CRLF3[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2495225	NM_015986.4(CRLF3):c.1270G>C (p.Gly424Arg)	CRLF3 (G424R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477925	NM_015986.4(CRLF3):c.1043G>A (p.Arg348Gln)	CRLF3 (R348Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528041	NM_015986.4(CRLF3):c.1030G>A (p.Asp344Asn)	CRLF3 (D344N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2360440	NM_015986.4(CRLF3):c.1012G>C (p.Glu338Gln)	CRLF3 (E338Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269557	NM_015986.4(CRLF3):c.961G>A (p.Val321Ile)	CRLF3 (V321I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279424	NM_015986.4(CRLF3):c.939T>G (p.Cys313Trp)	CRLF3 (C313W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2222029	NM_015986.4(CRLF3):c.922G>T (p.Ala308Ser)	CRLF3 (A308S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3077532	NM_015986.4(CRLF3):c.902C>T (p.Ser301Leu)	CRLF3 (S301L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3077531	NM_015986.4(CRLF3):c.809C>G (p.Ser270Cys)	CRLF3 (S270C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319600	NM_015986.4(CRLF3):c.706G>A (p.Val236Ile)	CRLF3 (V236I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588424	NM_015986.4(CRLF3):c.682G>A (p.Val228Ile)	CRLF3 (V228I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493906	NM_015986.4(CRLF3):c.676G>C (p.Val226Leu)	CRLF3 (V226L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461059	NM_015986.4(CRLF3):c.625C>G (p.Gln209Glu)	CRLF3 (Q209E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269251	NM_015986.4(CRLF3):c.229C>T (p.Leu77Phe)	CRLF3 (L77F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468245	NM_015986.4(CRLF3):c.112C>T (p.Arg38Cys)	CRLF3 (R38C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 815922	GRCh37/hg19 17q11.2(chr17:28952286-29150025)x3	CRLF3	Copy number gain	not provided	GUncertain significance
Select item 564424	GRCh37/hg19 17q11.2(chr17:28952286-29121921)x3	CRLF3	Copy number gain	not provided	GUncertain significance