"Ambry Genetics"[submitter] AND "CRTC1"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2304325	NM_015321.3(CRTC1):c.243+1113C>T	CRTC1 (A92V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077660	NM_015321.3(CRTC1):c.321G>C (p.Glu107Asp)	CRTC1 (E107D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275973	NM_015321.3(CRTC1):c.385G>A (p.Asp129Asn)	CRTC1 (D129N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077661	NM_015321.3(CRTC1):c.425C>T (p.Ala142Val)	CRTC1 (A142V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077662	NM_015321.3(CRTC1):c.485C>T (p.Pro162Leu)	CRTC1 (P162L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217750	NM_015321.3(CRTC1):c.601A>G (p.Lys201Glu)	CRTC1 (K201E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380355	NM_015321.3(CRTC1):c.880G>A (p.Gly294Ser)	CRTC1 (G294S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374378	NM_015321.3(CRTC1):c.919C>T (p.Arg307Cys)	CRTC1 (R307C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077663	NM_015321.3(CRTC1):c.949A>G (p.Ser317Gly)	CRTC1 (S333G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544534	NM_015321.3(CRTC1):c.977C>T (p.Ser326Leu)	CRTC1 (S326L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605951	NM_015321.3(CRTC1):c.1126G>A (p.Ala376Thr)	CRTC1 (A376T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077655	NM_015321.3(CRTC1):c.1172G>A (p.Arg391His)	CRTC1 (R391H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405403	NM_015321.3(CRTC1):c.1177C>T (p.Pro393Ser)	CRTC1 (P393S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252525	NM_015321.3(CRTC1):c.1181C>T (p.Pro394Leu)	CRTC1 (P394L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613902	NM_015321.3(CRTC1):c.1271C>A (p.Ser424Tyr)	CRTC1 (S424Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589933	NM_015321.3(CRTC1):c.1277C>A (p.Pro426Gln)	CRTC1 (P426Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077656	NM_015321.3(CRTC1):c.1490A>G (p.Gln497Arg)	CRTC1 (Q497R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487948	NM_015321.3(CRTC1):c.1528A>G (p.Met510Val)	CRTC1 (M526V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208637	NM_015321.3(CRTC1):c.1589C>T (p.Ser530Leu)	CRTC1 (S530L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292704	NM_015321.3(CRTC1):c.1594G>A (p.Ala532Thr)	CRTC1 (A532T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077658	NM_015321.3(CRTC1):c.1613C>T (p.Thr538Met)	CRTC1 (T538M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367389	NM_015321.3(CRTC1):c.1753G>T (p.Gly585Cys)	CRTC1 (G585C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300692	NM_015321.3(CRTC1):c.1792G>A (p.Asp598Asn)	CRTC1 (D614N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077659	NM_015321.3(CRTC1):c.1834A>C (p.Met612Leu)	CRTC1 (M612L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277118	NM_015321.3(CRTC1):c.1867C>T (p.Pro623Ser)	CRTC1 (P639S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25