NM_001085377.2(MCC):c.814A>G (p.Ile272Val) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Apr 4, 2023
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:: RCV004308108.1

Allele description [Variation Report for NM_001085377.2(MCC):c.814A>G (p.Ile272Val)]

NM_001085377.2(MCC):c.814A>G (p.Ile272Val)

Gene:

MCC:MCC regulator of WNT signaling pathway [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

5q22.2

Genomic location:

Preferred name:

NM_001085377.2(MCC):c.814A>G (p.Ile272Val)

HGVS:

NC_000005.10:g.113143288T>C
NG_012265.1:g.350543A>G
NG_012265.2:g.350165A>G
NM_001085377.2:c.814A>GMANE SELECT
NM_002387.3:c.244A>G
NP_001078846.2:p.Ile272Val
NP_002378.2:p.Ile82Val
NC_000005.9:g.112478985T>C
NM_001085377.1:c.814A>G

Protein change:

I272V

Molecular consequence:

NM_001085377.2:c.814A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_002387.3:c.244A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

Recent activity

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Bmp6 protein [Danio rerio]
Bmp6 protein [Danio rerio]
gi|182890726|gb|AAI65212.1|

Protein
Lauraceae internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA ge...
Lauraceae internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene and internal transcribed spacer 2, complete sequence; and 26S ribosomal RNA gene, partial sequence.
PopSet: 14090722

PopSet
bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted [Danio re...
bloc1s5 biogenesis of lysosomal organelles complex-1, subunit 5, muted [Danio rerio]
Gene ID:324781

Gene

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003964128	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Apr 4, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003964128

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Apr 4, 2023)

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, SCV003964128.2

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

Description

The c.814A>G (p.I272V) alteration is located in exon 5 (coding exon 5) of the MCC gene. This alteration results from a A to G substitution at nucleotide position 814, causing the isoleucine (I) at amino acid position 272 to be replaced by a valine (V). 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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