ClinVar

NM_000162.5(GCK):c.1020-95G>A

Gene:

GCK:glucokinase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7p13

Genomic location:

• Chr7: 44145825 (on Assembly GRCh38)
• Chr7: 44185424 (on Assembly GRCh37)

Preferred name:

NM_000162.5(GCK):c.1020-95G>A

HGVS:

• NC_000007.14:g.44145825C>T
• NG_008847.2:g.57346G>A
• NM_000162.5:c.1020-95G>AMANE SELECT
• NM_001354800.1:c.1020-95G>A
• NM_001354801.1:c.9-95G>A
• NM_001354802.1:c.-122+84G>A
• NM_001354803.2:c.54-95G>A
• NM_033507.3:c.1023-95G>A
• NM_033508.3:c.1017-95G>A
• LRG_1074t1:c.1020-95G>A
• LRG_1074t2:c.1023-95G>A
• LRG_1074:g.57346G>A
• NC_000007.13:g.44185424C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs540085721

NCBI 1000 Genomes Browser:

rs540085721

Molecular consequence:

• NM_000162.5:c.1020-95G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354800.1:c.1020-95G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354801.1:c.9-95G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354802.1:c.-122+84G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354803.2:c.54-95G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_033507.3:c.1023-95G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_033508.3:c.1017-95G>A - intron variant - [Sequence Ontology: SO:0001627]