NM_001388067.1(MIPOL1):c.952A>G (p.Met318Val) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: May 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:: RCV004082672.1

Allele description [Variation Report for NM_001388067.1(MIPOL1):c.952A>G (p.Met318Val)]

NM_001388067.1(MIPOL1):c.952A>G (p.Met318Val)

Gene:

MIPOL1:mirror-image polydactyly 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

14q21.1

Genomic location:

Preferred name:

NM_001388067.1(MIPOL1):c.952A>G (p.Met318Val)

HGVS:

NC_000014.9:g.37422870A>G
NG_027724.1:g.229958A>G
NG_027724.2:g.229935A>G
NM_001195296.2:c.952A>G
NM_001195297.2:c.952A>G
NM_001388067.1:c.952A>GMANE SELECT
NM_001388068.1:c.952A>G
NM_001388069.1:c.952A>G
NM_001388070.1:c.859A>G
NM_001388071.1:c.859A>G
NM_001388072.1:c.859A>G
NM_001388073.1:c.844A>G
NM_001388074.1:c.751A>G
NM_001388075.1:c.751A>G
NM_001388077.1:c.952A>G
NM_001412440.1:c.952A>G
NM_138731.6:c.952A>G
NM_138731.7:c.952A>G
NP_001182225.1:p.Met318Val
NP_001182226.1:p.Met318Val
NP_001374996.1:p.Met318Val
NP_001374997.1:p.Met318Val
NP_001374998.1:p.Met318Val
NP_001374999.1:p.Met287Val
NP_001375000.1:p.Met287Val
NP_001375001.1:p.Met287Val
NP_001375002.1:p.Met282Val
NP_001375003.1:p.Met251Val
NP_001375004.1:p.Met251Val
NP_001375006.1:p.Met318Val
NP_001399369.1:p.Met318Val
NP_620059.1:p.Met318Val
NC_000014.8:g.37892075A>G
NM_001195296.1:c.952A>G

Protein change:

M251V

Molecular consequence:

NM_001195296.2:c.952A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001195297.2:c.952A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001388067.1:c.952A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001388068.1:c.952A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001388069.1:c.952A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001388070.1:c.859A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001388071.1:c.859A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001388072.1:c.859A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001388073.1:c.844A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001388074.1:c.751A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001388075.1:c.751A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001388077.1:c.952A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001412440.1:c.952A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_138731.7:c.952A>G - 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
SCV003543947	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (May 25, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003543947

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(May 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, SCV003543947.2

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

Description

The c.952A>G (p.M318V) alteration is located in exon 13 (coding exon 9) of the MIPOL1 gene. This alteration results from a A to G substitution at nucleotide position 952, causing the methionine (M) at amino acid position 318 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 24, 2024

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