All variants in the HRAS gene

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

4 entries on 1 page. Showing entries 1 - 4.
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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.37G>T r.(?) p.(Gly13Cys) - pathogenic g.534286C>A g.534286C>A HRAS(NM_001130442.1):c.37G>T (p.(Gly13Cys)) - HRAS_000011 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Nijmegen
+/. - c.37G>T r.(?) p.(Gly13Cys) - pathogenic g.534286C>A g.534286C>A HRAS(NM_001130442.1):c.37G>T (p.(Gly13Cys)) - HRAS_000011 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
+/. - c.37G>T r.(?) p.(Gly13Cys) - pathogenic g.534286C>A - - - HRAS_000011 - - - - De novo - - - - - Sha Hong
+/. - c.37G>T r.(?) p.(Gly13Cys) - pathogenic g.534286C>A - - - HRAS_000011 - - - - De novo - - - 0 - Simin Zheng
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