ClinVar

NM_033331.4(CDC14B):c.38C>T (p.Ala13Val)

Gene:

CDC14B:cell division cycle 14B [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9q22.33

Genomic location:

• Chr9: 96619341 (on Assembly GRCh38)
• Chr9: 99381623 (on Assembly GRCh37)

Preferred name:

NM_033331.4(CDC14B):c.38C>T (p.Ala13Val)

HGVS:

• NC_000009.12:g.96619341G>A
• NG_116904.1:g.448G>A
• NM_001351567.3:c.38C>T
• NM_003671.5:c.38C>T
• NM_033331.4:c.38C>TMANE SELECT
• NP_001338496.1:p.Ala13Val
• NP_003662.1:p.Ala13Val
• NP_201588.1:p.Ala13Val
• NC_000009.11:g.99381623G>A
• NM_033331.2:c.38C>T
• NR_147239.2:n.503C>T

This HGVS expression did not pass validation

Protein change:

A13V

Molecular consequence:

• NM_001351567.3:c.38C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_003671.5:c.38C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_033331.4:c.38C>T - missense variant - [Sequence Ontology: SO:0001583]
• NR_147239.2:n.503C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]