ClinVar

NM_033360.4(KRAS):c.219G>A (p.Arg73=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

12p12.1

Genomic location:

• Chr12: 25227305 (on Assembly GRCh38)
• Chr12: 25380239 (on Assembly GRCh37)

Preferred name:

NM_033360.4(KRAS):c.219G>A (p.Arg73=)

HGVS:

• NC_000012.12:g.25227305C>T
• NG_007524.1:g.28616G>A
• NG_007524.2:g.28699G>A
• NM_001369786.1:c.219G>A
• NM_001369787.1:c.219G>A
• NM_004985.5:c.219G>AMANE SELECT
• NM_033360.4:c.219G>A
• NP_001356715.1:p.Arg73=
• NP_001356716.1:p.Arg73=
• NP_004976.2:p.Arg73=
• NP_203524.1:p.Arg73=
• LRG_344t1:c.219G>A
• LRG_344t2:c.219G>A
• LRG_344:g.28699G>A
• LRG_344p1:p.Arg73=
• LRG_344p2:p.Arg73=
• NC_000012.11:g.25380239C>T
• NM_033360.2:c.219G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs104886027

NCBI 1000 Genomes Browser:

rs104886027

Molecular consequence:

• NM_001369786.1:c.219G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001369787.1:c.219G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_004985.5:c.219G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_033360.4:c.219G>A - synonymous variant - [Sequence Ontology: SO:0001819]