chr1-8714392-T-C

Position:

• chr1-8714392-T-C

Variant summary

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

The NM_001042681.2(RERE):​c.-144-57951A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.223 in 152,116 control chromosomes in the GnomAD database, including 4,682 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 (4682 hom., cov: 31)
• Consequence: RERE NM_001042681.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0340

Genes affected

RERE (HGNC:9965): (arginine-glutamic acid dipeptide repeats) This gene encodes a member of the atrophin family of arginine-glutamic acid (RE) dipeptide repeat-containing proteins. The encoded protein co-localizes with a transcription factor in the nucleus, and its overexpression triggers apoptosis. A similar protein in mouse associates with histone deacetylase and is thought to function as a transcriptional co-repressor during embryonic development. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.307 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
RERE	NM_001042681.2	c.-144-57951A>G		intron_variant		ENST00000400908.7
RERE	NM_012102.4	c.-144-57951A>G		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
RERE	ENST00000400908.7	c.-144-57951A>G		intron_variant		1	NM_001042681.2	P1

Frequencies

GnomAD3 genomes AF: 0.223 AC: 33856 AN: 151998 Hom.: 4682 Cov.: 31

Gnomad AFR AF: 0.0833

Gnomad AMI AF: 0.370

Gnomad AMR AF: 0.183

Gnomad ASJ AF: 0.180

Gnomad EAS AF: 0.0652

Gnomad SAS AF: 0.201

Gnomad FIN AF: 0.352

Gnomad MID AF: 0.237

Gnomad NFE AF: 0.311

Gnomad OTH AF: 0.211

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

GnomAD4 genome AF: 0.223 AC: 33855 AN: 152116 Hom.: 4682 Cov.: 31 AF XY: 0.222 AC XY: 16483 AN XY: 74352

Gnomad4 AFR AF: 0.0831

Gnomad4 AMR AF: 0.183

Gnomad4 ASJ AF: 0.180

Gnomad4 EAS AF: 0.0658

Gnomad4 SAS AF: 0.200

Gnomad4 FIN AF: 0.352

Gnomad4 NFE AF: 0.311

Gnomad4 OTH AF: 0.211

Alfa AF: 0.282 Hom.: 8351

Bravo AF: 0.204

Asia WGS AF: 0.160 AC: 558 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.96
DANN	Benign	0.29

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs953043; hg19: chr1-8774451;