NM_024596.5(MCPH1):c.182A>G (p.Asp61Gly) AND not specified

Clinical significance:Likely benign (Last evaluated: Mar 31, 2015)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000177335.1

Allele description [Variation Report for NM_024596.5(MCPH1):c.182A>G (p.Asp61Gly)]

NM_024596.5(MCPH1):c.182A>G (p.Asp61Gly)

Gene:
MCPH1:microcephalin 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
8p23.1
Genomic location:
Preferred name:
NM_024596.5(MCPH1):c.182A>G (p.Asp61Gly)
HGVS:
  • NC_000008.11:g.6414832A>G
  • NG_016619.2:g.13241A>G
  • NM_001172574.1:c.182A>G
  • NM_001172575.1:c.182A>G
  • NM_001322042.2:c.182A>G
  • NM_001322043.1:c.176A>G
  • NM_001322045.1:c.80A>G
  • NM_001363979.1:c.182A>G
  • NM_001363980.2:c.182A>G
  • NM_024596.5:c.182A>GMANE SELECT
  • NP_001166045.1:p.Asp61Gly
  • NP_001166046.1:p.Asp61Gly
  • NP_001308971.2:p.Asp61Gly
  • NP_001308972.1:p.Asp59Gly
  • NP_001308974.1:p.Asp27Gly
  • NP_001350908.1:p.Asp61Gly
  • NP_001350909.1:p.Asp61Gly
  • NP_078872.3:p.Asp61Gly
  • NC_000008.10:g.6272353A>G
  • NM_024596.3:c.182A>G
  • NM_024596.4:c.182A>G
  • NR_136159.1:n.258A>G
Protein change:
D27G
Links:
dbSNP: rs61749465
NCBI 1000 Genomes Browser:
rs61749465
Molecular consequence:
  • NM_001172574.1:c.182A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001172575.1:c.182A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001322042.2:c.182A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001322043.1:c.176A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001322045.1:c.80A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001363979.1:c.182A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001363980.2:c.182A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_024596.5:c.182A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NR_136159.1:n.258A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Observations:
1

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000229182EGL Genetic Diagnostics, Eurofins Clinical Diagnosticscriteria provided, single submitter
Likely benign
(Mar 31, 2015)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot providednot providednot providedclinical testing

Details of each submission

From EGL Genetic Diagnostics, Eurofins Clinical Diagnostics, SCV000229182.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot provided1not providednot providednot provided

Last Updated: Oct 30, 2020

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