ClinVar for Gene (Select 5651) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3068205	NM_002772.3(TMPRSS15):c.2765-2A>G	TMPRSS15	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 3064855	NM_002772.3(TMPRSS15):c.2809delinsATCA (p.Ser937delinsIleThr)	TMPRSS15	Indel (inframe_indel)	not provided	GUncertain significance
Select item 3062431	GRCh37/hg19 21q11.2-22.3(chr21:15023401-48097372)x3	ABCG1, ADAMTS1 +216 more	Copy number gain	not specified	GPathogenic
Select item 3061454	NM_002772.3(TMPRSS15):c.881-4G>C	TMPRSS15	Single nucleotide variant (intron variant)	TMPRSS15-related condition	GLikely benign
Select item 3017426	NM_002772.3(TMPRSS15):c.1396C>A (p.Gln466Lys)	TMPRSS15 (Q466K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3016960	NM_002772.3(TMPRSS15):c.2032+8T>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3013835	NM_002772.3(TMPRSS15):c.3003C>T (p.Pro1001=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3013170	NM_002772.3(TMPRSS15):c.1922-8C>G	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2993418	NM_002772.3(TMPRSS15):c.1890C>T (p.Asn630=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2975956	NM_002772.3(TMPRSS15):c.2668+14del	TMPRSS15	Deletion (intron variant)	not provided	GBenign
Select item 2973638	NM_002772.3(TMPRSS15):c.9G>A (p.Ser3=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2969617	NM_002772.3(TMPRSS15):c.645C>T (p.Asp215=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2960297	NM_002772.3(TMPRSS15):c.45C>T (p.Ser15=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2959836	NM_002772.3(TMPRSS15):c.142C>A (p.Arg48=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2919191	NM_002772.3(TMPRSS15):c.2091C>T (p.Ser697=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2906919	NM_002772.3(TMPRSS15):c.1452C>T (p.Asn484=)	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 2902554	NM_002772.3(TMPRSS15):c.1494A>G (p.Thr498=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2901838	NM_002772.3(TMPRSS15):c.324C>T (p.Asn108=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2900115	NM_002772.3(TMPRSS15):c.2272T>C (p.Leu758=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2897908	NM_002772.3(TMPRSS15):c.1431T>G (p.Val477=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2893828	NM_002772.3(TMPRSS15):c.588G>A (p.Thr196=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2893239	NM_002772.3(TMPRSS15):c.2481G>A (p.Val827=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2893169	NM_002772.3(TMPRSS15):c.180G>A (p.Ala60=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2889540	NM_002772.3(TMPRSS15):c.925A>G (p.Asn309Asp)	TMPRSS15 (N309D)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2889157	NM_002772.3(TMPRSS15):c.498C>G (p.Asp166Glu)	TMPRSS15 (D166E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2887010	NM_002772.3(TMPRSS15):c.544A>G (p.Ile182Val)	TMPRSS15 (I182V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2885915	NM_002772.3(TMPRSS15):c.27T>C (p.Ser9=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2881798	NM_002772.3(TMPRSS15):c.1171+11T>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2880654	NM_002772.3(TMPRSS15):c.1381A>T (p.Asn461Tyr)	TMPRSS15 (N461Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2880389	NM_002772.3(TMPRSS15):c.2412T>C (p.Tyr804=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2878878	NM_002772.3(TMPRSS15):c.198C>T (p.Ser66=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2878602	NM_002772.3(TMPRSS15):c.2388G>A (p.Trp796Ter)	TMPRSS15 (W796*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2877794	NM_002772.3(TMPRSS15):c.1564+20A>G	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2877536	NM_002772.3(TMPRSS15):c.532+14A>T	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 2876976	NM_002772.3(TMPRSS15):c.1080A>C (p.Leu360=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2876930	NM_002772.3(TMPRSS15):c.142C>T (p.Arg48Ter)	TMPRSS15 (R48*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2875860	NM_002772.3(TMPRSS15):c.1395A>C (p.Gly465=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2875704	NM_002772.3(TMPRSS15):c.2373C>T (p.Ala791=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2874152	NM_002772.3(TMPRSS15):c.2532T>C (p.His844=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2873442	NM_002772.3(TMPRSS15):c.2262-8T>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2873439	NM_002772.3(TMPRSS15):c.1236C>T (p.Leu412=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2872751	NM_002772.3(TMPRSS15):c.277-15T>G	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2872440	NM_002772.3(TMPRSS15):c.496+18T>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2872064	NM_002772.3(TMPRSS15):c.1781-5A>T	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2871758	NM_002772.3(TMPRSS15):c.1172-14dup	TMPRSS15	Duplication (intron variant)	not provided	GBenign
Select item 2871745	NM_002772.3(TMPRSS15):c.345-20T>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2871467	NM_002772.3(TMPRSS15):c.897T>G (p.Thr299=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2870688	NM_002772.3(TMPRSS15):c.1172-15T>A	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869688	NM_002772.3(TMPRSS15):c.1654+10T>A	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869685	NM_002772.3(TMPRSS15):c.1565-18C>T	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869535	NM_002772.3(TMPRSS15):c.1216C>T (p.Arg406Ter)	TMPRSS15 (R406*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2869044	NM_002772.3(TMPRSS15):c.1635C>T (p.Ser545=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2868345	NM_002772.3(TMPRSS15):c.2262-9C>A	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867834	NM_002772.3(TMPRSS15):c.2265A>G (p.Gln755=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2867766	NM_002772.3(TMPRSS15):c.2764+11A>T	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2866743	NM_002772.3(TMPRSS15):c.903T>C (p.Pro301=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2865092	NM_002772.3(TMPRSS15):c.1677A>G (p.Gln559=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2862140	NM_002772.3(TMPRSS15):c.1655-15C>T	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2858931	NM_002772.3(TMPRSS15):c.108T>C (p.Ile36=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2857282	NM_002772.3(TMPRSS15):c.302A>G (p.Asn101Ser)	TMPRSS15 (N101S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2854829	NM_002772.3(TMPRSS15):c.743A>G (p.Glu248Gly)	TMPRSS15 (E248G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2843798	NM_002772.3(TMPRSS15):c.2312-10A>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2843723	NM_002772.3(TMPRSS15):c.2328G>A (p.Leu776=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2842721	NM_002772.3(TMPRSS15):c.276+2T>C	TMPRSS15	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 2840847	NM_002772.3(TMPRSS15):c.1781-6G>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2838794	NM_002772.3(TMPRSS15):c.1921+20A>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2836767	NM_002772.3(TMPRSS15):c.105A>G (p.Leu35=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2835787	NM_002772.3(TMPRSS15):c.664+18C>T	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2831066	NM_002772.3(TMPRSS15):c.1125T>G (p.Ser375=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2820803	NM_002772.3(TMPRSS15):c.2364A>T (p.Gly788=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2818632	NM_002772.3(TMPRSS15):c.552C>A (p.Cys184Ter)	TMPRSS15 (C184*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2814681	NM_002772.3(TMPRSS15):c.2785C>T (p.Gln929Ter)	TMPRSS15 (Q929*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2813895	NM_002772.3(TMPRSS15):c.242A>G (p.Asp81Gly)	TMPRSS15 (D81G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2812316	NM_002772.3(TMPRSS15):c.2292G>A (p.Arg764=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2807428	NM_002772.3(TMPRSS15):c.1565-12T>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2806706	NM_002772.3(TMPRSS15):c.1021+14del	TMPRSS15	Deletion (intron variant)	not provided	GLikely benign
Select item 2806137	NM_002772.3(TMPRSS15):c.497-2A>G	TMPRSS15	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 2803758	NM_002772.3(TMPRSS15):c.146-19T>G	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2800144	NM_002772.3(TMPRSS15):c.1731C>T (p.Asn577=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2799530	NM_002772.3(TMPRSS15):c.493C>G (p.Leu165Val)	TMPRSS15 (L165V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2798763	NM_002772.3(TMPRSS15):c.2487-12T>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2798112	NM_002772.3(TMPRSS15):c.2128C>T (p.Gln710Ter)	TMPRSS15 (Q710*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2797191	NM_002772.3(TMPRSS15):c.345-16del	TMPRSS15	Deletion (intron variant)	not provided	GLikely benign
Select item 2796713	NM_002772.3(TMPRSS15):c.344+1G>A	TMPRSS15	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 2790426	NM_002772.3(TMPRSS15):c.145+11T>G	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2789391	NM_002772.3(TMPRSS15):c.664+20C>G	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2786343	NM_002772.3(TMPRSS15):c.2165+15T>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2784383	NM_002772.3(TMPRSS15):c.1922-15A>T	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2784153	NM_002772.3(TMPRSS15):c.1564+8A>G	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2783620	NM_002772.3(TMPRSS15):c.2165+5G>C	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2783538	NM_002772.3(TMPRSS15):c.2319A>G (p.Gly773=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2783490	NM_002772.3(TMPRSS15):c.2312-16C>G	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2783437	NM_002772.3(TMPRSS15):c.2382G>A (p.Gly794=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2781855	NM_002772.3(TMPRSS15):c.768C>T (p.Ile256=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2780902	NM_002772.3(TMPRSS15):c.146-16T>G	TMPRSS15	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2779646	NM_002772.3(TMPRSS15):c.2565C>T (p.Val855=)	TMPRSS15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2779527	NM_002772.3(TMPRSS15):c.1516C>T (p.Leu506Phe)	TMPRSS15 (L506F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2779395	NM_002772.3(TMPRSS15):c.1831A>G (p.Arg611Gly)	TMPRSS15 (R611G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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