NM_001163735.2(MYO19):c.2864G>A (p.Arg955Lys) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 2, 2024
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:: RCV004649911.1

Allele description [Variation Report for NM_001163735.2(MYO19):c.2864G>A (p.Arg955Lys)]

NM_001163735.2(MYO19):c.2864G>A (p.Arg955Lys)

Genes:

MYO19:myosin XIX [Gene - OMIM - HGNC]
ZNHIT3:zinc finger HIT-type containing 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17q12

Genomic location:

Preferred name:

NM_001163735.2(MYO19):c.2864G>A (p.Arg955Lys)

HGVS:

NC_000017.11:g.36496300C>T
NM_001163735.2:c.2864G>AMANE SELECT
NM_001281432.2:c.287-1306C>T
NM_025109.6:c.2264G>A
NP_001157207.1:p.Arg955Lys
NP_079385.2:p.Arg755Lys
NC_000017.10:g.34852144C>T
NM_001163735.1:c.2864G>A

Protein change:

R755K

Molecular consequence:

NM_001281432.2:c.287-1306C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001163735.2:c.2864G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_025109.6:c.2264G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

Recent activity

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DUF5017 domain-containing protein [Sphingobacterium thermophilum]
DUF5017 domain-containing protein [Sphingobacterium thermophilum]
gi|2730949613|ref|WP_345062880.1|

Protein
redoxin domain-containing protein [Sphingobacterium thermophilum]
redoxin domain-containing protein [Sphingobacterium thermophilum]
gi|2730951245|ref|WP_345064512.1|

Protein
intraflagellar transport protein 122 homolog isoform 1 [Rattus norvegicus]
intraflagellar transport protein 122 homolog isoform 1 [Rattus norvegicus]
gi|828747766|ref|NP_001296450.1|

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV005142450	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jun 2, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV005142450

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jun 2, 2024)

germline

clinical testing

Citation Link

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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

Details of each submission

From Ambry Genetics, SCV005142450.1

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

Description

The c.2864G>A (p.R955K) alteration is located in exon 26 (coding exon 24) of the MYO19 gene. This alteration results from a G to A substitution at nucleotide position 2864, causing the arginine (R) at amino acid position 955 to be replaced by a lysine (K). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	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: Nov 3, 2024

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