.9:g.55663260C>T
NM_000363.4:c.575G>A
P19429:p.Arg192His

Protein change:

R192H; ARG192HIS

Links:

UniProtKB: P19429#VAR_016084; OMIM: 191044.0006; dbSNP: rs104894729

NCBI 1000 Genomes Browser:

rs104894729

Molecular consequence:

NM_000363.5:c.575G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: SUDDEN INFANT DEATH SYNDROME (SIDS)
Synonyms:: Sudden Infant Death
Identifiers:: EFO: EFO_0005303; MeSH: D013398; MedGen: C0038644; OMIM: 272120

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003835493	Baylor Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Pathogenic (Aug 8, 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

SCV003835493

Baylor Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Pathogenic
(Aug 8, 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

Nothing to display

Details of each submission

From Baylor Genetics, SCV003835493.1

#	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: Sep 29, 2024

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