"Ambry Genetics"[submitter] AND "ODR4"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3204065	NM_017847.6(ODR4):c.227C>G (p.Ala76Gly)	ODR4 (A76G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204066	NM_017847.6(ODR4):c.326G>A (p.Arg109His)	ODR4 (R109H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3204067	NM_017847.6(ODR4):c.803C>T (p.Ser268Phe)	ODR4 (S236F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305455	NM_017847.6(ODR4):c.1000+2014C>T	OCLM, ODR4 (P5S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328260	NM_017847.6(ODR4):c.1000+2015C>T	OCLM, ODR4 (P5L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212827	NM_017847.6(ODR4):c.1000+2056A>G	OCLM, ODR4 (I19V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302841	NM_017847.6(ODR4):c.1000+2075T>C	OCLM, ODR4 (I25T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2403140	NM_017847.6(ODR4):c.1000+2087G>A	OCLM, ODR4 (S29N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302132	NM_017847.6(ODR4):c.1000+2119A>G	OCLM, ODR4	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3204063	NM_017847.6(ODR4):c.1126G>A (p.Glu376Lys)	ODR4 (E376K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204064	NM_017847.6(ODR4):c.1309G>A (p.Ala437Thr)	ODR4 (A414T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance