U.S. flag

An official website of the United States government

NM_005334.3(HCFC1):c.3550G>A (p.Gly1184Arg) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 23, 2018
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:
RCV000081292.16

Allele description [Variation Report for NM_005334.3(HCFC1):c.3550G>A (p.Gly1184Arg)]

NM_005334.3(HCFC1):c.3550G>A (p.Gly1184Arg)

Gene:
HCFC1:host cell factor C1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Xq28
Genomic location:
Preferred name:
NM_005334.3(HCFC1):c.3550G>A (p.Gly1184Arg)
HGVS:
  • NC_000023.11:g.153954849C>T
  • NG_012513.1:g.21520G>A
  • NM_005334.3:c.3550G>AMANE SELECT
  • NP_005325.2:p.Gly1184Arg
  • NP_005325.2:p.Gly1184Arg
  • NC_000023.10:g.153220300C>T
  • NM_005334.2:c.3550G>A
Protein change:
G1184R
Links:
dbSNP: rs398124207
NCBI 1000 Genomes Browser:
rs398124207
Molecular consequence:
  • NM_005334.3:c.3550G>A - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000113200Eurofins Ntd Llc (ga)
criteria provided, single submitter

(EGL ClinVar v180209 classification definitions)		Uncertain significance
(Aug 23, 2018) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot providednot providednot providedclinical testing

Details of each submission

From Eurofins Ntd Llc (ga), SCV000113200.8

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

Last Updated: Sep 29, 2024