Related gene-specific medical variations for Gene (Select 200539) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3394313	NM_144994.8(ANKRD23):c.731A>G (p.Asp244Gly)	ANKRD23, LOC129934370 (D244G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3394300	NM_144994.8(ANKRD23):c.752T>C (p.Val251Ala)	ANKRD23, LOC129934370 (V251A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124046	NM_144994.8(ANKRD23):c.872G>C (p.Arg291Pro)	ANKRD23, LOC129934369 (R291P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124039	NM_144994.8(ANKRD23):c.769A>C (p.Lys257Gln)	ANKRD23, LOC129934370 (K257Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477565	NM_144994.8(ANKRD23):c.859C>A (p.Gln287Lys)	ANKRD23, LOC129934369 (Q287K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295801	NM_144994.8(ANKRD23):c.764G>T (p.Ser255Ile)	ANKRD23, LOC129934370 (S255I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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