"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "CTNND2"[ge - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 809732	NM_001332.4(CTNND2):c.3232C>T (p.Arg1078Trp)	CTNND2 (R766W +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3025344	NM_001332.4(CTNND2):c.2952C>T (p.Ala984=)	CTNND2, LOC126807316	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 722905	NM_001332.4(CTNND2):c.2464-5G>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 714949	NM_001332.4(CTNND2):c.2316G>A (p.Ser772=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 2655296	NM_001332.4(CTNND2):c.2160-8C>A	CTNND2	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2655297	NM_001332.4(CTNND2):c.2099A>G (p.Asp700Gly)	CTNND2 (D267G +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2655298	NM_001332.4(CTNND2):c.2087C>T (p.Ser696Leu)	CTNND2 (S263L +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2655299	NM_001332.4(CTNND2):c.1943C>T (p.Thr648Met)	CTNND2 (T215M +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2673006	NM_001332.4(CTNND2):c.1549A>G (p.Ser517Gly)	CTNND2 (S180G +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 444649	NM_001332.4(CTNND2):c.1520A>C (p.Gln507Pro)	CTNND2 (Q507P +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3026983	NM_001332.4(CTNND2):c.1499C>G (p.Ala500Gly)	CTNND2 (A163G +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3026005	NM_001332.4(CTNND2):c.1428C>T (p.His476=)	CTNND2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 872811	NM_001332.4(CTNND2):c.1174G>A (p.Ala392Thr)	CTNND2 (A301T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1176481	NM_001332.4(CTNND2):c.916C>A (p.Arg306Ser)	CTNND2 (R215S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 521010	NM_001332.4(CTNND2):c.803C>A (p.Pro268Gln)	CTNND2 (P268Q +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1298981	NM_001332.4(CTNND2):c.772_801del (p.Thr258_Ser267del)	CTNND2	Deletion (inframe_deletion +1 more)	not provided	GUncertain significance
Select item 1320597	NM_001332.4(CTNND2):c.656CGC[10] (p.Pro225_Pro226dup)	CTNND2	Microsatellite (inframe_insertion +1 more)	not provided	GLikely benign
Select item 1241651	NM_001332.4(CTNND2):c.656CGC[9] (p.Pro226dup)	CTNND2	Microsatellite (inframe_insertion +1 more)	CTNND2-related condition +2 more	GBenign/Likely benign
Select item 430945	NM_001332.4(CTNND2):c.671C>T (p.Pro224Leu)	CTNND2 (P224L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1317661	NM_001332.4(CTNND2):c.655G>A (p.Ala219Thr)	CTNND2 (A128T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 716339	NM_001332.4(CTNND2):c.594G>A (p.Thr198=)	CTNND2	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign/Likely benign
Select item 3026731	NM_001332.4(CTNND2):c.579A>C (p.Thr193=)	CTNND2	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2655300	NM_001332.4(CTNND2):c.9G>C (p.Ala3=)	CTNND2	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 1262174	NM_001332.4(CTNND2):c.-9G>A	CTNND2	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign

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Items: 24