CSRNP2[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2247440	NM_030809.3(CSRNP2):c.293G>A (p.Arg98His)	CSRNP2 (R98H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3078376	NM_030809.3(CSRNP2):c.209A>G (p.Gln70Arg)	CSRNP2 (Q70R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474752	NM_030809.3(CSRNP2):c.188G>A (p.Arg63Lys)	CSRNP2 (R63K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3078375	NM_030809.3(CSRNP2):c.185G>A (p.Arg62Gln)	CSRNP2 (R62Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512679	NM_030809.3(CSRNP2):c.170G>A (p.Arg57Gln)	CSRNP2 (R57Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484633	NM_030809.3(CSRNP2):c.127C>G (p.Pro43Ala)	CSRNP2 (P43A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395974	NM_030809.3(CSRNP2):c.125A>G (p.Asn42Ser)	CSRNP2 (N42S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483832	NM_030809.3(CSRNP2):c.36G>T (p.Lys12Asn)	CSRNP2 (K12N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3078377	NM_030809.3(CSRNP2):c.20C>T (p.Ser7Leu)	CSRNP2 (S7L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511526	NM_030809.3(CSRNP2):c.14C>T (p.Thr5Met)	CSRNP2 (T5M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance