ClinVar

NM_020631.6(PLEKHG5):c.1647G>A (p.Glu549=)

Gene:

PLEKHG5:pleckstrin homology and RhoGEF domain containing G5 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p36.31

Genomic location:

• Chr1: 6470539 (on Assembly GRCh38)
• Chr1: 6530599 (on Assembly GRCh37)

Preferred name:

NM_020631.6(PLEKHG5):c.1647G>A (p.Glu549=)

HGVS:

• NC_000001.11:g.6470539C>T
• NG_007978.1:g.54471G>A
• NG_029910.1:g.657G>A
• NM_001042663.3:c.1758G>A
• NM_001042664.2:c.1647G>A
• NM_001042665.2:c.1647G>A
• NM_001265592.2:c.1758G>A
• NM_001265593.2:c.1854G>A
• NM_001265594.3:c.1647G>A
• NM_020631.6:c.1647G>AMANE SELECT
• NM_198681.4:c.1647G>A
• NP_001036128.2:p.Glu586=
• NP_001036129.1:p.Glu549=
• NP_001036130.1:p.Glu549=
• NP_001252521.2:p.Glu586=
• NP_001252522.1:p.Glu618=
• NP_001252523.1:p.Glu549=
• NP_065682.2:p.Glu549=
• NP_065682.2:p.Glu549=
• NP_941374.3:p.Glu549=
• LRG_262t1:c.1647G>A
• LRG_262:g.54471G>A
• LRG_262p1:p.Glu549=
• NC_000001.10:g.6530599C>T
• NM_020631.3:c.1647G>A
• NM_020631.4:c.1647G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs770781624

NCBI 1000 Genomes Browser:

rs770781624

Molecular consequence:

• NM_001042663.3:c.1758G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001042664.2:c.1647G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001042665.2:c.1647G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001265592.2:c.1758G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001265593.2:c.1854G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001265594.3:c.1647G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_020631.6:c.1647G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_198681.4:c.1647G>A - synonymous variant - [Sequence Ontology: SO:0001819]