ClinVar

NM_000399.5(EGR2):c.1066G>A (p.Glu356Lys)

Gene:

EGR2:early growth response 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

10q21.3

Genomic location:

• Chr10: 62813572 (on Assembly GRCh38)
• Chr10: 64573332 (on Assembly GRCh37)

Preferred name:

NM_000399.5(EGR2):c.1066G>A (p.Glu356Lys)

HGVS:

• NC_000010.11:g.62813572C>T
• NG_008936.2:g.111329G>A
• NM_000399.5:c.1066G>AMANE SELECT
• NM_001136177.3:c.1066G>A
• NM_001136178.2:c.1066G>A
• NM_001136179.3:c.916G>A
• NM_001321037.2:c.916G>A
• NP_000390.2:p.Glu356Lys
• NP_001129649.1:p.Glu356Lys
• NP_001129650.1:p.Glu356Lys
• NP_001129651.1:p.Glu306Lys
• NP_001307966.1:p.Glu306Lys
• LRG_239t1:c.1066G>A
• LRG_239:g.111329G>A
• NC_000010.10:g.64573332C>T
• NM_000399.3:c.1066G>A

This HGVS expression did not pass validation

Protein change:

E306K

Links:

dbSNP: rs751448371

NCBI 1000 Genomes Browser:

rs751448371

Molecular consequence:

• NM_000399.5:c.1066G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001136177.3:c.1066G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001136178.2:c.1066G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001136179.3:c.916G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001321037.2:c.916G>A - missense variant - [Sequence Ontology: SO:0001583]