"Ambry Genetics"[submitter] AND "FYTTD1"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2604612	NM_032288.7(FYTTD1):c.56C>G (p.Pro19Arg)	FYTTD1 (P19R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461316	NM_032288.7(FYTTD1):c.62C>A (p.Ala21Asp)	FYTTD1 (A21D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337195	NM_032288.7(FYTTD1):c.130G>A (p.Glu44Lys)	FYTTD1 (E44K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097638	NM_032288.7(FYTTD1):c.214T>C (p.Trp72Arg)	FYTTD1 (W72R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097639	NM_032288.7(FYTTD1):c.216G>C (p.Trp72Cys)	FYTTD1 (W46C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2479095	NM_032288.7(FYTTD1):c.297T>G (p.Asn99Lys)	FYTTD1 (N99K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2387846	NM_032288.7(FYTTD1):c.544C>A (p.His182Asn)	FYTTD1 (H156N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097640	NM_032288.7(FYTTD1):c.584G>A (p.Arg195Lys)	FYTTD1 (R195K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2300445	NM_032288.7(FYTTD1):c.641C>G (p.Ala214Gly)	FYTTD1 (A188G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346103	NM_032288.7(FYTTD1):c.687T>G (p.Ile229Met)	FYTTD1 (I203M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2510228	NM_032288.7(FYTTD1):c.727C>T (p.Pro243Ser)	FYTTD1 (P243S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622390	NM_032288.7(FYTTD1):c.838A>G (p.Ile280Val)	FYTTD1 (I254V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457913	NM_032288.7(FYTTD1):c.934A>G (p.Ser312Gly)	FYTTD1 (S312G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance