ClinVar

NM_016203.4(PRKAG2):c.*365G>A

Gene:

PRKAG2:protein kinase AMP-activated non-catalytic subunit gamma 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7q36.1

Genomic location:

• Chr7: 151556836 (on Assembly GRCh38)
• Chr7: 151253922 (on Assembly GRCh37)

Preferred name:

NM_016203.4(PRKAG2):c.*365G>A

HGVS:

• NC_000007.14:g.151556836C>T
• NG_007486.2:g.325396G>A
• NM_001040633.2:c.*365G>A
• NM_001304527.2:c.*365G>A
• NM_001304531.2:c.*365G>A
• NM_001363698.2:c.*365G>A
• NM_016203.4:c.*365G>AMANE SELECT
• NM_024429.2:c.*365G>A
• LRG_430t1:c.*365G>A
• LRG_430:g.325396G>A
• NC_000007.13:g.151253922C>T
• NG_007486.1:g.325395G>A
• NM_016203.3:c.*365G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs886062098

NCBI 1000 Genomes Browser:

rs886062098

Molecular consequence:

• NM_001040633.2:c.*365G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001304527.2:c.*365G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001304531.2:c.*365G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001363698.2:c.*365G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_016203.4:c.*365G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_024429.2:c.*365G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]