View all transcript variants in gene NRAS

Information The variants shown are described using the NM_002524.4 transcript reference sequence.

8 entries on 1 page. Showing entries 1 - 8.
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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>A p.(Gly12Asp) missense_variant - 2/7 possibly_damaging(0.726) r.(?) deleterious(0) 1 Unknown subst g.115258747C>T - 5.580 - NRAS_000003 MSCV_0000069 - - ; - - - -
./. c.35G>C p.(Gly12Ala) missense_variant - 2/7 benign(0.267) r.(?) deleterious(0.02) 1 Unknown subst g.115258747C>G - 5.580 - NRAS_000002 MSCV_0000068 NA - ; - - - -
./. c.35G>T p.(Gly12Val) missense_variant - 2/7 possibly_damaging(0.902) r.(?) deleterious(0) 1 Unknown subst g.115258747C>A - 5.580 - NRAS_000001 MSCV_0000067 NA - ; - - - -
?/? c.101C>T p.(Pro34Leu) missense_variant - 2/7 probably_damaging(0.999) r.(?) deleterious(0.02) 1 Unknown subst g.115258681G>A - 5.450 - NRAS_000007 MSCV_0000066 - - ; - - - -
./. c.101C>T p.(Pro34Leu) - - - - r.(?) - 1 Unknown - g.115258681G>A - - - NRAS_000007 MSCV_0000066 - - ; clinvar; - - - -
./. c.182A>C p.(Gln61Pro) missense_variant - 3/7 possibly_damaging(0.713) r.(?) deleterious(0) 1 Unknown subst g.115256529T>G - 5.080 - NRAS_000006 MSCV_0000065 NA - ; - - - -
?/? c.182A>G p.(Gln61Arg) missense_variant - 3/7 benign(0.006) r.(?) deleterious(0.03) 1 Unknown subst g.115256529T>C - 5.080 - NRAS_000005 MSCV_0000064 - - ; - - - -
./. c.182A>T p.(Gln61Leu) missense_variant - 3/7 benign(0.109) r.(?) deleterious(0) 1 Unknown subst g.115256529T>A - 5.080 - NRAS_000004 MSCV_0000063 NA - ; - - - -
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