ClinVar

NM_024877.4(CCNP):c.152G>A (p.Gly51Asp)

Genes:

LOC130064442:ATAC-STARR-seq lymphoblastoid silent region 10618 [Gene]
CCNP:cyclin P [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.2

Genomic location:

• Chr19: 40226490 (on Assembly GRCh38)
• Chr19: 40732397 (on Assembly GRCh37)

Preferred name:

NM_024877.4(CCNP):c.152G>A (p.Gly51Asp)

HGVS:

• NC_000019.10:g.40226490C>T
• NG_141394.1:g.68C>T
• NG_198859.1:g.214C>T
• NM_001144029.1:c.152G>A
• NM_001411133.1:c.152G>A
• NM_024877.4:c.152G>AMANE SELECT
• NP_001137501.1:p.Gly51Asp
• NP_001398062.1:p.Gly51Asp
• NP_079153.2:p.Gly51Asp
• NC_000019.9:g.40732397C>T
• NM_024877.3:c.152G>A

This HGVS expression did not pass validation

Protein change:

G51D

Molecular consequence:

• NM_001144029.1:c.152G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001411133.1:c.152G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_024877.4:c.152G>A - missense variant - [Sequence Ontology: SO:0001583]