View all transcript variants in gene HRAS

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

9 entries on 1 page. Showing entries 1 - 9.
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Effect     

AscendingDNA change (cDNA)     

Protein     

GVS function     

Position     

Exon     

PolyPhen     

RNA change     

SIFT     

Type     

DNA change (genomic) (hg19)     

Published as     

GERP     

Segregation     

DB-ID     

dbSNP ID     

Frequency     

Sources     

Reference     

Variant remarks     

Genetic origin     

Owner     
./. c.34G>A p.(Gly12Ser) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.993) r.(?) deleterious(0.02) subst g.534289C>T - 3.000 - HRAS_000006 rs104894229 - ; 11150980;17412879;20660566;16443854;19382114;22926243;16329078;17054105;18039947;19371735;{PMID - - LOVD
./. c.34G>C p.(Gly12Arg) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.999) r.(?) deleterious(0.01) subst g.534289C>G - 3.000 - HRAS_000005 rs104894229 - ; 11150980;17412879;20660566;16443854;19382114;22926243;16329078;17054105;18039947;19371735;{PMID - - LOVD
?/? c.34G>T p.(Gly12Cys) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.999) r.(?) deleterious(0.04) subst g.534289C>A - 3.000 - HRAS_000004 rs104894229 - ; 11150980;17412879;20660566;16443854;19382114;22926243;16329078;17054105;18039947;19371735;{PMID - - LOVD
./. c.35G>A p.(Gly12Asp) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.995) r.(?) deleterious(0) subst g.534288C>T - 3.000 - HRAS_000003 rs104894230 - ; 16170316;22499344;16443854;20658932;17412879;18039947;6092966;6330729;17979197;21344638;{PMID:171 - - LOVD
./. c.35G>C p.(Gly12Ala) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.979) r.(?) deleterious(0.03) subst g.534288C>G - 3.000 - HRAS_000002 rs104894230 - ; 16170316;22499344;16443854;20658932;17412879;18039947;6092966;6330729;17979197;21344638;{PMID:171 - - LOVD
?/? c.35G>T p.(Gly12Val) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.998) r.(?) deleterious(0) subst g.534288C>A - 3.000 - HRAS_000001 rs104894230 - ; 16170316;22499344;16443854;20658932;17412879;18039947;6092966;6330729;17979197;21344638;{PMID:171 - - LOVD
./. c.37G>A p.(Gly13Ser) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.993) r.(?) deleterious(0.02) subst g.534286C>T - 3.000 - HRAS_000009 NA - ; - - - LOVD
?/? c.37G>C p.(Gly13Arg) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.999) r.(?) deleterious(0) subst g.534286C>G - 3.000 - HRAS_000008 - - ; - - - LOVD
./. c.37G>T p.(Gly13Cys) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.999) r.(?) deleterious(0.05) subst g.534286C>A - 3.000 - HRAS_000007 NA - ; - - - LOVD
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