"Ambry Genetics"[submitter] AND "LOC101927954"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278588	NM_001083536.2(FGD3):c.847G>T (p.Val283Leu)	FGD3, LOC101927954 (V283L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2355409	NM_001083536.2(FGD3):c.857A>G (p.Asn286Ser)	FGD3, LOC101927954 (N286S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2232590	NM_001083536.2(FGD3):c.863C>T (p.Thr288Met)	FGD3, LOC101927954 (T288M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3094628	NM_001083536.2(FGD3):c.925G>T (p.Asp309Tyr)	FGD3, LOC101927954 (D309Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3094629	NM_001083536.2(FGD3):c.928T>C (p.Tyr310His)	FGD3, LOC101927954 (Y310H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2261331	NM_001083536.2(FGD3):c.962G>A (p.Arg321Gln)	FGD3, LOC101927954 (R321Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3094630	NM_001083536.2(FGD3):c.985G>A (p.Glu329Lys)	FGD3, LOC101927954 (E329K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224263	NM_001083536.2(FGD3):c.992T>C (p.Ile331Thr)	FGD3, LOC101927954 (I331T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094615	NM_001083536.2(FGD3):c.1024A>G (p.Ile342Val)	FGD3, LOC101927954 (I342V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517427	NM_001083536.2(FGD3):c.1087G>A (p.Asp363Asn)	FGD3, LOC101927954 (D363N)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2345046	NM_001083536.2(FGD3):c.1156A>T (p.Thr386Ser)	FGD3, LOC101927954 (T386S)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3094616	NM_001083536.2(FGD3):c.1159C>T (p.Pro387Ser)	FGD3, LOC101927954 (P387S)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2306026	NM_001083536.2(FGD3):c.1169G>A (p.Arg390His)	FGD3, LOC101927954 (R390H)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance