VCV001497395.6 - ClinVar

NM_001368809.2(AMPD2):c.1202C>T (p.Thr401Met)

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.

(4)

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.

Uncertain significance

criteria provided, multiple submitters, no conflicts

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_001368809.2(AMPD2):c.1202C>T (p.Thr401Met)

Variation ID: 1497395 Accession: VCV001497395.6

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 1p13.3 1: 109628204 (GRCh38) [ NCBI UCSC ] 1: 110170826 (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	Mar 28, 2022	Feb 4, 2024	Apr 11, 2023

HGVS

Nucleotide	Protein	Molecular consequence
NM_001368809.2:c.1202C>T MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_001355738.1:p.Thr401Met	missense
NM_001257361.2:c.1010C>T	NP_001244290.1:p.Thr337Met	missense
NM_001308170.1:c.1139C>T	NP_001295099.1:p.Thr380Met	missense
NM_004037.9:c.1202C>T	NP_004028.4:p.Thr401Met	missense
NM_139156.4:c.1121C>T	NP_631895.1:p.Thr374Met	missense
NC_000001.11:g.109628204C>T
NC_000001.10:g.110170826C>T
NG_034075.1:g.13392C>T

... more HGVS ... less HGVS

Protein change

T337M, T380M, T401M, T374M

Other names

Canonical SPDI

NC_000001.11:109628203: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.

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

The Genome Aggregation Database (gnomAD) 0.00001

Exome Aggregation Consortium (ExAC) 0.00002

The Genome Aggregation Database (gnomAD), exomes 0.00002

Links

dbSNP: rs751131036 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.
AMPD2		-	-	GRCh38 GRCh37	298	434
LOC126805822	-	-	-	GRCh38	-	111

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.
Hereditary spastic paraplegia 63 Pontocerebellar hypoplasia type 9	Uncertain significance (1)	criteria provided, single submitter	Aug 14, 2021	RCV002019820.4
not provided	Uncertain significance (1)	criteria provided, single submitter	Nov 15, 2022	RCV003138025.3
Pontocerebellar hypoplasia type 9	Uncertain significance (1)	criteria provided, single submitter	Apr 11, 2023	RCV003348736.1
Hereditary spastic paraplegia 63	Uncertain significance (1)	criteria provided, single submitter	Apr 11, 2023	RCV003348735.1

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.
Uncertain significance (Aug 14, 2021)	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015)) Method: clinical testing	Pontocerebellar hypoplasia type 9 Hereditary spastic paraplegia 63 Affected status: unknown Allele origin: germline	Labcorp Genetics (formerly Invitae), Labcorp Accession: SCV002285550.1 First in ClinVar: Mar 28, 2022 Last updated: Mar 28, 2022
Uncertain significance (Apr 11, 2023)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	Pontocerebellar hypoplasia type 9 Affected status: no Allele origin: germline	Genome-Nilou Lab Accession: SCV004050577.1 First in ClinVar: Oct 28, 2023 Last updated: Oct 28, 2023
Uncertain significance (Apr 11, 2023)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	Hereditary spastic paraplegia 63 Affected status: no Allele origin: germline	Genome-Nilou Lab Accession: SCV004050576.1 First in ClinVar: Oct 28, 2023 Last updated: Oct 28, 2023
Uncertain significance (Nov 15, 2022)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	not provided Affected status: unknown Allele origin: germline	Revvity Omics, Revvity Accession: SCV003826274.2 First in ClinVar: Mar 04, 2023 Last updated: Feb 04, 2024

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 rs751131036 ...

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 Sep 29, 2024

ClinVar Genomic variation as it relates to human health

NM_001368809.2(AMPD2):c.1202C>T (p.Thr401Met)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for rs751131036 ...