SERPINA5[gene] and "single gene"[properties] - ClinVar

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Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2390124	NM_000624.6(SERPINA5):c.62G>A (p.Arg21His)	SERPINA5 (R21H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160343	NM_000624.6(SERPINA5):c.73C>T (p.Arg25Trp)	SERPINA5 (R25W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514374	NM_000624.6(SERPINA5):c.109G>A (p.Gly37Ser)	SERPINA5 (G37S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614495	NM_000624.6(SERPINA5):c.155T>C (p.Leu52Pro)	SERPINA5 (L52P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258515	NM_000624.6(SERPINA5):c.158A>T (p.Tyr53Phe)	SERPINA5 (Y53F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160338	NM_000624.6(SERPINA5):c.185G>A (p.Ser62Asn)	SERPINA5 (S62N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354487	NM_000624.6(SERPINA5):c.265A>T (p.Met89Leu)	SERPINA5 (M89L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556190	NM_000624.6(SERPINA5):c.294C>A (p.Asn98Lys)	SERPINA5 (N98K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484144	NM_000624.6(SERPINA5):c.331T>A (p.Phe111Ile)	SERPINA5 (F111I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381619	NM_000624.6(SERPINA5):c.343C>A (p.Leu115Ile)	SERPINA5 (L115I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160340	NM_000624.6(SERPINA5):c.401T>A (p.Phe134Tyr)	SERPINA5 (F134Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548653	NM_000624.6(SERPINA5):c.406G>A (p.Asp136Asn)	SERPINA5 (D136N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160341	NM_000624.6(SERPINA5):c.439A>G (p.Ser147Gly)	SERPINA5 (S147G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317556	NM_000624.6(SERPINA5):c.451A>G (p.Thr151Ala)	SERPINA5 (T151A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273984	NM_000624.6(SERPINA5):c.482A>T (p.Asn161Ile)	SERPINA5 (N161I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317555	NM_000624.6(SERPINA5):c.566A>G (p.Lys189Arg)	SERPINA5 (K189R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317553	NM_000624.6(SERPINA5):c.589G>A (p.Val197Met)	SERPINA5 (V197M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2608223	NM_000624.6(SERPINA5):c.622A>G (p.Lys208Glu)	SERPINA5 (K208E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160342	NM_000624.6(SERPINA5):c.635G>A (p.Ser212Asn)	SERPINA5 (S212N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 776855	NM_000624.6(SERPINA5):c.649G>C (p.Gly217Arg)	SERPINA5 (G217R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2530017	NM_000624.6(SERPINA5):c.652A>T (p.Thr218Ser)	SERPINA5 (T218S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2644480	NM_000624.6(SERPINA5):c.682G>C (p.Glu228Gln)	SERPINA5 (E228Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2490617	NM_000624.6(SERPINA5):c.686C>T (p.Thr229Ile)	SERPINA5 (T229I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552994	NM_000624.6(SERPINA5):c.692T>C (p.Val231Ala)	SERPINA5 (V231A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370896	NM_000624.6(SERPINA5):c.742C>G (p.Arg248Gly)	SERPINA5 (R248G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472377	NM_000624.6(SERPINA5):c.747C>A (p.Asn249Lys)	SERPINA5 (N249K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160344	NM_000624.6(SERPINA5):c.892C>A (p.Gln298Lys)	SERPINA5 (Q298K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460678	NM_000624.6(SERPINA5):c.932C>T (p.Ser311Phe)	SERPINA5 (S311F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512508	NM_000624.6(SERPINA5):c.949G>A (p.Val317Ile)	SERPINA5 (V317I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2521784	NM_000624.6(SERPINA5):c.955C>T (p.Pro319Ser)	SERPINA5 (P319S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317557	NM_000624.6(SERPINA5):c.958A>G (p.Ser320Gly)	SERPINA5 (S320G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 722623	NM_000624.6(SERPINA5):c.1002C>T (p.Ser334=)	SERPINA5	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2222813	NM_000624.6(SERPINA5):c.1003G>A (p.Gly335Ser)	SERPINA5 (G335S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552118	NM_000624.6(SERPINA5):c.1075G>A (p.Gly359Arg)	SERPINA5 (G359R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317554	NM_000624.6(SERPINA5):c.1120T>A (p.Ser374Thr)	SERPINA5 (S374T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340104	NM_000624.6(SERPINA5):c.1155C>A (p.Asn385Lys)	SERPINA5 (N385K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273776	NM_000624.6(SERPINA5):c.1174A>G (p.Ile392Val)	SERPINA5 (I392V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160336	NM_000624.6(SERPINA5):c.1192C>T (p.Leu398Phe)	SERPINA5 (L398F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160337	NM_000624.6(SERPINA5):c.1204A>G (p.Lys402Glu)	SERPINA5 (K402E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375975	NM_000624.6(SERPINA5):c.1213C>T (p.Arg405Cys)	SERPINA5 (R405C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 40