ClinVar

NM_005138.3(SCO2):c.69T>C (p.Pro23=)

Genes:

NCAPH2:non-SMC condensin II complex subunit H2 [Gene - OMIM - HGNC]
SCO2:synthesis of cytochrome C oxidase 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

22q13.33

Genomic location:

• Chr22: 50524343 (on Assembly GRCh38)
• Chr22: 50962772 (on Assembly GRCh37)

Preferred name:

NM_005138.3(SCO2):c.69T>C (p.Pro23=)

HGVS:

• NC_000022.11:g.50524343A>G
• NG_011860.1:g.10743T>C
• NG_016235.1:g.7097T>C
• NG_021419.1:g.21128A>G
• NM_001169109.2:c.69T>C
• NM_001169110.1:c.69T>C
• NM_001169111.2:c.69T>C
• NM_001185011.2:c.*968A>G
• NM_005138.3:c.69T>CMANE SELECT
• NM_152299.4:c.*968A>GMANE SELECT
• NP_001162580.1:p.Pro23=
• NP_001162581.1:p.Pro23=
• NP_001162582.1:p.Pro23=
• NP_005129.2:p.Pro23=
• LRG_727:g.10743T>C
• NC_000022.10:g.50962772A>G

This HGVS expression did not pass validation

Molecular consequence:

• NM_001185011.2:c.*968A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_152299.4:c.*968A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001169109.2:c.69T>C - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001169110.1:c.69T>C - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001169111.2:c.69T>C - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_005138.3:c.69T>C - synonymous variant - [Sequence Ontology: SO:0001819]