"Ambry Genetics"[submitter] AND "SERPIND1"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2240949	NM_000185.4(SERPIND1):c.40A>G (p.Ile14Val)	PI4KA, SERPIND1 (I14V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160467	NM_000185.4(SERPIND1):c.71C>T (p.Pro24Leu)	PI4KA, SERPIND1 (P24L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2320647	NM_000185.4(SERPIND1):c.229G>A (p.Asp77Asn)	PI4KA, SERPIND1 (D77N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244253	NM_000185.4(SERPIND1):c.512G>A (p.Gly171Glu)	PI4KA, SERPIND1 (G171E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2255600	NM_000185.4(SERPIND1):c.532C>T (p.His178Tyr)	PI4KA, SERPIND1 (H178Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160466	NM_000185.4(SERPIND1):c.584T>C (p.Ile195Thr)	PI4KA, SERPIND1 (I195T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470000	NM_000185.4(SERPIND1):c.622C>T (p.Arg208Cys)	PI4KA, SERPIND1 (R208C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608699	NM_000185.4(SERPIND1):c.800T>G (p.Met267Arg)	PI4KA, SERPIND1 (M267R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160468	NM_000185.4(SERPIND1):c.848C>G (p.Pro283Arg)	PI4KA, SERPIND1 (P283R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490816	NM_000185.4(SERPIND1):c.863T>C (p.Met288Thr)	PI4KA, SERPIND1 (M288T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 393085	NM_000185.4(SERPIND1):c.980A>C (p.Gln327Pro)	PI4KA, SERPIND1 (Q327P)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3160465	NM_000185.4(SERPIND1):c.1181T>C (p.Leu394Pro)	PI4KA, SERPIND1 (L394P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2229137	NM_000185.4(SERPIND1):c.1207T>C (p.Tyr403His)	PI4KA, SERPIND1 (Y403H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2260829	NM_000185.4(SERPIND1):c.1396C>G (p.Gln466Glu)	PI4KA, SERPIND1 (Q466E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance