NM_001130438.3(SPTAN1):c.6660C>T (p.Asn2220=) AND not specified

Germline classification:: Benign/Likely benign (2 submissions)
Last evaluated:: Feb 7, 2013
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV000147651.15

Allele description [Variation Report for NM_001130438.3(SPTAN1):c.6660C>T (p.Asn2220=)]

NM_001130438.3(SPTAN1):c.6660C>T (p.Asn2220=)

Gene:

SPTAN1:spectrin alpha, non-erythrocytic 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9q34.11

Genomic location:

Preferred name:

NM_001130438.3(SPTAN1):c.6660C>T (p.Asn2220=)

Other names:

p.N2220N:AAC>AAT

HGVS:

NC_000009.12:g.128627469C>T
NG_027748.1:g.79912C>T
NM_001130438.3:c.6660C>TMANE SELECT
NM_001195532.2:c.6585C>T
NM_001363759.2:c.6660C>T
NM_001363765.2:c.6600C>T
NM_003127.4:c.6645C>T
NP_001123910.1:p.Asn2220=
NP_001182461.1:p.Asn2195=
NP_001350688.1:p.Asn2220=
NP_001350694.1:p.Asn2200=
NP_003118.2:p.Asn2215=
NC_000009.11:g.131389748C>T
NM_001130438.2:c.6660C>T

Links:

dbSNP: rs112955915

NCBI 1000 Genomes Browser:

rs112955915

Molecular consequence:

NM_001130438.3:c.6660C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001195532.2:c.6585C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001363759.2:c.6660C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001363765.2:c.6600C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_003127.4:c.6645C>T - synonymous variant - [Sequence Ontology: SO:0001819]

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
SCV000171864	GeneDx	criteria provided, single submitter (GeneDx Variant Classification (06012015))	Benign (Feb 7, 2013)	germline	clinical testing	Citation Link,
SCV000195100	Genetic Services Laboratory, University of Chicago	criteria provided, single submitter (ACMG Guidelines, 2007)	Likely benign (Sep 7, 2012)	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

SCV000171864

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification (06012015))

Benign
(Feb 7, 2013)

germline

clinical testing

Citation Link,

SCV000195100

Genetic Services Laboratory, University of Chicago

criteria provided, single submitter

(ACMG Guidelines, 2007)

Likely benign
(Sep 7, 2012)

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
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.

Richards CS, Bale S, Bellissimo DB, Das S, Grody WW, Hegde MR, Lyon E, Ward BE; Molecular Subcommittee of the ACMG Laboratory Quality Assurance Committee..

Genet Med. 2008 Apr;10(4):294-300. doi: 10.1097/GIM.0b013e31816b5cae.

PubMed [citation]

PMID:: 18414213

Details of each submission

From GeneDx, SCV000171864.12

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

Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Genetic Services Laboratory, University of Chicago, SCV000195100.1

#	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: Apr 15, 2024

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