ClinVar

NM_002524.5(NRAS):c.183A>T (p.Gln61His)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

1p13.2

Genomic location:

• Chr1: 114713907 (on Assembly GRCh38)
• Chr1: 115256528 (on Assembly GRCh37)

Preferred name:

NM_002524.5(NRAS):c.183A>T (p.Gln61His)

HGVS:

• NC_000001.11:g.114713907T>A
• NG_007572.1:g.7988A>T
• NM_002524.5:c.183A>TMANE SELECT
• NP_002515.1:p.Gln61His
• LRG_92t1:c.183A>T
• LRG_92:g.7988A>T
• NC_000001.10:g.115256528T>A
• NM_002524.3:c.183A>T
• NM_002524.4:c.183A>T

This HGVS expression did not pass validation

Protein change:

Q61H

Links:

dbSNP: rs121913255

NCBI 1000 Genomes Browser:

rs121913255

Molecular consequence:

• NM_002524.5:c.183A>T - missense variant - [Sequence Ontology: SO:0001583]