"Ambry Genetics"[submitter] AND "ZBTB25"[gene] - ClinVar

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

Search results

Items: 48

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1951427	NM_005956.4(MTHFD1):c.2347G>A (p.Val783Met)	MTHFD1, ZBTB25 (V783M)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3215065	NM_005956.4(MTHFD1):c.2470G>A (p.Asp824Asn)	MTHFD1, ZBTB25 (D824N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2208635	NM_004857.3(AKAP5):c.28G>A (p.Val10Ile)	AKAP5, ZBTB25 (V10I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541951	NM_004857.3(AKAP5):c.48G>C (p.Lys16Asn)	AKAP5, ZBTB25 (K16N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2308049	NM_004857.3(AKAP5):c.124A>C (p.Lys42Gln)	AKAP5, ZBTB25 (K42Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106049	NM_004857.3(AKAP5):c.136G>T (p.Ala46Ser)	AKAP5, ZBTB25 (A46S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221567	NM_004857.3(AKAP5):c.167C>T (p.Ala56Val)	AKAP5, ZBTB25 (A56V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2203965	NM_004857.3(AKAP5):c.227G>T (p.Arg76Leu)	AKAP5, ZBTB25 (R76L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106052	NM_004857.3(AKAP5):c.232G>T (p.Ala78Ser)	AKAP5, ZBTB25 (A78S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542341	NM_004857.3(AKAP5):c.272G>T (p.Arg91Met)	AKAP5, ZBTB25 (R91M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106055	NM_004857.3(AKAP5):c.286A>C (p.Lys96Gln)	AKAP5, ZBTB25 (K96Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2479858	NM_004857.3(AKAP5):c.319C>T (p.Pro107Ser)	AKAP5, ZBTB25 (P107S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213110	NM_004857.3(AKAP5):c.383C>T (p.Pro128Leu)	AKAP5, ZBTB25 (P128L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607583	NM_004857.3(AKAP5):c.497A>C (p.Gln166Pro)	AKAP5, ZBTB25 (Q166P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254311	NM_004857.3(AKAP5):c.498G>C (p.Gln166His)	AKAP5, ZBTB25 (Q166H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330526	NM_004857.3(AKAP5):c.517G>C (p.Ala173Pro)	AKAP5, ZBTB25 (A173P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278760	NM_004857.3(AKAP5):c.628A>T (p.Ile210Phe)	AKAP5, ZBTB25 (I210F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609059	NM_004857.3(AKAP5):c.659A>C (p.His220Pro)	AKAP5, ZBTB25 (H220P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296483	NM_004857.3(AKAP5):c.749T>C (p.Leu250Pro)	AKAP5, ZBTB25 (L250P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526201	NM_004857.3(AKAP5):c.772C>G (p.Gln258Glu)	AKAP5, ZBTB25 (Q258E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466174	NM_004857.3(AKAP5):c.842G>A (p.Ser281Asn)	AKAP5, ZBTB25 (S281N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481156	NM_004857.3(AKAP5):c.976A>C (p.Lys326Gln)	AKAP5, ZBTB25 (K326Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106036	NM_004857.3(AKAP5):c.1003A>G (p.Met335Val)	AKAP5, ZBTB25 (M335V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471336	NM_004857.3(AKAP5):c.1117G>A (p.Val373Ile)	AKAP5, ZBTB25 (V373I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404789	NM_004857.3(AKAP5):c.1135G>A (p.Gly379Ser)	AKAP5, ZBTB25 (G379S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533217	NM_004857.3(AKAP5):c.1171C>T (p.Leu391Phe)	AKAP5, ZBTB25 (L391F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3191968	NM_006977.5(ZBTB25):c.1015T>C (p.Cys339Arg)	ZBTB25 (C339R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3191975	NM_006977.5(ZBTB25):c.995C>A (p.Thr332Lys)	ZBTB25 (T332K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2515615	NM_006977.5(ZBTB25):c.973G>C (p.Val325Leu)	ZBTB25 (V364L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615940	NM_006977.5(ZBTB25):c.941G>A (p.Arg314Gln)	ZBTB25 (R314Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362066	NM_006977.5(ZBTB25):c.940C>T (p.Arg314Trp)	ZBTB25 (R314W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3191974	NM_006977.5(ZBTB25):c.884G>A (p.Arg295His)	ZBTB25 (R334H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2364875	NM_006977.5(ZBTB25):c.881G>A (p.Cys294Tyr)	ZBTB25 (C294Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3191973	NM_006977.5(ZBTB25):c.851C>G (p.Pro284Arg)	ZBTB25 (P284R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340120	NM_006977.5(ZBTB25):c.802G>A (p.Gly268Ser)	ZBTB25 (G307S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208292	NM_006977.5(ZBTB25):c.717A>C (p.Leu239Phe)	ZBTB25 (L278F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2464442	NM_006977.5(ZBTB25):c.621A>T (p.Arg207Ser)	ZBTB25 (R246S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239327	NM_006977.5(ZBTB25):c.614A>T (p.Gln205Leu)	ZBTB25 (Q244L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471859	NM_006977.5(ZBTB25):c.604T>G (p.Ser202Ala)	ZBTB25 (S202A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3191971	NM_006977.5(ZBTB25):c.575C>T (p.Ala192Val)	ZBTB25 (A231V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459733	NM_006977.5(ZBTB25):c.520A>G (p.Ile174Val)	ZBTB25 (I174V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2542824	NM_006977.5(ZBTB25):c.494A>G (p.His165Arg)	ZBTB25 (H204R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3191970	NM_006977.5(ZBTB25):c.281G>A (p.Arg94His)	ZBTB25 (R133H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2410666	NM_006977.5(ZBTB25):c.240G>A (p.Met80Ile)	ZBTB25 (M119I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359025	NM_006977.5(ZBTB25):c.235A>G (p.Ile79Val)	ZBTB25 (I118V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349353	NM_006977.5(ZBTB25):c.88A>G (p.Ile30Val)	ZBTB25 (I69V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191972	NM_006977.5(ZBTB25):c.76T>C (p.Cys26Arg)	ZBTB25 (C26R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191969	NM_006977.5(ZBTB25):c.11C>T (p.Ala4Val)	ZBTB25 (A4V +1 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: 48