"Ambry Genetics"[submitter] AND "LOC130062059"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2523574	NM_024619.4(FN3KRP):c.28G>C (p.Gly10Arg)	FN3KRP, LOC130062059 (G10R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398771	NM_024619.4(FN3KRP):c.49A>T (p.Thr17Ser)	FN3KRP, LOC130062059 (T17S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095973	NM_024619.4(FN3KRP):c.61G>C (p.Gly21Arg)	FN3KRP, LOC130062059 (G21R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225145	NM_024619.4(FN3KRP):c.77G>A (p.Ser26Asn)	FN3KRP, LOC130062059 (S26N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244001	NM_024619.4(FN3KRP):c.79C>G (p.Gln27Glu)	FN3KRP, LOC130062059 (Q27E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2236414	NM_024619.4(FN3KRP):c.94G>C (p.Asp32His)	FN3KRP, LOC130062059 (D32H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620831	NM_024619.4(FN3KRP):c.101A>G (p.Asp34Gly)	FN3KRP, LOC130062059 (D34G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279382	NM_024619.4(FN3KRP):c.106G>A (p.Gly36Arg)	FN3KRP, LOC130062059 (G36R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance