"Ambry Genetics"[submitter] AND "ODF2L"[gene] - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2327197	NM_001366781.1(ODF2L):c.1862C>T (p.Ser621Leu)	ODF2L (S529L +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254190	NM_001366781.1(ODF2L):c.1847A>G (p.Asn616Ser)	ODF2L (N485S +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527225	NM_001366781.1(ODF2L):c.1806+664C>T	ODF2L (P423L +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2351611	NM_001366781.1(ODF2L):c.1798A>G (p.Met600Val)	ODF2L (M416V +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204054	NM_001366781.1(ODF2L):c.1738T>A (p.Leu580Ile)	ODF2L (L386I +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343458	NM_001366781.1(ODF2L):c.1711A>G (p.Arg571Gly)	ODF2L (R571G +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342740	NM_001366781.1(ODF2L):c.1475A>G (p.Glu492Gly)	ODF2L (E308G +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552643	NM_001366781.1(ODF2L):c.1396G>A (p.Asp466Asn)	ODF2L (D335N +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3204052	NM_001366781.1(ODF2L):c.1352A>C (p.His451Pro)	ODF2L (H451P +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407785	NM_001366781.1(ODF2L):c.1290G>T (p.Glu430Asp)	ODF2L (E260D +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482958	NM_001366781.1(ODF2L):c.1179G>T (p.Leu393Phe)	ODF2L (L422F +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462730	NM_001366781.1(ODF2L):c.1142C>A (p.Thr381Asn)	ODF2L (T279N +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204051	NM_001366781.1(ODF2L):c.1127A>G (p.Glu376Gly)	ODF2L (E235G +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230277	NM_001366781.1(ODF2L):c.1045A>G (p.Thr349Ala)	ODF2L (T191A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204050	NM_001366781.1(ODF2L):c.1036C>G (p.Leu346Val)	ODF2L (L307V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262946	NM_001366781.1(ODF2L):c.1027A>G (p.Thr343Ala)	ODF2L (T304A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204060	NM_001366781.1(ODF2L):c.980G>T (p.Cys327Phe)	ODF2L (C157F +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332679	NM_001366781.1(ODF2L):c.980G>A (p.Cys327Tyr)	ODF2L (C157Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204059	NM_001366781.1(ODF2L):c.949A>G (p.Lys317Glu)	ODF2L (K186E +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263325	NM_001366781.1(ODF2L):c.928A>G (p.Ile310Val)	ODF2L (I179V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204058	NM_001366781.1(ODF2L):c.914T>C (p.Met305Thr)	ODF2L (M147T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374520	NM_001366781.1(ODF2L):c.857G>A (p.Ser286Asn)	ODF2L (S155N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461775	NM_001366781.1(ODF2L):c.845A>G (p.Asn282Ser)	ODF2L (N112S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313249	NM_001366781.1(ODF2L):c.821T>G (p.Leu274Trp)	ODF2L (L116W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204057	NM_001366781.1(ODF2L):c.813A>T (p.Glu271Asp)	ODF2L (E101D +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204056	NM_001366781.1(ODF2L):c.812A>T (p.Glu271Val)	ODF2L (E140V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466789	NM_001366781.1(ODF2L):c.806A>G (p.Asp269Gly)	ODF2L (D138G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558911	NM_001366781.1(ODF2L):c.739A>C (p.Lys247Gln)	ODF2L (K116Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292964	NM_001366781.1(ODF2L):c.685A>G (p.Ile229Val)	ODF2L (I190V +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2589588	NM_001366781.1(ODF2L):c.677A>G (p.Asn226Ser)	ODF2L (N226S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523170	NM_001366781.1(ODF2L):c.595G>A (p.Glu199Lys)	ODF2L (E199K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289139	NM_001366781.1(ODF2L):c.575A>G (p.Gln192Arg)	ODF2L (Q192R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3204055	NM_001366781.1(ODF2L):c.529C>T (p.Arg177Cys)	ODF2L (R46C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2231552	NM_001366781.1(ODF2L):c.251A>G (p.Asn84Ser)	ODF2L (N84S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2591924	NM_001366781.1(ODF2L):c.74A>G (p.Glu25Gly)	ODF2L (E25G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 35