Related gene-specific medical variations for Gene (Select 338692) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3123213	NM_207354.3(ANKRD13D):c.52C>T (p.Arg18Trp)	ANKRD13D, LOC130006179 (R18W)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3123205	NM_207354.3(ANKRD13D):c.37C>G (p.Leu13Val)	ANKRD13D, LOC130006179 (L13V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3123202	NM_207354.3(ANKRD13D):c.32A>C (p.His11Pro)	ANKRD13D, LOC130006179 (H11P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2613799	NM_207354.3(ANKRD13D):c.23T>G (p.Phe8Cys)	ANKRD13D, LOC130006179 (F8C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 92041	NM_207354.3(ANKRD13D):c.251G>T (p.Gly84Val)	ANKRD13D (G84V)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance

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