ClinVar

NM_002880.4(RAF1):c.834+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: 12604123 (on Assembly GRCh38)
• Chr3: 12645622 (on Assembly GRCh37)

Preferred name:

NM_002880.4(RAF1):c.834+13C>T

HGVS:

• NC_000003.12:g.12604123G>A
• NG_007467.1:g.65057C>T
• NM_001354689.3:c.834+13C>T
• NM_001354690.3:c.834+13C>T
• NM_001354691.3:c.591+13C>T
• NM_001354692.3:c.591+13C>T
• NM_001354693.3:c.735+13C>T
• NM_001354694.3:c.591+13C>T
• NM_001354695.3:c.492+13C>T
• NM_002880.4:c.834+13C>TMANE SELECT
• LRG_413t2:c.834+13C>T
• LRG_413:g.65057C>T
• NC_000003.11:g.12645622G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs748478768

NCBI 1000 Genomes Browser:

rs748478768

Molecular consequence:

• NM_001354689.3:c.834+13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354690.3:c.834+13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354691.3:c.591+13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354692.3:c.591+13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354693.3:c.735+13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354694.3:c.591+13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354695.3:c.492+13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_002880.4:c.834+13C>T - intron variant - [Sequence Ontology: SO:0001627]