ClinVar

NM_033360.4(KRAS):c.*37A>G

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

12p12.1

Genomic location:

• Chr12: 25209879 (on Assembly GRCh38)
• Chr12: 25362813 (on Assembly GRCh37)

Preferred name:

NM_033360.4(KRAS):c.*37A>G

HGVS:

• NC_000012.12:g.25209879T>C
• NG_007524.2:g.46125A>G
• NM_001369786.1:c.*37A>G
• NM_001369787.1:c.483A>G
• NM_004985.5:c.483A>GMANE SELECT
• NM_033360.4:c.*37A>G
• NP_001356716.1:p.Arg161=
• NP_004976.2:p.Arg161=
• LRG_344t1:c.483A>G
• LRG_344t2:c.*37A>G
• LRG_344:g.46125A>G
• LRG_344p1:p.Arg161=
• NC_000012.11:g.25362813T>C
• NG_007524.1:g.46042A>G
• NM_004985.3:c.483A>G

This HGVS expression did not pass validation

Links:

dbSNP: rs730880380

NCBI 1000 Genomes Browser:

rs730880380

Molecular consequence:

• NM_001369786.1:c.*37A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_033360.4:c.*37A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001369787.1:c.483A>G - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_004985.5:c.483A>G - synonymous variant - [Sequence Ontology: SO:0001819]