VCV002616148.2 - ClinVar

NM_153816.6(SNX14):c.1903C>T (p.Pro635Ser)

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.

Uncertain significance

criteria provided, single submitter

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_153816.6(SNX14):c.1903C>T (p.Pro635Ser)

Variation ID: 2616148 Accession: VCV002616148.2

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 6q14.3 6: 85528354 (GRCh38) [ NCBI UCSC ] 6: 86238072 (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	Oct 28, 2023	May 1, 2024	Aug 4, 2023

HGVS

Nucleotide	Protein	Molecular consequence
NM_153816.6:c.1903C>T MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_722523.1:p.Pro635Ser	missense
NM_001297614.3:c.1876C>T	NP_001284543.1:p.Pro626Ser	missense
NM_001304479.2:c.1747C>T	NP_001291408.1:p.Pro583Ser	missense
NM_001350532.2:c.1966C>T	NP_001337461.1:p.Pro656Ser	missense
NM_001350533.2:c.1900C>T	NP_001337462.1:p.Pro634Ser	missense
NM_001350534.2:c.1873C>T	NP_001337463.1:p.Pro625Ser	missense
NM_001350535.2:c.1900C>T	NP_001337464.1:p.Pro634Ser	missense
NM_001350536.2:c.1771C>T	NP_001337465.1:p.Pro591Ser	missense
NM_001350537.2:c.1768C>T	NP_001337466.1:p.Pro590Ser	missense
NM_001350538.2:c.1759C>T	NP_001337467.1:p.Pro587Ser	missense
NM_001350539.2:c.1744C>T	NP_001337468.1:p.Pro582Ser	missense
NM_001350540.2:c.1903C>T	NP_001337469.1:p.Pro635Ser	missense
NM_001350541.2:c.1876C>T	NP_001337470.1:p.Pro626Ser	missense
NM_001350542.2:c.1615C>T	NP_001337471.1:p.Pro539Ser	missense
NM_001350543.2:c.1612C>T	NP_001337472.1:p.Pro538Ser	missense
NM_001350544.2:c.1603C>T	NP_001337473.1:p.Pro535Ser	missense
NM_001350545.2:c.1459C>T	NP_001337474.1:p.Pro487Ser	missense
NM_001350546.2:c.1459C>T	NP_001337475.1:p.Pro487Ser	missense
NM_001350547.2:c.853C>T	NP_001337476.1:p.Pro285Ser	missense
NM_001350548.2:c.748C>T	NP_001337477.1:p.Pro250Ser	missense
NM_001350549.2:c.748C>T	NP_001337478.1:p.Pro250Ser	missense
NM_001350550.2:c.748C>T	NP_001337479.1:p.Pro250Ser	missense
NM_001350551.2:c.748C>T	NP_001337480.1:p.Pro250Ser	missense
NM_001350552.2:c.748C>T	NP_001337481.1:p.Pro250Ser	missense
NM_001350553.2:c.721C>T	NP_001337482.1:p.Pro241Ser	missense
NM_020468.6:c.1744C>T	NP_065201.1:p.Pro582Ser	missense
NR_146774.2:n.1785C>T		non-coding transcript variant
NR_146775.2:n.1788C>T		non-coding transcript variant
NR_146776.2:n.1911C>T		non-coding transcript variant
NR_146777.2:n.2039C>T		non-coding transcript variant
NR_146778.2:n.2043C>T		non-coding transcript variant
NR_146779.2:n.2040C>T		non-coding transcript variant
NC_000006.12:g.85528354G>A
NC_000006.11:g.86238072G>A
NG_047171.1:g.70803C>T

... more HGVS ... less HGVS

Protein change

P538S, P587S, P626S, P635S, P250S, P285S, P535S, P590S, P591S, P625S, P487S, P583S, P656S, P241S, P539S, P582S, P634S

Other names

Canonical SPDI

NC_000006.12:85528353:G:A

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.
SNX14		-	-	GRCh38 GRCh37	287	309

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.
Inborn genetic diseases	Uncertain significance (1)	criteria provided, single submitter	Aug 4, 2023	RCV003371573.2

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.
Uncertain significance (Aug 04, 2023)	criteria provided, single submitter (Ambry Variant Classification Scheme 2023) Method: clinical testing	Inborn genetic diseases Affected status: unknown Allele origin: germline	Ambry Genetics Accession: SCV004081502.2 First in ClinVar: Oct 28, 2023 Last updated: May 01, 2024	Comment: The c.1903C>T (p.P635S) alteration is located in exon 20 (coding exon 20) of the SNX14 gene. This alteration results from a C to T substitution … (more) The c.1903C>T (p.P635S) alteration is located in exon 20 (coding exon 20) of the SNX14 gene. This alteration results from a C to T substitution at nucleotide position 1903, causing the proline (P) at amino acid position 635 to be replaced by a serine (S). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. (less)

Comment:

The c.1903C>T (p.P635S) alteration is located in exon 20 (coding exon 20) of the SNX14 gene. This alteration results from a C to T substitution at nucleotide position 1903, causing the proline (P) at amino acid position 635 to be replaced by a serine (S). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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.

Comment:

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 this variant ...

Record last updated Jul 15, 2024

ClinVar Genomic variation as it relates to human health

NM_153816.6(SNX14):c.1903C>T (p.Pro635Ser)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...