ClinVar

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:

• Chr16: 68329187 (on Assembly GRCh38)
• Chr16: 68363090 (on Assembly GRCh37)

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

This HGVS expression did not pass validation

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]