ASGR2[gene] and "single gene"[properties] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 786837	NM_001201352.2(ASGR2):c.909C>T (p.Gly303=)	ASGR2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 721041	NM_001201352.2(ASGR2):c.906C>T (p.Thr302=)	ASGR2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2516959	NM_001201352.2(ASGR2):c.833C>T (p.Pro278Leu)	ASGR2 (P259L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317987	NM_001201352.2(ASGR2):c.811G>C (p.Glu271Gln)	ASGR2 (E271Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130300	NM_001201352.2(ASGR2):c.796G>A (p.Glu266Lys)	ASGR2 (E266K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342640	NM_001201352.2(ASGR2):c.790G>A (p.Gly264Arg)	ASGR2 (G245R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490044	NM_001201352.2(ASGR2):c.767T>G (p.Val256Gly)	ASGR2 (V242G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303181	NM_001201352.2(ASGR2):c.709G>C (p.Gly237Arg)	ASGR2 (G242R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469562	NM_001201352.2(ASGR2):c.700G>A (p.Asp234Asn)	ASGR2 (D215N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130298	NM_001201352.2(ASGR2):c.680A>G (p.Asn227Ser)	ASGR2 (N208S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378555	NM_001201352.2(ASGR2):c.668C>T (p.Thr223Met)	ASGR2 (T223M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532372	NM_001201352.2(ASGR2):c.529G>A (p.Val177Met)	ASGR2 (V158M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130297	NM_001201352.2(ASGR2):c.506G>A (p.Arg169Lys)	ASGR2 (R150K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317995	NM_001201352.2(ASGR2):c.463G>C (p.Val155Leu)	ASGR2 (V141L +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3130296	NM_001201352.2(ASGR2):c.457C>T (p.Arg153Cys)	ASGR2 (R158C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130295	NM_001201352.2(ASGR2):c.448G>A (p.Val150Met)	ASGR2 (V136M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511994	NM_001201352.2(ASGR2):c.346G>A (p.Val116Met)	ASGR2 (V102M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130294	NM_001201352.2(ASGR2):c.322G>C (p.Ala108Pro)	ASGR2 (A108P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130293	NM_001201352.2(ASGR2):c.311C>T (p.Thr104Met)	ASGR2 (T85M +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2269721	NM_001201352.2(ASGR2):c.299C>T (p.Ser100Leu)	ASGR2 (S86L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267645	NM_001201352.2(ASGR2):c.265C>T (p.Arg89Trp)	ASGR2 (R89W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2624391	NM_001201352.2(ASGR2):c.241+11C>A	ASGR2 (H65Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615982	NM_001201352.2(ASGR2):c.191T>C (p.Leu64Pro)	ASGR2 (L45P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400247	NM_001201352.2(ASGR2):c.109A>G (p.Asn37Asp)	ASGR2 (N37D)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign

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Items: 24