ClinVar

NM_000352.6(ABCC8):c.1882G>A (p.Glu628Lys)

Gene:

ABCC8:ATP binding cassette subfamily C member 8 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p15.1

Genomic location:

• Chr11: 17428606 (on Assembly GRCh38)
• Chr11: 17450153 (on Assembly GRCh37)

Preferred name:

NM_000352.6(ABCC8):c.1882G>A (p.Glu628Lys)

HGVS:

• NC_000011.10:g.17428606C>T
• NG_008867.1:g.53297G>A
• NM_000352.6:c.1882G>AMANE SELECT
• NM_001287174.3:c.1882G>A
• NM_001351295.2:c.1882G>A
• NM_001351296.2:c.1879G>A
• NM_001351297.2:c.1879G>A
• NP_000343.2:p.Glu628Lys
• NP_001274103.1:p.Glu628Lys
• NP_001338224.1:p.Glu628Lys
• NP_001338225.1:p.Glu627Lys
• NP_001338226.1:p.Glu627Lys
• LRG_790t1:c.1882G>A
• LRG_790t2:c.1882G>A
• LRG_790:g.53297G>A
• LRG_790p1:p.Glu628Lys
• LRG_790p2:p.Glu628Lys
• NC_000011.9:g.17450153C>T
• NM_001287174.1:c.1882G>A
• NR_147094.2:n.1948G>A

This HGVS expression did not pass validation

Protein change:

E627K

Links:

dbSNP: rs565662182

NCBI 1000 Genomes Browser:

rs565662182

Molecular consequence:

• NM_000352.6:c.1882G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001287174.3:c.1882G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001351295.2:c.1882G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001351296.2:c.1879G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001351297.2:c.1879G>A - missense variant - [Sequence Ontology: SO:0001583]
• NR_147094.2:n.1948G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]