ClinVar

NM_033360.4(KRAS):c.*3269C>T

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

12p12.1

Genomic location:

• Chr12: 25206647 (on Assembly GRCh38)
• Chr12: 25359581 (on Assembly GRCh37)

Preferred name:

NM_033360.4(KRAS):c.*3269C>T

HGVS:

• NC_000012.12:g.25206647G>A
• NG_007524.2:g.49357C>T
• NM_001369786.1:c.*3269C>T
• NM_001369787.1:c.*3148C>T
• NM_004985.5:c.*3148C>TMANE SELECT
• NM_033360.4:c.*3269C>T
• LRG_344t1:c.*3148C>T
• LRG_344t2:c.*3269C>T
• LRG_344:g.49357C>T
• NC_000012.11:g.25359581G>A
• NG_007524.1:g.49274C>T
• NM_004985.3:c.*3148C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs886049183

NCBI 1000 Genomes Browser:

rs886049183

Molecular consequence:

• NM_001369786.1:c.*3269C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001369787.1:c.*3148C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_004985.5:c.*3148C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_033360.4:c.*3269C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]