ATF2[gene] and "single gene"[properties] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 750476	NM_001880.4(ATF2):c.1503G>A (p.Gln501=)	ATF2	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3130787	NM_001880.4(ATF2):c.1496A>G (p.Gln499Arg)	ATF2 (Q441R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2496301	NM_001880.4(ATF2):c.1406C>T (p.Ala469Val)	ATF2 (A411V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2472578	NM_001880.4(ATF2):c.1404G>C (p.Lys468Asn)	ATF2 (K450N +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2399635	NM_001880.4(ATF2):c.1397C>T (p.Thr466Ile)	ATF2 (T408I +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2623578	NM_001880.4(ATF2):c.1375A>G (p.Thr459Ala)	ATF2 (T401A +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2385631	NM_001880.4(ATF2):c.1324T>A (p.Ser442Thr)	ATF2 (S442T +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 775788	NM_001880.4(ATF2):c.1320C>T (p.Asp440=)	ATF2	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 2339468	NM_001880.4(ATF2):c.1312T>A (p.Ser438Thr)	ATF2 (S420T +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2226289	NM_001880.4(ATF2):c.1282G>A (p.Gly428Ser)	ATF2 (G370S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 450692	NM_001880.4(ATF2):c.1086T>G (p.Asn362Lys)	ATF2 (N362K +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 775789	NM_001880.4(ATF2):c.1044C>T (p.Asn348=)	ATF2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 218554	NM_001880.4(ATF2):c.1013G>A (p.Ser338Asn)	ATF2 (S338N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619079	NM_001880.4(ATF2):c.964A>G (p.Thr322Ala)	ATF2 (T264A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2462880	NM_001880.4(ATF2):c.935C>T (p.Pro312Leu)	ATF2 (P294L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494601	NM_001880.4(ATF2):c.659A>G (p.His220Arg)	ATF2 (H202R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2233284	NM_001880.4(ATF2):c.518A>G (p.Asn173Ser)	ATF2 (N115S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531358	NM_001880.4(ATF2):c.476C>A (p.Pro159His)	ATF2 (P141H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491411	NM_001880.4(ATF2):c.421C>G (p.Pro141Ala)	ATF2 (P123A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301784	NM_001880.4(ATF2):c.153G>T (p.Met51Ile)	ATF2 (M51I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2532344	NM_001880.4(ATF2):c.11A>G (p.Lys4Arg)	ATF2 (K4R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance

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Items: 21