VCV002681780.1 - ClinVar

NM_024426.6(WT1):c.1504G>C (p.Asp502His)

Germline

Classification

The aggregate germline classification for this variant, typically for a monogenic or Mendelian disorder as in the ACMG/AMP guidelines, or for response to a drug. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the aggregate classification.

(1)

Stars represent the aggregate review status, or the level of review supporting the aggregate germline classification for this VCV record. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status. The number of submissions which contribute to this review status is shown in parentheses.

Likely pathogenic

criteria provided, single submitter

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_024426.6(WT1):c.1504G>C (p.Asp502His)

Variation ID: 2681780 Accession: VCV002681780.1

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 11p13 11: 32389123 (GRCh38) [ NCBI UCSC ] 11: 32410669 (GRCh37) [ NCBI UCSC ]

Timeline in ClinVar

	First in ClinVar Help The date this variant first appeared in ClinVar with each type of classification.	Last submission Help The date of the most recent submission for each type of classification for this variant.	Last evaluated Help The most recent date that a submitter evaluated this variant for each type of classification.
Germline	Jun 23, 2024	Jun 23, 2024	Dec 1, 2023

HGVS

Nucleotide	Protein	Molecular consequence
NM_024426.6:c.1504G>C MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_077744.4:p.Asp502His	missense
NM_000378.6:c.1444G>C	NP_000369.4:p.Asp482His	missense
NM_001198551.2:c.844G>C	NP_001185480.1:p.Asp282His	missense
NM_001198552.2:c.802G>C	NP_001185481.1:p.Asp268His	missense
NM_001367854.1:c.316G>C	NP_001354783.1:p.Asp106His	missense
NM_001407044.1:c.1489G>C	NP_001393973.1:p.Asp497His	missense
NM_001407045.1:c.1453G>C	NP_001393974.1:p.Asp485His	missense
NM_001407046.1:c.1411G>C	NP_001393975.1:p.Asp471His	missense
NM_001407047.1:c.1372G>C	NP_001393976.1:p.Asp458His	missense
NM_001407048.1:c.1363G>C	NP_001393977.1:p.Asp455His	missense
NM_001407049.1:c.1360G>C	NP_001393978.1:p.Asp454His	missense
NM_001407050.1:c.1330G>C	NP_001393979.1:p.Asp444His	missense
NM_001407051.1:c.742G>C	NP_001393980.1:p.Asp248His	missense
NM_024424.5:c.1495G>C	NP_077742.3:p.Asp499His	missense
NM_024425.2:c.1438G>C	NP_077743.2:p.Asp480His	missense
NR_160306.1:n.1836G>C		non-coding transcript variant
NR_176266.1:n.1776G>C		non-coding transcript variant
NC_000011.10:g.32389123C>G
NC_000011.9:g.32410669C>G
NG_009272.1:g.51419G>C
LRG_525:g.51419G>C
LRG_525t1:c.1489G>C	LRG_525p1:p.Asp497His
LRG_525t2:c.844G>C	LRG_525p2:p.Asp282His

... more HGVS ... less HGVS

Protein change

D106H, D248H, D268H, D282H, D444H, D454H, D455H, D458H, D471H, D480H, D482H, D485H, D497H, D499H, D502H

Other names

Canonical SPDI

NC_000011.10:32389122:C:G

Functional consequence Help The effect of the variant on RNA or protein function, based on experimental evidence from submitters.

Global minor allele frequency (GMAF) Help The global minor allele frequency calculated by the 1000 Genomes Project. The minor allele at this location is indicated in parentheses and may be different from the allele represented by this VCV record.

Allele frequency Help The frequency of the allele represented by this VCV record.

Links

VarSome

Genes

Gene	OMIM	ClinGen Gene Dosage Sensitivity Curation		Variation Viewer Help Links to Variation Viewer, a genome browser to view variation data from NCBI databases.	Related variants
Gene	OMIM	HI score Help The haploinsufficiency score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.	TS score Help The triplosensitivity score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.		Within gene Help The number of variants in ClinVar that are contained within this gene, with a link to view the list of variants.	All Help The number of variants in ClinVar for this gene, including smaller variants within the gene and larger CNVs that overlap or fully contain the gene.
WT1		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	914	1672

Conditions - Germline

Condition Help The condition for this variant-condition (RCV) record in ClinVar.	Classification Help The aggregate germline classification for this variant-condition (RCV) record in ClinVar. The number of submissions that contribute to this aggregate classification is shown in parentheses. (# of submissions)	Review status Help The aggregate review status for this variant-condition (RCV) record in ClinVar. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status.	Last evaluated Help The most recent date that a submitter evaluated this variant for the condition.	Variation/condition record Help The RCV accession number, with most recent version number, for the variant-condition record, with a link to the RCV web page.
Nephrotic syndrome, type 4	Likely pathogenic (1)	criteria provided, single submitter	Dec 1, 2023	RCV004577627.1

Submissions - Germline

Classification Help The submitted germline classification for each SCV record. (Last evaluated)	Review status Help Stars represent the review status, or the level of review supporting the submitted (SCV) record. This value is calculated by NCBI based on data from the submitter. Read our rules for calculating the review status. This column also includes a link to the submitter’s assertion criteria if provided, and the collection method. (Assertion criteria)	Condition Help The condition for the classification, provided by the submitter for this submitted (SCV) record. This column also includes the affected status and allele origin of individuals observed with this variant.	Submitter Help The submitting organization for this submitted (SCV) record. This column also includes the SCV accession and version number, the date this SCV first appeared in ClinVar, and the date that this SCV was last updated in ClinVar.	More information Help This column includes more information supporting the classification, including citations, the comment on classification, and detailed evidence provided as observations of the variant by the submitter.
Likely pathogenic (Dec 01, 2023)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	Nephrotic syndrome, type 4 Affected status: yes Allele origin: de novo	Precision Medicine Center, Zhengzhou University Accession: SCV004218505.1 First in ClinVar: Jun 23, 2024 Last updated: Jun 23, 2024	Publications: PubMed (1) PubMed: 25741868 Comment: PS2,PM2_p,PP3 Sex: male

Germline Functional Evidence

There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar.

Citations for germline classification of this variant

Title	Author	Journal	Year	Link
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	Genetics in medicine : official journal of the American College of Medical Genetics	2015	PMID: 25741868

Text-mined citations for this variant ...

Record last updated Jun 30, 2024

ClinVar Genomic variation as it relates to human health

NM_024426.6(WT1):c.1504G>C (p.Asp502His)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...