ClinVar

NM_017547.4(FOXRED1):c.183C>T (p.Pro61=)

Gene:

FOXRED1:FAD dependent oxidoreductase domain containing 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q24.2

Genomic location:

• Chr11: 126271534 (on Assembly GRCh38)
• Chr11: 126141429 (on Assembly GRCh37)

Preferred name:

NM_017547.4(FOXRED1):c.183C>T (p.Pro61=)

HGVS:

• NC_000011.10:g.126271534C>T
• NG_028029.1:g.7495C>T
• NM_001425160.1:c.183C>T
• NM_001425161.1:c.183C>T
• NM_001425163.1:c.183C>T
• NM_001425164.1:c.183C>T
• NM_001425165.1:c.183C>T
• NM_001425166.1:c.183C>T
• NM_001425167.1:c.183C>T
• NM_001425169.1:c.-348C>T
• NM_001425170.1:c.-328C>T
• NM_001425171.1:c.-375C>T
• NM_001425174.1:c.-356C>T
• NM_001425175.1:c.-356C>T
• NM_017547.4:c.183C>TMANE SELECT
• NP_001412089.1:p.Pro61=
• NP_001412090.1:p.Pro61=
• NP_001412092.1:p.Pro61=
• NP_001412093.1:p.Pro61=
• NP_001412094.1:p.Pro61=
• NP_001412095.1:p.Pro61=
• NP_001412096.1:p.Pro61=
• NP_060017.1:p.Pro61=
• NC_000011.9:g.126141429C>T
• NR_037648.2:n.360C>T
• NR_189143.1:n.236C>T

This HGVS expression did not pass validation

Molecular consequence:

• NR_037648.2:n.360C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_001425160.1:c.183C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001425161.1:c.183C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001425163.1:c.183C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001425164.1:c.183C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001425165.1:c.183C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001425166.1:c.183C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001425167.1:c.183C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_017547.4:c.183C>T - synonymous variant - [Sequence Ontology: SO:0001819]