rs7799265

Variant names:

• chr7-28392857-C-G
• rs7799265
• ENST00000396299.6:c.-25+93416C>G

Your query was ambiguous. Multiple possible variants found:

• chr7-28392857-C-G
• chr7-28392857-C-T

Variant summary

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

The ENST00000396299.6(CREB5):​c.-25+93416C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0789 in 152,222 control chromosomes in the GnomAD database, including 521 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 0.079 (521 hom., cov: 32)
• Consequence: CREB5 ENST00000396299.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.447
• Publications: 2 publications found

Genes affected

CREB5 (HGNC:16844): (cAMP responsive element binding protein 5) The product of this gene belongs to the CRE (cAMP response element)-binding protein family. Members of this family contain zinc-finger and bZIP DNA-binding domains. The encoded protein specifically binds to CRE as a homodimer or a heterodimer with c-Jun or CRE-BP1, and functions as a CRE-dependent trans-activator. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

ACMG classification

Our verdict: Benign. The variant received -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 = 0.129 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CREB5	NM_182899.5	c.-25+93416C>G		intron_variant	Intron 1 of 9		NP_878902.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CREB5	ENST00000396299.6	c.-25+93416C>G		intron_variant	Intron 1 of 9	1		ENSP00000379593.2

Frequencies

GnomAD3 genomes AF: 0.0789 AC: 12004 AN: 152104 Hom.: 521 Cov.: 32

Gnomad AFR AF: 0.102

Gnomad AMI AF: 0.0406

Gnomad AMR AF: 0.0850

Gnomad ASJ AF: 0.0988

Gnomad EAS AF: 0.00231

Gnomad SAS AF: 0.137

Gnomad FIN AF: 0.0805

Gnomad MID AF: 0.117

Gnomad NFE AF: 0.0647

Gnomad OTH AF: 0.0688

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

GnomAD4 genome AF: 0.0789 AC: 12014 AN: 152222 Hom.: 521 Cov.: 32 AF XY: 0.0807 AC XY: 6004 AN XY: 74410

African (AFR) AF: 0.102 AC: 4237 AN: 41532

American (AMR) AF: 0.0848 AC: 1296 AN: 15278

Ashkenazi Jewish (ASJ) AF: 0.0988 AC: 343 AN: 3472

East Asian (EAS) AF: 0.00251 AC: 13 AN: 5188

South Asian (SAS) AF: 0.138 AC: 664 AN: 4822

European-Finnish (FIN) AF: 0.0805 AC: 852 AN: 10586

Middle Eastern (MID) AF: 0.0986 AC: 29 AN: 294

European-Non Finnish (NFE) AF: 0.0647 AC: 4399 AN: 68022

Other (OTH) AF: 0.0681 AC: 144 AN: 2116

Alfa AF: 0.0357 Hom.: 30

Bravo AF: 0.0788

Asia WGS AF: 0.0670 AC: 232 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	0.29
DANN	Benign	0.47
PhyloP100		-0.45
Mutation Taster		=100/0	polymorphism (auto)

Splicing

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

Other links and lift over

dbSNP: rs7799265; hg19: chr7-28432476;