ClinVar

NM_000162.5(GCK):c.1020-10C>T

Gene:

GCK:glucokinase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7p13

Genomic location:

• Chr7: 44145740 (on Assembly GRCh38)
• Chr7: 44185339 (on Assembly GRCh37)

Preferred name:

NM_000162.5(GCK):c.1020-10C>T

HGVS:

• NC_000007.14:g.44145740G>A
• NG_008847.2:g.57431C>T
• NM_000162.5:c.1020-10C>TMANE SELECT
• NM_001354800.1:c.1020-10C>T
• NM_001354801.1:c.9-10C>T
• NM_001354802.1:c.-121-10C>T
• NM_001354803.2:c.54-10C>T
• NM_033507.3:c.1023-10C>T
• NM_033508.3:c.1017-10C>T
• LRG_1074t1:c.1020-10C>T
• LRG_1074t2:c.1023-10C>T
• LRG_1074:g.57431C>T
• NC_000007.13:g.44185339G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs193922257

NCBI 1000 Genomes Browser:

rs193922257

Molecular consequence:

• NM_000162.5:c.1020-10C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354800.1:c.1020-10C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354801.1:c.9-10C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354802.1:c.-121-10C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001354803.2:c.54-10C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_033507.3:c.1023-10C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_033508.3:c.1017-10C>T - intron variant - [Sequence Ontology: SO:0001627]