X-147912049-C-CGCGGCGGCG

Position:

• chrX-147912049-C-CGCGGCGGCG

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP6_Moderate BA1

The NM_002024.6(FMR1):​c.-108_-100dup variant causes a 5 prime UTR change involving the alteration of a non-conserved nucleotide. Variant has been reported in ClinVar as Benign (★).

• Frequency:
  • Genomes: 𝑓 0.10 (118 hom., 774 hem., cov: 2)
  • Exomes 𝑓: 0.045 (9 hom. 186 hem.)
  • Failed GnomAD Quality Control
• Consequence: FMR1 NM_002024.6 5_prime_UTR
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 0.618

Genes affected

FMR1 (HGNC:3775): (fragile X messenger ribonucleoprotein 1) The protein encoded by this gene binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm. A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome. Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1). Multiple alternatively spliced transcript variants that encode different protein isoforms and which are located in different cellular locations have been described for this gene. [provided by RefSeq, May 2010]

ACMG classification

Verdict is Benign. Variant got -10 ACMG points.

• BP6: Variant X-147912049-C-CGCGGCGGCG is Benign according to our data. Variant chrX-147912049-C-CGCGGCGGCG is described in ClinVar as [Benign]. Clinvar id is 763962.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.136 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
FMR1	NM_002024.6	c.-108_-100dup		5_prime_UTR_variant	1/17	ENST00000370475.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
FMR1	ENST00000370475.9	c.-108_-100dup		5_prime_UTR_variant	1/17	1	NM_002024.6	P3

Frequencies

GnomAD3 genomes AF: 0.103 AC: 3603 AN: 35043 Hom.: 117 Cov.: 2 AF XY: 0.134 AC XY: 774 AN XY: 5791

Gnomad AFR AF: 0.0426

Gnomad AMI AF: 0.0447

Gnomad AMR AF: 0.0693

Gnomad ASJ AF: 0.0778

Gnomad EAS AF: 0.0141

Gnomad SAS AF: 0.0728

Gnomad FIN AF: 0.181

Gnomad MID AF: 0.0580

Gnomad NFE AF: 0.140

Gnomad OTH AF: 0.0989

GnomAD4 exome Data not reliable, filtered out with message: AS_VQSR AF: 0.0452 AC: 281 AN: 6216 Hom.: 9 Cov.: 0 AF XY: 0.0561 AC XY: 186 AN XY: 3316

Gnomad4 AFR exome AF: 0.0303

Gnomad4 AMR exome AF: 0.00

Gnomad4 ASJ exome AF: 0.0313

Gnomad4 EAS exome AF: 0.167

Gnomad4 SAS exome AF: 0.00

Gnomad4 FIN exome AF: 0.00

Gnomad4 NFE exome AF: 0.0455

Gnomad4 OTH exome AF: 0.0765

GnomAD4 genome AF: 0.103 AC: 3605 AN: 35041 Hom.: 118 Cov.: 2 AF XY: 0.134 AC XY: 774 AN XY: 5795

Gnomad4 AFR AF: 0.0427

Gnomad4 AMR AF: 0.0692

Gnomad4 ASJ AF: 0.0778

Gnomad4 EAS AF: 0.0141

Gnomad4 SAS AF: 0.0729

Gnomad4 FIN AF: 0.181

Gnomad4 NFE AF: 0.140

Gnomad4 OTH AF: 0.0985

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

Labcorp Genetics (formerly Invitae), Labcorp

Dec 31, 2019

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Computational scores

Source: dbNSFP v4.3

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs193922936; hg19: chrX-146993567;