View all transcript variants in gene HRAS

Information The variants shown are described using the NM_176795.3 transcript reference sequence.

1 entry on 1 page. Showing entry 1.
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Effect     

AscendingDNA change (cDNA)     

Protein     

GVS function     

Position     

Exon     

PolyPhen     

RNA change     

SIFT     

Chr     

Allele     

Type     

DNA change (genomic) (hg19)     

Published as     

GERP     

Segregation     

DB-ID     

MSCV     

dbSNP ID     

Frequency     

Sources     

Reference     

Variant remarks     

Genetic origin     

Owner     
./. c.35G>C p.(Gly12Ala) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.979) r.(?) deleterious(0.03) 11 Unknown subst g.534288C>G - 3.000 - HRAS_000002 MSCV_0000273 rs104894230 - ; 16170316;22499344;16443854;20658932;17412879;18039947;6092966;6330729;17979197;21344638;{PMID:171 - - -
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