ClinVar

NM_004985.5(KRAS):c.112-9C>T

Gene:

KRAS:KRAS proto-oncogene, GTPase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

12p12.1

Genomic location:

• Chr12: 25227421 (on Assembly GRCh38)
• Chr12: 25380355 (on Assembly GRCh37)

Preferred name:

NM_004985.5(KRAS):c.112-9C>T

HGVS:

• NC_000012.12:g.25227421G>A
• NG_007524.2:g.28583C>T
• NM_001369786.1:c.112-9C>T
• NM_001369787.1:c.112-9C>T
• NM_004985.5:c.112-9C>TMANE SELECT
• NM_033360.4:c.112-9C>T
• LRG_344t1:c.112-9C>T
• LRG_344t2:c.112-9C>T
• LRG_344:g.28583C>T
• NC_000012.11:g.25380355G>A
• NG_007524.1:g.28500C>T
• NM_004985.3:c.112-9C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs727504298

NCBI 1000 Genomes Browser:

rs727504298

Molecular consequence:

• NM_001369786.1:c.112-9C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001369787.1:c.112-9C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_004985.5:c.112-9C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_033360.4:c.112-9C>T - intron variant - [Sequence Ontology: SO:0001627]

Observations:

1