ANKRD7[gene] and "single gene"[properties] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2343937	NM_019644.4(ANKRD7):c.65G>A (p.Arg22Gln)	ANKRD7 (R22Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342512	NM_019644.4(ANKRD7):c.65G>C (p.Arg22Pro)	ANKRD7 (R22P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126948	NM_019644.4(ANKRD7):c.76T>G (p.Leu26Val)	ANKRD7 (L26V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273120	NM_019644.4(ANKRD7):c.133C>T (p.Leu45Phe)	ANKRD7 (L45F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246683	NM_019644.4(ANKRD7):c.182C>T (p.Thr61Ile)	ANKRD7 (T61I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387276	NM_019644.4(ANKRD7):c.202G>A (p.Ala68Thr)	ANKRD7 (A68T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126944	NM_019644.4(ANKRD7):c.240G>C (p.Glu80Asp)	ANKRD7 (E80D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298125	NM_019644.4(ANKRD7):c.349G>A (p.Asp117Asn)	ANKRD7 (D117N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126945	NM_019644.4(ANKRD7):c.370C>T (p.Arg124Cys)	ANKRD7 (R124C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396245	NM_019644.4(ANKRD7):c.371G>A (p.Arg124His)	ANKRD7 (R124H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126946	NM_019644.4(ANKRD7):c.517A>G (p.Met173Val)	ANKRD7 (M173V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126947	NM_019644.4(ANKRD7):c.550G>A (p.Val184Met)	ANKRD7 (V184M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355405	NM_019644.4(ANKRD7):c.667G>A (p.Val223Met)	ANKRD7 (V223M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2613499	NM_019644.4(ANKRD7):c.679C>A (p.Leu227Met)	ANKRD7 (L227M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance