NM_014871.6(PAN2):c.1347G>C (p.Arg449Ser) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Sep 13, 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:: RCV004366003.1

Allele description [Variation Report for NM_014871.6(PAN2):c.1347G>C (p.Arg449Ser)]

NM_014871.6(PAN2):c.1347G>C (p.Arg449Ser)

Gene:

PAN2:poly(A) specific ribonuclease subunit PAN2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

12q13.3

Genomic location:

Preferred name:

NM_014871.6(PAN2):c.1347G>C (p.Arg449Ser)

HGVS:

NC_000012.12:g.56326325C>G
NM_001127460.4:c.1347G>C
NM_001166279.3:c.1347G>C
NM_001394699.1:c.1347G>C
NM_001394700.1:c.1347G>C
NM_001394701.1:c.1347G>C
NM_001394702.1:c.1347G>C
NM_001394703.1:c.1347G>C
NM_001394704.1:c.1347G>C
NM_001394705.1:c.1347G>C
NM_001394706.1:c.1347G>C
NM_001394707.1:c.1347G>C
NM_001394708.1:c.930G>C
NM_014871.6:c.1347G>CMANE SELECT
NP_001120932.2:p.Arg449Ser
NP_001159751.2:p.Arg449Ser
NP_001381628.1:p.Arg449Ser
NP_001381629.1:p.Arg449Ser
NP_001381630.1:p.Arg449Ser
NP_001381631.1:p.Arg449Ser
NP_001381632.1:p.Arg449Ser
NP_001381633.1:p.Arg449Ser
NP_001381634.1:p.Arg449Ser
NP_001381635.1:p.Arg449Ser
NP_001381636.1:p.Arg449Ser
NP_001381637.1:p.Arg310Ser
NP_055686.4:p.Arg449Ser
NC_000012.11:g.56720109C>G
NM_001127460.2:c.1347G>C

Protein change:

R310S

Molecular consequence:

NM_001127460.4:c.1347G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001166279.3:c.1347G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001394699.1:c.1347G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001394700.1:c.1347G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001394701.1:c.1347G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001394702.1:c.1347G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001394703.1:c.1347G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001394704.1:c.1347G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001394705.1:c.1347G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001394706.1:c.1347G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001394707.1:c.1347G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001394708.1:c.930G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_014871.6:c.1347G>C - missense variant - [Sequence Ontology: SO:0001583]

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
SCV004091172	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Sep 13, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004091172

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Sep 13, 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, SCV004091172.2

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

Description

The c.1347G>C (p.R449S) alteration is located in exon 8 (coding exon 7) of the PAN2 gene. This alteration results from a G to C substitution at nucleotide position 1347, causing the arginine (R) at amino acid position 449 to be replaced by a serine (S). 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 24, 2024

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