rs1515274

Variant names:

• chr2-179627905-A-G
• rs1515274
• NM_152520.6:c.299-82936T>C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_152520.6(ZNF385B):​c.299-82936T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.154 in 152,098 control chromosomes in the GnomAD database, including 1,951 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 0.15 (1951 hom., cov: 32)
• Consequence: ZNF385B NM_152520.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0820
• Publications: 6 publications found

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

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.238 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ZNF385B	NM_152520.6	c.299-82936T>C		intron_variant	Intron 3 of 9	ENST00000410066.7	NP_689733.4

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ZNF385B	ENST00000410066.7	c.299-82936T>C		intron_variant	Intron 3 of 9	1	NM_152520.6	ENSP00000386845.2

Frequencies

GnomAD3 genomes AF: 0.154 AC: 23411 AN: 151980 Hom.: 1948 Cov.: 32

Gnomad AFR AF: 0.126

Gnomad AMI AF: 0.0702

Gnomad AMR AF: 0.232

Gnomad ASJ AF: 0.198

Gnomad EAS AF: 0.249

Gnomad SAS AF: 0.154

Gnomad FIN AF: 0.146

Gnomad MID AF: 0.241

Gnomad NFE AF: 0.146

Gnomad OTH AF: 0.165

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

GnomAD4 genome AF: 0.154 AC: 23433 AN: 152098 Hom.: 1951 Cov.: 32 AF XY: 0.156 AC XY: 11617 AN XY: 74346

African (AFR) AF: 0.126 AC: 5233 AN: 41510

American (AMR) AF: 0.232 AC: 3543 AN: 15260

Ashkenazi Jewish (ASJ) AF: 0.198 AC: 686 AN: 3472

East Asian (EAS) AF: 0.249 AC: 1284 AN: 5160

South Asian (SAS) AF: 0.155 AC: 745 AN: 4816

European-Finnish (FIN) AF: 0.146 AC: 1547 AN: 10580

Middle Eastern (MID) AF: 0.241 AC: 71 AN: 294

European-Non Finnish (NFE) AF: 0.146 AC: 9913 AN: 67980

Other (OTH) AF: 0.164 AC: 347 AN: 2114

Alfa AF: 0.156 Hom.: 3258

Bravo AF: 0.162

Asia WGS AF: 0.218 AC: 754 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	4.3
DANN	Benign	0.62
PhyloP100		0.082
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs1515274; hg19: chr2-180492632;