NM_019023.5(PRMT7):c.89T>C (p.Ile30Thr) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Feb 12, 2024
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:: RCV004515331.1

Allele description [Variation Report for NM_019023.5(PRMT7):c.89T>C (p.Ile30Thr)]

NM_019023.5(PRMT7):c.89T>C (p.Ile30Thr)

Gene:

PRMT7:protein arginine methyltransferase 7 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q22.1

Genomic location:

Preferred name:

NM_019023.5(PRMT7):c.89T>C (p.Ile30Thr)

HGVS:

NC_000016.10:g.68316068T>C
NG_054896.1:g.10095T>C
NG_054896.2:g.10051T>C
NM_001184824.4:c.89T>C
NM_001290018.2:c.89T>C
NM_001351143.3:c.89T>C
NM_001351144.3:c.89T>C
NM_001378018.1:c.89T>C
NM_001378020.1:c.28T>C
NM_001378021.1:c.-112T>C
NM_001378022.1:c.-112T>C
NM_001378023.1:c.-112T>C
NM_019023.5:c.89T>CMANE SELECT
NP_001171753.1:p.Ile30Thr
NP_001276947.1:p.Ile30Thr
NP_001338072.1:p.Ile30Thr
NP_001338073.1:p.Ile30Thr
NP_001364947.1:p.Ile30Thr
NP_001364949.1:p.Leu10=
NP_061896.1:p.Ile30Thr
NC_000016.9:g.68349971T>C
NM_019023.2:c.89T>C
NR_147056.3:n.253T>C
NR_147057.3:n.388T>C
NR_147058.3:n.388T>C
NR_165365.1:n.388T>C
NR_165366.1:n.253T>C
NR_165367.1:n.253T>C
NR_165368.1:n.388T>C
NR_165369.1:n.253T>C
NR_165370.1:n.253T>C
NR_165371.1:n.388T>C
NR_165372.1:n.388T>C
NR_165373.1:n.388T>C

Protein change:

I30T

Molecular consequence:

NM_001378021.1:c.-112T>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001378022.1:c.-112T>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001378023.1:c.-112T>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001184824.4:c.89T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001290018.2:c.89T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001351143.3:c.89T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001351144.3:c.89T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001378018.1:c.89T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_019023.5:c.89T>C - missense variant - [Sequence Ontology: SO:0001583]
NR_147056.3:n.253T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_147057.3:n.388T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_147058.3:n.388T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_165365.1:n.388T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_165366.1:n.253T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_165367.1:n.253T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_165368.1:n.388T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_165369.1:n.253T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_165370.1:n.253T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_165371.1:n.388T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_165372.1:n.388T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_165373.1:n.388T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NM_001378020.1:c.28T>C - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

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wt, no stress, 37C, 60 min
wt, no stress, 37C, 60 min

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV005011751	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Feb 12, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV005011751

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Feb 12, 2024)

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, SCV005011751.1

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

Description

The c.89T>C (p.I30T) alteration is located in exon 3 (coding exon 1) of the PRMT7 gene. This alteration results from a T to C substitution at nucleotide position 89, causing the isoleucine (I) at amino acid position 30 to be replaced by a threonine (T). 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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