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NM_001184880.2(PCDH19):c.402C>A (p.Ile134=) AND Inborn genetic diseases

Germline classification:
Benign (1 submission)
Last evaluated:
Jan 8, 2016
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:
RCV002311588.9

Allele description [Variation Report for NM_001184880.2(PCDH19):c.402C>A (p.Ile134=)]

NM_001184880.2(PCDH19):c.402C>A (p.Ile134=)

Gene:
PCDH19:protocadherin 19 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Xq22.1
Genomic location:
Preferred name:
NM_001184880.2(PCDH19):c.402C>A (p.Ile134=)
Other names:
p.I134I:ATC>ATA
HGVS:
  • NC_000023.11:g.100408196G>T
  • NG_021319.1:g.7078C>A
  • NM_001105243.2:c.402C>A
  • NM_001184880.2:c.402C>AMANE SELECT
  • NM_020766.3:c.402C>A
  • NP_001098713.1:p.Ile134=
  • NP_001171809.1:p.Ile134=
  • NP_065817.2:p.Ile134=
  • LRG_843t1:c.402C>A
  • LRG_843:g.7078C>A
  • LRG_843p1:p.Ile134=
  • NC_000023.10:g.99663194G>T
  • NM_001105243.1:c.402C>A
  • NM_001184880.1:c.402C>A
  • NP_001171809.1:p.(=)
Links:
dbSNP: rs41300169
NCBI 1000 Genomes Browser:
rs41300169
Molecular consequence:
  • NM_001105243.2:c.402C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001184880.2:c.402C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_020766.3:c.402C>A - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:
Inborn genetic diseases
Identifiers:
MeSH: D030342; MedGen: C0950123

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000845867Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Benign
(Jan 8, 2016) 		germlineclinical testing

Citation Link

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Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Ambry Genetics, SCV000845867.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This alteration is classified as benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Nov 24, 2024