chr10-79256139-C-T

Position:

• chr10-79256139-C-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_020338.4(ZMIZ1):​c.281-21042C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.297 in 152,118 control chromosomes in the GnomAD database, including 7,536 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.30 (7536 hom., cov: 32)
• Consequence: ZMIZ1 NM_020338.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.200

Genes affected

ZMIZ1 (HGNC:16493): (zinc finger MIZ-type containing 1) This gene encodes a member of the PIAS (protein inhibitor of activated STAT) family of proteins. The encoded protein regulates the activity of various transcription factors, including the androgen receptor, Smad3/4, and p53. The encoded protein may also play a role in sumoylation. A translocation between this locus on chromosome 10 and the protein tyrosine kinase ABL1 locus on chromosome 9 has been associated with acute lymphoblastic leukemia. [provided by RefSeq, Mar 2010]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.386 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
ZMIZ1	NM_020338.4	c.281-21042C>T		intron_variant		ENST00000334512.10	NP_065071.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
ZMIZ1	ENST00000334512.10	c.281-21042C>T		intron_variant		5	NM_020338.4	ENSP00000334474	P1
ZMIZ1	ENST00000472035.5	n.70+12401C>T		intron_variant, non_coding_transcript_variant		2

Frequencies

GnomAD3 genomes AF: 0.297 AC: 45166 AN: 151998 Hom.: 7530 Cov.: 32

Gnomad AFR AF: 0.147

Gnomad AMI AF: 0.197

Gnomad AMR AF: 0.304

Gnomad ASJ AF: 0.438

Gnomad EAS AF: 0.193

Gnomad SAS AF: 0.401

Gnomad FIN AF: 0.280

Gnomad MID AF: 0.404

Gnomad NFE AF: 0.383

Gnomad OTH AF: 0.337

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.297 AC: 45187 AN: 152118 Hom.: 7536 Cov.: 32 AF XY: 0.295 AC XY: 21959 AN XY: 74344

Gnomad4 AFR AF: 0.147

Gnomad4 AMR AF: 0.304

Gnomad4 ASJ AF: 0.438

Gnomad4 EAS AF: 0.193

Gnomad4 SAS AF: 0.401

Gnomad4 FIN AF: 0.280

Gnomad4 NFE AF: 0.383

Gnomad4 OTH AF: 0.337

Alfa AF: 0.373 Hom.: 24846

Bravo AF: 0.289

Asia WGS AF: 0.325 AC: 1130 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	9.2
DANN	Benign	0.74

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs11593576; hg19: chr10-81015896;