ClinVar for Gene (Select 7018) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3354388	NM_001063.4(TF):c.967A>G (p.Lys323Glu)	TF (K196E +2 more)	Single nucleotide variant (missense variant)	TF-related disorder	GUncertain significance
Select item 3338974	NM_001063.4(TF):c.1108G>A (p.Glu370Lys)	TF (E243K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325586	NM_001063.4(TF):c.1277T>C (p.Val426Ala)	TF (V299A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325585	NM_001063.4(TF):c.1253C>G (p.Ala418Gly)	TF (A291G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325584	NM_001063.4(TF):c.2023G>A (p.Val675Ile)	TF (V548I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325583	NM_001063.4(TF):c.2086C>T (p.Arg696Cys)	TF (R696C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325582	NM_001063.4(TF):c.212T>C (p.Ile71Thr)	TF (I71T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3242060	NM_001063.4(TF):c.113G>A (p.Cys38Tyr)	TF (C38Y)	Single nucleotide variant (missense variant +2 more)	Atransferrinemia	GUncertain significance
Select item 3176438	NM_001063.4(TF):c.860A>G (p.Asn287Ser)	TF (N160S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176437	NM_001063.4(TF):c.714C>G (p.Asp238Glu)	TF (D111E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176436	NM_001063.4(TF):c.659A>G (p.Asp220Gly)	TF (D176G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176435	NM_001063.4(TF):c.485G>A (p.Arg162His)	TF (R118H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176433	NM_001063.4(TF):c.1424G>A (p.Arg475Lys)	TF (R431K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176432	NM_001063.4(TF):c.1303G>A (p.Asp435Asn)	TF (D308N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176431	NM_001063.4(TF):c.1118A>G (p.Lys373Arg)	TF (K246R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3023457	NM_001063.4(TF):c.216+18A>G	TF	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3022425	NM_001063.4(TF):c.2062+20T>C	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3021978	NM_001063.4(TF):c.217-9C>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3021940	NM_001063.4(TF):c.1048+11G>A	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3018470	NM_001063.4(TF):c.681G>A (p.Ser227=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3017841	NM_001063.4(TF):c.1200C>A (p.Ile400=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3014980	NM_001063.4(TF):c.567G>A (p.Leu189=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3014500	NM_001063.4(TF):c.957C>T (p.His319=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3013657	NM_001063.4(TF):c.1194C>G (p.Ala398=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3012145	NM_001063.4(TF):c.503-14T>C	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3011892	NM_001063.4(TF):c.912C>T (p.Phe304=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3011761	NM_001063.4(TF):c.2007C>T (p.Tyr669=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3009864	NM_001063.4(TF):c.2063-13C>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3008818	NM_001063.4(TF):c.1821C>G (p.Val607=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3008443	NM_001063.4(TF):c.1743G>A (p.Leu581=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3008036	NM_001063.4(TF):c.1622+9T>G	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3007480	NM_001063.4(TF):c.1587C>T (p.Asn529=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3005973	NM_001063.4(TF):c.954C>T (p.Ala318=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3005942	NM_001063.4(TF):c.1905G>A (p.Ser635=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3005938	NM_001063.4(TF):c.1331-14T>C	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3005382	NM_001063.4(TF):c.636-5C>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3005230	NM_001063.4(TF):c.871-18_871-17del	TF	Deletion (intron variant)	not provided	GLikely benign
Select item 3004585	NM_001063.4(TF):c.1000C>T (p.Leu334=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3004404	NM_001063.4(TF):c.252T>C (p.Gly84=)	TF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3003571	NM_001063.4(TF):c.1476C>T (p.His492=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3003398	NM_001063.4(TF):c.684T>A (p.Thr228=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3002567	NM_001063.4(TF):c.549G>C (p.Gly183=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3002491	NM_001063.4(TF):c.870+10C>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3002200	NM_001063.4(TF):c.1623-18A>G	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3001171	NM_001063.4(TF):c.2010A>G (p.Leu670=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2997943	NM_001063.4(TF):c.691+18A>G	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2997317	NM_001063.4(TF):c.285C>T (p.Asn95=)	TF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2994995	NM_001063.4(TF):c.2052C>T (p.Cys684=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2993466	NM_001063.4(TF):c.1857A>T (p.Ile619=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2991736	NM_001063.4(TF):c.492T>C (p.Pro164=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2991474	NM_001063.4(TF):c.318A>G (p.Ser106=)	TF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2991214	NM_001063.4(TF):c.318A>C (p.Ser106=)	TF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2987412	NM_001063.4(TF):c.60C>G (p.Val20=)	TF	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2986960	NM_001063.4(TF):c.1330+18A>G	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2986825	NM_001063.4(TF):c.2082T>C (p.Thr694=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2986766	NM_001063.4(TF):c.1512C>T (p.Ala504=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2986074	NM_001063.4(TF):c.2063-18CTCTG[3]	TF	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2985879	NM_001063.4(TF):c.43+15G>A	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2984418	NM_001063.4(TF):c.216+19A>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2983988	NM_001063.4(TF):c.1938G>A (p.Lys646=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2983385	NM_001063.4(TF):c.354T>C (p.Ala118=)	TF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2980201	NM_001063.4(TF):c.756G>A (p.Lys252=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2979471	NM_001063.4(TF):c.1873-20A>G	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2979320	NM_001063.4(TF):c.1487-19C>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2979229	NM_001063.4(TF):c.1048+16G>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2979116	NM_001063.4(TF):c.1688-4C>G	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2978927	NM_001063.4(TF):c.43+15G>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2977617	NM_001063.4(TF):c.2097A>G (p.Ter699=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2976208	NM_001063.4(TF):c.43+9G>C	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2974454	NM_001063.4(TF):c.240A>G (p.Thr80=)	TF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2974382	NM_001063.4(TF):c.828C>A (p.Gly276=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2971526	NM_001063.4(TF):c.691+13C>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2971472	NM_001063.4(TF):c.1048+8C>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2970549	NM_001063.4(TF):c.810C>T (p.Val270=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2969820	NM_001063.4(TF):c.1331-4G>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2969784	NM_001063.4(TF):c.1455G>T (p.Leu485=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2969778	NM_001063.4(TF):c.93G>A (p.Ser31=)	TF	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2969165	NM_001063.4(TF):c.1179C>T (p.Thr393=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2969162	NM_001063.4(TF):c.1812C>T (p.His604=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2968962	NM_001063.4(TF):c.105C>T (p.Ala35=)	TF	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2967254	NM_001063.4(TF):c.1203+12C>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2967085	NM_001063.4(TF):c.1806G>A (p.Pro602=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2966608	NM_001063.4(TF):c.1204-12G>A	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2966071	NM_001063.4(TF):c.1331-11C>A	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2965661	NM_001063.4(TF):c.1191C>T (p.Ile397=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2965293	NM_001063.4(TF):c.1965A>G (p.Val655=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2964421	NM_001063.4(TF):c.300G>A (p.Val100=)	TF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2963786	NM_001063.4(TF):c.1203+15C>A	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2963608	NM_001063.4(TF):c.1929G>A (p.Ser643=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2962146	NM_001063.4(TF):c.1203+9C>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961484	NM_001063.4(TF):c.692-18T>A	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2960913	NM_001063.4(TF):c.1203+19C>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2960591	NM_001063.4(TF):c.636-20G>C	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2960079	NM_001063.4(TF):c.1431T>C (p.Ala477=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2958342	NM_001063.4(TF):c.615C>T (p.Phe205=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2957997	NM_001063.4(TF):c.635+20C>T	TF	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2957857	NM_001063.4(TF):c.306G>A (p.Glu102=)	TF	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2957723	NM_001063.4(TF):c.1845C>T (p.Cys615=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2957616	NM_001063.4(TF):c.561C>T (p.Pro187=)	TF	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2956803	NM_001063.4(TF):c.216+16C>T	TF	Single nucleotide variant (intron variant)	not provided	GBenign

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