All variants in the HRAS gene

Information The variants shown are described using the NM_005343.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
+/. - c.38G>T r.(?) p.(Gly13Val) - pathogenic g.534285C>A g.534285C>A 38G>A (Gly13Val) - HRAS_000020 - PubMed: Lefebvre 2021 - - Germline/De novo (untested) - - - 0 - Johan den Dunnen
+?/. - c.38G>T r.(?) p.(Gly13Val) - likely pathogenic g.534285C>A - HRAS(NM_005343.2):c.38G>T (p.(Gly13Val)) - HRAS_000020 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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