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NM_182628.3(CFAP100):c.1459G>T (p.Asp487Tyr) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 13, 2023
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:
RCV004428662.1

Allele description [Variation Report for NM_182628.3(CFAP100):c.1459G>T (p.Asp487Tyr)]

NM_182628.3(CFAP100):c.1459G>T (p.Asp487Tyr)

Gene:
CFAP100:cilia and flagella associated protein 100 [Gene - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
3q21.3
Genomic location:
Preferred name:
NM_182628.3(CFAP100):c.1459G>T (p.Asp487Tyr)
HGVS:
  • NC_000003.12:g.126434212G>T
  • NM_182628.3:c.1459G>TMANE SELECT
  • NP_872434.2:p.Asp487Tyr
  • NC_000003.11:g.126153055G>T
  • NM_182628.2:c.1459G>T
Protein change:
D487Y
Molecular consequence:
  • NM_182628.3:c.1459G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004925615Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Oct 13, 2023) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV004925615.1

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

Description

The c.1459G>T (p.D487Y) alteration is located in exon 15 (coding exon 14) of the CFAP100 gene. This alteration results from a G to T substitution at nucleotide position 1459, causing the aspartic acid (D) at amino acid position 487 to be replaced by a tyrosine (Y). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 1, 2024