ClinVar Miner

List of variants in gene FLT4 studied for colonic neoplasm

Included ClinVar conditions (19):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
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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