ZBTB8OS[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2664871	GRCh38/hg38 1p36.33-35.1(chr1:99125-34026935)x3	LOC129929105, LOC129929106 +2149 more	Copy number gain	Trisomy 12p	GPathogenic
Select item 149963	GRCh38/hg38 1p36.11-34.2(chr1:24381206-41401517)x3	LOC129929733, LOC129929734 +1145 more	Copy number gain	See cases	GPathogenic
Select item 146124	GRCh38/hg38 1p35.3-35.1(chr1:28424867-33122854)x1	LOC129929998, LOC129929999 +293 more	Copy number loss	See cases	GPathogenic
Select item 59931	GRCh38/hg38 1p35.2-35.1(chr1:30766758-33359428)x1	A3GALT2, ADGRB2 +214 more	Copy number loss	See cases	GPathogenic
Select item 2593105	NM_178547.5(ZBTB8OS):c.476C>T (p.Pro159Leu)	ZBTB8OS (P114L +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3192222	NM_178547.5(ZBTB8OS):c.457G>A (p.Val153Ile)	ZBTB8OS (G140D +12 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3192221	NM_178547.5(ZBTB8OS):c.398C>T (p.Ser133Leu)	ZBTB8OS (S157L +8 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3192220	NM_178547.5(ZBTB8OS):c.293A>G (p.Tyr98Cys)	ZBTB8OS (Y62C +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2281083	NM_178547.5(ZBTB8OS):c.232G>A (p.Val78Ile)	ZBTB8OS (V83I +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2397221	NM_178547.5(ZBTB8OS):c.220C>G (p.Gln74Glu)	ZBTB8OS (Q17E +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2406640	NM_178547.5(ZBTB8OS):c.217C>T (p.Leu73Phe)	ZBTB8OS (L16F +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2555305	NM_178547.5(ZBTB8OS):c.158T>C (p.Phe53Ser)	ZBTB8OS (F13S +4 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2685410	GRCh37/hg19 1p35.1(chr1:33099109-33528691)x1	HPCA, AK2 +9 more	Copy number loss	not provided	GUncertain significance
Select item 814067	GRCh37/hg19 1p35.2-35.1(chr1:30819875-34380419)x3	TMEM54, RBBP4 +51 more	Copy number gain	not provided	GLikely pathogenic
Select item 635767	GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3	ANGPTL7, C1orf127 +783 more	Copy number gain	Intellectual disability, mild +1 more	GUncertain significance
Select item 625764	GRCh37/hg19 1p35.1-34.3(chr1:32859415-36454915)	YARS1, ZBTB8A +41 more	Copy number loss	not provided	GPathogenic
Select item 442387	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)	BCAS2, CNTN2 +2014 more	Copy number gain	See cases	GPathogenic
Select item 442386	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3	FAM76A, FAM78B +2014 more	Copy number gain	See cases	GPathogenic