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NM_019023.5(PRMT7):c.391+13C>T AND not provided

Germline classification:
Benign (1 submission)
Last evaluated:
Nov 4, 2023
Review status:
Somatic classification
of clinical impact:
None
Review status:
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
no assertion criteria provided
Record status:
current
Accession:
RCV002194691.6

Allele description [Variation Report for NM_019023.5(PRMT7):c.391+13C>T]

NM_019023.5(PRMT7):c.391+13C>T

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.391+13C>T
HGVS:
  • NC_000016.10:g.68329187C>T
  • NG_054896.1:g.23214C>T
  • NM_001184824.4:c.241+13C>T
  • NM_001290018.2:c.391+13C>T
  • NM_001351143.3:c.391+13C>T
  • NM_001351144.3:c.391+13C>T
  • NM_001378018.1:c.391+13C>T
  • NM_001378020.1:c.184+4355C>T
  • NM_001378021.1:c.154+13C>T
  • NM_001378022.1:c.154+13C>T
  • NM_001378023.1:c.154+13C>T
  • NM_019023.5:c.391+13C>TMANE SELECT
  • NC_000016.9:g.68363090C>T
...more
Links:
dbSNP: rs113721763
NCBI 1000 Genomes Browser:
rs113721763
Molecular consequence:
  • NM_001184824.4:c.241+13C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001290018.2:c.391+13C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001351143.3:c.391+13C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001351144.3:c.391+13C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001378018.1:c.391+13C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001378020.1:c.184+4355C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001378021.1:c.154+13C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001378022.1:c.154+13C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001378023.1:c.154+13C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_019023.5:c.391+13C>T - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV002354652Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Benign
(Nov 4, 2023)
germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Last Updated: Sep 29, 2024

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