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.81T>C r.(?) p.(His27=) - benign g.534242A>G g.534242A>G HRAS(NM_005343.2):c.81T>C (p.H27=), HRAS(NM_176795.4):c.81T>C (p.H27=) - HRAS_000017 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_AMC
-/. - c.81T>C r.(?) p.(His27=) - benign g.534242A>G g.534242A>G HRAS(NM_005343.2):c.81T>C (p.H27=), HRAS(NM_176795.4):c.81T>C (p.H27=) - HRAS_000017 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Rotterdam
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