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.
Legend  

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.34G>C p.(Gly12Arg) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.999) r.(?) deleterious(0.01) 11 Unknown subst g.534289C>G - 3.000 - HRAS_000005 - rs104894229 - ; 11150980;17412879;20660566;16443854;19382114;22926243;16329078;17054105;18039947;19371735;{PMID - - -
Legend