NM_001146105.2(PARP9):c.1108A>G (p.Ile370Val) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Oct 3, 2023
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:: RCV004502710.1

Allele description [Variation Report for NM_001146105.2(PARP9):c.1108A>G (p.Ile370Val)]

NM_001146105.2(PARP9):c.1108A>G (p.Ile370Val)

Gene:

PARP9:poly(ADP-ribose) polymerase family member 9 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3q21.1

Genomic location:

Preferred name:

NM_001146105.2(PARP9):c.1108A>G (p.Ile370Val)

HGVS:

NC_000003.12:g.122550802T>C
NM_001146102.2:c.1213A>G
NM_001146103.2:c.1108A>G
NM_001146104.2:c.1108A>G
NM_001146105.2:c.1108A>GMANE SELECT
NM_001146106.3:c.1108A>G
NM_001387871.1:c.1213A>G
NM_001387872.1:c.1213A>G
NM_001387873.1:c.1147A>G
NM_001387874.1:c.1147A>G
NM_001387875.1:c.1108A>G
NM_001387876.1:c.1108A>G
NM_001387877.1:c.1108A>G
NM_001387878.1:c.1213A>G
NM_001387879.1:c.1213A>G
NM_001387880.1:c.1213A>G
NM_001387881.1:c.1108A>G
NM_001387882.1:c.1108A>G
NM_001387883.1:c.1108A>G
NM_001387884.1:c.1108A>G
NM_001387885.1:c.1108A>G
NM_001387886.1:c.1108A>G
NM_001387887.1:c.1108A>G
NM_031458.3:c.1213A>G
NP_001139574.1:p.Ile405Val
NP_001139575.1:p.Ile370Val
NP_001139576.1:p.Ile370Val
NP_001139577.1:p.Ile370Val
NP_001139578.1:p.Ile370Val
NP_001374800.1:p.Ile405Val
NP_001374801.1:p.Ile405Val
NP_001374802.1:p.Ile383Val
NP_001374803.1:p.Ile383Val
NP_001374804.1:p.Ile370Val
NP_001374805.1:p.Ile370Val
NP_001374806.1:p.Ile370Val
NP_001374807.1:p.Ile405Val
NP_001374808.1:p.Ile405Val
NP_001374809.1:p.Ile405Val
NP_001374810.1:p.Ile370Val
NP_001374811.1:p.Ile370Val
NP_001374812.1:p.Ile370Val
NP_001374813.1:p.Ile370Val
NP_001374814.1:p.Ile370Val
NP_001374815.1:p.Ile370Val
NP_001374816.1:p.Ile370Val
NP_113646.2:p.Ile405Val
NC_000003.11:g.122269649T>C
NM_031458.2:c.1213A>G
NR_170857.1:n.1543A>G
NR_170858.1:n.1543A>G
NR_170859.1:n.1250A>G
NR_170860.1:n.1253A>G
NR_170861.1:n.1355A>G
NR_170862.1:n.1253A>G
NR_170863.1:n.1253A>G
NR_170864.1:n.1253A>G
NR_170865.1:n.1387A>G

Protein change:

I370V

Molecular consequence:

NM_001146102.2:c.1213A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001146103.2:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001146104.2:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001146105.2:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001146106.3:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387871.1:c.1213A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387872.1:c.1213A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387873.1:c.1147A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387874.1:c.1147A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387875.1:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387876.1:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387877.1:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387878.1:c.1213A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387879.1:c.1213A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387880.1:c.1213A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387881.1:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387882.1:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387883.1:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387884.1:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387885.1:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387886.1:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001387887.1:c.1108A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_031458.3:c.1213A>G - missense variant - [Sequence Ontology: SO:0001583]
NR_170857.1:n.1543A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_170858.1:n.1543A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_170859.1:n.1250A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_170860.1:n.1253A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_170861.1:n.1355A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_170862.1:n.1253A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_170863.1:n.1253A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_170864.1:n.1253A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_170865.1:n.1387A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004998712	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Oct 3, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004998712

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Oct 3, 2023)

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, SCV004998712.1

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

Description

The c.1213A>G (p.I405V) alteration is located in exon 6 (coding exon 5) of the PARP9 gene. This alteration results from a A to G substitution at nucleotide position 1213, causing the isoleucine (I) at amino acid position 405 to be replaced by a valine (V). 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: May 7, 2024

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