"PreventionGenetics, part of Exact Sciences"[submitter] AND "PDCD10"[g - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 590685	NM_007217.4(PDCD10):c.634G>T (p.Ala212Ser)	PDCD10 (A212S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 590684	NM_007217.4(PDCD10):c.586C>T (p.Arg196Ter)	PDCD10 (R196*)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic
Select item 344108	NM_007217.4(PDCD10):c.574G>A (p.Val192Ile)	PDCD10 (V192I)	Single nucleotide variant (missense variant)	Cerebral cavernous malformation 3 +2 more	GConflicting classifications of pathogenicity
Select item 590683	NM_007217.4(PDCD10):c.558-2A>T	PDCD10	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 590682	NM_007217.4(PDCD10):c.535A>G (p.Lys179Glu)	PDCD10 (K179E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 536234	NM_007217.4(PDCD10):c.510C>G (p.Tyr170Ter)	PDCD10 (Y170*)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 590681	NM_007217.4(PDCD10):c.501del (p.Phe167fs)	PDCD10 (F167fs)	Deletion (frameshift variant)	not provided	GLikely pathogenic
Select item 590680	NM_007217.4(PDCD10):c.496G>T (p.Glu166Ter)	PDCD10 (E166*)	Single nucleotide variant (nonsense)	not provided	GLikely pathogenic
Select item 468331	NM_007217.4(PDCD10):c.474+5G>A	PDCD10	Single nucleotide variant (intron variant)	Cerebral arteriovenous malformation +6 more	GPathogenic/Likely pathogenic
Select item 2628404	NM_007217.4(PDCD10):c.462C>A (p.Tyr154Ter)	PDCD10 (Y154*)	Single nucleotide variant (nonsense)	PDCD10-related disorder	GLikely pathogenic
Select item 590678	NM_007217.4(PDCD10):c.396-2A>T	PDCD10	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 590679	NM_007217.4(PDCD10):c.396-3C>G	PDCD10	Single nucleotide variant (intron variant)	not provided	GPathogenic
Select item 590677	NM_007217.4(PDCD10):c.395+2T>G	PDCD10	Single nucleotide variant (splice donor variant)	not provided	GPathogenic
Select item 590676	NM_007217.4(PDCD10):c.395+1G>A	PDCD10	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 468330	NM_007217.4(PDCD10):c.322C>T (p.Arg108Ter)	PDCD10 (R108*)	Single nucleotide variant (nonsense)	PDCD10-related disorder +2 more	GPathogenic
Select item 590675	NM_007217.4(PDCD10):c.283C>T (p.Arg95Ter)	PDCD10 (R95*)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic
Select item 590674	NM_145859.1(PDCD10):c.269_270delAG	PDCD10	Microsatellite	not provided	GLikely pathogenic
Select item 590673	NM_007217.4(PDCD10):c.269-1G>C	PDCD10	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 590672	NM_007217.4(PDCD10):c.268+1del	PDCD10	Deletion (splice donor variant)	not provided	GLikely pathogenic
Select item 590671	NM_007217.4(PDCD10):c.183CAT[1] (p.Ile63del)	PDCD10 (I63del)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 590670	NM_007217.4(PDCD10):c.150+1G>T	PDCD10	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 447923	NM_007217.4(PDCD10):c.150+1G>A	PDCD10	Single nucleotide variant (splice donor variant)	not provided	GPathogenic/Likely pathogenic
Select item 3058354	NM_007217.4(PDCD10):c.150G>A (p.Lys50=)	PDCD10	Single nucleotide variant (synonymous variant)	PDCD10-related disorder	GUncertain significance
Select item 590669	NM_007217.4(PDCD10):c.117del (p.Ala40fs)	PDCD10 (A40fs)	Deletion (frameshift variant)	not provided	GLikely pathogenic
Select item 372445	NM_007217.4(PDCD10):c.103C>T (p.Arg35Ter)	PDCD10 (R35*)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic
Select item 590667	NM_007217.4(PDCD10):c.-284C>T	PDCD10	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 590668	NM_007217.4(PDCD10):c.-308T>C	LOC129937857, PDCD10	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GBenign
Select item 369413	NM_007217.4(PDCD10):c.-438G>C	LOC129937857, PDCD10 +1 more	Single nucleotide variant (5 prime UTR variant)	SERPINI1-related disorder +2 more	GConflicting classifications of pathogenicity

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Items: 28