"Invitae"[submitter] AND "TG"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2781284	NM_003235.5(TG):c.6C>T (p.Ala2=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2860363	NM_003235.5(TG):c.9G>C (p.Leu3=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2989569	NM_003235.5(TG):c.12C>A (p.Val4=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2749478	NM_003235.5(TG):c.30G>A (p.Leu10=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2727459	NM_003235.5(TG):c.54G>A (p.Ser18=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 726990	NM_003235.5(TG):c.60T>C (p.Asn20=)	TG	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3005979	NM_003235.5(TG):c.67+7T>C	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2968886	NM_003235.5(TG):c.67+10G>T	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2785520	NM_003235.5(TG):c.67+13G>A	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2959419	NM_003235.5(TG):c.67+17T>C	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3011502	NM_003235.5(TG):c.68-6T>C	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2864375	NM_003235.5(TG):c.68-4C>A	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2844374	NM_003235.5(TG):c.73C>T (p.Gln25Ter)	TG (Q25*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2777589	NM_003235.5(TG):c.78G>C (p.Val26=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 452123	NM_003235.5(TG):c.85C>T (p.Gln29Ter)	TG (Q29*)	Single nucleotide variant (nonsense)	not provided	GPathogenic/Likely pathogenic
Select item 2791603	NM_003235.5(TG):c.90C>T (p.Pro30=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 774249	NM_003235.5(TG):c.105G>A (p.Glu35=)	TG	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2979251	NM_003235.5(TG):c.108G>T (p.Leu36=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2966016	NM_003235.5(TG):c.117A>G (p.Glu39=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2898164	NM_003235.5(TG):c.120G>A (p.Thr40=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2895237	NM_003235.5(TG):c.132G>A (p.Lys44=)	TG	Single nucleotide variant (synonymous variant)	TG-related condition +1 more	GLikely benign
Select item 909867	NM_003235.5(TG):c.138A>G (p.Ala46=)	TG	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 756068	NM_003235.5(TG):c.138A>C (p.Ala46=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 436995	NM_003235.5(TG):c.144C>T (p.Tyr48=)	TG	Single nucleotide variant (synonymous variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 2789679	NM_003235.5(TG):c.147G>C (p.Val49=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2817507	NM_003235.5(TG):c.150C>G (p.Pro50=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2791451	NM_003235.5(TG):c.151C>T (p.Gln51Ter)	TG (Q51*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 3006427	NM_003235.5(TG):c.171C>T (p.Ser57=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 709816	NM_003235.5(TG):c.176+9T>C	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2956644	NM_003235.5(TG):c.176+12G>A	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2980823	NM_003235.5(TG):c.176+20C>T	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2879853	NM_003235.5(TG):c.177-19G>A	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2821708	NM_003235.5(TG):c.177-13G>A	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2992581	NM_003235.5(TG):c.177-11C>T	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 756127	NM_003235.5(TG):c.195C>T (p.Asn65=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 361907	NM_003235.5(TG):c.198C>T (p.Asp66=)	TG	Single nucleotide variant (synonymous variant)	TG-related condition +2 more	GConflicting classifications of pathogenicity
Select item 781146	NM_003235.5(TG):c.199G>A (p.Gly67Ser)	TG (G67S)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2756955	NM_003235.5(TG):c.225C>A (p.Ala75=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2889163	NM_003235.5(TG):c.228C>T (p.Asn76=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 436996	NM_003235.5(TG):c.229G>A (p.Gly77Ser)	TG (G77S)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 2840124	NM_003235.5(TG):c.246C>G (p.Gly82=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3011286	NM_003235.5(TG):c.252G>A (p.Arg84=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2856005	NM_003235.5(TG):c.253C>T (p.Gln85Ter)	TG (Q85*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2976894	NM_003235.5(TG):c.274+1G>A	TG	Single nucleotide variant (splice donor variant)	not provided	GPathogenic
Select item 2735213	NM_003235.5(TG):c.274+2T>G	TG	Single nucleotide variant (splice donor variant)	not provided	GPathogenic
Select item 2869980	NM_003235.5(TG):c.274+13G>A	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2965621	NM_003235.5(TG):c.274+14G>C	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2839563	NM_003235.5(TG):c.274+15G>A	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2757278	NM_003235.5(TG):c.274+15G>C	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2781902	NM_003235.5(TG):c.274+16G>A	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2964533	NM_003235.5(TG):c.274+17G>A	TG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2972462	NM_003235.5(TG):c.274+19C>T	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2873653	NM_003235.5(TG):c.274+19_274+20insTTACACTTACAAGGGAGTAAGGG	TG	Insertion (intron variant)	not provided	GLikely benign
Select item 2968801	NM_003235.5(TG):c.274+20G>C	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2958108	NM_003235.5(TG):c.274+20G>A	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2963277	NM_003235.5(TG):c.275-17G>A	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3008176	NM_003235.5(TG):c.275-16C>T	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2715778	NM_003235.5(TG):c.275-15T>C	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2972621	NM_003235.5(TG):c.275-14C>G	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2861571	NM_003235.5(TG):c.275-13C>T	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2744453	NM_003235.5(TG):c.275-13C>G	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2968933	NM_003235.5(TG):c.275-9T>C	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2824423	NM_003235.5(TG):c.279G>C (p.Leu93=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2779538	NM_003235.5(TG):c.282A>G (p.Ser94=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2750279	NM_003235.5(TG):c.288T>C (p.Cys96=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2907533	NM_003235.5(TG):c.295C>T (p.Gln99Ter)	TG (Q99*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 3023020	NM_003235.5(TG):c.300A>G (p.Lys100=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2808824	NM_003235.5(TG):c.301C>T (p.Gln101Ter)	TG (Q101*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2735187	NM_003235.5(TG):c.324C>T (p.Tyr108=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 774464	NM_003235.5(TG):c.325A>G (p.Ile109Val)	TG (I109V)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2992750	NM_003235.5(TG):c.339C>T (p.Asp113=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2709901	NM_003235.5(TG):c.345C>A (p.Ser115=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 910761	NM_003235.5(TG):c.353C>T (p.Pro118Leu)	TG (P118L)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2770776	NM_003235.5(TG):c.354T>C (p.Pro118=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2799066	NM_003235.5(TG):c.355C>T (p.Gln119Ter)	TG (Q119*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 752414	NM_003235.5(TG):c.366T>C (p.Asp122=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 762444	NM_003235.5(TG):c.372G>A (p.Gly124=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2882275	NM_003235.5(TG):c.378C>T (p.Tyr126=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2960954	NM_003235.5(TG):c.380C>T (p.Ala127Val)	TG (A127V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2996779	NM_003235.5(TG):c.381G>A (p.Ala127=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2713273	NM_003235.5(TG):c.396T>C (p.Asp132=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2699703	NM_003235.5(TG):c.399G>A (p.Val133=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2713686	NM_003235.5(TG):c.416G>A (p.Trp139Ter)	TG (W139*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 735018	NM_003235.5(TG):c.426C>T (p.Asp142=)	TG	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2861136	NM_003235.5(TG):c.429A>G (p.Ala143=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2891046	NM_003235.5(TG):c.447T>C (p.Tyr149=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 911984	NM_003235.5(TG):c.455G>A (p.Arg152His)	TG (R152H)	Single nucleotide variant (missense variant)	Iodotyrosyl coupling defect +2 more	GConflicting classifications of pathogenicity
Select item 2797237	NM_003235.5(TG):c.474G>A (p.Lys158=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2989640	NM_003235.5(TG):c.475C>A (p.Arg159=)	TG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1028100	NM_003235.5(TG):c.475C>T (p.Arg159Ter)	TG (R159*)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 2696557	NM_003235.5(TG):c.478+11C>T	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2751374	NM_003235.5(TG):c.478+14A>G	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2960778	NM_003235.5(TG):c.478+15G>C	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 258995	NM_003235.5(TG):c.478+15G>A	TG	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 2903520	NM_003235.5(TG):c.478+16C>T	TG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2963098	NM_003235.5(TG):c.478+17G>A	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2956051	NM_003235.5(TG):c.478+20T>C	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2987298	NM_003235.5(TG):c.479-18T>A	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3011477	NM_003235.5(TG):c.479-16T>C	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3008289	NM_003235.5(TG):c.479-15C>T	TG	Single nucleotide variant (intron variant)	not provided	GLikely benign

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