List of variants in gene combination FLT4, LOC126807632 reported as uncertain significance for Carcinoma of colon

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
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

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