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NM_002299.4(LCT):c.3390G>A (p.Glu1130=)

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Interpretation:
Uncertain significance​

Review status:
criteria provided, single submitter
Submissions:
2 (Most recent: Feb 20, 2020)
Last evaluated:
Jan 13, 2018
Accession:
VCV000331187.4
Variation ID:
331187
Description:
single nucleotide variant
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NM_002299.4(LCT):c.3390G>A (p.Glu1130=)

Allele ID
284380
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
2q21.3
Genomic location
2: 135808957 (GRCh38) GRCh38 UCSC
2: 136566527 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
LRG_338t1:c.3390G>A
LRG_338:g.51213G>A
NC_000002.11:g.136566527C>T
... more HGVS
Protein change
-
Other names
-
Canonical SPDI
NC_000002.12:135808956:C:T
Functional consequence
-
Global minor allele frequency (GMAF)
-

Allele frequency
The Genome Aggregation Database (gnomAD), exomes 0.00000
Links
ClinGen: CA10612278
dbSNP: rs886054865
VarSome
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Aggregate interpretations per condition

Interpreted condition Interpretation Number of submissions Review status Last evaluated Variation/condition record
Uncertain significance 1 criteria provided, single submitter Jan 13, 2018 RCV000284711.3
Uncertain significance 1 criteria provided, single submitter Jun 14, 2016 RCV000376775.3
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Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
LCT - - GRCh38
GRCh37
184 199

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter More information
Uncertain significance
(Jun 14, 2016)
criteria provided, single submitter
Method: clinical testing
Lactose Intolerance
Affected status: unknown
Allele origin: germline
Illumina Laboratory Services,Illumina
Accession: SCV000416493.2
Submitted: (Oct 18, 2016)
Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
Method: clinical testing
Congenital lactase deficiency
Affected status: unknown
Allele origin: germline
Illumina Laboratory Services,Illumina
Accession: SCV000416494.3
Submitted: (Feb 20, 2020)
Comment:
This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated … (more)

Functional evidence

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There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar.

Citations for this variant

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There are no citations in ClinVar for this variation. If you know of citations for this variation, please consider submitting that information to ClinVar.

Text-mined citations for rs886054865...

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These citations are identified by LitVar using the rs number, so they may include citations for more than one variant at this location. Please review the LitVar results carefully for your variant of interest.

Record last updated Jan 08, 2022