Variant chr16-22534089-G-C details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Likely benign. Variant got -4 ACMG points: 0P and 4B. BP4_Strong

The NM_001395849.1(NPIPB5):c.1106G>C(p.Arg369Pro) variant causes a missense change involving the alteration of a non-conserved nucleotide. In-silico tool predicts a benign outcome for this variant. 13/17 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).

Frequency

Genomes: 𝑓 0.00055 ( 0 hom., cov: 8)

Exomes 𝑓: 0.000097 ( 0 hom. )

Failed GnomAD Quality Control

Consequence

NPIPB5
NM_001395849.1 missense

Scores

Clinical Significance

Uncertain significance criteria provided, single submitter U:1

Conservation

PhyloP100: -1.91

Variant links:

Genes affected

NPIPB5 (HGNC:37233): (nuclear pore complex interacting protein family member B5) Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

NPIPB5 links:

LOC105371131 (HGNC:):

LOC105371131 links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Likely_benign. Variant got -4 ACMG points.

BP4

Computational evidence support a benign effect (MetaRNN=0.03210807).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
NPIPB5	NM_001395849.1 linkuse as main transcript	c.1106G>C	p.Arg369Pro	missense_variant	7/7	ENST00000424340.7
LOC105371131	XR_007065022.1 linkuse as main transcript	n.150+3389C>G		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
NPIPB5	ENST00000424340.7 linkuse as main transcript	c.1106G>C	p.Arg369Pro	missense_variant	7/7	1	NM_001395849.1	P1

Frequencies

GnomAD3 genomes

AF:

0.00

AC:

AN:

52528

Hom.:

Cov.:

FAILED QC

Gnomad AFR

AF:

0.00152

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:

0.000365

Gnomad MID

AF:

0.00

Gnomad NFE

AF:

0.000123

Gnomad OTH

AF:

0.00139

GnomAD3 exomes

AF:

0.0000487

AC:

AN:

41102

Hom.:

AF XY:

0.00

AC XY:

AN XY:

20844

show subpopulations

Gnomad AFR exome

AF:

0.000254

Gnomad AMR exome

AF:

0.00

Gnomad ASJ exome

AF:

0.00

Gnomad EAS exome

AF:

0.00

Gnomad SAS exome

AF:

0.00

Gnomad FIN exome

AF:

0.00

Gnomad NFE exome

AF:

0.0000648

Gnomad OTH exome

AF:

0.00

GnomAD4 exome

Data not reliable, filtered out with message: AS_VQSR

AF:

0.0000973

AC:

102

AN:

1048388

Hom.:

Cov.:

AF XY:

0.000107

AC XY:

AN XY:

534612

show subpopulations

Gnomad4 AFR exome

AF:

0.000554

Gnomad4 AMR exome

AF:

0.00

Gnomad4 ASJ exome

AF:

0.00

Gnomad4 EAS exome

AF:

0.0000840

Gnomad4 SAS exome

AF:

0.000371

Gnomad4 FIN exome

AF:

0.0000277

Gnomad4 NFE exome

AF:

0.0000632

Gnomad4 OTH exome

AF:

0.000107

GnomAD4 genome

Data not reliable, filtered out with message: AS_VQSR

AF:

0.000552

AC:

AN:

52580

Hom.:

Cov.:

AF XY:

0.000672

AC XY:

AN XY:

25282

show subpopulations

Gnomad4 AFR

AF:

0.00152

Gnomad4 AMR

AF:

0.00

Gnomad4 ASJ

AF:

0.00

Gnomad4 EAS

AF:

0.00

Gnomad4 SAS

AF:

0.00

Gnomad4 FIN

AF:

0.000365

Gnomad4 NFE

AF:

0.000123

Gnomad4 OTH

AF:

0.00137

ExAC

AF:

0.0000644

AC:

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

LINK: link

Submissions by phenotype

not specified

Uncertain:1

Uncertain significance, criteria provided, single submitter

clinical testing

Ambry Genetics

Jul 14, 2023

The c.1106G>C (p.R369P) alteration is located in exon 7 (coding exon 7) of the NPIPB5 gene. This alteration results from a G to C substitution at nucleotide position 1106, causing the arginine (R) at amino acid position 369 to be replaced by a proline (P). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Benign

0.21

BayesDel_addAF

Benign

-0.42

BayesDel_noAF

Benign

-0.55

CADD

Benign

0.55

DANN

Benign

0.82

Eigen

Benign

-1.5

Eigen_PC

Benign

-1.5

FATHMM_MKL

Benign

0.026

M_CAP

Benign

0.0025

MetaRNN

Benign

0.032

T;T;T;T;T;T

MetaSVM

Benign

-0.95

MutationTaster

Benign

1.0

N;N

PROVEAN

Benign

3.2

N;.;N;N;N;.

REVEL

Benign

0.097

Sift

Benign

0.94

T;.;T;T;T;.

Sift4G

Benign

0.34

T;T;T;T;T;T

Polyphen

0.011

.;.;B;B;.;.

Vest4

0.14, 0.14, 0.15, 0.13

MutPred

0.20

Gain of methylation at K367 (P = 0.0454);Gain of methylation at K367 (P = 0.0454);Gain of methylation at K367 (P = 0.0454);Gain of methylation at K367 (P = 0.0454);Gain of methylation at K367 (P = 0.0454);.;

MVP

0.067

ClinPred

0.0079

Varity_R

0.12

gMVP

0.0036

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

Publications

LitVar

Below is the list of publications found by LitVar. It may be empty.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

LitVar

Other links and lift over