ClinVar

NM_002880.4(RAF1):c.1803+15T>G

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

3p25.2

Genomic location:

• Chr3: 12584832 (on Assembly GRCh38)
• Chr3: 12626331 (on Assembly GRCh37)

Preferred name:

NM_002880.4(RAF1):c.1803+15T>G

HGVS:

• NC_000003.12:g.12584832A>C
• NG_007467.1:g.84348T>G
• NM_001354689.3:c.1863+15T>G
• NM_001354690.3:c.1803+15T>G
• NM_001354691.3:c.1560+15T>G
• NM_001354692.3:c.1560+15T>G
• NM_001354693.3:c.1704+15T>G
• NM_001354694.3:c.1620+15T>G
• NM_001354695.3:c.1461+15T>G
• NM_002880.4:c.1803+15T>GMANE SELECT
• LRG_413t2:c.1863+15T>G
• LRG_413:g.84348T>G
• NC_000003.11:g.12626331A>C

This HGVS expression did not pass validation

Links:

dbSNP: rs778164265

NCBI 1000 Genomes Browser:

rs778164265

Molecular consequence:

• NM_001354689.3:c.1863+15T>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354690.3:c.1803+15T>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354691.3:c.1560+15T>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354692.3:c.1560+15T>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354693.3:c.1704+15T>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354694.3:c.1620+15T>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354695.3:c.1461+15T>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_002880.4:c.1803+15T>G - intron variant - [Sequence Ontology: SO:0001627]