ELK1[gene] and "single gene"[properties] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 782673	NM_001114123.3(ELK1):c.1254C>T (p.Pro418=)	ELK1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 714924	NM_001114123.3(ELK1):c.1158G>A (p.Ala386=)	ELK1 (A94T)	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2660433	NM_001114123.3(ELK1):c.1041T>C (p.Ala347=)	ELK1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3088286	NM_001114123.3(ELK1):c.1031G>C (p.Gly344Ala)	ELK1 (G344A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 749988	NM_001114123.3(ELK1):c.993G>A (p.Pro331=)	ELK1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3275144	NM_001114123.3(ELK1):c.991C>T (p.Pro331Ser)	ELK1 (P331S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601783	NM_001114123.3(ELK1):c.830C>T (p.Pro277Leu)	ELK1 (P277L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 810583	NM_001114123.3(ELK1):c.779del (p.Ala260fs)	ELK1 (A260fs)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 1339790	NM_001114123.3(ELK1):c.775G>T (p.Val259Phe)	ELK1 (V259F)	Single nucleotide variant (missense variant +1 more)	not provided	Gnot provided
Select item 3275146	NM_001114123.3(ELK1):c.761A>C (p.Lys254Thr)	ELK1 (K254T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 711108	NM_001114123.3(ELK1):c.672C>A (p.Pro224=)	ELK1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2660434	NM_001114123.3(ELK1):c.642C>T (p.Gly214=)	ELK1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2526653	NM_001114123.3(ELK1):c.640G>A (p.Gly214Ser)	ELK1 (G214S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372967	NM_001114123.3(ELK1):c.628G>T (p.Ala210Ser)	ELK1 (A210S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2660435	NM_001114123.3(ELK1):c.576C>G (p.Pro192=)	ELK1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1333081	NM_001114123.3(ELK1):c.548G>A (p.Ser183Asn)	ELK1 (S183N)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2543476	NM_001114123.3(ELK1):c.538G>A (p.Val180Met)	ELK1 (V180M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 714925	NM_001114123.3(ELK1):c.514C>G (p.Pro172Ala)	ELK1 (P172A)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2373982	NM_001114123.3(ELK1):c.506C>T (p.Pro169Leu)	ELK1 (P169L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306201	NM_001114123.3(ELK1):c.472C>T (p.Leu158Phe)	ELK1 (L158F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 780690	NM_001114123.3(ELK1):c.430G>A (p.Gly144Ser)	ELK1 (G144S)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 3088287	NM_001114123.3(ELK1):c.407G>T (p.Gly136Val)	ELK1 (G136V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3275145	NM_001114123.3(ELK1):c.361G>A (p.Ala121Thr)	ELK1 (A121T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331014	NM_001114123.3(ELK1):c.357A>G (p.Ile119Met)	ELK1 (I119M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 24