NM_025228.4:c.703-2804G>A

Variant names:

• chr1-209770144-G-A
• rs11119344
• NM_025228.4:c.703-2804G>A

Variant summary

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

The NM_025228.4(TRAF3IP3):​c.703-2804G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.179 in 152,168 control chromosomes in the GnomAD database, including 2,830 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 0.18 (2830 hom., cov: 33)
• Consequence: TRAF3IP3 NM_025228.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.323
• Publications: 6 publications found

Genes affected

TRAF3IP3 (HGNC:30766): (TRAF3 interacting protein 3) The gene encodes a protein that mediates cell growth by modulating the c-Jun N-terminal kinase signal transduction pathway. The encoded protein may also interact with a large multi-protein assembly containing the phosphatase 2A catalytic subunit. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.23 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_025228.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TRAF3IP3	NM_025228.4	MANE Select	c.703-2804G>A		intron	N/A	NP_079504.2
	TRAF3IP3	NM_001320143.2		c.703-2804G>A		intron	N/A	NP_001307072.1
	TRAF3IP3	NM_001320144.2		c.643-2804G>A		intron	N/A	NP_001307073.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TRAF3IP3	ENST00000367025.8	TSL:1 MANE Select	c.703-2804G>A		intron	N/A	ENSP00000355992.3
	TRAF3IP3	ENST00000367026.7	TSL:1	c.643-2804G>A		intron	N/A	ENSP00000355993.3
	TRAF3IP3	ENST00000478359.5	TSL:1	n.703-2804G>A		intron	N/A	ENSP00000417665.1

Frequencies

GnomAD3 genomes AF: 0.179 AC: 27210 AN: 152050 Hom.: 2832 Cov.: 33

Gnomad AFR AF: 0.0787

Gnomad AMI AF: 0.220

Gnomad AMR AF: 0.169

Gnomad ASJ AF: 0.239

Gnomad EAS AF: 0.0945

Gnomad SAS AF: 0.158

Gnomad FIN AF: 0.265

Gnomad MID AF: 0.228

Gnomad NFE AF: 0.233

Gnomad OTH AF: 0.194

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

GnomAD4 genome AF: 0.179 AC: 27209 AN: 152168 Hom.: 2830 Cov.: 33 AF XY: 0.179 AC XY: 13305 AN XY: 74366

African (AFR) AF: 0.0787 AC: 3269 AN: 41538

American (AMR) AF: 0.168 AC: 2569 AN: 15282

Ashkenazi Jewish (ASJ) AF: 0.239 AC: 830 AN: 3468

East Asian (EAS) AF: 0.0940 AC: 487 AN: 5182

South Asian (SAS) AF: 0.159 AC: 765 AN: 4816

European-Finnish (FIN) AF: 0.265 AC: 2799 AN: 10570

Middle Eastern (MID) AF: 0.238 AC: 70 AN: 294

European-Non Finnish (NFE) AF: 0.233 AC: 15816 AN: 67998

Other (OTH) AF: 0.191 AC: 403 AN: 2108

Alfa AF: 0.217 Hom.: 6164

Bravo AF: 0.167

Asia WGS AF: 0.116 AC: 405 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	9.5
DANN	Benign	0.72
PhyloP100		0.32
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: rs11119344; hg19: chr1-209943489;