ClinVar

NM_033360.4(KRAS):c.*2012T>C

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

12p12.1

Genomic location:

• Chr12: 25207904 (on Assembly GRCh38)
• Chr12: 25360838 (on Assembly GRCh37)

Preferred name:

NM_033360.4(KRAS):c.*2012T>C

HGVS:

• NC_000012.12:g.25207904A>G
• NG_007524.2:g.48100T>C
• NM_001369786.1:c.*2012T>C
• NM_001369787.1:c.*1891T>C
• NM_004985.5:c.*1891T>CMANE SELECT
• NM_033360.4:c.*2012T>C
• LRG_344t1:c.*1891T>C
• LRG_344t2:c.*2012T>C
• LRG_344:g.48100T>C
• NC_000012.11:g.25360838A>G
• NG_007524.1:g.48017T>C
• NM_004985.3:c.*1891T>C

This HGVS expression did not pass validation

Links:

dbSNP: rs886049190

NCBI 1000 Genomes Browser:

rs886049190

Molecular consequence:

• NM_001369786.1:c.*2012T>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001369787.1:c.*1891T>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_004985.5:c.*1891T>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_033360.4:c.*2012T>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]