NM_001281775.3(ZMYND8):c.639G>A (p.Met213Ile) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Oct 25, 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:: RCV004168056.1

Allele description [Variation Report for NM_001281775.3(ZMYND8):c.639G>A (p.Met213Ile)]

NM_001281775.3(ZMYND8):c.639G>A (p.Met213Ile)

Gene:

ZMYND8:zinc finger MYND-type containing 8 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

20q13.12

Genomic location:

Preferred name:

NM_001281775.3(ZMYND8):c.639G>A (p.Met213Ile)

HGVS:

NC_000020.11:g.47291817C>T
NM_001281771.3:c.564G>A
NM_001281772.3:c.579G>A
NM_001281773.3:c.579G>A
NM_001281774.3:c.579G>A
NM_001281775.3:c.639G>AMANE SELECT
NM_001281776.3:c.639G>A
NM_001281777.3:c.564G>A
NM_001281778.3:c.564G>A
NM_001281779.3:c.-297G>A
NM_001281780.3:c.-297G>A
NM_001281781.3:c.564G>A
NM_001281782.3:c.564G>A
NM_001281783.3:c.639G>A
NM_001281784.3:c.564G>A
NM_001363714.1:c.660G>A
NM_001363741.2:c.579G>A
NM_012408.6:c.639G>A
NM_183047.4:c.639G>A
NM_183048.4:c.564G>A
NP_001268700.1:p.Met188Ile
NP_001268701.1:p.Met193Ile
NP_001268702.1:p.Met193Ile
NP_001268703.1:p.Met193Ile
NP_001268704.1:p.Met213Ile
NP_001268705.1:p.Met213Ile
NP_001268706.1:p.Met188Ile
NP_001268707.1:p.Met188Ile
NP_001268710.1:p.Met188Ile
NP_001268711.1:p.Met188Ile
NP_001268712.1:p.Met213Ile
NP_001268713.1:p.Met188Ile
NP_001350643.1:p.Met220Ile
NP_001350670.1:p.Met193Ile
NP_036540.3:p.Met213Ile
NP_898868.1:p.Met213Ile
NP_898869.1:p.Met188Ile
NC_000020.10:g.45920561C>T
NM_183047.1:c.639G>A

Protein change:

M188I

Molecular consequence:

NM_001281779.3:c.-297G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001281780.3:c.-297G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001281771.3:c.564G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281772.3:c.579G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281773.3:c.579G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281774.3:c.579G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281775.3:c.639G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281776.3:c.639G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281777.3:c.564G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281778.3:c.564G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281781.3:c.564G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281782.3:c.564G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281783.3:c.639G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281784.3:c.564G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363714.1:c.660G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001363741.2:c.579G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_012408.6:c.639G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_183047.4:c.639G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_183048.4:c.564G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003654885	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Oct 25, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003654885

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Oct 25, 2022)

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	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV003654885.2

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

Description

The c.639G>A (p.M213I) alteration is located in exon 6 (coding exon 6) of the ZMYND8 gene. This alteration results from a G to A substitution at nucleotide position 639, causing the methionine (M) at amino acid position 213 to be replaced by an isoleucine (I). 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 10, 2024

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