ClinVar Miner

List of variants in gene KRAS reported as benign for not provided

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Gene type:
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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_004985.5(KRAS):c.451-5617= rs4362222 0.99825
NM_033360.4(KRAS):c.4+287A>G rs6487461 0.53272
NM_004985.5(KRAS):c.450+298_450+322del rs369535718 0.50586
NM_033360.4(KRAS):c.*298T>G rs712 0.45514
NM_004985.5(KRAS):c.519T>C (p.Asp173=) rs1137282 0.19563
NM_004985.5(KRAS):c.-12+162G>C rs61016093 0.17074
NM_033360.4(KRAS):c.450+92A>G rs76433096 0.14824
NM_004985.5(KRAS):c.450+308_450+322del rs1565883959 0.11591
NM_004985.5(KRAS):c.451-9G>A rs12313763 0.08467
NM_004985.5(KRAS):c.291-162A>C rs61762369 0.06157
NM_004985.5(KRAS):c.450+306_450+322del rs1565883960 0.06064
NM_004985.5(KRAS):c.450+298T>A rs200853468 0.04590
NM_033360.4(KRAS):c.-11-273A>G rs12305108 0.02959
NM_004985.5(KRAS):c.450+304_450+322del rs1565883961 0.02424
NM_004985.5(KRAS):c.450+300_450+322del rs1565883967 0.02356
NM_033360.4(KRAS):c.290+74T>G rs115908336 0.01631
NM_033360.4(KRAS):c.*1758_*1759del rs535478558 0.00456
NM_033360.4(KRAS):c.5-18A>G rs200189105 0.00100
NM_033360.4(KRAS):c.*4619T>C rs768891600 0.00035
NM_004985.5(KRAS):c.264A>G (p.Lys88=) rs370920665 0.00021
NM_004985.5(KRAS):c.451-5535A>C rs201170656 0.00019
NM_004985.5(KRAS):c.198A>G (p.Ala66=) rs200229810 0.00016
NM_033360.4(KRAS):c.*3672C>G rs188922523 0.00016
NM_033360.4(KRAS):c.*4036A>G rs886049179 0.00011
NM_033360.4(KRAS):c.4+5G>A rs201789109 0.00006
NM_033360.4(KRAS):c.249C>T (p.Ala83=) rs751117590 0.00002
NM_004985.5(KRAS):c.*1634A>G
NM_004985.5(KRAS):c.111+190A>T rs12228277
NM_004985.5(KRAS):c.528GAA[1] (p.Lys180del) rs397517043
NM_033360.4(KRAS):c.*4187del rs34719539
NM_033360.4(KRAS):c.290+97A>C rs11836509
NM_033360.4(KRAS):c.290+97A>T rs11836509
NM_033360.4(KRAS):c.450+40A>G rs2141505353

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