View unique 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     

Reported     

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     
./. 1 c.34G>A p.(Gly12Ser) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.993) r.(?) deleterious(0.02) 11 Unknown subst g.534289C>T - 3.000 - HRAS_000006 MSCV_0000278 rs104894229 - ; 11150980;17412879;20660566;16443854;19382114;22926243;16329078;17054105;18039947;19371735;{PMID - - -
./. 1 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 MSCV_0000277 rs104894229 - ; 11150980;17412879;20660566;16443854;19382114;22926243;16329078;17054105;18039947;19371735;{PMID - - -
?/? 1 c.34G>T p.(Gly12Cys) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.999) r.(?) deleterious(0.04) 11 Unknown subst g.534289C>A - 3.000 - HRAS_000004 MSCV_0000275 rs104894229 - ; 11150980;17412879;20660566;16443854;19382114;22926243;16329078;17054105;18039947;19371735;{PMID - - -
./. 1 c.35G>A p.(Gly12Asp) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.995) r.(?) deleterious(0) 11 Unknown subst g.534288C>T - 3.000 - HRAS_000003 MSCV_0000274 rs104894230 - ; 16170316;22499344;16443854;20658932;17412879;18039947;6092966;6330729;17979197;21344638;{PMID:171 - - -
./. 1 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 - - -
./., ?/? 2 c.35G>T p.(Gly12Val) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.998) r.(?) -, deleterious(0) 11 Unknown subst g.534288C>A - 3.000 - HRAS_000001 MSCV_0000271 rs104894230 - clinvar; 16170316;22499344;16443854;20658932;17412879;18039947;6092966;6330729;17979197;21344638;{PMID:171 - - -
./. 1 c.37G>A p.(Gly13Ser) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.993) r.(?) deleterious(0.02) 11 Unknown subst g.534286C>T - 3.000 - HRAS_000009 MSCV_0000269 NA - ; - - - -
?/? 1 c.37G>C p.(Gly13Arg) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.999) r.(?) deleterious(0) 11 Unknown subst g.534286C>G - 3.000 - HRAS_000008 MSCV_0000268 - - ; - - - -
./. 1 c.37G>T p.(Gly13Cys) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.999) r.(?) deleterious(0.05) 11 Unknown subst g.534286C>A - 3.000 - HRAS_000007 MSCV_0000267 NA - ; - - - -
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