ZNF615[gene] - ClinVar

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

Search results

Items: 60

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59116	GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	LOC130064925, LOC130064926 +1081 more	Copy number gain	See cases	GPathogenic
Select item 59117	GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	LOC130064903, LOC130064904 +1093 more	Copy number gain	See cases	GPathogenic
Select item 59126	GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	LOC130065082, LOC130065083 +806 more	Copy number gain	See cases	GPathogenic
Select item 146579	GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	OSCAR, PEG3 +782 more	Copy number gain	See cases	GPathogenic
Select item 57219	GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3	LOC130065034, LOC130065035 +761 more	Copy number gain	See cases	GPathogenic
Select item 59127	GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3	A1BG, A1BG-AS1 +647 more	Copy number gain	See cases	GPathogenic
Select item 155383	GRCh38/hg38 19q13.41(chr19:51202361-51993020)x3	C19orf84, CD33 +62 more	Copy number gain	See cases	GUncertain significance
Select item 154637	GRCh38/hg38 19q13.41(chr19:51769103-52124150)x3	FPR2, FPR3 +20 more	Copy number gain	See cases	GBenign
Select item 157458	NM_001005738.1(FPR2):c.290_344331dup	FPR2, FPR3 +20 more	Duplication	Gestational diabetes mellitus uncontrolled	Gnot provided
Select item 154882	GRCh38/hg38 19q13.41(chr19:51785545-52075049)x3	FPR3, LOC126862921 +16 more	Copy number gain	See cases	GLikely benign
Select item 58803	GRCh38/hg38 19q13.41(chr19:51824349-52113443)x3	FPR3, LOC126862921 +18 more	Copy number gain	See cases	GUncertain significance
Select item 147613	GRCh38/hg38 19q13.41(chr19:51865544-52113443)x3	LOC126862922, LOC126862923 +16 more	Copy number gain	See cases	GBenign
Select item 3258925	NM_001199324.2(ZNF615):c.2209C>T (p.His737Tyr)	ZNF615 (H737Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378829	NM_001199324.2(ZNF615):c.2188C>T (p.His730Tyr)	ZNF615 (H726Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478017	NM_001199324.2(ZNF615):c.2135A>G (p.Lys712Arg)	ZNF615 (K701R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297256	NM_001199324.2(ZNF615):c.2099T>C (p.Phe700Ser)	ZNF615 (F689S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224406	NM_001199324.2(ZNF615):c.2013C>A (p.Phe671Leu)	ZNF615 (F660L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197213	NM_001199324.2(ZNF615):c.1964G>A (p.Arg655Gln)	ZNF615 (R644Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607139	NM_001199324.2(ZNF615):c.1958A>T (p.His653Leu)	ZNF615 (H649L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554317	NM_001199324.2(ZNF615):c.1913A>T (p.Asn638Ile)	ZNF615 (N638I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205576	NM_001199324.2(ZNF615):c.1882A>C (p.Thr628Pro)	ZNF615 (T628P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258923	NM_001199324.2(ZNF615):c.1708C>T (p.Arg570Trp)	ZNF615 (R564W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258920	NM_001199324.2(ZNF615):c.1628G>A (p.Arg543Gln)	ZNF615 (R532Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197212	NM_001199324.2(ZNF615):c.1610G>A (p.Arg537Gln)	ZNF615 (R531Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241914	NM_001199324.2(ZNF615):c.1567T>C (p.Tyr523His)	ZNF615 (Y523H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595507	NM_001199324.2(ZNF615):c.1526G>A (p.Arg509His)	ZNF615 (R498H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523983	NM_001199324.2(ZNF615):c.1466A>G (p.His489Arg)	ZNF615 (H483R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197211	NM_001199324.2(ZNF615):c.1460G>A (p.Arg487Gln)	ZNF615 (R476Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258926	NM_001199324.2(ZNF615):c.1411G>A (p.Glu471Lys)	ZNF615 (E460K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328443	NM_001199324.2(ZNF615):c.1408A>C (p.Thr470Pro)	ZNF615 (T466P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222482	NM_001199324.2(ZNF615):c.1376G>A (p.Arg459Gln)	ZNF615 (R464Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258922	NM_001199324.2(ZNF615):c.1327G>A (p.Glu443Lys)	ZNF615 (E437K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258928	NM_001199324.2(ZNF615):c.1177A>T (p.Thr393Ser)	ZNF615 (T389S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249695	NM_001199324.2(ZNF615):c.1177A>G (p.Thr393Ala)	ZNF615 (T382A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592354	NM_001199324.2(ZNF615):c.1152A>G (p.Ile384Met)	ZNF615 (I380M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541960	NM_001199324.2(ZNF615):c.1150A>G (p.Ile384Val)	ZNF615 (I373V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197210	NM_001199324.2(ZNF615):c.1120C>T (p.His374Tyr)	ZNF615 (H368Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390322	NM_001199324.2(ZNF615):c.1082G>A (p.Gly361Glu)	ZNF615 (G350E +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589569	NM_001199324.2(ZNF615):c.1009T>G (p.Ser337Ala)	ZNF615 (S331A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467524	NM_001199324.2(ZNF615):c.989G>A (p.Ser330Asn)	ZNF615 (S319N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348739	NM_001199324.2(ZNF615):c.956G>A (p.Arg319Gln)	ZNF615 (R315Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390282	NM_001199324.2(ZNF615):c.920C>G (p.Ala307Gly)	ZNF615 (A301G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613449	NM_001199324.2(ZNF615):c.807A>C (p.Lys269Asn)	ZNF615 (K258N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258927	NM_001199324.2(ZNF615):c.736A>T (p.Ser246Cys)	ZNF615 (S235C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550523	NM_001199324.2(ZNF615):c.652A>C (p.Ser218Arg)	ZNF615 (S207R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258924	NM_001199324.2(ZNF615):c.641C>T (p.Ala214Val)	ZNF615 (A219V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377123	NM_001199324.2(ZNF615):c.623C>T (p.Thr208Ile)	ZNF615 (T202I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264984	NM_001199324.2(ZNF615):c.494A>G (p.Asn165Ser)	ZNF615 (N170S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484164	NM_001199324.2(ZNF615):c.305A>T (p.His102Leu)	ZNF615 (H102L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297190	NM_001199324.2(ZNF615):c.106G>A (p.Val36Met)	ZNF615 (V32M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197214	NM_001199324.2(ZNF615):c.28C>G (p.Leu10Val)	ZNF615 (L15V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2684892	GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3	ACP4, ADM5 +261 more	Copy number gain	not provided	GLikely pathogenic
Select item 1526670	GRCh37/hg19 19q13.33-13.41(chr19:49911081-53127438)	FPR3, ZNF577 +115 more	Copy number gain	not specified	GLikely pathogenic
Select item 980768	GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3	PPP1R15A, PPP2R1A +308 more	Copy number gain	not provided	GPathogenic
Select item 972980	GRCh37/hg19 19q13.32-13.42(chr19:47939842-54626871)	GRIN2D, GRWD1 +228 more	Copy number gain	not provided	Gnot provided
Select item 816084	GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3	C5AR1, C5AR2 +293 more	Copy number gain	not provided	GPathogenic
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	PGLYRP1, PGLYRP2 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	TMC4, TMED1 +1364 more	Copy number gain	See cases	GPathogenic
Select item 394342	GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3	A1BG, ACP4 +280 more	Copy number gain	See cases	GPathogenic
Select item 221886	GRCh37/hg19 19q13.41(chr19:52272131-52588718)x3	ZNF613, ZNF614 +8 more	Copy number gain	Premature ovarian failure	GBenign

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: 60