ClinVar

NM_005343.4(HRAS):c.411C>T (p.Tyr137=)

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: 533492 (on Assembly GRCh38)
• Chr11: 533492 (on Assembly GRCh37)

Preferred name:

NM_005343.4(HRAS):c.411C>T (p.Tyr137=)

HGVS:

• NC_000011.10:g.533492G>A
• NG_007666.1:g.7059C>T
• NM_001130442.3:c.411C>T
• NM_001318054.2:c.92C>T
• NM_005343.4:c.411C>TMANE SELECT
• NM_176795.5:c.411C>T
• NP_001123914.1:p.Tyr137=
• NP_001304983.1:p.Thr31Met
• NP_005334.1:p.Tyr137=
• NP_789765.1:p.Tyr137=
• LRG_506t1:c.411C>T
• LRG_506:g.7059C>T
• LRG_506p1:p.Tyr137=
• NC_000011.9:g.533492G>A
• NM_005343.2:c.411C>T

This HGVS expression did not pass validation

Protein change:

T31M

Links:

dbSNP: rs1471385417

NCBI 1000 Genomes Browser:

rs1471385417

Molecular consequence:

• NM_001318054.2:c.92C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001130442.3:c.411C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_005343.4:c.411C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_176795.5:c.411C>T - synonymous variant - [Sequence Ontology: SO:0001819]