Related gene-specific medical variations for Gene (Select 29109) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278835	NM_013241.3(FHOD1):c.836C>A (p.Thr279Asn)	FHOD1, LOC126862378 (T279N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095125	NM_013241.3(FHOD1):c.660G>C (p.Lys220Asn)	FHOD1, LOC126862378 (K220N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556070	NM_013241.3(FHOD1):c.724C>T (p.Arg242Cys)	FHOD1, LOC126862378 (R242C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2545008	NM_013241.3(FHOD1):c.548C>T (p.Ala183Val)	FHOD1, LOC126862378 (A183V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532166	NM_013241.3(FHOD1):c.434T>A (p.Ile145Asn)	FHOD1, LOC126862378 (I145N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519602	NM_013241.3(FHOD1):c.1052G>A (p.Arg351Gln)	FHOD1, LOC126862378 (R351Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507641	NM_013241.3(FHOD1):c.757G>A (p.Ala253Thr)	FHOD1, LOC126862378 (A253T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466291	NM_013241.3(FHOD1):c.1058G>T (p.Arg353Leu)	FHOD1, LOC126862378 (R353L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412520	NM_013241.3(FHOD1):c.553G>A (p.Gly185Ser)	FHOD1, LOC126862378 (G185S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380481	NM_013241.3(FHOD1):c.646C>G (p.Arg216Gly)	FHOD1, LOC126862378 (R216G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371445	NM_013241.3(FHOD1):c.1151G>A (p.Gly384Asp)	FHOD1, LOC130059190 (G384D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344523	NM_013241.3(FHOD1):c.407G>A (p.Arg136His)	FHOD1, LOC126862378 (R136H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223313	NM_013241.3(FHOD1):c.1246G>T (p.Ala416Ser)	FHOD1, LOC130059190 (A416S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 156714	NM_013241.3(FHOD1):c.635C>T (p.Ala212Val)	FHOD1, LOC126862378 (A212V)	Single nucleotide variant (missense variant)	not provided	Gnot provided