ClinVar

NM_001110792.2(MECP2):c.534C>T (p.Ser178=)

Gene:

MECP2:methyl-CpG binding protein 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xq28

Genomic location:

• ChrX: 154031330 (on Assembly GRCh38)
• ChrX: 153296781 (on Assembly GRCh37)

Preferred name:

NM_001110792.2(MECP2):c.534C>T (p.Ser178=)

HGVS:

• NC_000023.11:g.154031330G>A
• NG_007107.3:g.110774C>T
• NM_001110792.2:c.534C>TMANE SELECT
• NM_001316337.2:c.219C>T
• NM_001369391.2:c.219C>T
• NM_001369392.2:c.219C>T
• NM_001369393.2:c.219C>T
• NM_001369394.2:c.219C>T
• NM_001386137.1:c.-128-44C>T
• NM_001386138.1:c.-128-44C>T
• NM_001386139.1:c.-128-44C>T
• NM_004992.4:c.498C>T
• NP_001104262.1:p.Ser178=
• NP_001303266.1:p.Ser73=
• NP_001356320.1:p.Ser73=
• NP_001356321.1:p.Ser73=
• NP_001356322.1:p.Ser73=
• NP_001356323.1:p.Ser73=
• NP_004983.1:p.Ser166=
• LRG_764t1:c.534C>T
• LRG_764t2:c.498C>T
• LRG_764:g.110774C>T
• LRG_764p1:p.Ser178=
• LRG_764p2:p.Ser166=
• NC_000023.10:g.153296781G>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_001386137.1:c.-128-44C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001386138.1:c.-128-44C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001386139.1:c.-128-44C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001110792.2:c.534C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001316337.2:c.219C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001369391.2:c.219C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001369392.2:c.219C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001369393.2:c.219C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001369394.2:c.219C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_004992.4:c.498C>T - synonymous variant - [Sequence Ontology: SO:0001819]