ClinVar

NM_005343.4(HRAS):c.257A>C (p.Asn86Thr)

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: 533799 (on Assembly GRCh38)
• Chr11: 533799 (on Assembly GRCh37)

Preferred name:

NM_005343.4(HRAS):c.257A>C (p.Asn86Thr)

Other names:

p.N86T:AAC>ACC; NM_005343.3(HRAS):c.257A>C; p.Asn86Thr

HGVS:

• NC_000011.10:g.533799T>G
• NG_007666.1:g.6752A>C
• NM_001130442.3:c.257A>C
• NM_001318054.2:c.-63A>C
• NM_005343.4:c.257A>CMANE SELECT
• NM_176795.5:c.257A>C
• NP_001123914.1:p.Asn86Thr
• NP_005334.1:p.Asn86Thr
• NP_789765.1:p.Asn86Thr
• LRG_506t1:c.257A>C
• LRG_506:g.6752A>C
• LRG_506p1:p.Asn86Thr
• NC_000011.9:g.533799T>G
• NM_005343.2:c.257A>C
• NM_005343.3:c.257A>C

This HGVS expression did not pass validation

Protein change:

N86T

Links:

dbSNP: rs138272051

NCBI 1000 Genomes Browser:

rs138272051

Molecular consequence:

• NM_001318054.2:c.-63A>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001130442.3:c.257A>C - missense variant - [Sequence Ontology: SO:0001583]
• NM_005343.4:c.257A>C - missense variant - [Sequence Ontology: SO:0001583]
• NM_176795.5:c.257A>C - missense variant - [Sequence Ontology: SO:0001583]