ClinVar

NM_171982.5(TRIM35):c.443G>T (p.Cys148Phe)

Gene:

TRIM35:tripartite motif containing 35 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

8p21.2

Genomic location:

• Chr8: 27298552 (on Assembly GRCh38)
• Chr8: 27156069 (on Assembly GRCh37)

Preferred name:

NM_171982.5(TRIM35):c.443G>T (p.Cys148Phe)

HGVS:

• NC_000008.11:g.27298552C>A
• NM_001304495.2:c.436-4242G>T
• NM_001362813.2:c.443G>T
• NM_015066.2:c.443G>T
• NM_171982.5:c.443G>TMANE SELECT
• NP_001349742.1:p.Cys148Phe
• NP_055881.1:p.Cys148Phe
• NP_741983.2:p.Cys148Phe
• NC_000008.10:g.27156069C>A
• NM_171982.3:c.443G>T

This HGVS expression did not pass validation

Protein change:

C148F

Molecular consequence:

• NM_001304495.2:c.436-4242G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001362813.2:c.443G>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_015066.2:c.443G>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_171982.5:c.443G>T - missense variant - [Sequence Ontology: SO:0001583]