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NM_001178015.2(SLC4A10):c.858+1G>C AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 28, 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:
RCV003319634.1

Allele description [Variation Report for NM_001178015.2(SLC4A10):c.858+1G>C]

NM_001178015.2(SLC4A10):c.858+1G>C

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.858+1G>C
HGVS:
  • NC_000002.12:g.161872385G>C
  • NG_021401.1:g.253051G>C
  • NM_001178015.2:c.858+1G>CMANE SELECT
  • NM_001178016.2:c.891+1G>C
  • NM_001354440.2:c.858+1G>C
  • NM_001354441.2:c.891+1G>C
  • NM_001354442.2:c.891+1G>C
  • NM_001354443.2:c.894+1G>C
  • NM_001354444.2:c.855+1G>C
  • NM_001354445.2:c.891+1G>C
  • NM_001354446.2:c.858+1G>C
  • NM_001354447.2:c.894+1G>C
  • NM_001354448.2:c.888+1G>C
  • NM_001354449.2:c.855+1G>C
  • NM_001354450.2:c.858+1G>C
  • NM_001354451.2:c.855+1G>C
  • NM_001354453.2:c.711+1G>C
  • NM_001354455.2:c.279+1G>C
  • NM_001354460.2:c.894+1G>C
  • NM_001354461.2:c.894+1G>C
  • NM_022058.4:c.858+1G>C
  • NC_000002.11:g.162728895G>C
Molecular consequence:
  • NM_001178015.2:c.858+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001178016.2:c.891+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354440.2:c.858+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354441.2:c.891+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354442.2:c.891+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354443.2:c.894+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354444.2:c.855+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354445.2:c.891+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354446.2:c.858+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354447.2:c.894+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354448.2:c.888+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354449.2:c.855+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354450.2:c.858+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354451.2:c.855+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354453.2:c.711+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354455.2:c.279+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354460.2:c.894+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001354461.2:c.894+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_022058.4:c.858+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: CN517202

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004023513GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Uncertain significance
(Jun 28, 2022) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From GeneDx, SCV004023513.1

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

Description

Canonical splice site variant in a gene or region of a gene for which loss of function is not a well-established mechanism of disease; Not observed at significant frequency in large population cohorts (gnomAD); Variants in candidate genes are classified as variants of uncertain significance in accordance with ACMG guidelines (Richards et al., 2015); Has not been previously published as pathogenic or benign to our knowledge

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

Last Updated: Aug 13, 2023