ClinVar

NM_005343.4(HRAS):c.182A>T (p.Gln61Leu)

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: 533874 (on Assembly GRCh38)
• Chr11: 533874 (on Assembly GRCh37)

Preferred name:

NM_005343.4(HRAS):c.182A>T (p.Gln61Leu)

HGVS:

• NC_000011.10:g.533874T>A
• NG_007666.1:g.6677A>T
• NM_001130442.3:c.182A>T
• NM_001318054.2:c.-138A>T
• NM_005343.4:c.182A>TMANE SELECT
• NM_176795.5:c.182A>T
• NP_001123914.1:p.Gln61Leu
• NP_001123914.1:p.Gln61Leu
• NP_005334.1:p.Gln61Leu
• NP_789765.1:p.Gln61Leu
• LRG_506t1:c.182A>T
• LRG_506:g.6677A>T
• LRG_506p1:p.Gln61Leu
• NC_000011.9:g.533874T>A
• NM_001130442.2:c.182A>T
• NM_005343.2:c.182A>T

This HGVS expression did not pass validation

Protein change:

Q61L

Links:

dbSNP: rs121913233

NCBI 1000 Genomes Browser:

rs121913233

Molecular consequence:

• NM_001318054.2:c.-138A>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001130442.3:c.182A>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_005343.4:c.182A>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_176795.5:c.182A>T - missense variant - [Sequence Ontology: SO:0001583]