"PreventionGenetics, part of Exact Sciences"[submitter] AND "YTHDC2"[g - ClinVar

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Items: 46

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3046648	NM_022828.5(YTHDC2):c.-6A>G	YTHDC2	Single nucleotide variant (5 prime UTR variant)	YTHDC2-related disorder	GLikely benign
Select item 776057	NM_022828.5(YTHDC2):c.35C>T (p.Pro12Leu)	YTHDC2 (P12L)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GBenign
Select item 3037545	NM_022828.5(YTHDC2):c.188-6G>A	YTHDC2	Single nucleotide variant (intron variant)	YTHDC2-related disorder	GBenign
Select item 3057618	NM_022828.5(YTHDC2):c.676-8T>C	YTHDC2	Single nucleotide variant (intron variant)	YTHDC2-related disorder	GLikely benign
Select item 3057587	NM_022828.5(YTHDC2):c.783C>T (p.Ala261=)	YTHDC2	Single nucleotide variant (synonymous variant +1 more)	YTHDC2-related disorder	GLikely benign
Select item 3059374	NM_022828.5(YTHDC2):c.793C>A (p.Arg265=)	YTHDC2	Single nucleotide variant (synonymous variant +1 more)	YTHDC2-related disorder	GBenign
Select item 3051259	NM_022828.5(YTHDC2):c.794G>A (p.Arg265Gln)	YTHDC2 (R103Q +1 more)	Single nucleotide variant (missense variant +1 more)	YTHDC2-related disorder	GLikely benign
Select item 776058	NM_022828.5(YTHDC2):c.942C>T (p.Ile314=)	YTHDC2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3048472	NM_022828.5(YTHDC2):c.970T>C (p.Phe324Leu)	YTHDC2 (F162L +2 more)	Single nucleotide variant (missense variant)	YTHDC2-related disorder	GLikely benign
Select item 3041183	NM_022828.5(YTHDC2):c.972T>C (p.Phe324=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder	GBenign
Select item 708427	NM_022828.5(YTHDC2):c.1065C>G (p.Leu355=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder +1 more	GBenign
Select item 3056641	NM_022828.5(YTHDC2):c.1166A>T (p.Tyr389Phe)	YTHDC2 (Y227F +2 more)	Single nucleotide variant (missense variant)	YTHDC2-related disorder	GBenign
Select item 3041520	NM_022828.5(YTHDC2):c.1297C>T (p.Leu433=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder	GLikely benign
Select item 3050102	NM_022828.5(YTHDC2):c.1314G>A (p.Glu438=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder	GBenign
Select item 733689	NM_022828.5(YTHDC2):c.1452C>T (p.Ala484=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder +1 more	GBenign/Likely benign
Select item 776059	NM_022828.5(YTHDC2):c.1496-9T>C	YTHDC2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 3038560	NM_022828.5(YTHDC2):c.1689-5_1689-4dup	YTHDC2	Duplication (intron variant)	YTHDC2-related disorder	GBenign
Select item 3038830	NM_022828.5(YTHDC2):c.1689-8_1689-4del	YTHDC2	Deletion (intron variant)	YTHDC2-related disorder	GLikely benign
Select item 3042914	NM_022828.5(YTHDC2):c.1689-5_1689-3del	YTHDC2	Deletion (intron variant)	YTHDC2-related disorder	GLikely benign
Select item 3038046	NM_022828.5(YTHDC2):c.1689-4_1689-3del	YTHDC2	Deletion (intron variant)	YTHDC2-related disorder	GLikely benign
Select item 3060266	NM_022828.5(YTHDC2):c.1689-3C>T	YTHDC2	Single nucleotide variant (intron variant)	YTHDC2-related disorder	GBenign
Select item 3056221	NM_022828.5(YTHDC2):c.1689-3del	YTHDC2	Deletion (intron variant)	YTHDC2-related disorder	GLikely benign
Select item 3042060	NM_022828.5(YTHDC2):c.1689-3C>A	YTHDC2	Single nucleotide variant (intron variant)	YTHDC2-related disorder	GLikely benign
Select item 3059449	NM_022828.5(YTHDC2):c.1693A>T (p.Thr565Ser)	YTHDC2 (T265S +2 more)	Single nucleotide variant (missense variant)	YTHDC2-related disorder	GBenign
Select item 3060561	NM_022828.5(YTHDC2):c.1867+9G>A	YTHDC2	Single nucleotide variant (intron variant)	YTHDC2-related disorder	GBenign
Select item 3041384	NM_022828.5(YTHDC2):c.1899C>T (p.Asp633=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder	GBenign
Select item 3060554	NM_022828.5(YTHDC2):c.1951G>C (p.Asp651His)	YTHDC2 (D351H +2 more)	Single nucleotide variant (missense variant)	YTHDC2-related disorder	GBenign
Select item 3059238	NM_022828.5(YTHDC2):c.1955G>A (p.Ser652Asn)	YTHDC2 (S352N +2 more)	Single nucleotide variant (missense variant)	YTHDC2-related disorder	GBenign
Select item 3045233	NM_022828.5(YTHDC2):c.2428G>A (p.Val810Ile)	YTHDC2 (V510I +2 more)	Single nucleotide variant (missense variant)	YTHDC2-related disorder	GLikely benign
Select item 3060912	NM_022828.5(YTHDC2):c.2460T>C (p.Asp820=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder	GBenign
Select item 3060019	NM_022828.5(YTHDC2):c.2589A>G (p.Thr863=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder	GBenign
Select item 3043311	NM_022828.5(YTHDC2):c.3049-5A>T	YTHDC2	Single nucleotide variant (intron variant)	YTHDC2-related disorder	GLikely benign
Select item 3048515	NM_022828.5(YTHDC2):c.3061A>G (p.Asn1021Asp)	YTHDC2 (N1021D +2 more)	Single nucleotide variant (missense variant)	YTHDC2-related disorder	GLikely benign
Select item 3056194	NM_022828.5(YTHDC2):c.3081T>G (p.Ile1027Met)	YTHDC2 (I1027M +2 more)	Single nucleotide variant (missense variant)	YTHDC2-related disorder	GBenign
Select item 3041810	NM_022828.5(YTHDC2):c.3156T>C (p.Cys1052=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder	GLikely benign
Select item 3055550	NM_022828.5(YTHDC2):c.3234A>G (p.Ser1078=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder	GBenign
Select item 3053489	NM_022828.5(YTHDC2):c.3335A>G (p.His1112Arg)	YTHDC2 (H1112R +2 more)	Single nucleotide variant (missense variant)	YTHDC2-related disorder	GLikely benign
Select item 3060456	NM_022828.5(YTHDC2):c.3519T>G (p.Ser1173=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder	GBenign
Select item 3045008	NM_022828.5(YTHDC2):c.3522G>C (p.Gly1174=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder	GLikely benign
Select item 3044950	NM_022828.5(YTHDC2):c.3751T>C (p.Ser1251Pro)	YTHDC2 (S1089P +2 more)	Single nucleotide variant (missense variant)	YTHDC2-related disorder	GLikely benign
Select item 3057200	NM_022828.5(YTHDC2):c.3843G>A (p.Ser1281=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder	GBenign
Select item 710247	NM_022828.5(YTHDC2):c.3856A>G (p.Met1286Val)	YTHDC2 (M1124V +2 more)	Single nucleotide variant (missense variant)	YTHDC2-related disorder +1 more	GBenign
Select item 3043828	NM_022828.5(YTHDC2):c.4026C>T (p.Phe1342=)	YTHDC2	Single nucleotide variant (synonymous variant)	YTHDC2-related disorder	GBenign
Select item 3060952	NM_022828.5(YTHDC2):c.4030-7C>A	YTHDC2	Single nucleotide variant (intron variant)	YTHDC2-related disorder	GBenign
Select item 3060188	NM_022828.5(YTHDC2):c.4226T>A (p.Leu1409Gln)	YTHDC2 (L1109Q +2 more)	Single nucleotide variant (missense variant)	YTHDC2-related disorder	GBenign
Select item 3034726	NM_022828.5(YTHDC2):c.*1C>T	YTHDC2	Single nucleotide variant (3 prime UTR variant)	YTHDC2-related disorder	GLikely benign

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Items: 46