ClinVar Miner

List of variants in gene KRAS reported as uncertain significance for prostate cancer

Included ClinVar conditions (36):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP gnomAD frequency
NM_033360.4(KRAS):c.90C>T (p.Asp30=) rs113623140 0.00011
NM_004985.5(KRAS):c.-10C>G
NM_004985.5(KRAS):c.-11-10T>G
NM_004985.5(KRAS):c.-11-12T>A
NM_004985.5(KRAS):c.-11-12T>G
NM_004985.5(KRAS):c.-11-1G>C
NM_004985.5(KRAS):c.-11-21T>G
NM_004985.5(KRAS):c.-11-2A>C
NM_004985.5(KRAS):c.-11-2A>T
NM_004985.5(KRAS):c.-11-36C>T
NM_004985.5(KRAS):c.-11-4T>A
NM_004985.5(KRAS):c.-11-51del
NM_004985.5(KRAS):c.-11-7T>A
NM_004985.5(KRAS):c.-11-8A>C
NM_004985.5(KRAS):c.-11-8_-11-7insC
NM_004985.5(KRAS):c.-11G>A
NM_004985.5(KRAS):c.-6C>T
NM_004985.5(KRAS):c.107T>A (p.Ile36Lys)
NM_004985.5(KRAS):c.108delinsCC (p.Glu37fs)
NM_004985.5(KRAS):c.109G>T (p.Glu37Ter)
NM_004985.5(KRAS):c.109_110insC (p.Glu37fs)
NM_004985.5(KRAS):c.10T>A (p.Tyr4Asn)
NM_004985.5(KRAS):c.111+11T>C
NM_004985.5(KRAS):c.111+14del
NM_004985.5(KRAS):c.111+16A>G
NM_004985.5(KRAS):c.111+1G>C
NM_004985.5(KRAS):c.111+24A>G
NM_004985.5(KRAS):c.111+25T>C
NM_004985.5(KRAS):c.111+28C>T
NM_004985.5(KRAS):c.111+30G>T
NM_004985.5(KRAS):c.111+50T>A
NM_004985.5(KRAS):c.111+53A>G
NM_004985.5(KRAS):c.111+6T>C
NM_004985.5(KRAS):c.111+8T>C
NM_004985.5(KRAS):c.11A>T (p.Tyr4Phe)
NM_004985.5(KRAS):c.12T>A (p.Tyr4Ter)
NM_004985.5(KRAS):c.13A>G (p.Lys5Glu) rs193929331
NM_004985.5(KRAS):c.13A>T (p.Lys5Ter)
NM_004985.5(KRAS):c.16C>T (p.Leu6Phe)
NM_004985.5(KRAS):c.1del (p.Met1*)
NM_004985.5(KRAS):c.21_22insT (p.Val8fs)
NM_004985.5(KRAS):c.24dup (p.Val9fs)
NM_004985.5(KRAS):c.27T>A (p.Val9=)
NM_004985.5(KRAS):c.27T>G (p.Val9=)
NM_004985.5(KRAS):c.27_28insCTC (p.Val9_Gly10insLeu)
NM_004985.5(KRAS):c.29_30insT (p.Ala11fs)
NM_004985.5(KRAS):c.29_31del (p.Gly10del)
NM_004985.5(KRAS):c.30A>G (p.Gly10=) rs2135806293
NM_004985.5(KRAS):c.31G>T (p.Ala11Ser)
NM_004985.5(KRAS):c.33T>A (p.Ala11=)
NM_004985.5(KRAS):c.39C>T (p.Gly13=) rs397517040
NM_004985.5(KRAS):c.42A>T (p.Val14=)
NM_004985.5(KRAS):c.43G>T (p.Gly15Cys)
NM_004985.5(KRAS):c.4del (p.Thr2fs)
NM_004985.5(KRAS):c.50G>T (p.Ser17Ile)
NM_004985.5(KRAS):c.5C>G (p.Thr2Ser)
NM_004985.5(KRAS):c.62T>A (p.Ile21Lys)
NM_004985.5(KRAS):c.65A>C (p.Gln22Pro)
NM_004985.5(KRAS):c.6T>G (p.Thr2=)
NM_004985.5(KRAS):c.74A>T (p.Gln25Leu)
NM_004985.5(KRAS):c.75G>A (p.Gln25=)
NM_004985.5(KRAS):c.77A>C (p.Asn26Thr)
NM_004985.5(KRAS):c.80A>G (p.His27Arg)
NM_004985.5(KRAS):c.80A>T (p.His27Leu)
NM_004985.5(KRAS):c.84T>A (p.Phe28Leu)
NM_004985.5(KRAS):c.84del (p.Phe28fs)
NM_004985.5(KRAS):c.90C>A (p.Asp30Glu)
NM_004985.5(KRAS):c.91G>T (p.Glu31Ter)
NM_004985.5(KRAS):c.95A>C (p.Tyr32Ser)
NM_004985.5(KRAS):c.99T>C (p.Asp33=)
NM_004985.5(KRAS):c.9dup (p.Tyr4fs)
NM_033360.4(KRAS):c.-11delG

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