Related gene-specific medical variations for Gene (Select 110806306) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3021817	NR_001566.1(TERC):n.367C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 3015793	NR_001566.1(TERC):n.26_27insC	LOC110806306, TERC	Insertion (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 3014205	NR_001566.1(TERC):n.327TC[2]	LOC110806306, TERC	Microsatellite (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2981121	NR_001566.1(TERC):n.276T>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2915715	NR_001566.1(TERC):n.328del	LOC110806306, TERC	Deletion (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2913623	NR_001566.1(TERC):n.221G>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2912261	NR_001566.1(TERC):n.281A>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2902363	NR_001566.1(TERC):n.31G>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2861072	NR_001566.1(TERC):n.74C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2860949	NR_001566.1(TERC):n.261T>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2851362	NR_001566.1(TERC):n.2G>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2847940	NR_001566.1(TERC):n.284C>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2846098	NR_001566.1(TERC):n.55A>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2840076	NR_001566.1(TERC):n.62A>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2835501	NR_001566.1(TERC):n.286C>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2829379	NR_001566.1(TERC):n.45T>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2825576	NR_001566.1(TERC):n.355C>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2823729	NR_001566.1(TERC):n.4T>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2822064	NR_001566.1(TERC):n.25G>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2818331	NR_001566.1(TERC):n.221del	LOC110806306, TERC	Deletion (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2813316	NR_001566.1(TERC):n.84G>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2806781	NR_001566.1(TERC):n.365C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2800272	NR_001566.1(TERC):n.229C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2787205	NR_001566.1(TERC):n.232dup	TERC, LOC110806306	Duplication (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2771703	NR_001566.1(TERC):n.349T>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2761109	NR_001566.1(TERC):n.78G>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2756853	NR_001566.1(TERC):n.299C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2744757	NR_001566.1(TERC):n.105T>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2744221	NR_001566.1(TERC):n.247C>A	TERC, LOC110806306	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2744012	NR_001566.1(TERC):n.371A>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2737080	NR_001566.1(TERC):n.296C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2734587	NR_001566.1(TERC):n.108C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2734586	NR_001566.1(TERC):n.244C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2734585	NR_001566.1(TERC):n.287C>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2733764	NR_001566.1(TERC):n.85C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2733230	NR_001566.1(TERC):n.218C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2729669	NR_001566.1(TERC):n.121G>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2716777	NR_001566.1(TERC):n.177T>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2714419	NR_001566.1(TERC):n.364C>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2711150	NR_001566.1(TERC):n.303G>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2709303	NR_001566.1(TERC):n.305G>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2683780	NR_001566.1(TERC):n.61A>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	not provided +1 more	GUncertain significance
Select item 2629992	NR_001566.1(TERC):n.74_110del	LOC110806306, TERC	Deletion (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1 +1 more	GUncertain significance
Select item 2443277	NR_001566.1(TERC):n.234_235delinsTT	LOC110806306, TERC	Indel (non-coding transcript variant)	not specified	GUncertain significance
Select item 2420879	NR_001566.1(TERC):n.244C>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2199209	NR_001566.1(TERC):n.306T>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2194920	NR_001566.1(TERC):n.332C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2194681	NR_001566.1(TERC):n.141C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2188564	NR_001566.1(TERC):n.20T>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2182604	NR_001566.1(TERC):n.90C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2171755	NR_001566.1(TERC):n.359_361delinsAAG	LOC110806306, TERC	Indel (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2157288	NR_001566.1(TERC):n.19C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2154846	NR_001566.1(TERC):n.106C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2151943	NR_001566.1(TERC):n.210A>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2147463	NR_001566.1(TERC):n.190C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2146368	NR_001566.1(TERC):n.26G>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2146291	NR_001566.1(TERC):n.163G>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2139786	NR_001566.1(TERC):n.40T>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2132958	NR_001566.1(TERC):n.76G>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2131542	NR_001566.1(TERC):n.335G>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2130922	NR_001566.1(TERC):n.327T>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2126177	NR_001566.1(TERC):n.176dup	LOC110806306, TERC	Duplication (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2125942	NR_001566.1(TERC):n.279G>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2120824	NR_001566.1(TERC):n.253G>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2120146	NR_001566.1(TERC):n.155T>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2117745	NR_001566.1(TERC):n.72C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2105746	NR_001566.1(TERC):n.116C>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2101604	NR_001566.1(TERC):n.7C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2099633	NR_001566.1(TERC):n.43T>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2098214	NR_001566.1(TERC):n.114_115del	LOC110806306, TERC	Deletion (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GLikely pathogenic
Select item 2085050	NR_001566.1(TERC):n.192C>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2081070	NR_001566.1(TERC):n.26G>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2077265	NR_001566.1(TERC):n.44G>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2067519	NR_001566.1(TERC):n.149C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2059760	NR_001566.1(TERC):n.62A>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2059346	NR_001566.1(TERC):n.353G>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2049539	NR_001566.1(TERC):n.345G>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2043477	NR_001566.1(TERC):n.83T>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2034722	NR_001566.1(TERC):n.99T>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2029473	NR_001566.1(TERC):n.31G>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2024952	NR_001566.1(TERC):n.21G>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2022752	NR_001566.1(TERC):n.199C>A	TERC, LOC110806306	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2020151	NR_001566.1(TERC):n.275C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 2001725	NR_001566.1(TERC):n.65G>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 1996546	NR_001566.1(TERC):n.228G>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 1996056	NR_001566.1(TERC):n.211C>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 1977073	NR_001566.1(TERC):n.327T>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 1950225	NR_001566.1(TERC):n.184T>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 1948290	NR_001566.1(TERC):n.43dup	LOC110806306, TERC	Duplication (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 1940510	NR_001566.1(TERC):n.87C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 1923915	NR_001566.1(TERC):n.26G>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 1913090	NR_001566.1(TERC):n.32T>C	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 1913008	NR_001566.1(TERC):n.339G>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 1897164	NR_001566.1(TERC):n.18C>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 1896247	NR_001566.1(TERC):n.12G>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 1695964	NR_001566.1(TERC):n.234C>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Pulmonary fibrosis	GLikely risk allele
Select item 1695928	NR_001566.1(TERC):n.314_320dup	LOC110806306, TERC	Duplication (non-coding transcript variant)	Pulmonary fibrosis	GLikely risk allele
Select item 1693878	NR_001566.1(TERC):n.172A>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	not provided	GUncertain significance
Select item 1523182	NR_001566.1(TERC):n.211C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance
Select item 1519766	NR_001566.1(TERC):n.56C>G	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1	GUncertain significance

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