"Color Diagnostics, LLC DBA Color Health"[submitter] AND "TOE1"[gene] - ClinVar

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Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 509968	NM_001128425.2(MUTYH):c.36+20C>T	MUTYH, TOE1	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 371683	NM_001128425.2(MUTYH):c.36+20C>G	MUTYH, TOE1	Single nucleotide variant (5 prime UTR variant +1 more)	Familial adenomatous polyposis 2 +2 more	GLikely benign
Select item 182687	NM_001128425.2(MUTYH):c.36+20C>A	MUTYH, TOE1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 492036	NM_001128425.2(MUTYH):c.36+18T>C	MUTYH, TOE1	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 492035	NM_001128425.2(MUTYH):c.36+11C>G	MUTYH, TOE1	Single nucleotide variant (intron variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 138310	NM_025077.4(TOE1):c.-45G>A	MUTYH, TOE1	Single nucleotide variant (5 prime UTR variant +1 more)	Familial adenomatous polyposis 2 +3 more	GConflicting classifications of pathogenicity
Select item 464715	NM_001128425.2(MUTYH):c.36+10A>C	MUTYH, TOE1	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 920562	NM_001128425.2(MUTYH):c.36+9G>A	TOE1, MUTYH	Single nucleotide variant (5 prime UTR variant +1 more)	Familial adenomatous polyposis 2 +1 more	GLikely benign
Select item 628379	NM_001128425.2(MUTYH):c.36+9G>T	MUTYH, TOE1	Single nucleotide variant (5 prime UTR variant +1 more)	Familial adenomatous polyposis 2 +2 more	GLikely benign
Select item 492037	NM_001128425.2(MUTYH):c.36+7T>C	MUTYH, TOE1	Single nucleotide variant (5 prime UTR variant +1 more)	Familial adenomatous polyposis 2 +1 more	GLikely benign
Select item 464716	NM_001128425.2(MUTYH):c.36+6C>G	TOE1, MUTYH	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 573559	NM_001128425.2(MUTYH):c.36+4dup	MUTYH, TOE1	Duplication (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 246019	NM_001128425.2(MUTYH):c.36+4C>G	MUTYH, TOE1	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 234074	NM_001128425.2(MUTYH):c.36+3A>T	MUTYH, TOE1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 492030	NM_001128425.2(MUTYH):c.29G>C (p.Arg10Pro)	MUTYH, TOE1 (R10P)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 926570	NM_001128425.2(MUTYH):c.28C>T (p.Arg10Cys)	MUTYH, TOE1 (R10C)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 414151	NM_001128425.2(MUTYH):c.22C>T (p.Leu8=)	MUTYH, TOE1	Single nucleotide variant (5 prime UTR variant +2 more)	not specified +2 more	GLikely benign
Select item 142941	NM_001128425.2(MUTYH):c.17C>A (p.Ser6Tyr)	MUTYH, TOE1 (S6Y)	Single nucleotide variant (5 prime UTR variant +2 more)	Familial adenomatous polyposis 2 +4 more	GConflicting classifications of pathogenicity
Select item 919234	NM_001128425.2(MUTYH):c.13G>T (p.Val5Phe)	MUTYH, TOE1 (V5F)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 630514	NM_001128425.2(MUTYH):c.13G>A (p.Val5Ile)	TOE1, MUTYH (V5I)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 628380	NM_001128425.2(MUTYH):c.10C>T (p.Leu4Phe)	MUTYH, TOE1 (L4F)	Single nucleotide variant (5 prime UTR variant +2 more)	Familial adenomatous polyposis 2 +2 more	GUncertain significance
Select item 481801	NM_001128425.2(MUTYH):c.9G>T (p.Pro3=)	MUTYH, TOE1	Single nucleotide variant (5 prime UTR variant +2 more)	Familial adenomatous polyposis 2 +2 more	GLikely benign
Select item 464742	NM_001128425.2(MUTYH):c.9G>A (p.Pro3=)	MUTYH, TOE1	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 480012	NM_001128425.2(MUTYH):c.8C>G (p.Pro3Arg)	MUTYH, TOE1 (P3R)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 233944	NM_001128425.2(MUTYH):c.8C>T (p.Pro3Leu)	MUTYH, TOE1 (P3L)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 920563	NM_001128425.2(MUTYH):c.3G>A (p.Met1Ile)	TOE1, MUTYH (M1I)	Single nucleotide variant (5 prime UTR variant +3 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 230848	NM_001128425.2(MUTYH):c.2T>C (p.Met1Thr)	MUTYH, TOE1 (M1T +1 more)	Single nucleotide variant (missense variant +3 more)	not specified +3 more	GUncertain significance
Select item 859836	NM_001128425.2(MUTYH):c.1A>G (p.Met1Val)	MUTYH, TOE1 (M1V +1 more)	Single nucleotide variant (missense variant +3 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 619704	NM_001128425.2(MUTYH):c.-2C>G	TOE1, MUTYH (A2P)	Single nucleotide variant (missense variant +2 more)	Familial adenomatous polyposis 2 +2 more	GUncertain significance
Select item 1171396	NM_001128425.2(MUTYH):c.-3G>A	MUTYH, TOE1 (A2V)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 490028	NM_001128425.2(MUTYH):c.-3G>T	MUTYH, TOE1 (A2D)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 231593	NM_001128425.2(MUTYH):c.-4G>A	MUTYH, TOE1	Single nucleotide variant (synonymous variant +2 more)	not provided +2 more	GUncertain significance
Select item 2773696	NM_001128425.2(MUTYH):c.-7G>A	TOE1, MUTYH	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 925304	NM_001128425.2(MUTYH):c.-11T>C	TOE1, MUTYH (S5G)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 925955	NM_001128425.2(MUTYH):c.-13A>T	TOE1, MUTYH (S5R)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 380353	NM_001128425.2(MUTYH):c.-13A>C	MUTYH, TOE1 (S5R)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 920564	NM_001128425.2(MUTYH):c.-15T>C	MUTYH, TOE1 (D6G)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 628333	NM_001128425.2(MUTYH):c.-19A>G	MUTYH, TOE1	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance

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Items: 38