ClinVar Miner

List of variants in gene KRAS reported as uncertain significance for Noonan syndrome

Included ClinVar conditions (44):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_033360.4(KRAS):c.*986T>C rs559143985 0.00120
NM_033360.4(KRAS):c.*3766A>G rs529959450 0.00108
NM_033360.4(KRAS):c.*1826C>G rs539213224 0.00073
NM_033360.4(KRAS):c.*4619T>C rs768891600 0.00035
NM_033360.4(KRAS):c.*886A>G rs886049195 0.00033
NM_033360.4(KRAS):c.*314C>T rs150334904 0.00029
NM_033360.4(KRAS):c.*1831G>A rs531344668 0.00026
NM_004985.5(KRAS):c.264A>G (p.Lys88=) rs370920665 0.00021
NM_033360.4(KRAS):c.*4549G>C rs545014897 0.00020
NM_004985.5(KRAS):c.198A>G (p.Ala66=) rs200229810 0.00016
NM_033360.4(KRAS):c.*3575T>C rs749403585 0.00016
NM_033360.4(KRAS):c.*3672C>G rs188922523 0.00016
NM_033360.4(KRAS):c.*1752A>G rs763217196 0.00012
NM_033360.4(KRAS):c.*4036A>G rs886049179 0.00011
NM_033360.4(KRAS):c.*2012T>C rs886049190 0.00010
NM_033360.4(KRAS):c.*2577G>A rs886049186 0.00008
NM_033360.4(KRAS):c.*1622G>A rs886049194 0.00006
NM_033360.4(KRAS):c.*2605G>A rs779071703 0.00006
NM_033360.4(KRAS):c.*2815C>T rs886049185 0.00006
NM_033360.4(KRAS):c.*297C>T rs886049197 0.00006
NM_033360.4(KRAS):c.*2391_*2392insC rs886049188 0.00005
NM_033360.4(KRAS):c.*2446G>A rs886049187 0.00004
NM_033360.4(KRAS):c.*3620C>T rs886049181 0.00004
NM_033360.4(KRAS):c.*16T>C rs779184057 0.00002
NM_033360.4(KRAS):c.389C>T (p.Ala130Val) rs730880473 0.00002
NM_004985.5(KRAS):c.111+8T>G rs779370636 0.00001
NM_033360.4(KRAS):c.*1326C>T rs574966178 0.00001
NM_033360.4(KRAS):c.*1777A>G rs886049193 0.00001
NM_033360.4(KRAS):c.*2360A>G rs886049189 0.00001
NM_033360.4(KRAS):c.*4195G>A rs886049177 0.00001
NM_033360.4(KRAS):c.*4643G>A rs886049176 0.00001
NM_033360.4(KRAS):c.112-5C>T rs376520586 0.00001
NM_004985.5(KRAS):c.164T>G (p.Ile55Ser) rs1951406889
NM_004985.5(KRAS):c.388_389delinsAT (p.Ala130Ile) rs1951383854
NM_004985.5(KRAS):c.76A>C (p.Asn26His) rs794727277
NM_033360.4(KRAS):c.*101_*106del rs1339924833
NM_033360.4(KRAS):c.*180A>G rs886049198
NM_033360.4(KRAS):c.*1893A>G rs886049192
NM_033360.4(KRAS):c.*1967del rs886049191
NM_033360.4(KRAS):c.*3092_*3095del rs886049184
NM_033360.4(KRAS):c.*3269C>T rs886049183
NM_033360.4(KRAS):c.*3323T>C rs886049182
NM_033360.4(KRAS):c.*3803_*3804dup rs142323886
NM_033360.4(KRAS):c.*3875_*3878del rs886049180
NM_033360.4(KRAS):c.*4187del rs34719539
NM_033360.4(KRAS):c.*4604G>A rs577486152
NM_033360.4(KRAS):c.*491C>G rs886049196
NM_033360.4(KRAS):c.*659del rs756307694
NM_033360.4(KRAS):c.*671C>T rs566222739

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