6-37370573-A-T

Variant names:

• chr6-37370573-A-T
• rs195382
• NM_003958.4:c.976-939A>T

Variant summary

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

The NM_003958.4(RNF8):​c.976-939A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.134 in 152,104 control chromosomes in the GnomAD database, including 4,090 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 0.13 (4090 hom., cov: 32)
• Consequence: RNF8 NM_003958.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.00200
• Publications: 2 publications found

Genes affected

RNF8 (HGNC:10071): (ring finger protein 8) The protein encoded by this gene contains a RING finger motif and an FHA domain. This protein has been shown to interact with several class II ubiquitin-conjugating enzymes (E2), including UBE2E1/UBCH6, UBE2E2, and UBE2E3, and may act as an ubiquitin ligase (E3) in the ubiquitination of certain nuclear proteins. This protein is also known to play a role in the DNA damage response and depletion of this protein causes cell growth inhibition and cell cycle arrest. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.429 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_003958.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	RNF8	NM_003958.4	MANE Select	c.976-939A>T		intron	N/A	NP_003949.1
	RNF8	NM_183078.3		c.976-939A>T		intron	N/A	NP_898901.1
	RNF8	NR_046399.2		n.1264-939A>T		intron	N/A

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	RNF8	ENST00000373479.9	TSL:1 MANE Select	c.976-939A>T		intron	N/A	ENSP00000362578.4
	RNF8	ENST00000469731.5	TSL:5	c.976-939A>T		intron	N/A	ENSP00000418879.1
	RNF8	ENST00000498460.1	TSL:3	c.343-939A>T		intron	N/A	ENSP00000417599.1

Frequencies

GnomAD3 genomes AF: 0.134 AC: 20373 AN: 151986 Hom.: 4071 Cov.: 32

Gnomad AFR AF: 0.434

Gnomad AMI AF: 0.00219

Gnomad AMR AF: 0.0665

Gnomad ASJ AF: 0.0358

Gnomad EAS AF: 0.0897

Gnomad SAS AF: 0.0533

Gnomad FIN AF: 0.000378

Gnomad MID AF: 0.0506

Gnomad NFE AF: 0.00472

Gnomad OTH AF: 0.107

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

GnomAD4 genome AF: 0.134 AC: 20436 AN: 152104 Hom.: 4090 Cov.: 32 AF XY: 0.132 AC XY: 9818 AN XY: 74366

African (AFR) AF: 0.435 AC: 18006 AN: 41430

American (AMR) AF: 0.0668 AC: 1021 AN: 15284

Ashkenazi Jewish (ASJ) AF: 0.0358 AC: 124 AN: 3468

East Asian (EAS) AF: 0.0895 AC: 463 AN: 5172

South Asian (SAS) AF: 0.0527 AC: 254 AN: 4822

European-Finnish (FIN) AF: 0.000378 AC: 4 AN: 10594

Middle Eastern (MID) AF: 0.0578 AC: 17 AN: 294

European-Non Finnish (NFE) AF: 0.00472 AC: 321 AN: 68018

Other (OTH) AF: 0.106 AC: 224 AN: 2110

Alfa AF: 0.0801 Hom.: 307

Bravo AF: 0.154

Asia WGS AF: 0.0900 AC: 313 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	2.6
DANN	Benign	0.43
PhyloP100		-0.0020
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: rs195382; hg19: chr6-37338349;