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NM_012210.4(TRIM32):c.*1206T>C AND not provided

Germline classification:
Benign (1 submission)
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:
RCV004718543.1

Allele description [Variation Report for NM_012210.4(TRIM32):c.*1206T>C]

NM_012210.4(TRIM32):c.*1206T>C

Genes:
ASTN2:astrotactin 2 [Gene - OMIM - HGNC]
TRIM32:tripartite motif containing 32 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q33.1
Genomic location:
Preferred name:
NM_012210.4(TRIM32):c.*1206T>C
HGVS:
  • NC_000009.12:g.116700910T>C
  • NG_011619.1:g.18609T>C
  • NG_021409.2:g.719148A>G
  • NM_001099679.2:c.*1206T>C
  • NM_001365068.1:c.2806+24861A>GMANE SELECT
  • NM_001365069.1:c.2794+24861A>G
  • NM_001379048.1:c.*1206T>C
  • NM_001379049.1:c.*1206T>C
  • NM_001379050.1:c.*1206T>C
  • NM_012210.4:c.*1206T>CMANE SELECT
  • NM_014010.5:c.2653+24861A>G
  • LRG_211t1:c.*1206T>C
  • LRG_211:g.18609T>C
  • NC_000009.11:g.119463189T>C
  • NM_012210.3:c.*1206T>C
Links:
dbSNP: rs2281627
NCBI 1000 Genomes Browser:
rs2281627
Molecular consequence:
  • NM_001099679.2:c.*1206T>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001379048.1:c.*1206T>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001379049.1:c.*1206T>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001379050.1:c.*1206T>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_012210.4:c.*1206T>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001365068.1:c.2806+24861A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001365069.1:c.2794+24861A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_014010.5:c.2653+24861A>G - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005317873Breakthrough Genomics, Breakthrough Genomics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Benigngermlinenot provided

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providednot provided

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Breakthrough Genomics, Breakthrough Genomics, SCV005317873.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providednot provided PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024