Full data view for gene HRAS

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

10 entries on 1 page. Showing entries 1 - 10.
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Effect     

AscendingDNA change (cDNA)     

Protein     

GVS function     

Position     

Exon     

PolyPhen     

RNA change     

SIFT     

Allele     

Type     

DNA change (genomic) (hg19)     

Published as     

GERP     

Segregation     

DB-ID     

MSCV     

dbSNP ID     

Frequency     

Sources     

Reference     

Variant remarks     

Genetic origin     

Date     

Template     

Technique     

Tissue     

Description     

Disease     

Reference     

Gender     

Geographic origin     

Ethnic origin     

Population     

Consanguinity     

Age of death     

Cause of death     

Remarks     

Panel size     

Owner     
./. c.34G>A p.(Gly12Ser) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.993) r.(?) deleterious(0.02) Unknown subst g.534289C>T - 3.000 - HRAS_000006 MSCV_0000278 rs104894229 - ; 11150980;17412879;20660566;16443854;19382114;22926243;16329078;17054105;18039947;19371735;{PMID - - - - - - - - - - - - - - - - - - -
./. c.34G>C p.(Gly12Arg) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.999) r.(?) deleterious(0.01) Unknown subst g.534289C>G - 3.000 - HRAS_000005 MSCV_0000277 rs104894229 - ; 11150980;17412879;20660566;16443854;19382114;22926243;16329078;17054105;18039947;19371735;{PMID - - - - - - - - - - - - - - - - - - -
?/? c.34G>T p.(Gly12Cys) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.999) r.(?) deleterious(0.04) Unknown subst g.534289C>A - 3.000 - HRAS_000004 MSCV_0000275 rs104894229 - ; 11150980;17412879;20660566;16443854;19382114;22926243;16329078;17054105;18039947;19371735;{PMID - - - - - - - - - - - - - - - - - - -
./. c.35G>A p.(Gly12Asp) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.995) r.(?) deleterious(0) Unknown subst g.534288C>T - 3.000 - HRAS_000003 MSCV_0000274 rs104894230 - ; 16170316;22499344;16443854;20658932;17412879;18039947;6092966;6330729;17979197;21344638;{PMID:171 - - - - - - - - - - - - - - - - - - -
./. c.35G>C p.(Gly12Ala) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.979) r.(?) deleterious(0.03) Unknown subst g.534288C>G - 3.000 - HRAS_000002 MSCV_0000273 rs104894230 - ; 16170316;22499344;16443854;20658932;17412879;18039947;6092966;6330729;17979197;21344638;{PMID:171 - - - - - - - - - - - - - - - - - - -
?/? c.35G>T p.(Gly12Val) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.998) r.(?) deleterious(0) Unknown subst g.534288C>A - 3.000 - HRAS_000001 MSCV_0000271 rs104894230 - ; 16170316;22499344;16443854;20658932;17412879;18039947;6092966;6330729;17979197;21344638;{PMID:171 - - - - - - - - - - - - - - - - - - -
./. c.35G>T p.(Gly12Val) - - - - r.(?) - Unknown - g.534288C>A - - - HRAS_000001 MSCV_0000271 - - ; clinvar; - - - - - - - - - - - - - - - - - - - -
./. c.37G>A p.(Gly13Ser) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.993) r.(?) deleterious(0.02) Unknown subst g.534286C>T - 3.000 - HRAS_000009 MSCV_0000269 NA - ; - - - - - - - - - - - - - - - - - - - -
?/? c.37G>C p.(Gly13Arg) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.999) r.(?) deleterious(0) Unknown subst g.534286C>G - 3.000 - HRAS_000008 MSCV_0000268 - - ; - - - - - - - - - - - - - - - - - - - -
./. c.37G>T p.(Gly13Cys) missense_variant,NMD_transcript_variant - 2/7 probably_damaging(0.999) r.(?) deleterious(0.05) Unknown subst g.534286C>A - 3.000 - HRAS_000007 MSCV_0000267 NA - ; - - - - - - - - - - - - - - - - - - - -
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