"Ambry Genetics"[submitter] AND "RANBP10"[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2469744	NM_020850.3(RANBP10):c.1736C>T (p.Ser579Phe)	RANBP10 (S350F +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539483	NM_020850.3(RANBP10):c.1646C>T (p.Ser549Leu)	RANBP10 (S320L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589270	NM_020850.3(RANBP10):c.1585T>C (p.Tyr529His)	RANBP10 (Y442H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537654	NM_020850.3(RANBP10):c.1579C>T (p.Arg527Trp)	RANBP10 (R501W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151366	NM_020850.3(RANBP10):c.1504G>A (p.Gly502Arg)	RANBP10 (G532R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151364	NM_020850.3(RANBP10):c.1493G>A (p.Arg498Gln)	RANBP10 (R498Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151363	NM_020850.3(RANBP10):c.1353C>T (p.Ser451=)	RANBP10	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2363856	NM_020850.3(RANBP10):c.1304A>T (p.Asp435Val)	RANBP10 (D379V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251898	NM_020850.3(RANBP10):c.1267C>A (p.Pro423Thr)	RANBP10 (P367T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546882	NM_020850.3(RANBP10):c.1108C>T (p.Pro370Ser)	RANBP10 (P314S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619205	NM_020850.3(RANBP10):c.1072T>C (p.Ser358Pro)	RANBP10 (S129P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400402	NM_020850.3(RANBP10):c.1061G>A (p.Arg354Gln)	RANBP10 (R237Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151362	NM_020850.3(RANBP10):c.1058C>T (p.Ser353Phe)	RANBP10 (S124F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401422	NM_020850.3(RANBP10):c.1049G>A (p.Ser350Asn)	RANBP10 (S121N +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3151361	NM_020850.3(RANBP10):c.1046G>A (p.Arg349Gln)	RANBP10 (R349Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466249	NM_020850.3(RANBP10):c.1031C>T (p.Thr344Met)	RANBP10 (T227M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344488	NM_020850.3(RANBP10):c.947G>A (p.Arg316His)	RANBP10 (R199H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607252	NM_020850.3(RANBP10):c.916C>T (p.Arg306Cys)	RANBP10 (R306C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463870	NM_020850.3(RANBP10):c.868G>T (p.Ala290Ser)	RANBP10 (A173S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513529	NM_020850.3(RANBP10):c.848C>G (p.Thr283Ser)	RANBP10 (T283S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151368	NM_020850.3(RANBP10):c.796G>A (p.Val266Met)	RANBP10 (V266M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405382	NM_020850.3(RANBP10):c.745C>T (p.Arg249Trp)	RANBP10 (R132W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226962	NM_020850.3(RANBP10):c.713A>G (p.Gln238Arg)	RANBP10 (Q121R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151367	NM_020850.3(RANBP10):c.676A>G (p.Ile226Val)	RANBP10 (I109V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492257	NM_020850.3(RANBP10):c.659A>G (p.Gln220Arg)	RANBP10 (Q164R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490414	NM_020850.3(RANBP10):c.593C>T (p.Ala198Val)	RANBP10 (A142V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302171	NM_020850.3(RANBP10):c.547A>G (p.Thr183Ala)	RANBP10 (T183A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2533939	NM_020850.3(RANBP10):c.443A>T (p.His148Leu)	RANBP10 (H31L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2265447	NM_020850.3(RANBP10):c.383A>G (p.Asn128Ser)	RANBP10 (N128S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527907	NM_020850.3(RANBP10):c.226C>T (p.His76Tyr)	RANBP10 (H76Y)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2373832	NM_020850.3(RANBP10):c.83C>G (p.Pro28Arg)	RANBP10 (P28R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2272022	NM_020850.3(RANBP10):c.49G>A (p.Asp17Asn)	RANBP10 (D17N)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2408114	NM_020850.3(RANBP10):c.23C>T (p.Pro8Leu)	RANBP10 (P8L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3151365	NM_020850.3(RANBP10):c.14C>T (p.Thr5Met)	RANBP10 (T5M)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 34