NM_001098536.2(USP5):c.1843C>G (p.Pro615Ala) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Sep 7, 2022
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:: RCV004158438.1

Allele description [Variation Report for NM_001098536.2(USP5):c.1843C>G (p.Pro615Ala)]

NM_001098536.2(USP5):c.1843C>G (p.Pro615Ala)

Gene:

USP5:ubiquitin specific peptidase 5 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

12p13.31

Genomic location:

Preferred name:

NM_001098536.2(USP5):c.1843C>G (p.Pro615Ala)

HGVS:

NC_000012.12:g.6863266C>G
NG_011948.1:g.847C>G
NM_001098536.2:c.1843C>GMANE SELECT
NM_001382588.1:c.1717C>G
NM_001382589.1:c.1717C>G
NM_001382590.1:c.1705C>G
NM_001382591.1:c.1771C>G
NM_003481.3:c.1843C>G
NP_001092006.1:p.Pro615Ala
NP_001369517.1:p.Pro573Ala
NP_001369518.1:p.Pro573Ala
NP_001369519.1:p.Pro569Ala
NP_001369520.1:p.Pro591Ala
NP_003472.2:p.Pro615Ala
LRG_1126:g.847C>G
NC_000012.11:g.6972430C>G
NM_001098536.1:c.1843C>G
NR_168449.1:n.1873C>G
NR_168450.1:n.1688C>G
NR_168451.1:n.1803C>G
NR_168452.1:n.1873C>G
NR_168454.1:n.1698C>G
NR_168455.1:n.1914C>G
NR_168456.1:n.1914C>G
NR_168457.1:n.1785C>G
NR_168458.1:n.1999C>G

Protein change:

P569A

Molecular consequence:

NM_001098536.2:c.1843C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001382588.1:c.1717C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001382589.1:c.1717C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001382590.1:c.1705C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001382591.1:c.1771C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_003481.3:c.1843C>G - missense variant - [Sequence Ontology: SO:0001583]
NR_168449.1:n.1873C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_168450.1:n.1688C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_168451.1:n.1803C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_168452.1:n.1873C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_168454.1:n.1698C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_168455.1:n.1914C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_168456.1:n.1914C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_168457.1:n.1785C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_168458.1:n.1999C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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vh82e10.r1 Knowles Solter mouse E6 5d whole embryo Mus musculus cDNA clone IMAGE...
vh82e10.r1 Knowles Solter mouse E6 5d whole embryo Mus musculus cDNA clone IMAGE:893514 3', mRNA sequence
gi|2257388|gnl|dbEST|1162504|gb|AA5 .1|

Nucleotide
A930002I21Rik RIKEN cDNA A930002I21 gene [Mus musculus]
A930002I21Rik RIKEN cDNA A930002I21 gene [Mus musculus]
Gene ID:109226

Gene

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003644351	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Sep 7, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003644351

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Sep 7, 2022)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV003644351.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The c.1843C>G (p.P615A) alteration is located in exon 15 (coding exon 15) of the USP5 gene. This alteration results from a C to G substitution at nucleotide position 1843, causing the proline (P) at amino acid position 615 to be replaced by an alanine (A). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 3, 2024

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