NM_001228.5(CASP8):c.-26-8228T>C AND not provided

Germline classification:: Benign (2 submissions)
Last evaluated:: Nov 27, 2018
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:: RCV001643144.10

Allele description [Variation Report for NM_001228.5(CASP8):c.-26-8228T>C]

NM_001228.5(CASP8):c.-26-8228T>C

Genes:

CASP8:caspase 8 [Gene - OMIM - HGNC]
LOC128772255:melanoma risk locus-associated MPRA allelic enhancer 2:202122995 [Gene]

Variant type:

single nucleotide variant

Cytogenetic location:

2q33.1

Genomic location:

Preferred name:

NM_001228.5(CASP8):c.-26-8228T>C

HGVS:

NC_000002.12:g.201258233T>C
NG_007497.1:g.29776T>C
NG_149746.2:g.223T>C
NM_001080124.2:c.-26-8228T>C
NM_001080125.2:c.2T>C
NM_001228.5:c.-26-8228T>C
NM_001400642.1:c.2T>C
NM_001400645.1:c.-27+79T>C
NM_001400648.1:c.-26-8228T>C
NM_001400651.1:c.-26-8228T>C
NM_001400654.1:c.-1+79T>C
NM_001400655.1:c.-150T>C
NM_001400656.1:c.-27+79T>C
NM_001400657.1:c.1-8254T>C
NM_001400658.1:c.-27+79T>C
NM_001400660.1:c.1-8254T>C
NM_001400661.1:c.1-8254T>C
NM_001400662.1:c.-150T>C
NM_001400663.1:c.-26-8228T>C
NM_001400665.1:c.2T>C
NM_001400668.1:c.-27+79T>C
NM_001400669.1:c.-4-13283T>C
NM_001400677.1:c.-532-8254T>C
NM_001400678.1:c.-559+79T>C
NM_001400679.1:c.-26-8228T>C
NM_001400680.1:c.-637-8228T>C
NM_001400750.1:c.-682T>C
NM_001400751.1:c.-682T>C
NM_033355.4:c.1-8254T>C
NP_001073594.1:p.Met1Thr
NP_001387571.1:p.Met1Thr
NP_001387594.1:p.Met1Thr
LRG_34t1:c.-26-8228T>C
LRG_34:g.29776T>C
NC_000002.11:g.202122956T>C
NG_149746.1:g.134T>C
NM_001228.4:c.-26-8228T>C
NR_111983.2:n.199T>C
NR_174584.1:n.199T>C
NR_174592.1:n.199T>C
NR_174600.1:n.199T>C

Protein change:

M1T

Links:

dbSNP: rs3769824

NCBI 1000 Genomes Browser:

rs3769824

Molecular consequence:

NM_001400655.1:c.-150T>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001400662.1:c.-150T>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001400750.1:c.-682T>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001400751.1:c.-682T>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001080125.2:c.2T>C - initiator_codon_variant - [Sequence Ontology: SO:0001582]
NM_001400642.1:c.2T>C - initiator_codon_variant - [Sequence Ontology: SO:0001582]
NM_001400665.1:c.2T>C - initiator_codon_variant - [Sequence Ontology: SO:0001582]
NM_001080124.2:c.-26-8228T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001228.5:c.-26-8228T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400645.1:c.-27+79T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400648.1:c.-26-8228T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400651.1:c.-26-8228T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400654.1:c.-1+79T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400656.1:c.-27+79T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400657.1:c.1-8254T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400658.1:c.-27+79T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400660.1:c.1-8254T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400661.1:c.1-8254T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400663.1:c.-26-8228T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400668.1:c.-27+79T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400669.1:c.-4-13283T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400677.1:c.-532-8254T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400678.1:c.-559+79T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400679.1:c.-26-8228T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001400680.1:c.-637-8228T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_033355.4:c.1-8254T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001080125.2:c.2T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001400642.1:c.2T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001400665.1:c.2T>C - missense variant - [Sequence Ontology: SO:0001583]
NR_111983.2:n.199T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_174584.1:n.199T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_174592.1:n.199T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_174600.1:n.199T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001856772	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Benign (Nov 27, 2018)	germline	clinical testing	Citation Link,
SCV005238018	Breakthrough Genomics, Breakthrough Genomics	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign	germline	not provided	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001856772

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Benign
(Nov 27, 2018)

germline

clinical testing

Citation Link,

SCV005238018

Breakthrough Genomics, Breakthrough Genomics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign

germline

not provided

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	yes	not provided	not provided	not provided	not provided	not provided	clinical testing, not 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 GeneDx, SCV001856772.2

#	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

From Breakthrough Genomics, Breakthrough Genomics, SCV005238018.1

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

#	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: Nov 30, 2024

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Relating variation to medicine