All variants in the HRAS gene

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

3 entries on 1 page. Showing entries 1 - 3.
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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.357C>T r.(?) p.(Asp119=) - likely benign g.533546G>A g.533546G>A HRAS(NM_001318054.1):c.38C>T (p.T13I), HRAS(NM_176795.4):c.357C>T (p.D119=) - HRAS_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Nijmegen
-?/. - c.357C>T r.(?) p.(Asp119=) - likely benign g.533546G>A g.533546G>A HRAS(NM_001318054.1):c.38C>T (p.T13I), HRAS(NM_176795.4):c.357C>T (p.D119=) - HRAS_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-/. - c.357C>T r.(?) p.(Asp119=) - benign g.533546G>A g.533546G>A HRAS(NM_001318054.1):c.38C>T (p.T13I), HRAS(NM_176795.4):c.357C>T (p.D119=) - HRAS_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_AMC
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