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

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2244622	NM_176875.4(CCKBR):c.8T>G (p.Leu3Arg)	CCKBR (L3R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486721	NM_176875.4(CCKBR):c.76G>A (p.Ala26Thr)	CCKBR (A26T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 723129	NM_176875.4(CCKBR):c.109C>T (p.Leu37Phe)	CCKBR (L37F)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2507901	NM_176875.4(CCKBR):c.115T>G (p.Cys39Gly)	CCKBR (C39G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247565	NM_176875.4(CCKBR):c.142G>A (p.Gly48Arg)	CCKBR (G48R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343226	NM_176875.4(CCKBR):c.184G>A (p.Ala62Thr)	CCKBR (A62T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234580	NM_176875.4(CCKBR):c.190A>G (p.Ile64Val)	CCKBR (I64V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264459	NM_176875.4(CCKBR):c.192C>G (p.Ile64Met)	CCKBR (I64M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221978	NM_176875.4(CCKBR):c.218T>C (p.Met73Thr)	CCKBR (M73T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527665	NM_176875.4(CCKBR):c.226A>G (p.Ile76Val)	CCKBR (I76V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139696	NM_176875.4(CCKBR):c.229G>T (p.Val77Leu)	CCKBR (V77L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2207408	NM_176875.4(CCKBR):c.280C>T (p.Leu94Phe)	CCKBR (L94F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139697	NM_176875.4(CCKBR):c.301C>T (p.Leu101Phe)	CCKBR (L101F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2521501	NM_176875.4(CCKBR):c.317C>T (p.Ala106Val)	CCKBR (A106V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 769794	NM_176875.4(CCKBR):c.404-10C>G	CCKBR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3139698	NM_176875.4(CCKBR):c.406G>T (p.Val136Leu)	CCKBR (V136L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323002	NM_176875.4(CCKBR):c.439G>A (p.Ala147Thr)	CCKBR (A63T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139699	NM_176875.4(CCKBR):c.449T>C (p.Leu150Pro)	CCKBR (L150P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619432	NM_176875.4(CCKBR):c.1225T>C (p.Cys409Arg)	CCKBR (C409R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298326	NM_176875.4(CCKBR):c.1243G>A (p.Ala415Thr)	CCKBR (A331T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139695	NM_176875.4(CCKBR):c.1319C>T (p.Thr440Ile)	CCKBR (T440I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264458	NM_176875.4(CCKBR):c.1324A>G (p.Ser442Gly)	CCKBR (S511G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 22