ClinVar Miner

List of variants in gene KRAS studied for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 109
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HGVS dbSNP
NM_004985.5(KRAS):c.*1062G>A rs61763591
NM_004985.5(KRAS):c.*1083A>G rs7960917
NM_004985.5(KRAS):c.*1205C>T rs574966178
NM_004985.5(KRAS):c.*1418_*1420del rs200038818
NM_004985.5(KRAS):c.*1501G>A rs886049194
NM_004985.5(KRAS):c.*1540T>C rs61764366
NM_004985.5(KRAS):c.*1587T>C rs7973450
NM_004985.5(KRAS):c.*1627dup rs71065923
NM_004985.5(KRAS):c.*1631A>G rs763217196
NM_004985.5(KRAS):c.*1637_*1638del rs535478558
NM_004985.5(KRAS):c.*1638A>G rs4597149
NM_004985.5(KRAS):c.*1655C>T rs7973623
NM_004985.5(KRAS):c.*1656A>G rs886049193
NM_004985.5(KRAS):c.*1705C>G rs539213224
NM_004985.5(KRAS):c.*1710G>A rs531344668
NM_004985.5(KRAS):c.*1765T>C rs115968671
NM_004985.5(KRAS):c.*176C>T rs886049197
NM_004985.5(KRAS):c.*1772A>G rs886049192
NM_004985.5(KRAS):c.*177T>G rs712
NM_004985.5(KRAS):c.*1846del rs886049191
NM_004985.5(KRAS):c.*1891T>C rs886049190
NM_004985.5(KRAS):c.*193C>T rs150334904
NM_004985.5(KRAS):c.*2184A>G rs61764368
NM_004985.5(KRAS):c.*2239A>G rs886049189
NM_004985.5(KRAS):c.*2270_*2271insC rs886049188
NM_004985.5(KRAS):c.*2279dup rs56128001
NM_004985.5(KRAS):c.*2325G>A rs886049187
NM_004985.5(KRAS):c.*2371C>T rs61764369
NM_004985.5(KRAS):c.*2456G>A rs886049186
NM_004985.5(KRAS):c.*2484G>A rs779071703
NM_004985.5(KRAS):c.*2505T>G rs61764370
NM_004985.5(KRAS):c.*2694C>T rs886049185
NM_004985.5(KRAS):c.*2888A>G rs13096
NM_004985.5(KRAS):c.*2971_*2974del rs886049184
NM_004985.5(KRAS):c.*3148C>T rs886049183
NM_004985.5(KRAS):c.*3152G>A rs61764371
NM_004985.5(KRAS):c.*3202T>C rs886049182
NM_004985.5(KRAS):c.*3264del rs34176876
NM_004985.5(KRAS):c.*3377C>T rs1137188
NM_004985.5(KRAS):c.*3401T>A rs1137189
NM_004985.5(KRAS):c.*3454T>C rs749403585
NM_004985.5(KRAS):c.*3499C>T rs886049181
NM_004985.5(KRAS):c.*3502T>A rs61764372
NM_004985.5(KRAS):c.*3551C>G rs188922523
NM_004985.5(KRAS):c.*3645A>G rs529959450
NM_004985.5(KRAS):c.*3682_*3683dup rs142323886
NM_004985.5(KRAS):c.*3683dup rs142323886
NM_004985.5(KRAS):c.*370C>G rs886049196
NM_004985.5(KRAS):c.*3754_*3757del rs886049180
NM_004985.5(KRAS):c.*3760A>C rs1137196
NM_004985.5(KRAS):c.*3786A>G rs8720
NM_004985.5(KRAS):c.*3901A>C rs12587
NM_004985.5(KRAS):c.*3915A>G rs886049179
NM_004985.5(KRAS):c.*404T>C rs140080026
NM_004985.5(KRAS):c.*4065_*4066del rs34719539
NM_004985.5(KRAS):c.*4066del rs34719539
NM_004985.5(KRAS):c.*4074G>A rs886049177
NM_004985.5(KRAS):c.*4079T>A rs12245
NM_004985.5(KRAS):c.*4305_*4306dup rs61764373
NM_004985.5(KRAS):c.*4311A>G rs61764374
NM_004985.5(KRAS):c.*4428G>C rs545014897
NM_004985.5(KRAS):c.*4483G>A rs577486152
NM_004985.5(KRAS):c.*4498T>C rs768891600
NM_004985.5(KRAS):c.*4522G>A rs886049176
NM_004985.5(KRAS):c.*512T>C rs9266
NM_004985.5(KRAS):c.*538del rs756307694
NM_004985.5(KRAS):c.*550C>T rs566222739
NM_004985.5(KRAS):c.*59A>G rs886049198
NM_004985.5(KRAS):c.*765A>G rs886049195
NM_004985.5(KRAS):c.*824T>C rs61763589
NM_004985.5(KRAS):c.*865T>C rs559143985
NM_004985.5(KRAS):c.*973G>T rs61763590
NM_004985.5(KRAS):c.-128C>G rs886049199
NM_004985.5(KRAS):c.-160A>G rs727503111
NM_004985.5(KRAS):c.-176_-174CGG[4] rs886049200
NM_004985.5(KRAS):c.-180G>A rs886049201
NM_004985.5(KRAS):c.101C>G (p.Pro34Arg) rs104894366
NM_004985.5(KRAS):c.101C>T (p.Pro34Leu) rs104894366
NM_004985.5(KRAS):c.108A>G (p.Ile36Met) rs727503109
NM_004985.5(KRAS):c.112-5C>T rs376520586
NM_004985.5(KRAS):c.13A>G (p.Lys5Glu) rs193929331
NM_004985.5(KRAS):c.15A>T (p.Lys5Asn) rs104894361
NM_004985.5(KRAS):c.173C>T (p.Thr58Ile) rs104894364
NM_004985.5(KRAS):c.178G>A (p.Gly60Ser) rs104894359
NM_004985.5(KRAS):c.178G>C (p.Gly60Arg) rs104894359
NM_004985.5(KRAS):c.179G>T (p.Gly60Val) rs727503108
NM_004985.5(KRAS):c.182A>G (p.Gln61Arg) rs121913240
NM_004985.5(KRAS):c.183A>T (p.Gln61His) rs17851045
NM_004985.5(KRAS):c.194G>T (p.Ser65Ile) rs1555194026
NM_004985.5(KRAS):c.198A>G (p.Ala66=) rs200229810
NM_004985.5(KRAS):c.214A>T (p.Met72Leu) rs727504662
NM_004985.5(KRAS):c.264A>G (p.Lys88=) rs370920665
NM_004985.5(KRAS):c.347A>G (p.Asn116Ser) rs202247812
NM_004985.5(KRAS):c.351A>C (p.Lys117Asn) rs770248150
NM_004985.5(KRAS):c.389C>T (p.Ala130Val) rs730880473
NM_004985.5(KRAS):c.40G>A (p.Val14Ile) rs104894365
NM_004985.5(KRAS):c.440A>G (p.Lys147Arg) rs1135401776
NM_004985.5(KRAS):c.451-9G>A rs12313763
NM_004985.5(KRAS):c.454G>T (p.Val152Phe) rs397517041
NM_004985.5(KRAS):c.455T>G (p.Val152Gly) rs104894367
NM_004985.5(KRAS):c.458A>G (p.Asp153Gly) rs104894360
NM_004985.5(KRAS):c.458A>T (p.Asp153Val) rs104894360
NM_004985.5(KRAS):c.462T>C (p.Asp154=) rs779184057
NM_004985.5(KRAS):c.466T>A (p.Phe156Ile) rs397517042
NM_004985.5(KRAS):c.466T>G (p.Phe156Val) rs397517042
NM_004985.5(KRAS):c.490C>T (p.Arg164Ter) rs1555192443
NM_004985.5(KRAS):c.519T>C (p.Asp173=) rs1137282
NM_004985.5(KRAS):c.65A>G (p.Gln22Arg) rs727503110
NM_033360.4(KRAS):c.458A>T (p.Glu153Val)

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