dbSNP rs369210475: FANCE:c.1510-9T>C (chr6-35466235-T-C) – ACMG Classification: Likely_benign (-4 pts)

Variant summary

Our verdict is Likely benign. The variant received -4 ACMG points: 2P and 6B. PM2BP4_StrongBP6_Moderate

The NM_021922.3(FANCE):c.1510-9T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000000698 in 1,432,882 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: not found (cov: 32)

Exomes 𝑓: 7.0e-7 ( 0 hom. )

Consequence

FANCE
NM_021922.3 intron

Scores

Splicing: ADA: 0.00007299

Clinical Significance

Likely benign criteria provided, single submitter B:1

Conservation

PhyloP100: 0.240

Publications

0 publications found

Variant links:

Genes affected

FANCE (HGNC:3586): (FA complementation group E) The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group E. [provided by RefSeq, Jul 2008]

FANCE Gene-Disease associations (from GenCC):

Fanconi anemia complementation group E
Inheritance: AR Classification: DEFINITIVE, STRONG Submitted by: Labcorp Genetics (formerly Invitae), ClinGen, G2P
Fanconi anemia
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

FANCE links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Likely_benign. The variant received -4 ACMG points.

PM2

Very rare variant in population databases, with high coverage;

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.55).

BP6

Variant 6-35466235-T-C is Benign according to our data. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-35466235-T-C is described in CliVar as Likely_benign. Clinvar id is 414824.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
FANCE	NM_021922.3 link	c.1510-9T>C		intron_variant	Intron 9 of 9	ENST00000229769.3	NP_068741.1	Q9HB96

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
FANCE	ENST00000229769.3 link	c.1510-9T>C		intron_variant	Intron 9 of 9	1	NM_021922.3	ENSP00000229769.2		Q9HB96

Frequencies

GnomAD3 genomes

Cov.:

GnomAD4 exome

AF:

6.98e-7

AC:

AN:

1432882

Hom.:

Cov.:

AF XY:

0.00000140

AC XY:

AN XY:

714940

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

32908

American (AMR)

AF:

0.00

AC:

AN:

44690

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

25936

East Asian (EAS)

AF:

0.00

AC:

AN:

39580

South Asian (SAS)

AF:

0.00

AC:

AN:

85684

European-Finnish (FIN)

AF:

0.00

AC:

AN:

53396

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5706

European-Non Finnish (NFE)

AF:

0.00

AC:

AN:

1085528

Other (OTH)

AF:

0.0000168

AC:

AN:

59454

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.525

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

Cov.:

Alfa

AF:

0.00

Hom.:

Asia WGS

AF:

0.000289

AC:

AN:

3478

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

LINK: link

Submissions by phenotype

Fanconi anemia complementation group E

Benign:1

Apr 11, 2024

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.55

CADD

Benign

(source)

DANN

Benign

0.62

PhyloP100

0.24

Splicing

Name

Calibrated prediction

Score

Prediction

dbscSNV1_ADA

Benign

0.000073

dbscSNV1_RF

Benign

0.0020

SpliceAI score (max)

0.010

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

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over