Transcript #00000009 (NM_004985.4, KRAS gene)

Transcript name Kirsten rat sarcoma viral oncogene homolog, transcript variant b
Gene name KRAS (KRAS proto-oncogene, GTPase)
Chromosome 12
Transcript - NCBI ID NM_004985.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_004976.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

34 entries on 1 page. Showing entries 1 - 34.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
+/. 1 c.34G>A - r.(?) p.(Gly12Ser) - ClinVar
+/. - c.34G>C G12R r.(?) p.(Gly12Arg) - ClinVar
+/. - c.34G>C G12R r.(?) p.(Gly12Arg) - pathogenic
+/. - c.35G>A G12D r.(?) p.(Gly12Asp) - ClinVar
+/. - c.35G>A G12D r.(?) p.(Gly12Asp) - ClinVar
+/. 1 c.35G>A Codon 12 : GGT to GAT r.(?) p.(Gly12Asp) - ClinVar
+/. 1 c.35G>A Codon 12 : GGT to GAT r.(?) p.(Gly12Asp) - ClinVar
+/. 1 c.35G>A Codon 12 : GGT to GAT r.(?) p.(Gly12Asp) - ClinVar
+/. 1 c.35G>A Codon 12 : GGT to GAT r.(?) p.(Gly12Asp) - ClinVar
+/. - c.35G>A G12D r.(?) p.(Gly12Asp) - pathogenic
+/. 1 c.35G>A - r.(?) p.(Gly12Asp) - ClinVar
+/. - c.35G>A G12D r.(?) p.(Gly12Asp) missense Pathogenic
+/. - c.35G>A G12D r.(?) p.(Gly12Asp) missense Pathogenic
+/. - c.35G>C G12A r.(?) p.(Gly12Ala) - Pathogenic/Likely pathogenic
+/. - c.35G>C G12A r.(?) p.(Gly12Ala) - ClinVar
./. - c.35G>C G12A r.(?) p.(Gly12Ala) - ClinVar
+/. - c.35G>T G12V r.(?) p.(Gly12Val) - Pathogenic
+/. - c.35G>T G12V r.(?) p.(Gly12Val) - ClinVar
+/. - c.35G>T G12V r.(?) p.(Gly12Val) - ClinVar
+/. 1 c.35G>T Codon 12 : GGT to GTT r.(?) p.(Gly12Val) - ClinVar
+/. 1 c.35G>T Codon 12 : GGT to GTT r.(?) p.(Gly12Val) - ClinVar
+/. 1 c.35G>T - r.(?) p.(Gly12Val) - ClinVar
+/. - c.38G>A G13D r.(?) p.(Gly13Asp) - Pathogenic
+/. - c.38G>A G13D r.(?) p.(Gly13Asp) - ClinVar
+/. - c.38G>A G13D r.(?) p.(Gly13Asp) - ClinVar
+/. - c.38G>A G13D r.(?) p.(Gly13Asp) - ClinVar
+/. 1 c.38G>A Codon 13 : GGC to GAC r.(?) p.(Gly13Asp) - ClinVar
+/. 1 c.38G>A Codon 13 : GGC to GAC r.(?) p.(Gly13Asp) - ClinVar
+/. 1 c.38G>A - r.(?) p.(Gly13Asp) - ClinVar
+/. 1 c.38G>C - r.(?) p.(Gly13Ala) - ClinVar
+/. - c.40G>A V14I r.(?) p.(Val14Ile) - ClinVar
+/. - c.175G>A A59T r.(?) p.(Ala59Thr) missense Pathogenic / Likely pathogenic​
+/. - c.183A>C Q61H r.(?) p.(Gln61His) - Pathogenic/Likely pathogenic
./. - c.183A>C Q61H r.(?) p.(Gln61His) - ClinVar
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