ANKRD10[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2255409	NM_017664.4(ANKRD10):c.1198G>C (p.Val400Leu)	ANKRD10 (V400L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597362	NM_017664.4(ANKRD10):c.858C>G (p.Phe286Leu)	ANKRD10 (F286L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548836	NM_017664.4(ANKRD10):c.808G>A (p.Val270Ile)	ANKRD10 (V270I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122079	NM_017664.4(ANKRD10):c.752A>G (p.Lys251Arg)	ANKRD10 (K251R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380142	NM_017664.4(ANKRD10):c.712G>A (p.Val238Met)	ANKRD10 (V238M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3122075	NM_017664.4(ANKRD10):c.710C>T (p.Ala237Val)	ANKRD10 (A237V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482819	NM_017664.4(ANKRD10):c.655T>C (p.Ser219Pro)	ANKRD10 (S219P)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2264147	NM_017664.4(ANKRD10):c.512A>G (p.Gln171Arg)	ANKRD10 (Q171R)	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 2619026	NM_017664.4(ANKRD10):c.370G>A (p.Glu124Lys)	ANKRD10 (E124K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2381392	NM_017664.4(ANKRD10):c.362C>T (p.Pro121Leu)	ANKRD10 (P121L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256536	NM_017664.4(ANKRD10):c.296C>T (p.Ala99Val)	ANKRD10 (A99V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267361	NM_017664.4(ANKRD10):c.185T>C (p.Val62Ala)	ANKRD10 (V62A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2326993	NM_017664.4(ANKRD10):c.148C>G (p.Leu50Val)	ANKRD10 (L50V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214752	NM_017664.4(ANKRD10):c.40T>C (p.Phe14Leu)	ANKRD10 (F14L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122069	NM_017664.4(ANKRD10):c.5C>G (p.Ser2Trp)	ANKRD10 (S2W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance