U.S. flag

An official website of the United States government

NM_001372051.1(CASP8):c.339C>T (p.Ser113=) AND multiple conditions

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jul 27, 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:
RCV002504124.1

Allele description [Variation Report for NM_001372051.1(CASP8):c.339C>T (p.Ser113=)]

NM_001372051.1(CASP8):c.339C>T (p.Ser113=)

Gene:
CASP8:caspase 8 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q33.1
Genomic location:
Preferred name:
NM_001372051.1(CASP8):c.339C>T (p.Ser113=)
HGVS:
  • NC_000002.12:g.201271549C>T
  • NG_007497.1:g.43092C>T
  • NM_001080124.2:c.339C>T
  • NM_001080125.2:c.516C>T
  • NM_001228.5:c.435C>T
  • NM_001372051.1:c.339C>TMANE SELECT
  • NM_001400642.1:c.516C>T
  • NM_001400645.1:c.339C>T
  • NM_001400648.1:c.339C>T
  • NM_001400651.1:c.339C>T
  • NM_001400653.1:c.339C>T
  • NM_001400654.1:c.339C>T
  • NM_001400655.1:c.339C>T
  • NM_001400656.1:c.339C>T
  • NM_001400657.1:c.339C>T
  • NM_001400658.1:c.339C>T
  • NM_001400659.1:c.339C>T
  • NM_001400660.1:c.339C>T
  • NM_001400661.1:c.339C>T
  • NM_001400662.1:c.339C>T
  • NM_001400663.1:c.339C>T
  • NM_001400664.1:c.339C>T
  • NM_001400665.1:c.516C>T
  • NM_001400666.1:c.339C>T
  • NM_001400667.1:c.339C>T
  • NM_001400668.1:c.339C>T
  • NM_001400669.1:c.30C>T
  • NM_001400670.1:c.339C>T
  • NM_001400671.1:c.-194C>T
  • NM_001400672.1:c.-194C>T
  • NM_001400673.1:c.-194C>T
  • NM_001400674.1:c.-375C>T
  • NM_001400675.1:c.-194C>T
  • NM_001400676.1:c.-194C>T
  • NM_001400677.1:c.-194C>T
  • NM_001400678.1:c.-194C>T
  • NM_001400679.1:c.339C>T
  • NM_001400680.1:c.-273C>T
  • NM_001400750.1:c.-194C>T
  • NM_001400751.1:c.-194C>T
  • NM_033355.4:c.339C>T
  • NM_033356.4:c.339C>T
  • NP_001073593.1:p.Ser113=
  • NP_001073594.1:p.Ser172=
  • NP_001219.2:p.Ser145=
  • NP_001219.2:p.Ser145=
  • NP_001358980.1:p.Ser113=
  • NP_001387571.1:p.Ser172=
  • NP_001387574.1:p.Ser113=
  • NP_001387577.1:p.Ser113=
  • NP_001387580.1:p.Ser113=
  • NP_001387582.1:p.Ser113=
  • NP_001387583.1:p.Ser113=
  • NP_001387584.1:p.Ser113=
  • NP_001387585.1:p.Ser113=
  • NP_001387586.1:p.Ser113=
  • NP_001387587.1:p.Ser113=
  • NP_001387588.1:p.Ser113=
  • NP_001387589.1:p.Ser113=
  • NP_001387590.1:p.Ser113=
  • NP_001387591.1:p.Ser113=
  • NP_001387592.1:p.Ser113=
  • NP_001387593.1:p.Ser113=
  • NP_001387594.1:p.Ser172=
  • NP_001387595.1:p.Ser113=
  • NP_001387596.1:p.Ser113=
  • NP_001387597.1:p.Ser113=
  • NP_001387598.1:p.Ser10=
  • NP_001387599.1:p.Ser113=
  • NP_001387608.1:p.Ser113=
  • NP_203519.1:p.Ser113=
  • NP_203519.1:p.Ser113=
  • NP_203520.1:p.Ser113=
  • LRG_34t1:c.435C>T
  • LRG_34t2:c.339C>T
  • LRG_34t3:c.339C>T
  • LRG_34:g.43092C>T
  • LRG_34p1:p.Ser145=
  • LRG_34p2:p.Ser113=
  • LRG_34p3:p.Ser113=
  • NC_000002.11:g.202136272C>T
  • NM_001228.4:c.435C>T
  • NM_033355.3:c.339C>T
  • NR_111983.2:n.713C>T
  • NR_174583.1:n.554C>T
  • NR_174584.1:n.713C>T
  • NR_174585.1:n.485C>T
  • NR_174586.1:n.459C>T
  • NR_174588.1:n.622C>T
  • NR_174589.1:n.417C>T
  • NR_174590.1:n.554C>T
  • NR_174591.1:n.485C>T
  • NR_174592.1:n.687C>T
  • NR_174593.1:n.485C>T
  • NR_174594.1:n.528C>T
  • NR_174595.1:n.443C>T
  • NR_174596.1:n.443C>T
  • NR_174597.1:n.443C>T
  • NR_174598.1:n.622C>T
  • NR_174599.1:n.443C>T
  • NR_174600.1:n.713C>T
  • NR_174601.1:n.459C>T
  • NR_174602.1:n.443C>T
Links:
dbSNP: rs17860422
NCBI 1000 Genomes Browser:
rs17860422
Molecular consequence:
  • NM_001400671.1:c.-194C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001400672.1:c.-194C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001400673.1:c.-194C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001400674.1:c.-375C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001400675.1:c.-194C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001400676.1:c.-194C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001400677.1:c.-194C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001400678.1:c.-194C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001400680.1:c.-273C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001400750.1:c.-194C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001400751.1:c.-194C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NR_111983.2:n.713C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174583.1:n.554C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174584.1:n.713C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174585.1:n.485C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174586.1:n.459C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174588.1:n.622C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174589.1:n.417C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174590.1:n.554C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174591.1:n.485C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174592.1:n.687C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174593.1:n.485C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174594.1:n.528C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174595.1:n.443C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174596.1:n.443C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174598.1:n.622C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174599.1:n.443C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174600.1:n.713C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174601.1:n.459C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174602.1:n.443C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NM_001080124.2:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001080125.2:c.516C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001228.5:c.435C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001372051.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400642.1:c.516C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400645.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400648.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400651.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400653.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400654.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400655.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400656.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400657.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400658.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400659.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400660.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400661.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400662.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400663.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400664.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400665.1:c.516C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400666.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400667.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400668.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400669.1:c.30C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400670.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001400679.1:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_033355.4:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_033356.4:c.339C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:
Familial cancer of breast
Synonyms:
Breast cancer, familial; Hereditary breast cancer
Identifiers:
MONDO: MONDO:0016419; MedGen: C0346153; OMIM: 114480
Name:
Autoimmune lymphoproliferative syndrome type 2B
Synonyms:
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIB; Caspase-8 deficiency
Identifiers:
MONDO: MONDO:0011804; MedGen: C1846545; Orphanet: 275517; OMIM: 607271
Name:
Hepatocellular carcinoma (HCC)
Synonyms:
Primary carcinoma of liver; Hepatoma; LIVER CELL CARCINOMA; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0007256; MedGen: C2239176; OMIM: 114550; Human Phenotype Ontology: HP:0001402
Name:
Lung cancer
Synonyms:
Lung cancer, somatic; Malignant tumor of lung
Identifiers:
MONDO: MONDO:0008903; MedGen: C0242379; OMIM: 211980

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002811807Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely benign
(Jul 27, 2021) 		unknownclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot providednot providednot providednot providednot providedclinical testing

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 Fulgent Genetics, Fulgent Genetics, SCV002811807.1

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

Last Updated: Oct 20, 2024