ZNF267[gene] - ClinVar

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

Search results

Items: 51

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152605	GRCh38/hg38 16p12.2-11.2(chr16:23752047-31943755)x3	LOC130058732, LOC130058733 +504 more	Copy number gain	See cases	GPathogenic
Select item 144329	GRCh38/hg38 16p11.2-11.1(chr16:30691912-36160463)x3	AHSP, ARMC5 +136 more	Copy number gain	See cases	GPathogenic
Select item 3194778	NM_003414.6(ZNF267):c.23A>C (p.Asp8Ala)	ZNF267 (D8A)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2255996	NM_003414.6(ZNF267):c.140T>G (p.Val47Gly)	ZNF267 (V15G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623677	NM_003414.6(ZNF267):c.149C>T (p.Pro50Leu)	ZNF267 (P50L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484161	NM_003414.6(ZNF267):c.204G>C (p.Glu68Asp)	ZNF267 (E68D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335300	NM_003414.6(ZNF267):c.209C>T (p.Thr70Ile)	ZNF267 (T70I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 147205	GRCh38/hg38 16p11.2(chr16:31894396-33495702)x1	IGHV3OR16-8, LOC105369266 +8 more	Copy number loss	See cases	GBenign
Select item 2623216	NM_003414.6(ZNF267):c.264G>C (p.Glu88Asp)	ZNF267 (E88D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2549187	NM_003414.6(ZNF267):c.347G>C (p.Arg116Thr)	ZNF267 (R116T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194779	NM_003414.6(ZNF267):c.402T>A (p.Phe134Leu)	ZNF267 (F102L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316026	NM_003414.6(ZNF267):c.502G>A (p.Val168Ile)	ZNF267 (V168I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298621	NM_003414.6(ZNF267):c.524T>A (p.Leu175His)	ZNF267 (L143H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194781	NM_003414.6(ZNF267):c.646T>C (p.Tyr216His)	ZNF267 (Y184H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194782	NM_003414.6(ZNF267):c.656A>G (p.Asn219Ser)	ZNF267 (N187S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194783	NM_003414.6(ZNF267):c.659A>C (p.Asn220Thr)	ZNF267 (N220T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194784	NM_003414.6(ZNF267):c.679C>G (p.Gln227Glu)	ZNF267 (Q227E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194785	NM_003414.6(ZNF267):c.689G>A (p.Ser230Asn)	ZNF267 (S198N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346233	NM_003414.6(ZNF267):c.761T>A (p.Leu254His)	ZNF267 (L254H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2338673	NM_003414.6(ZNF267):c.763C>G (p.Gln255Glu)	ZNF267 (Q223E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596093	NM_003414.6(ZNF267):c.770T>C (p.Met257Thr)	ZNF267 (M257T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2646485	NM_003414.6(ZNF267):c.852A>G (p.Gln284=)	ZNF267	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2269832	NM_003414.6(ZNF267):c.941T>C (p.Ile314Thr)	ZNF267 (I314T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216693	NM_003414.6(ZNF267):c.998A>G (p.His333Arg)	ZNF267 (H333R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319228	NM_003414.6(ZNF267):c.1033A>G (p.Thr345Ala)	ZNF267 (T313A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369684	NM_003414.6(ZNF267):c.1036G>A (p.Glu346Lys)	ZNF267 (E314K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374101	NM_003414.6(ZNF267):c.1121A>G (p.Asp374Gly)	ZNF267 (D374G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366619	NM_003414.6(ZNF267):c.1124C>A (p.Thr375Asn)	ZNF267 (T343N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525242	NM_003414.6(ZNF267):c.1138T>A (p.Tyr380Asn)	ZNF267 (Y380N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512833	NM_003414.6(ZNF267):c.1186A>G (p.Ile396Val)	ZNF267 (I364V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194777	NM_003414.6(ZNF267):c.1376C>T (p.Thr459Ile)	ZNF267 (T427I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401499	NM_003414.6(ZNF267):c.1382A>G (p.Glu461Gly)	ZNF267 (E461G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395561	NM_003414.6(ZNF267):c.1423C>T (p.Arg475Cys)	ZNF267 (R443C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545026	NM_003414.6(ZNF267):c.1457A>G (p.His486Arg)	ZNF267 (H486R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328608	NM_003414.6(ZNF267):c.1676A>G (p.Tyr559Cys)	ZNF267 (Y559C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377758	NM_003414.6(ZNF267):c.1723C>A (p.Pro575Thr)	ZNF267 (P543T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364978	NM_003414.6(ZNF267):c.1867C>T (p.Arg623Trp)	ZNF267 (R591W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212404	NM_003414.6(ZNF267):c.2035C>T (p.Arg679Trp)	ZNF267 (R647W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2264138	NM_003414.6(ZNF267):c.2141G>C (p.Arg714Thr)	ZNF267 (R682T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256687	NM_003414.6(ZNF267):c.2154T>G (p.Cys718Trp)	ZNF267 (C686W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527671	NM_003414.6(ZNF267):c.2182A>G (p.Arg728Gly)	ZNF267 (R696G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 979443	GRCh37/hg19 16p11.2(chr16:30350747-31905898)x3	STX4, DCTPP1 +52 more	Copy number gain	not provided	GUncertain significance
Select item 813717	GRCh37/hg19 16p13.3-11.2(chr16:5805001-34230001)	ABAT, ABCC1 +250 more	Copy number gain	Microcephaly	GPathogenic
Select item 443126	GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3	CBLN1, CCDC102A +591 more	Copy number gain	See cases	GUncertain significance
Select item 443121	GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3	AARS1, ABAT +811 more	Copy number gain	See cases	GPathogenic
Select item 443120	GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)	CCL22, CCNF +811 more	Copy number gain	See cases	GPathogenic
Select item 395502	GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3	ABCC6, BCL7C +811 more	Copy number gain	See cases	GPathogenic
Select item 395300	GRCh37/hg19 16p11.2(chr16:28826162-29043901)x1	AHSP, ALDOA +99 more	Copy number loss	See cases	GLikely pathogenic
Select item 375693	maternal UPD(16p)	ALG1, BICDL2 +388 more	Complex	Hemimegalencephaly	GPathogenic
Select item 221519	GRCh37/hg19 16p11.2(chr16:31154186-31926800)x3	AHSP, ARMC5 +15 more	Copy number gain	Breast ductal adenocarcinoma	GUncertain significance
Select item 221391	GRCh37/hg19 16p13.3-11.2(chr16:1279324-31926800)x3	ABAT, ABCA3 +384 more	Copy number gain	Breast ductal adenocarcinoma	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: 51