ClinVar

NM_001323289.2(CDKL5):c.1721C>A (p.Pro574Gln)

Gene:

CDKL5:cyclin dependent kinase like 5 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xp22.13

Genomic location:

• ChrX: 18604645 (on Assembly GRCh38)
• ChrX: 18622765 (on Assembly GRCh37)

Preferred name:

NM_001323289.2(CDKL5):c.1721C>A (p.Pro574Gln)

HGVS:

• NC_000023.11:g.18604645C>A
• NG_008475.1:g.184041C>A
• NM_001037343.2:c.1721C>A
• NM_001323289.2:c.1721C>AMANE SELECT
• NM_003159.3:c.1721C>A
• NP_001032420.1:p.Pro574Gln
• NP_001310218.1:p.Pro574Gln
• NP_003150.1:p.Pro574Gln
• NC_000023.10:g.18622765C>A
• NM_003159.2:c.1721C>A

This HGVS expression did not pass validation

Protein change:

P574Q

Links:

dbSNP: rs199897804

NCBI 1000 Genomes Browser:

rs199897804

Molecular consequence:

• NM_001037343.2:c.1721C>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001323289.2:c.1721C>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_003159.3:c.1721C>A - missense variant - [Sequence Ontology: SO:0001583]