ClinVar

NM_000106.6(CYP2D6):c.794C>T (p.Ala265Val)

Gene:

CYP2D6:cytochrome P450 family 2 subfamily D member 6 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

22q13.2

Genomic location:

• Chr22: 42128223 (on Assembly GRCh38)
• Chr22: 42524225 (on Assembly GRCh37)

Preferred name:

NM_000106.6(CYP2D6):c.794C>T (p.Ala265Val)

HGVS:

• NC_000022.11:g.42128223G>A
• NG_008376.3:g.6769C>T
• NG_008376.4:g.7588C>T
• NM_000106.6:c.794C>TMANE SELECT
• NM_001025161.3:c.641C>T
• NP_000097.3:p.Ala265Val
• NP_001020332.2:p.Ala214Val
• LRG_303t1:c.794C>T
• LRG_303:g.7588C>T
• LRG_303p1:p.Ala265Val
• NC_000022.10:g.42524225G>A

This HGVS expression did not pass validation

Protein change:

A214V

Links:

dbSNP: rs1341003897

NCBI 1000 Genomes Browser:

rs1341003897

Molecular consequence:

• NM_000106.6:c.794C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001025161.3:c.641C>T - missense variant - [Sequence Ontology: SO:0001583]