ClinVar

NM_005343.4(HRAS):c.492G>A (p.Arg164=)

Genes:

HRAS:HRas proto-oncogene, GTPase [Gene - OMIM - HGNC]
LRRC56:leucine rich repeat containing 56 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p15.5

Genomic location:

• Chr11: 532714 (on Assembly GRCh38)
• Chr11: 532714 (on Assembly GRCh37)

Preferred name:

NM_005343.4(HRAS):c.492G>A (p.Arg164=)

HGVS:

• NC_000011.10:g.532714C>T
• NG_007666.1:g.7837G>A
• NM_001130442.3:c.492G>A
• NM_001318054.2:c.255G>A
• NM_005343.4:c.492G>AMANE SELECT
• NM_176795.5:c.*61G>A
• NP_001123914.1:p.Arg164=
• NP_001304983.1:p.Arg85=
• NP_005334.1:p.Arg164=
• LRG_506t1:c.492G>A
• LRG_506:g.7837G>A
• LRG_506p1:p.Arg164=
• NC_000011.9:g.532714C>T
• NM_005343.2:c.492G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs1461319720

NCBI 1000 Genomes Browser:

rs1461319720

Molecular consequence:

• NM_176795.5:c.*61G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001130442.3:c.492G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001318054.2:c.255G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_005343.4:c.492G>A - synonymous variant - [Sequence Ontology: SO:0001819]