10-101770141-TAAAAAAAAAAAAAAA-TAAAAAAAAAAAAA
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Variant summary
Our verdict is Benign. Variant got -8 ACMG points: 0P and 8B. BA1
The NM_033163.5(FGF8):c.*186_*187delTT variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0759 in 382,198 control chromosomes in the GnomAD database, including 2 homozygotes. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.
Frequency
Genomes: 𝑓 0.0031 ( 2 hom., cov: 0)
Exomes 𝑓: 0.11 ( 0 hom. )
Consequence
FGF8
NM_033163.5 3_prime_UTR
NM_033163.5 3_prime_UTR
Scores
Not classified
Clinical Significance
Not reported in ClinVar
Conservation
PhyloP100: 0.108
Genes affected
FGF8 (HGNC:3686): (fibroblast growth factor 8) The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein is known to be a factor that supports androgen and anchorage independent growth of mammary tumor cells. Overexpression of this gene has been shown to increase tumor growth and angiogensis. The adult expression of this gene is restricted to testes and ovaries. Temporal and spatial pattern of this gene expression suggests its function as an embryonic epithelial factor. Studies of the mouse and chick homologs revealed roles in midbrain and limb development, organogenesis, embryo gastrulation and left-right axis determination. The alternative splicing of this gene results in four transcript variants. [provided by RefSeq, Jul 2008]
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ACMG classification
Classification made for transcript
Verdict is Benign. Variant got -8 ACMG points.
BA1
GnomAdExome4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.141 is higher than 0.05.
Transcripts
RefSeq
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | TSL | MANE | Protein | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|---|
FGF8 | ENST00000320185 | c.*186_*187delTT | 3_prime_UTR_variant | Exon 6 of 6 | 1 | NM_033163.5 | ENSP00000321797.2 | |||
FGF8 | ENST00000344255 | c.*186_*187delTT | 3_prime_UTR_variant | Exon 6 of 6 | 1 | ENSP00000340039.3 | ||||
FGF8 | ENST00000469792.6 | n.*885_*886delTT | splice_region_variant, non_coding_transcript_exon_variant | Exon 5 of 5 | 5 | ENSP00000473299.1 | ||||
FGF8 | ENST00000469792.6 | n.*885_*886delTT | 3_prime_UTR_variant | Exon 5 of 5 | 5 | ENSP00000473299.1 |
Frequencies
GnomAD3 genomes AF: 0.00312 AC: 377AN: 120762Hom.: 2 Cov.: 0
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GnomAD4 exome AF: 0.110 AC: 28647AN: 261454Hom.: 0 AF XY: 0.111 AC XY: 14898AN XY: 134426
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GnomAD4 genome AF: 0.00313 AC: 378AN: 120744Hom.: 2 Cov.: 0 AF XY: 0.00344 AC XY: 197AN XY: 57194
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Find out detailed SpliceAI scores and Pangolin per-transcript scores at