TEAD4[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3175577	NM_003213.4(TEAD4):c.53C>T (p.Ser18Phe)	TEAD4 (S18F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484008	NM_003213.4(TEAD4):c.88G>T (p.Ala30Ser)	TEAD4 (A30S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2281428	NM_003213.4(TEAD4):c.131G>A (p.Ser44Asn)	TEAD4 (S44N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2403562	NM_003213.4(TEAD4):c.166G>A (p.Ala56Thr)	TEAD4 (A56T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546977	NM_003213.4(TEAD4):c.206C>T (p.Ser69Leu)	TEAD4 (S69L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395249	NM_003213.4(TEAD4):c.229C>T (p.Arg77Trp)	TEAD4 (R77W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212797	NM_003213.4(TEAD4):c.247C>T (p.Arg83Cys)	TEAD4 (R83C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175575	NM_003213.4(TEAD4):c.332G>C (p.Arg111Pro)	TEAD4 (R111P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493047	NM_003213.4(TEAD4):c.355G>C (p.Asp119His)	TEAD4 (D119H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2385091	NM_003213.4(TEAD4):c.454C>T (p.Arg152Trp)	TEAD4 (R152W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3175576	NM_003213.4(TEAD4):c.463G>A (p.Gly155Ser)	TEAD4 (G26S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341937	NM_003213.4(TEAD4):c.467G>A (p.Arg156His)	TEAD4 (R156H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3325182	NM_003213.4(TEAD4):c.528T>C (p.Asp176=)	TEAD4	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2511167	NM_003213.4(TEAD4):c.560T>C (p.Val187Ala)	TEAD4 (V144A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2642576	NM_003213.4(TEAD4):c.584-4G>T	TEAD4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2293829	NM_003213.4(TEAD4):c.602G>T (p.Gly201Val)	TEAD4 (G158V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213153	NM_003213.4(TEAD4):c.607G>A (p.Ala203Thr)	TEAD4 (A203T +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3325181	NM_003213.4(TEAD4):c.625C>T (p.Pro209Ser)	TEAD4 (P209S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175578	NM_003213.4(TEAD4):c.643C>G (p.Gln215Glu)	TEAD4 (Q86E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369003	NM_003213.4(TEAD4):c.655G>A (p.Val219Met)	TEAD4 (V176M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175579	NM_003213.4(TEAD4):c.718G>A (p.Asp240Asn)	TEAD4 (D111N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175580	NM_003213.4(TEAD4):c.742G>A (p.Val248Met)	TEAD4 (V205M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325183	NM_003213.4(TEAD4):c.790G>T (p.Ala264Ser)	TEAD4 (A221S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3175581	NM_003213.4(TEAD4):c.803G>T (p.Arg268Leu)	TEAD4 (R139L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370580	NM_003213.4(TEAD4):c.860G>A (p.Arg287Gln)	TEAD4 (R158Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325180	NM_003213.4(TEAD4):c.918C>G (p.Ile306Met)	TEAD4 (I263M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338922	NM_003213.4(TEAD4):c.970G>A (p.Glu324Lys)	TEAD4 (E195K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558713	NM_003213.4(TEAD4):c.1125C>G (p.His375Gln)	TEAD4 (H375Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2642577	NM_003213.4(TEAD4):c.1266C>T (p.His422=)	TEAD4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3175574	NM_003213.4(TEAD4):c.1276C>T (p.His426Tyr)	TEAD4 (H383Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 30