"PreventionGenetics, part of Exact Sciences"[submitter] AND "NFATC1"[g - ClinVar

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Items: 43

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3044671	NM_001278669.2(NFATC1):c.-16CGC[5]	NFATC1	Microsatellite (5 prime UTR variant)	NFATC1-related disorder	GBenign
Select item 712225	NM_001278669.2(NFATC1):c.105C>T (p.Gly35=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	NFATC1-related disorder +1 more	GBenign
Select item 3053678	NM_001278669.2(NFATC1):c.127+4036_127+4040dup	LOC130062776, NFATC1 (M1fs)	Duplication (frameshift variant +2 more)	NFATC1-related disorder	GBenign
Select item 3055115	NM_001278669.2(NFATC1):c.127+4098_127+4106del	LOC130062776, NFATC1	Deletion (inframe deletion +2 more)	NFATC1-related disorder	GUncertain significance
Select item 789237	NM_001278669.2(NFATC1):c.153C>T (p.Asn51=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 1659336	NM_001278669.2(NFATC1):c.202C>A (p.Pro68Thr)	NFATC1 (P55T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 785825	NM_001278669.2(NFATC1):c.204G>A (p.Pro68=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 3043417	NM_001278669.2(NFATC1):c.213C>T (p.Asn71=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	NFATC1-related disorder	GLikely benign
Select item 1600213	NM_001278669.2(NFATC1):c.267C>T (p.Tyr89=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 781420	NM_001278669.2(NFATC1):c.291C>T (p.Pro97=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 3049518	NM_001278669.2(NFATC1):c.292G>T (p.Ala98Ser)	NFATC1 (A85S +1 more)	Single nucleotide variant (missense variant +1 more)	NFATC1-related disorder	GUncertain significance
Select item 777309	NM_001278669.2(NFATC1):c.294G>A (p.Ala98=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	NFATC1-related disorder +1 more	GBenign
Select item 718803	NM_001278669.2(NFATC1):c.723G>A (p.Ser241=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 1593761	NM_001278669.2(NFATC1):c.1069C>G (p.Leu357Val)	NFATC1 (L344V +1 more)	Single nucleotide variant (missense variant +1 more)	NFATC1-related disorder +1 more	GBenign/Likely benign
Select item 3041203	NM_001278669.2(NFATC1):c.1089G>A (p.Pro363=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	NFATC1-related disorder	GLikely benign
Select item 3040516	NM_001278669.2(NFATC1):c.1101G>A (p.Ala367=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	NFATC1-related disorder	GLikely benign
Select item 1536393	NM_001278669.2(NFATC1):c.1104C>T (p.Pro368=)	NFATC1	Single nucleotide variant (intron variant +1 more)	not provided +1 more	GBenign
Select item 791508	NM_001278669.2(NFATC1):c.1205T>C (p.Leu402Pro)	NFATC1 (L389P +1 more)	Single nucleotide variant (missense variant +1 more)	NFATC1-related disorder +1 more	GBenign/Likely benign
Select item 2636804	NM_001278669.2(NFATC1):c.1222A>G (p.Met408Val)	NFATC1 (M395V +1 more)	Single nucleotide variant (missense variant +1 more)	NFATC1-related disorder	GUncertain significance
Select item 2064128	NM_001278669.2(NFATC1):c.1226+8G>A	NFATC1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1674086	NM_001278669.2(NFATC1):c.1326C>T (p.Tyr442=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	NFATC1-related disorder +1 more	GBenign/Likely benign
Select item 2043919	NM_001278669.2(NFATC1):c.1386+6C>T	NFATC1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 731768	NM_001278669.2(NFATC1):c.1446C>T (p.Asp482=)	NFATC1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 782919	NM_001278669.2(NFATC1):c.1521C>T (p.His507=)	NFATC1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1600898	NM_001278669.2(NFATC1):c.1527C>T (p.Ala509=)	NFATC1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 724417	NM_001278669.2(NFATC1):c.1589+8G>A	NFATC1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 3043438	NM_001278669.2(NFATC1):c.1825G>A (p.Val609Met)	NFATC1 (V137M +2 more)	Single nucleotide variant (missense variant)	NFATC1-related disorder	GLikely benign
Select item 1664128	NM_001278669.2(NFATC1):c.1851T>C (p.Ser617=)	NFATC1	Single nucleotide variant (synonymous variant)	NFATC1-related disorder +1 more	GBenign
Select item 1654169	NM_001278669.2(NFATC1):c.1983G>A (p.Pro661=)	NFATC1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1668933	NM_001278669.2(NFATC1):c.1986A>G (p.Pro662=)	NFATC1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3043330	NM_001278669.2(NFATC1):c.2010C>T (p.Ser670=)	NFATC1	Single nucleotide variant (synonymous variant)	NFATC1-related disorder	GLikely benign
Select item 1602470	NM_001278669.2(NFATC1):c.2092+9A>C	NFATC1 (I688L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 2648829	NM_001278669.2(NFATC1):c.2092+20C>T	NFATC1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3051100	NM_001278669.2(NFATC1):c.2213C>A (p.Pro738His)	NFATC1 (P266H +2 more)	Single nucleotide variant (missense variant +1 more)	NFATC1-related disorder	GLikely benign
Select item 2039153	NM_001278669.2(NFATC1):c.2239G>A (p.Gly747Ser)	NFATC1 (G275S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 1601079	NM_001278669.2(NFATC1):c.2280G>A (p.Ala760=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 1602345	NM_001278669.2(NFATC1):c.2289C>T (p.Gly763=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 787471	NM_001278669.2(NFATC1):c.2290G>A (p.Val764Met)	NFATC1 (V292M +2 more)	Single nucleotide variant (missense variant +1 more)	NFATC1-related disorder +1 more	GBenign
Select item 2154755	NM_001278669.2(NFATC1):c.2307C>T (p.His769=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3051946	NM_001278669.2(NFATC1):c.2349G>A (p.Pro783=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	NFATC1-related disorder	GLikely benign
Select item 784751	NM_001278669.2(NFATC1):c.2372C>T (p.Pro791Leu)	NFATC1 (P778L +2 more)	Single nucleotide variant (missense variant +1 more)	NFATC1-related disorder +1 more	GBenign
Select item 2074985	NM_001278669.2(NFATC1):c.2382C>T (p.Ala794=)	NFATC1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 1600611	NM_001278669.2(NFATC1):c.2383G>A (p.Gly795Arg)	NFATC1 (G323R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign

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Items: 43