VCV000083162.4 - ClinVar

NM_000038.6(APC):c.1627-315C>T

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.

(2)

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.

Benign

criteria provided, single submitter

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_000038.6(APC):c.1627-315C>T

Variation ID: 83162 Accession: VCV000083162.4

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 5q22.2 5: 112828541 (GRCh38) [ NCBI UCSC ] 5: 112164238 (GRCh37) [ NCBI UCSC ] 5: 112192137 (NCBI36) [ 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	Oct 31, 2013	Sep 12, 2021	Jan 10, 2019

HGVS

Nucleotide	Protein	Molecular consequence
NM_000038.6:c.1627-315C>T MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.		intron variant
NM_001127510.3:c.1627-315C>T		intron variant
NM_001127511.3:c.1573-315C>T		intron variant
NM_001354895.2:c.1627-315C>T		intron variant
NM_001354896.2:c.1681-315C>T		intron variant
NM_001354897.2:c.1657-315C>T		intron variant
NM_001354898.2:c.1552-315C>T		intron variant
NM_001354899.2:c.1543-315C>T		intron variant
NM_001354900.2:c.1504-315C>T		intron variant
NM_001354901.2:c.1450-315C>T		intron variant
NM_001354902.2:c.1354-315C>T		intron variant
NM_001354903.2:c.1324-315C>T		intron variant
NM_001354904.2:c.1249-315C>T		intron variant
NM_001354905.2:c.1147-315C>T		intron variant
NM_001354906.2:c.778-315C>T		intron variant
NC_000005.10:g.112828541C>T
NC_000005.9:g.112164238C>T
NC_000005.8:g.112192137C>T
NG_008481.4:g.141021C>T
LRG_130:g.141021C>T

... more HGVS ... less HGVS

Protein change

Other names

Canonical SPDI

NC_000005.10:112828540:C:T

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.

0.32588 (C)

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

The Genome Aggregation Database (gnomAD) 0.60209

Trans-Omics for Precision Medicine (TOPMed) 0.62128

1000 Genomes Project 30x 0.66958

1000 Genomes Project 0.67412

Links

ClinGen: CA005396 dbSNP: rs187075 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.
APC		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	14965	15103

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.
Familial colorectal cancer	other (1)	no assertion criteria provided	-	RCV000074152.1
not provided	Benign (1)	criteria provided, single submitter	Jan 10, 2019	RCV001636633.3

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.
Benign (Jan 10, 2019)	criteria provided, single submitter (GeneDx Variant Classification Process June 2021) Method: clinical testing	Not Provided Affected status: yes Allele origin: germline	GeneDx Accession: SCV001849235.1 First in ClinVar: Sep 12, 2021 Last updated: Sep 12, 2021
cancer (-)	no assertion criteria provided Method: not provided	Familial colorectal cancer Affected status: not provided Allele origin: unknown	Systems Biology Platform Zhejiang California International NanoSystems Institute Accession: SCV000105745.1 First in ClinVar: Oct 31, 2013 Last updated: Oct 31, 2013	Comment: Converted during submission to other.

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

There are no citations for germline classification of this variant in ClinVar. If you know of citations for this variation, please consider submitting that information to ClinVar.

Text-mined citations for rs187075 ...

These citations are identified by LitVar using the rs number, so they may include citations for more than one variant at this location. Please review the LitVar results carefully for your variant of interest.

Record last updated Jun 10, 2024

ClinVar Genomic variation as it relates to human health

NM_000038.6(APC):c.1627-315C>T

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for rs187075 ...