Variant 2-162174974-G-T details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_ModerateBP6_Very_StrongBS2

The NM_004460.5(FAP):c.1870-8C>A variant causes a splice region, intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00452 in 1,591,836 control chromosomes in the GnomAD database, including 36 homozygotes. In-silico tool predicts a benign outcome for this variant. 2/3 splice prediction tools predict no significant impact on normal splicing. Variant has been reported in ClinVar as Benign (★★).

Frequency

Genomes: 𝑓 0.0025 ( 2 hom., cov: 32)

Exomes 𝑓: 0.0047 ( 34 hom. )

Consequence

FAP
NM_004460.5 splice_region, intron

Scores

Splicing: ADA: 0.5620

Clinical Significance

Benign criteria provided, multiple submitters, no conflicts B:2

Conservation

PhyloP100: 1.99

Variant links:

Genes affected

FAP (HGNC:3590): (fibroblast activation protein alpha) The protein encoded by this gene is a homodimeric integral membrane gelatinase belonging to the serine protease family. It is selectively expressed in reactive stromal fibroblasts of epithelial cancers, granulation tissue of healing wounds, and malignant cells of bone and soft tissue sarcomas. This protein is thought to be involved in the control of fibroblast growth or epithelial-mesenchymal interactions during development, tissue repair, and epithelial carcinogenesis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2014]

FAP links:

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ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -14 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.25).

BP6

Variant 2-162174974-G-T is Benign according to our data. Variant chr2-162174974-G-T is described in ClinVar as [Benign]. Clinvar id is 711802.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BS2

High Homozygotes in GnomAd4 at 2 AR gene

Transcripts

RefSeq

Gene	Transcript	HGVSc	Effect	MANE	Protein	UniProt
FAP	NM_004460.5 link	c.1870-8C>A	splice_region_variant, intron_variant	ENST00000188790.9	NP_004451.2	Q12884-1
FAP	NM_001291807.3 link	c.1795-8C>A	splice_region_variant, intron_variant		NP_001278736.1	Q12884B4DLR2
FAP	XM_011510796.4 link	c.1840-8C>A	splice_region_variant, intron_variant		XP_011509098.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
FAP	ENST00000188790.9 link	c.1870-8C>A		splice_region_variant, intron_variant		1	NM_004460.5	ENSP00000188790.4		Q12884-1

Frequencies

GnomAD3 genomes

AF:

0.00245

AC:

373

AN:

152080

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.000893

Gnomad AMI

AF:

0.00

Gnomad AMR

AF:

0.00177

Gnomad ASJ

AF:

0.00433

Gnomad EAS

AF:

0.000386

Gnomad SAS

AF:

0.00726

Gnomad FIN

AF:

0.00104

Gnomad MID

AF:

0.00316

Gnomad NFE

AF:

0.00351

Gnomad OTH

AF:

0.00287

GnomAD3 exomes

AF:

0.00388

AC:

967

AN:

248944

Hom.:

AF XY:

0.00433

AC XY:

582

AN XY:

134498

show subpopulations

Gnomad AFR exome

AF:

0.000927

Gnomad AMR exome

AF:

0.00179

Gnomad ASJ exome

AF:

0.00682

Gnomad EAS exome

AF:

0.00

Gnomad SAS exome

AF:

0.0100

Gnomad FIN exome

AF:

0.000742

Gnomad NFE exome

AF:

0.00426

Gnomad OTH exome

AF:

0.00396

GnomAD4 exome

AF:

0.00474

AC:

6820

AN:

1439638

Hom.:

Cov.:

AF XY:

0.00490

AC XY:

3518

AN XY:

717528

show subpopulations

Gnomad4 AFR exome

AF:

0.000639

Gnomad4 AMR exome

AF:

0.00169

Gnomad4 ASJ exome

AF:

0.00657

Gnomad4 EAS exome

AF:

0.00

Gnomad4 SAS exome

AF:

0.0100

Gnomad4 FIN exome

AF:

0.00101

Gnomad4 NFE exome

AF:

0.00495

Gnomad4 OTH exome

AF:

0.00361

GnomAD4 genome

AF:

0.00245

AC:

373

AN:

152198

Hom.:

Cov.:

AF XY:

0.00228

AC XY:

170

AN XY:

74416

show subpopulations

Gnomad4 AFR

AF:

0.000890

Gnomad4 AMR

AF:

0.00177

Gnomad4 ASJ

AF:

0.00433

Gnomad4 EAS

AF:

0.000387

Gnomad4 SAS

AF:

0.00726

Gnomad4 FIN

AF:

0.00104

Gnomad4 NFE

AF:

0.00351

Gnomad4 OTH

AF:

0.00284

Alfa

AF:

0.00326

Hom.:

Bravo

AF:

0.00230

Asia WGS

AF:

0.00289

AC:

AN:

3478

ClinVar

Significance: Benign

Submissions summary: Benign:2

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not provided

Benign:2

Benign, criteria provided, single submitter	not provided	Breakthrough Genomics, Breakthrough Genomics	-	- -
Benign, criteria provided, single submitter	clinical testing	Labcorp Genetics (formerly Invitae), Labcorp	May 30, 2018	- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.25

CADD

Benign

DANN

Benign

0.92

Splicing

Name

Calibrated prediction

Score

Prediction

dbscSNV1_ADA

Benign

0.56

dbscSNV1_RF

Benign

0.44

SpliceAI score (max)

0.51

Details are displayed if max score is > 0.2

DS_AL_spliceai

0.51

Position offset: -8

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