NM_024422.6(DSC2):c.630+256_630+257dup AND not provided

Germline classification:: Benign (1 submission)
Last evaluated:: Aug 18, 2019
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:: RCV001540906.2

Allele description [Variation Report for NM_024422.6(DSC2):c.630+256_630+257dup]

NM_024422.6(DSC2):c.630+256_630+257dup

Gene:

DSC2:desmocollin 2 [Gene - OMIM - HGNC]

Variant type:

Duplication

Cytogenetic location:

18q12.1

Genomic location:

Preferred name:

NM_024422.6(DSC2):c.630+256_630+257dup

HGVS:

NC_000018.10:g.31089182_31089183dup
NG_008208.2:g.18260_18261dup
NM_004949.5:c.630+256_630+257dup
NM_024422.6:c.630+256_630+257dupMANE SELECT
LRG_400:g.18260_18261dup
NC_000018.9:g.28669145_28669146dup

Links:

dbSNP: rs768405529

NCBI 1000 Genomes Browser:

rs768405529

Molecular consequence:

NM_004949.5:c.630+256_630+257dup - intron variant - [Sequence Ontology: SO:0001627]
NM_024422.6:c.630+256_630+257dup - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

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SURP and G-patch domain-containing protein 1 [Homo sapiens]
SURP and G-patch domain-containing protein 1 [Homo sapiens]
gi|33469964|ref|NP_757386.2|

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001758837	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Benign (Aug 18, 2019)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001758837

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Benign
(Aug 18, 2019)

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

Details of each submission

From GeneDx, SCV001758837.1

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

#	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

Last Updated: Dec 24, 2023

ClinVar

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