19-57678391-T-C
Variant summary
Our verdict is Likely benign. Variant got -2 ACMG points: 2P and 4B. PM2BP4_Strong
The NM_152677.4(ZSCAN4):c.788T>C(p.Phe263Ser) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0000657 in 1,613,988 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. 14/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).
Frequency
Consequence
NM_152677.4 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Likely_benign. Variant got -2 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
ZSCAN4 | NM_152677.4 | c.788T>C | p.Phe263Ser | missense_variant | 5/5 | ENST00000318203.9 | |
ZSCAN4 | NM_001384833.1 | c.788T>C | p.Phe263Ser | missense_variant | 7/7 | ||
ZSCAN4 | XM_017026458.1 | c.788T>C | p.Phe263Ser | missense_variant | 5/5 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
ZSCAN4 | ENST00000318203.9 | c.788T>C | p.Phe263Ser | missense_variant | 5/5 | 2 | NM_152677.4 | P1 |
Frequencies
GnomAD3 genomes ? AF: 0.0000855 AC: 13AN: 152110Hom.: 0 Cov.: 32
GnomAD3 exomes AF: 0.0000716 AC: 18AN: 251364Hom.: 0 AF XY: 0.0000589 AC XY: 8AN XY: 135852
GnomAD4 exome AF: 0.0000636 AC: 93AN: 1461878Hom.: 0 Cov.: 31 AF XY: 0.0000633 AC XY: 46AN XY: 727236
GnomAD4 genome ? AF: 0.0000855 AC: 13AN: 152110Hom.: 0 Cov.: 32 AF XY: 0.0000807 AC XY: 6AN XY: 74308
ClinVar
Submissions by phenotype
not specified Uncertain:1
Uncertain significance, criteria provided, single submitter | clinical testing | Ambry Genetics | Sep 30, 2021 | The c.788T>C (p.F263S) alteration is located in exon 5 (coding exon 3) of the ZSCAN4 gene. This alteration results from a T to C substitution at nucleotide position 788, causing the phenylalanine (F) at amino acid position 263 to be replaced by a serine (S). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. - |
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at