ClinVar

NM_019023.5(PRMT7):c.928-7G>A

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

16q22.1

Genomic location:

• Chr16: 68345668 (on Assembly GRCh38)
• Chr16: 68379571 (on Assembly GRCh37)

Preferred name:

NM_019023.5(PRMT7):c.928-7G>A

HGVS:

• NC_000016.10:g.68345668G>A
• NG_054896.1:g.39695G>A
• NG_054896.2:g.39651G>A
• NM_001184824.4:c.778-7G>A
• NM_001290018.2:c.928-7G>A
• NM_001351143.3:c.928-7G>A
• NM_001351144.3:c.928-7G>A
• NM_001378018.1:c.928-7G>A
• NM_001378020.1:c.721-7G>A
• NM_001378021.1:c.691-7G>A
• NM_001378022.1:c.691-7G>A
• NM_001378023.1:c.691-7G>A
• NM_019023.5:c.928-7G>AMANE SELECT
• NC_000016.9:g.68379571G>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_001184824.4:c.778-7G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001290018.2:c.928-7G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001351143.3:c.928-7G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001351144.3:c.928-7G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001378018.1:c.928-7G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001378020.1:c.721-7G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001378021.1:c.691-7G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001378022.1:c.691-7G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001378023.1:c.691-7G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_019023.5:c.928-7G>A - intron variant - [Sequence Ontology: SO:0001627]