NM_005866.4(SIGMAR1):c.61G>A (p.Val21Met) AND multiple conditions

This record was updated by the submitter. Please see the current version.

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Aug 31, 2021
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:: RCV001297404.4

Allele description

NM_005866.4(SIGMAR1):c.61G>A (p.Val21Met)

Gene:

SIGMAR1:sigma non-opioid intracellular receptor 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9p13.3

Genomic location:

Preferred name:

NM_005866.4(SIGMAR1):c.61G>A (p.Val21Met)

HGVS:

NC_000009.12:g.34637637C>T
NG_029945.2:g.5135G>A
NM_001282205.2:c.61G>A
NM_001282206.2:c.-193G>A
NM_001282207.2:c.61G>A
NM_001282208.2:c.61G>A
NM_001282209.2:c.61G>A
NM_005866.2:c.61G>A
NM_005866.4:c.61G>AMANE SELECT
NM_147157.3:c.61G>A
NP_001269134.1:p.Val21Met
NP_001269136.1:p.Val21Met
NP_001269137.1:p.Val21Met
NP_001269138.1:p.Val21Met
NP_005857.1:p.Val21Met
NP_671513.1:p.Val21Met
NC_000009.11:g.34637634C>T
NR_104108.2:n.151G>A

Protein change:

V21M

Links:

dbSNP: rs1396152845

NCBI 1000 Genomes Browser:

rs1396152845

Molecular consequence:

NM_001282206.2:c.-193G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001282205.2:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001282207.2:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001282208.2:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001282209.2:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_005866.4:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_147157.3:c.61G>A - missense variant - [Sequence Ontology: SO:0001583]
NR_104108.2:n.151G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Autosomal recessive distal spinal muscular atrophy 2
Synonyms:: NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; Hereditary motor neuropathy, Jerash type; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0011585; MedGen: C1854023; Orphanet: 139552; OMIM: 605726

Name:: Amyotrophic lateral sclerosis type 16
Synonyms:: Amyotrophic lateral sclerosis 16, juvenile
Identifiers:: MONDO: MONDO:0013715; MedGen: C3280587; Orphanet: 300605; OMIM: 614373

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001486416	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Aug 31, 2021)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001486416

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Aug 31, 2021)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group, Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Invitae, SCV001486416.2

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

#	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 29, 2022

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