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NM_020754.4(ARHGAP31):c.2364A>T (p.Pro788=) AND not specified

Germline classification:
Likely benign (1 submission)
Last evaluated:
Nov 25, 2015
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:
RCV000348214.4

Allele description [Variation Report for NM_020754.4(ARHGAP31):c.2364A>T (p.Pro788=)]

NM_020754.4(ARHGAP31):c.2364A>T (p.Pro788=)

Gene:
ARHGAP31:Rho GTPase activating protein 31 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
3q13.33
Genomic location:
Preferred name:
NM_020754.4(ARHGAP31):c.2364A>T (p.Pro788=)
HGVS:
  • NC_000003.12:g.119414293A>T
  • NG_007665.2:g.124921A>T
  • NM_020754.4:c.2364A>TMANE SELECT
  • NP_065805.2:p.Pro788=
  • NC_000003.11:g.119133140A>T
  • NM_020754.3:c.2364A>T
Links:
dbSNP: rs61746581
NCBI 1000 Genomes Browser:
rs61746581
Molecular consequence:
  • NM_020754.4:c.2364A>T - synonymous variant - [Sequence Ontology: SO:0001819]
Observations:
1

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000337790Eurofins Ntd Llc (ga)
criteria provided, single submitter

(EGL Classification Definitions 2015)		Likely benign
(Nov 25, 2015) 		germlineclinical testing

Citation Link

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Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot providednot providednot providedclinical testing

Details of each submission

From Eurofins Ntd Llc (ga), SCV000337790.4

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

Last Updated: Oct 13, 2024