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NM_001174089.2(SLC4A11):c.132G>C (p.Glu44Asp) AND Inborn genetic diseases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 18, 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:
RCV004683788.1

Allele description [Variation Report for NM_001174089.2(SLC4A11):c.132G>C (p.Glu44Asp)]

NM_001174089.2(SLC4A11):c.132G>C (p.Glu44Asp)

Gene:
SLC4A11:solute carrier family 4 member 11 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
20p13
Genomic location:
Preferred name:
NM_001174089.2(SLC4A11):c.132G>C (p.Glu44Asp)
HGVS:
  • NC_000020.11:g.3234851C>G
  • NG_017072.1:g.9391G>C
  • NM_001174089.2:c.132G>CMANE SELECT
  • NM_001174090.2:c.261G>C
  • NM_001363745.2:c.132G>C
  • NM_001400277.1:c.75G>C
  • NM_001400278.1:c.75G>C
  • NM_001400279.1:c.75G>C
  • NM_001400280.1:c.261G>C
  • NM_032034.4:c.180G>C
  • NP_001167560.1:p.Glu44Asp
  • NP_001167561.1:p.Glu87Asp
  • NP_001350674.1:p.Glu44Asp
  • NP_001387206.1:p.Glu25Asp
  • NP_001387207.1:p.Glu25Asp
  • NP_001387208.1:p.Glu25Asp
  • NP_001387209.1:p.Glu87Asp
  • NP_114423.1:p.Glu60Asp
  • NC_000020.10:g.3215497C>G
  • NM_032034.3:c.180G>C
  • NR_135000.1:n.300G>C
  • NR_174470.1:n.690G>C
  • NR_174471.1:n.690G>C
Protein change:
E25D
Molecular consequence:
  • NM_001174089.2:c.132G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001174090.2:c.261G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001363745.2:c.132G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001400277.1:c.75G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001400278.1:c.75G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001400279.1:c.75G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001400280.1:c.261G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_032034.4:c.180G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NR_135000.1:n.300G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174470.1:n.690G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_174471.1:n.690G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Inborn genetic diseases
Identifiers:
MeSH: D030342; MedGen: C0950123

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005169079Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Mar 18, 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, SCV005169079.1

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

Description

The c.180G>C (p.E60D) alteration is located in exon 2 (coding exon 2) of the SLC4A11 gene. This alteration results from a G to C substitution at nucleotide position 180, causing the glutamic acid (E) at amino acid position 60 to be replaced by an aspartic acid (D). 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: Aug 11, 2024