"PreventionGenetics, part of Exact Sciences"[submitter] AND "DIP2C"[ge - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1598742	NM_014974.3(DIP2C):c.4653T>C (p.Tyr1551=)	DIP2C	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1645706	NM_014974.3(DIP2C):c.4569C>T (p.Gly1523=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder +1 more	GBenign
Select item 1542347	NM_014974.3(DIP2C):c.4320A>G (p.Val1440=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder +1 more	GLikely benign
Select item 2629927	NM_014974.3(DIP2C):c.4318G>A (p.Val1440Ile)	DIP2C (V1440I)	Single nucleotide variant (missense variant)	DIP2C-related disorder	GUncertain significance
Select item 1600373	NM_014974.3(DIP2C):c.4294+7G>T	DIP2C	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 2719038	NM_014974.3(DIP2C):c.4120-9C>T	DIP2C	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 3050735	NM_014974.3(DIP2C):c.4098G>C (p.Leu1366=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder	GLikely benign
Select item 1593649	NM_014974.3(DIP2C):c.3981C>T (p.His1327=)	DIP2C	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1673071	NM_014974.3(DIP2C):c.3822A>G (p.Ala1274=)	DIP2C	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1555833	NM_014974.3(DIP2C):c.3584+9C>T	DIP2C	Single nucleotide variant (intron variant)	DIP2C-related disorder +1 more	GBenign/Likely benign
Select item 3035275	NM_014974.3(DIP2C):c.3411C>T (p.Leu1137=)	DIP2C, LOC126860805	Single nucleotide variant (synonymous variant)	DIP2C-related disorder	GLikely benign
Select item 1587129	NM_014974.3(DIP2C):c.3320C>T (p.Thr1107Met)	LOC126860805, DIP2C (T1107M)	Single nucleotide variant (missense variant)	DIP2C-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 1603559	NM_014974.3(DIP2C):c.3180G>A (p.Pro1060=)	DIP2C	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1545970	NM_014974.3(DIP2C):c.3109+5A>G	DIP2C	Single nucleotide variant (intron variant)	DIP2C-related disorder +1 more	GBenign
Select item 3043987	NM_014974.3(DIP2C):c.2511C>T (p.Asp837=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder	GLikely benign
Select item 1555107	NM_014974.3(DIP2C):c.2508C>T (p.His836=)	DIP2C	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1454560	NM_014974.3(DIP2C):c.2415C>T (p.Asn805=)	DIP2C, LOC126860806	Single nucleotide variant (synonymous variant)	DIP2C-related disorder +1 more	GLikely benign
Select item 1533348	NM_014974.3(DIP2C):c.1918A>C (p.Ser640Arg)	DIP2C (S640R)	Single nucleotide variant (missense variant)	DIP2C-related disorder +1 more	GLikely benign
Select item 1645858	NM_014974.3(DIP2C):c.1866C>T (p.Gly622=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder +1 more	GBenign
Select item 771174	NM_014974.3(DIP2C):c.1863C>T (p.Asp621=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder +1 more	GBenign
Select item 1592697	NM_014974.3(DIP2C):c.1557A>G (p.Thr519=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder +1 more	GLikely benign
Select item 1532507	NM_014974.3(DIP2C):c.1495-7G>A	DIP2C	Single nucleotide variant (intron variant)	DIP2C-related disorder +1 more	GLikely benign
Select item 3049817	NM_014974.3(DIP2C):c.1385-4C>T	DIP2C	Single nucleotide variant (intron variant)	DIP2C-related disorder	GLikely benign
Select item 1545960	NM_014974.3(DIP2C):c.1248G>A (p.Pro416=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder +1 more	GBenign
Select item 1242047	NM_014974.3(DIP2C):c.970C>T (p.Leu324=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder +1 more	GBenign
Select item 3041704	NM_014974.3(DIP2C):c.870G>A (p.Pro290=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder	GLikely benign
Select item 1345487	NM_014974.3(DIP2C):c.698C>T (p.Ala233Val)	DIP2C (A233V)	Single nucleotide variant (missense variant)	DIP2C-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 1582719	NM_014974.3(DIP2C):c.627C>T (p.Asp209=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder +1 more	GLikely benign
Select item 1942038	NM_014974.3(DIP2C):c.456C>G (p.Thr152=)	DIP2C	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2631191	NM_014974.3(DIP2C):c.424T>G (p.Ser142Ala)	DIP2C (S142A)	Single nucleotide variant (missense variant)	DIP2C-related disorder	GUncertain significance
Select item 724891	NM_014974.3(DIP2C):c.408C>T (p.Gly136=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder +1 more	GBenign/Likely benign
Select item 708364	NM_014974.3(DIP2C):c.395-5C>A	DIP2C	Single nucleotide variant (intron variant)	DIP2C-related disorder +1 more	GBenign/Likely benign
Select item 1666523	NM_014974.3(DIP2C):c.395-9_395-7del	DIP2C	Microsatellite (intron variant)	not provided +1 more	GLikely benign
Select item 2630287	NM_014974.3(DIP2C):c.231A>T (p.Arg77=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder	GUncertain significance
Select item 1534431	NM_014974.3(DIP2C):c.210C>T (p.Ser70=)	DIP2C	Single nucleotide variant (synonymous variant)	DIP2C-related disorder +1 more	GBenign/Likely benign

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Items: 35