16-23608057-T-C

Variant names:

Variant summary

Our verdict is Likely benign. The variant received -5 ACMG points: 0P and 5B. BP4_StrongBP6

The NM_024675.4(PALB2):c.3202-45A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0000208 in 1,587,370 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 (no stars).

Frequency

Genomes: 𝑓 0.000020 ( 0 hom., cov: 31)

Exomes 𝑓: 0.000021 ( 0 hom. )

Consequence

PALB2
NM_024675.4 intron

Scores

Clinical Significance

Likely benign no assertion criteria provided B:1

Conservation

PhyloP100: -1.96

Publications

1 publications found

Variant links:

Genes affected

PALB2 (HGNC:26144): (partner and localizer of BRCA2) This gene encodes a protein that may function in tumor suppression. This protein binds to and colocalizes with the breast cancer 2 early onset protein (BRCA2) in nuclear foci and likely permits the stable intranuclear localization and accumulation of BRCA2. [provided by RefSeq, Jul 2008]

PALB2 Gene-Disease associations (from GenCC):

hereditary breast carcinoma
Inheritance: AD Classification: DEFINITIVE Submitted by: ClinGen, Ambry Genetics
Fanconi anemia complementation group N
Inheritance: AR Classification: DEFINITIVE, STRONG Submitted by: G2P, Labcorp Genetics (formerly Invitae), ClinGen, Ambry Genetics
pancreatic cancer, susceptibility to, 3
Inheritance: AD Classification: STRONG Submitted by: Genomics England PanelApp, Labcorp Genetics (formerly Invitae)
familial ovarian cancer
Inheritance: AD Classification: MODERATE Submitted by: ClinGen
Fanconi anemia
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet
hereditary nonpolyposis colon cancer
Inheritance: AD Classification: LIMITED Submitted by: ClinGen

PALB2 links:

ENSG00000261723 (HGNC:58305):

ENSG00000261723 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Likely_benign. The variant received -5 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.83).

BP6

Variant 16-23608057-T-C is Benign according to our data. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-23608057-T-C is described in CliVar as Likely_benign. Clinvar id is 126724.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PALB2	NM_024675.4 link	c.3202-45A>G		intron_variant	Intron 11 of 12	ENST00000261584.9	NP_078951.2	Q86YC2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PALB2	ENST00000261584.9 link	c.3202-45A>G		intron_variant	Intron 11 of 12	1	NM_024675.4	ENSP00000261584.4		Q86YC2

Frequencies

GnomAD3 genomes

AF:

0.0000198

AC:

AN:

151826

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.00

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:

0.0000441

Gnomad OTH

AF:

0.00

GnomAD2 exomes

AF:

0.0000243

AC:

AN:

246982

AF XY:

0.0000149

show subpopulations

Gnomad AFR exome

AF:

0.00

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:

0.0000539

Gnomad OTH exome

AF:

0.00

GnomAD4 exome

AF:

0.0000209

AC:

AN:

1435544

Hom.:

Cov.:

AF XY:

0.0000238

AC XY:

AN XY:

715582

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

32856

American (AMR)

AF:

0.00

AC:

AN:

44448

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

25934

East Asian (EAS)

AF:

0.00

AC:

AN:

39554

South Asian (SAS)

AF:

0.00

AC:

AN:

85594

European-Finnish (FIN)

AF:

0.00

AC:

AN:

53298

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5722

European-Non Finnish (NFE)

AF:

0.0000248

AC:

AN:

1088556

Other (OTH)

AF:

0.0000504

AC:

AN:

59582

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.520

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome 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

GnomAD4 genome

AF:

0.0000198

AC:

AN:

151826

Hom.:

Cov.:

AF XY:

0.0000135

AC XY:

AN XY:

74142

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

41294

American (AMR)

AF:

0.00

AC:

AN:

15236

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

3472

East Asian (EAS)

AF:

0.00

AC:

AN:

5184

South Asian (SAS)

AF:

0.00

AC:

AN:

4806

European-Finnish (FIN)

AF:

0.00

AC:

AN:

10542

Middle Eastern (MID)

AF:

0.00

AC:

AN:

316

European-Non Finnish (NFE)

AF:

0.0000441

AC:

AN:

67970

Other (OTH)

AF:

0.00

AC:

AN:

2094

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.575

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:

0.00

Hom.:

Bravo

AF:

0.0000453

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: no assertion criteria provided

LINK: link

Submissions by phenotype

Familial cancer of breast

Benign:1

May 13, 2019

Leiden Open Variation Database

Significance:Likely benign

Review Status:no assertion criteria provided

Collection Method:curation

Curators: Marc Tischkowitz, Arleen D. Auerbach. Submitter to LOVD: Marc Tischkowitz. -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.83

CADD

Benign

0.051

(source)

DANN

Benign

0.51

PhyloP100

-2.0

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

You must be logged in to view publications. This limit was set because tens of millions (!) of queries from AI bots are generated daily.

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