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NM_000503.6(EYA1):c.1325A>G (p.Lys442Arg) AND Branchiootorenal syndrome 1

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jan 1, 2022
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:
RCV002071021.1

Allele description [Variation Report for NM_000503.6(EYA1):c.1325A>G (p.Lys442Arg)]

NM_000503.6(EYA1):c.1325A>G (p.Lys442Arg)

Gene:
EYA1:EYA transcriptional coactivator and phosphatase 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
8q13.3
Genomic location:
Preferred name:
NM_000503.6(EYA1):c.1325A>G (p.Lys442Arg)
HGVS:
  • NC_000008.11:g.71216727T>C
  • NG_011735.3:g.336404A>G
  • NM_000503.6:c.1325A>GMANE SELECT
  • NM_001288574.2:c.1307A>G
  • NM_001288575.2:c.959A>G
  • NM_001370333.1:c.1412A>G
  • NM_001370334.1:c.1325A>G
  • NM_001370335.1:c.1325A>G
  • NM_001370336.1:c.1304A>G
  • NM_172058.4:c.1325A>G
  • NM_172059.5:c.1307A>G
  • NP_000494.2:p.Lys442Arg
  • NP_001275503.1:p.Lys436Arg
  • NP_001275504.1:p.Lys320Arg
  • NP_001357262.1:p.Lys471Arg
  • NP_001357263.1:p.Lys442Arg
  • NP_001357264.1:p.Lys442Arg
  • NP_001357265.1:p.Lys435Arg
  • NP_742055.1:p.Lys442Arg
  • NP_742056.2:p.Lys436Arg
  • NC_000008.10:g.72128962T>C
  • NM_000503.5:c.1325A>G
Protein change:
K320R
Links:
dbSNP: rs2128853814
NCBI 1000 Genomes Browser:
rs2128853814
Molecular consequence:
  • NM_000503.6:c.1325A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001288574.2:c.1307A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001288575.2:c.959A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370333.1:c.1412A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370334.1:c.1325A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370335.1:c.1325A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001370336.1:c.1304A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_172058.4:c.1325A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_172059.5:c.1307A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Branchiootorenal syndrome 1
Identifiers:
MONDO: MONDO:0007236; MedGen: C4551702; Orphanet: 107; OMIM: 113650

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002320807Provincial Medical Genetics Program of British Columbia, University of British Columbia
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Jan 1, 2022) 		de novoclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedde novoyesnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Provincial Medical Genetics Program of British Columbia, University of British Columbia, SCV002320807.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1de novoyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Dec 24, 2023