Related gene-specific medical variations for Gene (Select 83697) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3165161	NM_031467.3(SLC4A9):c.2633T>C (p.Ile878Thr)	ANKHD1-DT, SLC4A9 (I878T +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3165160	NM_031467.3(SLC4A9):c.2578A>G (p.Arg860Gly)	ANKHD1-DT, SLC4A9 (R797G +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2470520	NM_031467.3(SLC4A9):c.2758G>C (p.Glu920Gln)	ANKHD1-DT, SLC4A9 (E920Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294747	NM_031467.3(SLC4A9):c.2660T>C (p.Phe887Ser)	ANKHD1-DT, SLC4A9 (F824S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285669	NM_031467.3(SLC4A9):c.2641A>C (p.Thr881Pro)	ANKHD1-DT, SLC4A9 (T881P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236764	NM_031467.3(SLC4A9):c.2710G>A (p.Val904Ile)	ANKHD1-DT, SLC4A9 (V841I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221458	NM_031467.3(SLC4A9):c.2786T>C (p.Leu929Pro)	ANKHD1-DT, SLC4A9 (L915P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215704	NM_031467.3(SLC4A9):c.2866A>C (p.Ile956Leu)	ANKHD1-DT, SLC4A9 (I893L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205561	NM_031467.3(SLC4A9):c.2692C>G (p.Arg898Gly)	ANKHD1-DT, SLC4A9 (R898G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance