ClinVar Miner

List of variants reported as uncertain significance for colonic neoplasm by Immunobiology Lab; University of Kashmir

Included ClinVar conditions (19):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 35
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HGVS dbSNP
NM_002019.4(FLT1):c.2439_2466del (p.Tyr815fs) rs796052115
NM_002253.3(KDR):c.2380G>A (p.Gly794Arg) rs795902896
NM_002253.3(KDR):c.2509+20T>A rs795902897
NM_002253.3(KDR):c.2510-27del rs795902898
NM_002253.3(KDR):c.2544G>T (p.Val848=) rs795902899
NM_002253.3(KDR):c.2598A>C (p.Ala866=) rs795939486
NM_002253.3(KDR):c.2615-23C>T rs778886056
NM_002253.3(KDR):c.2656C>A (p.Leu886Ile) rs794729676
NM_002253.3(KDR):c.2676T>A (p.Ile892=) rs794729677
NM_002253.3(KDR):c.2705T>A (p.Leu902Gln) rs794729678
NM_002253.3(KDR):c.2721G>C (p.Lys907Asn) rs200773668
NM_002253.3(KDR):c.3405-4C>T rs370501217
NM_002253.3(KDR):c.3441C>G (p.Pro1147=) rs795939487
NM_002253.3(KDR):c.3465G>A (p.Glu1155=) rs795939488
NM_002253.3(KDR):c.3487C>T (p.Leu1163Phe) rs761176323
NM_182925.5(FLT4):c.2407-6C>G rs796052107
NM_182925.5(FLT4):c.2407-7C>T rs796052108
NM_182925.5(FLT4):c.2414A>C (p.His805Pro) rs796052106
NM_182925.5(FLT4):c.2433C>A (p.Gly811=) rs796052105
NM_182925.5(FLT4):c.2470C>A (p.Leu824Met) rs796052104
NM_182925.5(FLT4):c.2496C>G (p.Ser832=) rs796052103
NM_182925.5(FLT4):c.2498A>C (p.Tyr833Ser) rs796052102
NM_182925.5(FLT4):c.2502T>A (p.Asp834Glu) rs796052101
NM_182925.5(FLT4):c.2507G>A (p.Ser836Asn) rs796052100
NM_182925.5(FLT4):c.2519del (p.Phe840fs) rs796052099
NM_182925.5(FLT4):c.2542+12A>G rs751737827
NM_182925.5(FLT4):c.2542+18del rs796052098
NM_182925.5(FLT4):c.2542+20del rs796052097
NM_182925.5(FLT4):c.2647+31del rs796052109
NM_182925.5(FLT4):c.3002-9A>C rs796052114
NM_182925.5(FLT4):c.3056del (p.Phe1019fs) rs796052113
NM_182925.5(FLT4):c.3064del (p.Ala1022fs) rs796052112
NM_182925.5(FLT4):c.3065C>T (p.Ala1022Val) rs56364366
NM_182925.5(FLT4):c.3072del (p.Met1025fs) rs796052111
NM_182925.5(FLT4):c.3076del (p.Glu1026fs) rs796052110

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