rs10201348

chr2-179651355-A-G

Variant summary

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

The NM_152520.6(ZNF385B):c.299-106386T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.217 in 152,074 control chromosomes in the GnomAD database, including 5,116 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 0.22 (5116 hom., cov: 32)
• Consequence: ZNF385B NM_152520.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.492

Genes affected

ZNF385B (HGNC:26332): (zinc finger protein 385B) Enables p53 binding activity. Involved in intrinsic apoptotic signaling pathway by p53 class mediator. Located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.8).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.434 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
ZNF385B	NM_152520.6	c.299-106386T>C		intron_variant		ENST00000410066.7

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
ZNF385B	ENST00000410066.7	c.299-106386T>C		intron_variant		1	NM_152520.6	P1
ZNF385B	ENST00000409343.5	c.25+94358T>C		intron_variant		2
ZNF385B	ENST00000463918.1	n.106+8722T>C		intron_variant, non_coding_transcript_variant		3
ZNF385B	ENST00000475539.5	n.142+94358T>C		intron_variant, non_coding_transcript_variant		4

Frequencies

GnomAD3 genomes AF: 0.217 AC: 33019 AN: 151956 Hom.: 5116 Cov.: 32

Gnomad AFR AF: 0.439

Gnomad AMI AF: 0.292

Gnomad AMR AF: 0.187

Gnomad ASJ AF: 0.156

Gnomad EAS AF: 0.152

Gnomad SAS AF: 0.0928

Gnomad FIN AF: 0.0714

Gnomad MID AF: 0.161

Gnomad NFE AF: 0.129

Gnomad OTH AF: 0.193

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

GnomAD4 genome AF: 0.217 AC: 33045 AN: 152074 Hom.: 5116 Cov.: 32 AF XY: 0.213 AC XY: 15827 AN XY: 74360

Gnomad4 AFR AF: 0.439

Gnomad4 AMR AF: 0.186

Gnomad4 ASJ AF: 0.156

Gnomad4 EAS AF: 0.152

Gnomad4 SAS AF: 0.0929

Gnomad4 FIN AF: 0.0714

Gnomad4 NFE AF: 0.129

Gnomad4 OTH AF: 0.190

Alfa AF: 0.164 Hom.: 577

Bravo AF: 0.240

Asia WGS AF: 0.148 AC: 513 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.80
Cadd	Benign	5.1
Dann	Benign	0.78

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: rs10201348; hg19: chr2-180516082;