rs12464423

Variant names:

Your query was ambiguous. Multiple possible variants found:

Variant summary

Our verdict is Benign. The variant received -17 ACMG points: 0P and 17B. BP4_StrongBP6_Very_StrongBP7BS1

The NM_015650.4(TRAF3IP1):c.885G>A(p.Lys295Lys) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000517 in 1,409,386 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).

Frequency

Genomes: 𝑓 0.00023 ( 0 hom., cov: 31)

Exomes 𝑓: 0.00055 ( 0 hom. )

Consequence

TRAF3IP1
NM_015650.4 synonymous

Scores

Clinical Significance

Likely benign criteria provided, multiple submitters, no conflicts B:2

Conservation

PhyloP100: 0.0600

Publications

25 publications found

Variant links:

Genes affected

TRAF3IP1 (HGNC:17861): (TRAF3 interacting protein 1) The protein encoded by this gene interacts with TNF receptor-associated factor 3, tethering it to cytoskeletal microtubules. The encoded protein is also an inhibitor of the innate type I IFN response. Defects in this gene are a cause of Senior-Loken syndrome 9. [provided by RefSeq, Mar 2017]

TRAF3IP1 Gene-Disease associations (from GenCC):

Senior-Loken syndrome 9
Inheritance: AR Classification: DEFINITIVE, STRONG Submitted by: G2P, Labcorp Genetics (formerly Invitae)
Senior-Loken syndrome
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet
short rib-polydactyly syndrome, Majewski type
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

TRAF3IP1 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Benign. The variant received -17 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.61).

BP6

Variant 2-238329312-G-A is Benign according to our data. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-238329312-G-A is described in CliVar as Likely_benign. Clinvar id is 1113790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BP7

Synonymous conserved (PhyloP=0.06 with no splicing effect.

BS1

Variant frequency is greater than expected in population nfe. GnomAdExome4 allele frequency = 0.000552 (694/1257358) while in subpopulation NFE AF = 0.000667 (672/1007726). AF 95% confidence interval is 0.000625. There are 0 homozygotes in GnomAdExome4. There are 335 alleles in the male GnomAdExome4 subpopulation. Median coverage is 36. This position passed quality control check.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TRAF3IP1	NM_015650.4 link	c.885G>A	p.Lys295Lys	synonymous_variant	Exon 5 of 17	ENST00000373327.5	NP_056465.2	Q8TDR0-1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	UniProt
TRAF3IP1	ENST00000373327.5 link	c.885G>A	p.Lys295Lys	synonymous_variant	Exon 5 of 17	1	NM_015650.4	ENSP00000362424.4	Q8TDR0-1
TRAF3IP1	ENST00000391993.7 link	c.885G>A	p.Lys295Lys	synonymous_variant	Exon 5 of 15	1		ENSP00000375851.3	Q8TDR0-2
TRAF3IP1	ENST00000409739.2 link	n.*754G>A		non_coding_transcript_exon_variant	Exon 5 of 5	3		ENSP00000386648.2	H7BZ10
TRAF3IP1	ENST00000409739.2 link	n.*754G>A		3_prime_UTR_variant	Exon 5 of 5	3		ENSP00000386648.2	H7BZ10

Frequencies

GnomAD3 genomes

AF:

0.000230

AC:

AN:

152028

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.000193

Gnomad AMI

AF:

0.00

Gnomad AMR

AF:

0.00

Gnomad ASJ

AF:

0.00

Gnomad EAS

AF:

0.00

Gnomad SAS

AF:

0.00

Gnomad FIN

AF:

0.00

Gnomad MID

AF:

0.00

Gnomad NFE

AF:

0.000397

Gnomad OTH

AF:

0.00

GnomAD2 exomes

AF:

0.000244

AC:

AN:

147800

AF XY:

0.000266

show subpopulations

Gnomad AFR exome

AF:

0.000157

Gnomad AMR exome

AF:

0.00

Gnomad ASJ exome

AF:

0.00

Gnomad EAS exome

AF:

0.00

Gnomad FIN exome

AF:

0.00

Gnomad NFE exome

AF:

0.000445

Gnomad OTH exome

AF:

0.000325

GnomAD4 exome

AF:

0.000552

AC:

694

AN:

1257358

Hom.:

Cov.:

AF XY:

0.000551

AC XY:

335

AN XY:

608150

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

27686

American (AMR)

AF:

0.00

AC:

AN:

22536

Ashkenazi Jewish (ASJ)

AF:

0.0000575

AC:

AN:

17386

East Asian (EAS)

AF:

0.00

AC:

AN:

35222

South Asian (SAS)

AF:

0.00

AC:

AN:

45130

European-Finnish (FIN)

AF:

0.0000220

AC:

AN:

45488

Middle Eastern (MID)

AF:

0.00

AC:

AN:

4942

European-Non Finnish (NFE)

AF:

0.000667

AC:

672

AN:

1007726

Other (OTH)

AF:

0.000390

AC:

AN:

51242

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.480

Heterozygous variant carriers

116

155

194

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Variant carriers

120

150

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

AF:

0.000230

AC:

AN:

152028

Hom.:

Cov.:

AF XY:

0.000175

AC XY:

AN XY:

74238

show subpopulations

African (AFR)

AF:

0.000193

AC:

AN:

41414

American (AMR)

AF:

0.00

AC:

AN:

15248

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

3472

East Asian (EAS)

AF:

0.00

AC:

AN:

5186

South Asian (SAS)

AF:

0.00

AC:

AN:

4826

European-Finnish (FIN)

AF:

0.00

AC:

AN:

10572

Middle Eastern (MID)

AF:

0.00

AC:

AN:

316

European-Non Finnish (NFE)

AF:

0.000397

AC:

AN:

67992

Other (OTH)

AF:

0.00

AC:

AN:

2090

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.492

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Genome Het

Variant carriers

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

Alfa

AF:

0.00000572

Hom.:

16662

ClinVar

Significance: Likely benign

Submissions summary: Benign:2

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not provided

Benign:2

Jan 08, 2025

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Mar 01, 2025

CeGaT Center for Human Genetics Tuebingen

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

TRAF3IP1: BP4, BP7 -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.61

CADD

Benign

6.1

(source)

DANN

Benign

0.49

PhyloP100

0.060

Mutation Taster

=100/0

polymorphism

(source)

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.020

Details are displayed if max score is > 0.2

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

Publications

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over