NM_000159.4(GCDH):c.572T>C (p.Met191Thr) AND not provided

Clinical significance:Likely pathogenic (Last evaluated: Apr 20, 2015)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000724678.1

Allele description [Variation Report for NM_000159.4(GCDH):c.572T>C (p.Met191Thr)]

NM_000159.4(GCDH):c.572T>C (p.Met191Thr)

Gene:
GCDH:glutaryl-CoA dehydrogenase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
19p13.13
Genomic location:
Preferred name:
NM_000159.4(GCDH):c.572T>C (p.Met191Thr)
HGVS:
  • NC_000019.10:g.12896058T>C
  • NG_009292.1:g.9899T>C
  • NM_000159.4:c.572T>CMANE SELECT
  • NM_013976.5:c.572T>C
  • NP_000150.1:p.Met191Thr
  • NP_039663.1:p.Met191Thr
  • NC_000019.9:g.13006872T>C
  • NM_000159.2:c.572T>C
  • NM_000159.3:c.572T>C
  • NR_102316.1:n.735T>C
  • NR_102317.1:n.988T>C
  • Q92947:p.Met191Thr
Protein change:
M191T
Links:
UniProtKB: Q92947#VAR_000378; dbSNP: rs149120354
NCBI 1000 Genomes Browser:
rs149120354
Molecular consequence:
  • NM_000159.4:c.572T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_013976.5:c.572T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NR_102316.1:n.735T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_102317.1:n.988T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Observations:
1

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000232017EGL Genetic Diagnostics, Eurofins Clinical Diagnosticscriteria provided, single submitter
Likely pathogenic
(Apr 20, 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, SCV000232017.5

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

Last Updated: Nov 27, 2021

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