NM_012134.3(LMOD1):c.995T>C (p.Met332Thr) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 2, 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:: RCV004286880.1

Allele description [Variation Report for NM_012134.3(LMOD1):c.995T>C (p.Met332Thr)]

NM_012134.3(LMOD1):c.995T>C (p.Met332Thr)

Gene:

LMOD1:leiomodin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q32.1

Genomic location:

Preferred name:

NM_012134.3(LMOD1):c.995T>C (p.Met332Thr)

HGVS:

NC_000001.11:g.201900018A>G
NM_012134.3:c.995T>CMANE SELECT
NP_036266.2:p.Met332Thr
NC_000001.10:g.201869146A>G
NM_012134.2:c.995T>C

Protein change:

M332T

Molecular consequence:

NM_012134.3:c.995T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

Recent activity

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proteasome core particle subunit beta 6 [Saccharomyces cerevisiae S288C]
proteasome core particle subunit beta 6 [Saccharomyces cerevisiae S288C]
gi|6319430|ref|NP_009512.1|

Protein
PREDICTED: Homo sapiens ring finger protein 32 (RNF32), transcript variant X27, ...
PREDICTED: Homo sapiens ring finger protein 32 (RNF32), transcript variant X27, mRNA
gi|2217365663|ref|XM_047419905.1|

Nucleotide
Cryptosporiopsis rhizophila strain PB 103 internal transcribed spacer 1, partial...
Cryptosporiopsis rhizophila strain PB 103 internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene, complete sequence; and internal transcribed spacer 2, partial sequence
gi|365822718|gb|JN655662.1|

Nucleotide
unnamed protein product, partial [Mus musculus]
unnamed protein product, partial [Mus musculus]
gi|74199074|dbj|BAE30750.1|

Protein
Poulsenia armata voucher KD3566 internal transcribed spacer 1, partial sequence;...
Poulsenia armata voucher KD3566 internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene, complete sequence; and internal transcribed spacer 2, partial sequence; chloroplast
gi|1735118566|gb|MK914529.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003913364	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Mar 2, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003913364

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Mar 2, 2023)

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, SCV003913364.2

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

Description

The c.995T>C (p.M332T) alteration is located in exon 2 (coding exon 2) of the LMOD1 gene. This alteration results from a T to C substitution at nucleotide position 995, causing the methionine (M) at amino acid position 332 to be replaced by a threonine (T). 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: Oct 26, 2024

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