ClinVar

NM_000914.4(OPRM1):c.-394C>A

Gene:

OPRM1:opioid receptor mu 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6q25.2

Genomic location:

• Chr6: 154039151 (on Assembly GRCh38)
• Chr6: 154360286 (on Assembly GRCh37)

Preferred name:

NM_000914.4(OPRM1):c.-394C>A

HGVS:

• NC_000006.12:g.154039151C>A
• NG_021208.2:g.33651C>A
• NM_000914.4:c.-394C>A
• NM_001008504.3:c.-394C>A
• NM_001145279.4:c.1-10C>A
• NM_001145280.4:c.-11+28133C>A
• NM_001145281.3:c.47+28592C>A
• NM_001285522.1:c.-394C>A
• NM_001285523.2:c.-394C>A
• NM_001285524.1:c.-10C>A
• LRG_1007:g.33651C>A
• NC_000006.11:g.154360286C>A

This HGVS expression did not pass validation

Links:

dbSNP: rs1583169385

NCBI 1000 Genomes Browser:

rs1583169385

Molecular consequence:

• NM_001285522.1:c.-394C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001285524.1:c.-10C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001145279.4:c.1-10C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001145280.4:c.-11+28133C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001145281.3:c.47+28592C>A - intron variant - [Sequence Ontology: SO:0001627]