NM_000202.8(IDS):c.641C>T (p.Thr214Met) AND not specified

Clinical significance:Benign (Last evaluated: Jul 8, 2014)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000078368.4

Allele description [Variation Report for NM_000202.8(IDS):c.641C>T (p.Thr214Met)]

NM_000202.8(IDS):c.641C>T (p.Thr214Met)

Genes:
LOC106050102:IDS recombination region [Gene]
IDS:iduronate 2-sulfatase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Xq28
Genomic location:
Preferred name:
NM_000202.8(IDS):c.641C>T (p.Thr214Met)
HGVS:
  • NC_000023.11:g.149498174G>A
  • NG_011900.3:g.12161C>T
  • NG_042264.1:g.11529G>A
  • NM_000202.8:c.641C>TMANE SELECT
  • NM_001166550.4:c.371C>T
  • NM_006123.5:c.641C>T
  • NP_000193.1:p.Thr214Met
  • NP_000193.1:p.Thr214Met
  • NP_000193.1:p.Thr214Met
  • NP_000193.1:p.Thr214Met
  • NP_001160022.1:p.Thr124Met
  • NP_006114.1:p.Thr214Met
  • NC_000023.10:g.148579705G>A
  • NM_000202.5:c.641C>T
  • NM_000202.6:c.641C>T
  • NR_104128.2:n.810C>T
Protein change:
T124M
Links:
dbSNP: rs61736892
NCBI 1000 Genomes Browser:
rs61736892
Molecular consequence:
  • NM_000202.8:c.641C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001166550.4:c.371C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_006123.5:c.641C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NR_104128.2:n.810C>T - 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
SCV000110214EGL Genetic Diagnostics, Eurofins Clinical Diagnosticscriteria provided, single submitter
Benign
(Jul 8, 2014)
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, SCV000110214.8

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

Last Updated: Sep 18, 2021

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