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NM_032219.4(SLC49A3):c.1634C>A (p.Pro545Gln) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 19, 2024
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:
RCV004674803.1

Allele description [Variation Report for NM_032219.4(SLC49A3):c.1634C>A (p.Pro545Gln)]

NM_032219.4(SLC49A3):c.1634C>A (p.Pro545Gln)

Genes:
MYL5:myosin light chain 5 [Gene - OMIM - HGNC]
SLC49A3:solute carrier family 49 member 3 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
4p16.3
Genomic location:
Preferred name:
NM_032219.4(SLC49A3):c.1634C>A (p.Pro545Gln)
HGVS:
  • NC_000004.12:g.682004G>T
  • NG_171399.1:g.387G>T
  • NM_001294341.2:c.1637C>A
  • NM_001294342.2:c.1280C>A
  • NM_001363650.2:c.*10G>T
  • NM_001378059.1:c.1346C>A
  • NM_001378060.1:c.1343C>A
  • NM_001378061.1:c.1400C>A
  • NM_001378062.1:c.1277C>A
  • NM_001395441.1:c.*10G>T
  • NM_001395442.1:c.*10G>T
  • NM_001395443.1:c.*10G>T
  • NM_001395444.1:c.*10G>T
  • NM_001395445.1:c.*10G>T
  • NM_001395446.1:c.*10G>T
  • NM_001395447.1:c.*10G>T
  • NM_001395448.1:c.*10G>T
  • NM_001395449.1:c.*10G>T
  • NM_002477.2:c.*10G>TMANE SELECT
  • NM_032219.4:c.1634C>AMANE SELECT
  • NP_001281270.1:p.Pro546Gln
  • NP_001281271.1:p.Pro427Gln
  • NP_001364988.1:p.Pro449Gln
  • NP_001364989.1:p.Pro448Gln
  • NP_001364990.1:p.Pro467Gln
  • NP_001364991.1:p.Pro426Gln
  • NP_115595.2:p.Pro545Gln
  • NC_000004.11:g.675793G>T
  • NM_032219.2:c.1634C>A
Protein change:
P426Q
Molecular consequence:
  • NM_001363650.2:c.*10G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001395441.1:c.*10G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001395442.1:c.*10G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001395443.1:c.*10G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001395444.1:c.*10G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001395445.1:c.*10G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001395446.1:c.*10G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001395447.1:c.*10G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001395448.1:c.*10G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001395449.1:c.*10G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_002477.2:c.*10G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001294341.2:c.1637C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001294342.2:c.1280C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001378059.1:c.1346C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001378060.1:c.1343C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001378061.1:c.1400C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001378062.1:c.1277C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_032219.4:c.1634C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005169050Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Mar 19, 2024) 		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, SCV005169050.1

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

Description

The c.1634C>A (p.P545Q) alteration is located in exon 10 (coding exon 10) of the MFSD7 gene. This alteration results from a C to A substitution at nucleotide position 1634, causing the proline (P) at amino acid position 545 to be replaced by a glutamine (Q). 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