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NM_001178015.2(SLC4A10):c.1402C>A (p.His468Asn) AND Inborn genetic diseases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 13, 2022
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:
RCV002844951.2

Allele description [Variation Report for NM_001178015.2(SLC4A10):c.1402C>A (p.His468Asn)]

NM_001178015.2(SLC4A10):c.1402C>A (p.His468Asn)

Gene:
SLC4A10:solute carrier family 4 member 10 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q24.2
Genomic location:
Preferred name:
NM_001178015.2(SLC4A10):c.1402C>A (p.His468Asn)
HGVS:
  • NC_000002.12:g.161900971C>A
  • NG_021401.1:g.281637C>A
  • NM_001178015.2:c.1402C>AMANE SELECT
  • NM_001178016.2:c.1345C>A
  • NM_001354440.2:c.1402C>A
  • NM_001354441.2:c.1435C>A
  • NM_001354442.2:c.1435C>A
  • NM_001354443.2:c.1348C>A
  • NM_001354444.2:c.1399C>A
  • NM_001354445.2:c.1345C>A
  • NM_001354446.2:c.1312C>A
  • NM_001354447.2:c.1348C>A
  • NM_001354448.2:c.1342C>A
  • NM_001354449.2:c.1309C>A
  • NM_001354450.2:c.1312C>A
  • NM_001354451.2:c.1309C>A
  • NM_001354453.2:c.1165C>A
  • NM_001354455.2:c.733C>A
  • NM_001354460.2:c.1438C>A
  • NM_001354461.2:c.1438C>A
  • NM_022058.4:c.1312C>A
  • NP_001171486.1:p.His468Asn
  • NP_001171487.1:p.His449Asn
  • NP_001341369.1:p.His468Asn
  • NP_001341370.1:p.His479Asn
  • NP_001341371.1:p.His479Asn
  • NP_001341372.1:p.His450Asn
  • NP_001341373.1:p.His467Asn
  • NP_001341374.1:p.His449Asn
  • NP_001341375.1:p.His438Asn
  • NP_001341376.1:p.His450Asn
  • NP_001341377.1:p.His448Asn
  • NP_001341378.1:p.His437Asn
  • NP_001341379.1:p.His438Asn
  • NP_001341380.1:p.His437Asn
  • NP_001341382.1:p.His389Asn
  • NP_001341384.1:p.His245Asn
  • NP_001341389.1:p.His480Asn
  • NP_001341390.1:p.His480Asn
  • NP_071341.2:p.His438Asn
  • NC_000002.11:g.162757481C>A
  • NM_001178015.1:c.1402C>A
Protein change:
H245N
Molecular consequence:
  • NM_001178015.2:c.1402C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001178016.2:c.1345C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354440.2:c.1402C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354441.2:c.1435C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354442.2:c.1435C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354443.2:c.1348C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354444.2:c.1399C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354445.2:c.1345C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354446.2:c.1312C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354447.2:c.1348C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354448.2:c.1342C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354449.2:c.1309C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354450.2:c.1312C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354451.2:c.1309C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354453.2:c.1165C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354455.2:c.733C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354460.2:c.1438C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354461.2:c.1438C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_022058.4:c.1312C>A - missense variant - [Sequence Ontology: SO:0001583]

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
SCV003606896Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Apr 13, 2022) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV003606896.2

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

Description

The c.1402C>A (p.H468N) alteration is located in exon 12 (coding exon 12) of the SLC4A10 gene. This alteration results from a C to A substitution at nucleotide position 1402, causing the histidine (H) at amino acid position 468 to be replaced by an asparagine (N). 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 1, 2024