ClinVar

NM_002880.4(RAF1):c.1194-13C>T

Gene:

RAF1:Raf-1 proto-oncogene, serine/threonine kinase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p25.2

Genomic location:

• Chr3: 12590987 (on Assembly GRCh38)
• Chr3: 12632486 (on Assembly GRCh37)

Preferred name:

NM_002880.4(RAF1):c.1194-13C>T

HGVS:

• NC_000003.12:g.12590987G>A
• NG_007467.1:g.78193C>T
• NM_001354689.3:c.1254-13C>T
• NM_001354690.3:c.1194-13C>T
• NM_001354691.3:c.951-13C>T
• NM_001354692.3:c.951-13C>T
• NM_001354693.3:c.1095-13C>T
• NM_001354694.3:c.1011-13C>T
• NM_001354695.3:c.852-13C>T
• NM_002880.4:c.1194-13C>TMANE SELECT
• LRG_413t2:c.1254-13C>T
• LRG_413:g.78193C>T
• NC_000003.11:g.12632486G>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_001354689.3:c.1254-13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354690.3:c.1194-13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354691.3:c.951-13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354692.3:c.951-13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354693.3:c.1095-13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354694.3:c.1011-13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354695.3:c.852-13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_002880.4:c.1194-13C>T - intron variant - [Sequence Ontology: SO:0001627]