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NM_003844.4(TNFRSF10A):c.355G>A (p.Gly119Ser) AND not provided

Germline classification:
Uncertain significance (2 submissions)
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
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:
RCV000087209.4

Allele description [Variation Report for NM_003844.4(TNFRSF10A):c.355G>A (p.Gly119Ser)]

NM_003844.4(TNFRSF10A):c.355G>A (p.Gly119Ser)

Gene:
TNFRSF10A:TNF receptor superfamily member 10a [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
8p21.3
Genomic location:
Preferred name:
NM_003844.4(TNFRSF10A):c.355G>A (p.Gly119Ser)
HGVS:
  • NC_000008.11:g.23212164C>T
  • NG_032107.1:g.18004G>A
  • NM_003844.4:c.355G>AMANE SELECT
  • NP_003835.3:p.Gly119Ser
  • NC_000008.10:g.23069677C>T
  • NM_003844.3:c.355G>A
Protein change:
G119S
Links:
dbSNP: rs483352726
NCBI 1000 Genomes Browser:
rs483352726
Molecular consequence:
  • NM_003844.4:c.355G>A - missense variant - [Sequence Ontology: SO:0001583]

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
SCV000155175Richard Lifton Laboratory, Yale University School of Medicine
no assertion criteria provided
unknownsomaticnot provided

Description

TNFRSF10A:p.G119S

SCV000155175

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedsomaticnot providednot providednot providednot provided2not providedliterature only

Details of each submission

From Richard Lifton Laboratory, Yale University School of Medicine, SCV000120071.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providednot providednot provided

Description

Converted during submission to Uncertain significance.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1somaticnot provided1not providednot providednot providednot providednot providednot provided

From Richard Lifton Laboratory, Yale University School of Medicine, SCV000155175.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providednot providednot provided

Description

Converted during submission to Uncertain significance.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1somaticnot provided1not providednot providednot providednot providednot providednot provided

Flagged submissions

Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000120071Richard Lifton Laboratory, Yale University School of Medicine
flagged submission
Reason: This record appears to be redundant with a more recent record from the same submitter.
Notes: SCV000120071 appears to be redundant with SCV000155175.
unknownsomaticnot provided

Last Updated: Dec 9, 2023