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NM_198580.3(SLC27A1):c.1741C>T (p.Arg581Trp) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 28, 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:
RCV004456743.1

Allele description [Variation Report for NM_198580.3(SLC27A1):c.1741C>T (p.Arg581Trp)]

NM_198580.3(SLC27A1):c.1741C>T (p.Arg581Trp)

Genes:
PGLS-DT:PGLS divergent transcript [Gene - HGNC]
SLC27A1:solute carrier family 27 member 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
19p13.11
Genomic location:
Preferred name:
NM_198580.3(SLC27A1):c.1741C>T (p.Arg581Trp)
HGVS:
  • NC_000019.10:g.17501377C>T
  • NM_198580.3:c.1741C>TMANE SELECT
  • NP_940982.1:p.Arg581Trp
  • NC_000019.9:g.17612186C>T
  • NM_198580.1:c.1741C>T
Protein change:
R581W
Molecular consequence:
  • NM_198580.3:c.1741C>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
SCV004950342Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Dec 28, 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, SCV004950342.1

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

Description

The c.1741C>T (p.R581W) alteration is located in exon 11 (coding exon 11) of the SLC27A1 gene. This alteration results from a C to T substitution at nucleotide position 1741, causing the arginine (R) at amino acid position 581 to be replaced by a tryptophan (W). 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: May 7, 2024