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NM_024426.6(WT1):c.813G>C (p.Pro271=) AND multiple conditions

Germline classification:
Likely benign (1 submission)
Last evaluated:
Oct 27, 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:
RCV001454642.8

Allele description [Variation Report for NM_024426.6(WT1):c.813G>C (p.Pro271=)]

NM_024426.6(WT1):c.813G>C (p.Pro271=)

Gene:
WT1:WT1 transcription factor [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11p13
Genomic location:
Preferred name:
NM_024426.6(WT1):c.813G>C (p.Pro271=)
HGVS:
  • NC_000011.10:g.32428030C>G
  • NG_009272.1:g.12512G>C
  • NG_122166.1:g.213C>G
  • NM_000378.6:c.813G>C
  • NM_001198551.2:c.162G>C
  • NM_001198552.2:c.162G>C
  • NM_001407044.1:c.813G>C
  • NM_001407045.1:c.813G>C
  • NM_001407046.1:c.813G>C
  • NM_001407047.1:c.690G>C
  • NM_001407048.1:c.813G>C
  • NM_001407049.1:c.813G>C
  • NM_001407050.1:c.690G>C
  • NM_001407051.1:c.51G>C
  • NM_024424.5:c.813G>C
  • NM_024425.2:c.798G>C
  • NM_024426.6:c.813G>CMANE SELECT
  • NP_000369.4:p.Pro271=
  • NP_001185480.1:p.Pro54=
  • NP_001185480.1:p.Pro54=
  • NP_001185481.1:p.Pro54=
  • NP_001393973.1:p.Pro271=
  • NP_001393974.1:p.Pro271=
  • NP_001393975.1:p.Pro271=
  • NP_001393976.1:p.Pro230=
  • NP_001393977.1:p.Pro271=
  • NP_001393978.1:p.Pro271=
  • NP_001393979.1:p.Pro230=
  • NP_001393980.1:p.Pro17=
  • NP_077742.3:p.Pro271=
  • NP_077743.2:p.Pro266=
  • NP_077744.3:p.Pro266=
  • NP_077744.4:p.Pro271=
  • LRG_525t1:c.798G>C
  • LRG_525t2:c.162G>C
  • LRG_525:g.12512G>C
  • LRG_525p1:p.Pro266=
  • LRG_525p2:p.Pro54=
  • NC_000011.9:g.32449576C>G
  • NM_001198551.1:c.162G>C
  • NM_024426.3:c.798G>C
  • NM_024426.4:c.798G>C
  • NR_160306.1:n.992G>C
  • NR_176266.1:n.992G>C
Links:
dbSNP: rs1341857958
NCBI 1000 Genomes Browser:
rs1341857958
Molecular consequence:
  • NR_160306.1:n.992G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_176266.1:n.992G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NM_000378.6:c.813G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001198551.2:c.162G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001198552.2:c.162G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407044.1:c.813G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407045.1:c.813G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407046.1:c.813G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407047.1:c.690G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407048.1:c.813G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407049.1:c.813G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407050.1:c.690G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407051.1:c.51G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_024424.5:c.813G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_024425.2:c.798G>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_024426.6:c.813G>C - synonymous variant - [Sequence Ontology: SO:0001819]

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
Name:
Frasier syndrome
Identifiers:
MONDO: MONDO:0007635; MeSH: D052159; MedGen: C0950122; Orphanet: 347; OMIM: 136680
Name:
Wilms tumor 1 (WT1)
Synonyms:
Wilms tumor, somatic
Identifiers:
MONDO: MONDO:0008679; MedGen: CN033288; Orphanet: 654; OMIM: 194070
Name:
11p partial monosomy syndrome (WAGR)
Synonyms:
CHROMOSOME 11p13 DELETION SYNDROME; WAGR syndrome; WAGR Complex; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0008681; MedGen: C0206115; Orphanet: 893; OMIM: 194072

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001658377Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Likely benign
(Oct 27, 2023) 		germlineclinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV001658377.4

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

Last Updated: Sep 29, 2024