TMPRSS15[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2118032	NM_002772.3(TMPRSS15):c.3038G>A (p.Trp1013Ter)	TMPRSS15 (W1013*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2058153	NM_002772.3(TMPRSS15):c.3034G>A (p.Glu1012Lys)	TMPRSS15 (E1012K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3179903	NM_002772.3(TMPRSS15):c.3032C>T (p.Thr1011Ile)	TMPRSS15 (T1011I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2127725	NM_002772.3(TMPRSS15):c.3025A>G (p.Arg1009Gly)	TMPRSS15 (R1009G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1973483	NM_002772.3(TMPRSS15):c.3016A>G (p.Arg1006Gly)	TMPRSS15 (R1006G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2715807	NM_002772.3(TMPRSS15):c.3015C>G (p.Ala1005=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2076344	NM_002772.3(TMPRSS15):c.3004G>A (p.Gly1002Arg)	TMPRSS15 (G1002R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3013835	NM_002772.3(TMPRSS15):c.3003C>T (p.Pro1001=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2054818	NM_002772.3(TMPRSS15):c.2999G>A (p.Arg1000His)	TMPRSS15 (R1000H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2125905	NM_002772.3(TMPRSS15):c.2998C>T (p.Arg1000Cys)	TMPRSS15 (R1000C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2068350	NM_002772.3(TMPRSS15):c.2998C>A (p.Arg1000Ser)	TMPRSS15 (R1000S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2265836	NM_002772.3(TMPRSS15):c.2987C>T (p.Ala996Val)	TMPRSS15 (A996V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2005688	NM_002772.3(TMPRSS15):c.2959G>A (p.Gly987Ser)	TMPRSS15 (G987S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2011611	NM_002772.3(TMPRSS15):c.2953C>G (p.Leu985Val)	TMPRSS15 (L985V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2040424	NM_002772.3(TMPRSS15):c.2944A>G (p.Arg982Gly)	TMPRSS15 (R982G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2175430	NM_002772.3(TMPRSS15):c.2928G>C (p.Met976Ile)	TMPRSS15 (M976I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2540386	NM_002772.3(TMPRSS15):c.2927T>C (p.Met976Thr)	TMPRSS15 (M976T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3327330	NM_002772.3(TMPRSS15):c.2912C>T (p.Ser971Leu)	TMPRSS15 (S971L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2197345	NM_002772.3(TMPRSS15):c.2907G>A (p.Gly969=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3327331	NM_002772.3(TMPRSS15):c.2906G>A (p.Gly969Glu)	TMPRSS15 (G969E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 722982	NM_002772.3(TMPRSS15):c.2905G>A (p.Gly969Arg)	TMPRSS15 (G969R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2104267	NM_002772.3(TMPRSS15):c.2905-20T>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2068213	NM_002772.3(TMPRSS15):c.2904+6G>T	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3179902	NM_002772.3(TMPRSS15):c.2895T>A (p.Asp965Glu)	TMPRSS15 (D1010E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611549	NM_002772.3(TMPRSS15):c.2887G>A (p.Gly963Arg)	TMPRSS15 (G963R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2085786	NM_002772.3(TMPRSS15):c.2848A>T (p.Ile950Phe)	TMPRSS15 (I950F)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2597778	NM_002772.3(TMPRSS15):c.2828A>G (p.Gln943Arg)	TMPRSS15 (Q943R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2420761	NM_002772.3(TMPRSS15):c.2827C>T (p.Gln943Ter)	TMPRSS15 (Q943*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1977959	NM_002772.3(TMPRSS15):c.2825A>G (p.Gln942Arg)	TMPRSS15 (Q942R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3064855	NM_002772.3(TMPRSS15):c.2809delinsATCA (p.Ser937delinsIleThr)	TMPRSS15	Indel (inframe_indel)	not provided	GUncertain significance
Select item 1251988	NM_002772.3(TMPRSS15):c.2808_2809insATCA (p.Ser937fs)	TMPRSS15 (S937fs)	Insertion (frameshift variant)	Enterokinase deficiency	GPathogenic
Select item 1995358	NM_002772.3(TMPRSS15):c.2808A>G (p.Leu936=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2133611	NM_002772.3(TMPRSS15):c.2803C>T (p.Leu935Phe)	TMPRSS15 (L935F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3327345	NM_002772.3(TMPRSS15):c.2795A>G (p.Asp932Gly)	TMPRSS15 (D932G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2814681	NM_002772.3(TMPRSS15):c.2785C>T (p.Gln929Ter)	TMPRSS15 (Q929*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 3068205	NM_002772.3(TMPRSS15):c.2765-2A>G	TMPRSS15	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 2025486	NM_002772.3(TMPRSS15):c.2765-3C>A	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1971787	NM_002772.3(TMPRSS15):c.2765-15C>T	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1976616	NM_002772.3(TMPRSS15):c.2764+14_2764+16delinsAAA	TMPRSS15	Indel (intron variant)	not provided	GUncertain significance
Select item 1970972	NM_002772.3(TMPRSS15):c.2764+16C>A	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1970973	NM_002772.3(TMPRSS15):c.2764+15T>A	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1970975	NM_002772.3(TMPRSS15):c.2764+14C>A	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2867766	NM_002772.3(TMPRSS15):c.2764+11A>T	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1996634	NM_002772.3(TMPRSS15):c.2764+11A>G	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 773611	NM_002772.3(TMPRSS15):c.2764+10C>A	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 773612	NM_002772.3(TMPRSS15):c.2764+9T>A	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 773613	NM_002772.3(TMPRSS15):c.2764+7T>A	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2877335	NM_002772.3(TMPRSS15):c.2751G>A (p.Thr917=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2417028	NM_002772.3(TMPRSS15):c.2750C>T (p.Thr917Met)	TMPRSS15 (T917M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2692830	NM_002772.3(TMPRSS15):c.2744G>A (p.Trp915Ter)	TMPRSS15 (W915*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2127164	NM_002772.3(TMPRSS15):c.2738C>T (p.Ala913Val)	TMPRSS15 (A913V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3327335	NM_002772.3(TMPRSS15):c.2734A>G (p.Ile912Val)	TMPRSS15 (I912V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2198072	NM_002772.3(TMPRSS15):c.2725A>T (p.Asn909Tyr)	TMPRSS15 (N909Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 790438	NM_002772.3(TMPRSS15):c.2716C>G (p.Pro906Ala)	TMPRSS15 (P906A)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 2009657	NM_002772.3(TMPRSS15):c.2715T>C (p.Pro905=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 4167	NM_002772.3(TMPRSS15):c.2707_2708del (p.Val903fs)	TMPRSS15 (V903fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2072938	NM_002772.3(TMPRSS15):c.2706A>G (p.Gln902=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 786439	NM_002772.3(TMPRSS15):c.2704C>G (p.Gln902Glu)	TMPRSS15 (Q902E)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 1941449	NM_002772.3(TMPRSS15):c.2694G>A (p.Pro898=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2127166	NM_002772.3(TMPRSS15):c.2688T>C (p.Cys896=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3327334	NM_002772.3(TMPRSS15):c.2684T>C (p.Ile895Thr)	TMPRSS15 (I895T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2145148	NM_002772.3(TMPRSS15):c.2677C>G (p.Gln893Glu)	TMPRSS15 (Q893E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1972682	NM_002772.3(TMPRSS15):c.2669-11T>A	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2101426	NM_002772.3(TMPRSS15):c.2669-13C>G	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1970982	NM_002772.3(TMPRSS15):c.2668+14dup	TMPRSS15	Duplication (intron variant)	not provided	GBenign
Select item 2975956	NM_002772.3(TMPRSS15):c.2668+14del	TMPRSS15	Deletion (intron variant)	not provided	GBenign
Select item 2060047	NM_002772.3(TMPRSS15):c.2668+11_2668+14del	TMPRSS15	Deletion (intron variant)	not provided	GLikely benign
Select item 2116072	NM_002772.3(TMPRSS15):c.2653A>C (p.Lys885Gln)	TMPRSS15 (K885Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2095995	NM_002772.3(TMPRSS15):c.2652T>C (p.Phe884=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2094886	NM_002772.3(TMPRSS15):c.2647G>C (p.Glu883Gln)	TMPRSS15 (E883Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 743659	NM_002772.3(TMPRSS15):c.2625C>T (p.Asn875=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2186732	NM_002772.3(TMPRSS15):c.2619G>A (p.Lys873=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2082473	NM_002772.3(TMPRSS15):c.2612G>A (p.Arg871Gln)	TMPRSS15 (R871Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2139742	NM_002772.3(TMPRSS15):c.2611C>T (p.Arg871Ter)	TMPRSS15 (R871*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2181643	NM_002772.3(TMPRSS15):c.2599_2600insGATTAATAGATGAAATTGTC (p.His867fs)	TMPRSS15 (H867fs)	Insertion (frameshift variant)	not provided	GPathogenic
Select item 2127002	NM_002772.3(TMPRSS15):c.2595C>A (p.Asn865Lys)	TMPRSS15 (N865K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2110390	NM_002772.3(TMPRSS15):c.2579A>G (p.Asp860Gly)	TMPRSS15 (D860G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1972321	NM_002772.3(TMPRSS15):c.2576T>G (p.Ile859Arg)	TMPRSS15 (I859R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2588927	NM_002772.3(TMPRSS15):c.2570G>A (p.Arg857Gln)	TMPRSS15 (R857Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 4165	NM_002772.3(TMPRSS15):c.2569C>T (p.Arg857Ter)	TMPRSS15 (R857*)	Single nucleotide variant (nonsense)	Enterokinase deficiency	GPathogenic
Select item 2779646	NM_002772.3(TMPRSS15):c.2565C>T (p.Val855=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2079156	NM_002772.3(TMPRSS15):c.2539T>C (p.Ser847Pro)	TMPRSS15 (S847P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 782931	NM_002772.3(TMPRSS15):c.2536A>C (p.Lys846Gln)	TMPRSS15 (K846Q)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2874152	NM_002772.3(TMPRSS15):c.2532T>C (p.His844=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2030242	NM_002772.3(TMPRSS15):c.2514del (p.Ala839fs)	TMPRSS15 (A839fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2414283	NM_002772.3(TMPRSS15):c.2505C>A (p.Ser835=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2719606	NM_002772.3(TMPRSS15):c.2487-9_2487-7dup	TMPRSS15	Duplication (intron variant)	not provided	GLikely benign
Select item 2798763	NM_002772.3(TMPRSS15):c.2487-12T>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1974526	NM_002772.3(TMPRSS15):c.2487-17_2487-15del	TMPRSS15	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2628751	NM_002772.3(TMPRSS15):c.2486+1G>A	TMPRSS15	Single nucleotide variant (splice donor variant)	Enterokinase deficiency +2 more	GLikely pathogenic
Select item 2044107	NM_002772.3(TMPRSS15):c.2483A>G (p.Tyr828Cys)	TMPRSS15 (Y828C)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2893239	NM_002772.3(TMPRSS15):c.2481G>A (p.Val827=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2171311	NM_002772.3(TMPRSS15):c.2478C>T (p.Cys826=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2905759	NM_002772.3(TMPRSS15):c.2466C>T (p.Ser822=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2199799	NM_002772.3(TMPRSS15):c.2443G>A (p.Val815Ile)	TMPRSS15 (V815I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1997513	NM_002772.3(TMPRSS15):c.2441_2442dup (p.Val815fs)	TMPRSS15 (V815fs)	Microsatellite (frameshift variant)	not provided	GPathogenic
Select item 2100279	NM_002772.3(TMPRSS15):c.2438C>T (p.Ser813Phe)	TMPRSS15 (S813F)	Single nucleotide variant (missense variant)	TMPRSS15-related disorder +1 more	GUncertain significance
Select item 2128377	NM_002772.3(TMPRSS15):c.2434G>T (p.Ala812Ser)	TMPRSS15 (A812S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3327328	NM_002772.3(TMPRSS15):c.2431G>A (p.Gly811Ser)	TMPRSS15 (G811S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1901422	NM_002772.3(TMPRSS15):c.2415C>T (p.Gly805=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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