IGF2BP1[gene] and "single gene"[properties] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 789658	NM_006546.4(IGF2BP1):c.176-3T>C	IGF2BP1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2261333	NM_006546.4(IGF2BP1):c.232C>A (p.Gln78Lys)	IGF2BP1 (Q78K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 726908	NM_006546.4(IGF2BP1):c.318A>G (p.Thr106=)	IGF2BP1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 3285497	NM_006546.4(IGF2BP1):c.438C>A (p.Asn146Lys)	IGF2BP1 (N146K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622400	NM_006546.4(IGF2BP1):c.547G>C (p.Val183Leu)	IGF2BP1 (V183L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2300512	NM_006546.4(IGF2BP1):c.563C>T (p.Pro188Leu)	IGF2BP1 (P188L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528692	NM_006546.4(IGF2BP1):c.655C>T (p.Arg219Cys)	IGF2BP1 (R219C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3285496	NM_006546.4(IGF2BP1):c.667A>G (p.Lys223Glu)	IGF2BP1 (K223E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 781305	NM_006546.4(IGF2BP1):c.708C>T (p.Asn236=)	IGF2BP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2384315	NM_006546.4(IGF2BP1):c.748C>T (p.Pro250Ser)	IGF2BP1 (P250S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 720405	NM_006546.4(IGF2BP1):c.795T>A (p.His265Gln)	IGF2BP1 (H265Q)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2540569	NM_006546.4(IGF2BP1):c.820G>T (p.Ala274Ser)	IGF2BP1 (A135S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108538	NM_006546.4(IGF2BP1):c.826G>A (p.Glu276Lys)	IGF2BP1 (E276K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294892	NM_006546.4(IGF2BP1):c.875T>C (p.Ile292Thr)	IGF2BP1 (I292T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280360	NM_006546.4(IGF2BP1):c.997A>G (p.Ile333Val)	IGF2BP1 (I194V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332306	NM_006546.4(IGF2BP1):c.1018G>A (p.Glu340Lys)	IGF2BP1 (E340K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315710	NM_006546.4(IGF2BP1):c.1031T>C (p.Met344Thr)	IGF2BP1 (M205T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476972	NM_006546.4(IGF2BP1):c.1042C>T (p.Arg348Trp)	IGF2BP1 (R348W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339139	NM_006546.4(IGF2BP1):c.1069G>C (p.Ala357Pro)	IGF2BP1 (A357P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108534	NM_006546.4(IGF2BP1):c.1076G>A (p.Ser359Asn)	IGF2BP1 (S359N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285495	NM_006546.4(IGF2BP1):c.1144G>A (p.Ala382Thr)	IGF2BP1 (A243T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383074	NM_006546.4(IGF2BP1):c.1154C>A (p.Pro385Gln)	IGF2BP1 (P246Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272530	NM_006546.4(IGF2BP1):c.1163G>A (p.Ser388Asn)	IGF2BP1 (S249N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347486	NM_006546.4(IGF2BP1):c.1168G>A (p.Val390Ile)	IGF2BP1 (V251I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108535	NM_006546.4(IGF2BP1):c.1187A>G (p.Tyr396Cys)	IGF2BP1 (Y257C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537227	NM_006546.4(IGF2BP1):c.1210G>A (p.Glu404Lys)	IGF2BP1 (E265K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285498	NM_006546.4(IGF2BP1):c.1376C>T (p.Pro459Leu)	IGF2BP1 (P459L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321843	NM_006546.4(IGF2BP1):c.1478G>A (p.Arg493His)	IGF2BP1 (R354H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108537	NM_006546.4(IGF2BP1):c.1691A>G (p.His564Arg)	IGF2BP1 (H425R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473885	NM_006546.4(IGF2BP1):c.1723C>T (p.Arg575Trp)	IGF2BP1 (R575W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1264098	NM_006546.4(IGF2BP1):c.*6013T>C	IGF2BP1	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign

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Items: 31