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NM_024426.6(WT1):c.406C>A (p.Pro136Thr) AND Drash syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 25, 2023
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:
RCV003471039.1

Allele description [Variation Report for NM_024426.6(WT1):c.406C>A (p.Pro136Thr)]

NM_024426.6(WT1):c.406C>A (p.Pro136Thr)

Genes:
WT1:WT1 transcription factor [Gene - OMIM - HGNC]
LOC107982234:WT1/WT1-AS bi-directional promoter region [Gene]
Variant type:
single nucleotide variant
Cytogenetic location:
11p13
Genomic location:
Preferred name:
NM_024426.6(WT1):c.406C>A (p.Pro136Thr)
HGVS:
  • NC_000011.10:g.32434955G>T
  • NG_009272.1:g.5587C>A
  • NG_050766.1:g.4208G>T
  • NM_000378.6:c.406C>A
  • NM_024424.5:c.406C>A
  • NM_024426.6:c.406C>AMANE SELECT
  • NP_000369.4:p.Pro136Thr
  • NP_077742.3:p.Pro136Thr
  • NP_077744.4:p.Pro136Thr
  • LRG_525:g.5587C>A
  • NC_000011.9:g.32456501G>T
  • NR_160306.1:n.585C>A
Protein change:
P136T
Links:
dbSNP: rs748045691
NCBI 1000 Genomes Browser:
rs748045691
Molecular consequence:
  • NM_000378.6:c.406C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_024424.5:c.406C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_024426.6:c.406C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_160306.1:n.585C>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Drash syndrome (DDS)
Synonyms:
WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM; Wilms tumor and pseudohermaphroditism; Nephropathy, wilms tumor, and genital anomalies; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0008682; MedGen: C0950121; Orphanet: 220; OMIM: 194080

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004206918Baylor Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Jun 25, 2023) 		unknownclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot 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 Baylor Genetics, SCV004206918.1

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

Last Updated: Sep 29, 2024