chr12-130349232-C-T
Variant summary
Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_StrongBP6_ModerateBS1BS2
The NM_004764.5(PIWIL1):c.735-7C>T variant causes a splice region, splice polypyrimidine tract, intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0125 in 1,609,448 control chromosomes in the GnomAD database, including 159 homozygotes. In-silico tool predicts a benign outcome for this variant. 3/3 splice prediction tools predict no significant impact on normal splicing. Variant has been reported in ClinVar as Benign (★).
Frequency
Consequence
NM_004764.5 splice_region, splice_polypyrimidine_tract, intron
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Benign. Variant got -14 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
PIWIL1 | NM_004764.5 | c.735-7C>T | splice_region_variant, splice_polypyrimidine_tract_variant, intron_variant | ENST00000245255.7 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
PIWIL1 | ENST00000245255.7 | c.735-7C>T | splice_region_variant, splice_polypyrimidine_tract_variant, intron_variant | 1 | NM_004764.5 | P1 | |||
PIWIL1 | ENST00000540672.2 | n.992-7C>T | splice_region_variant, splice_polypyrimidine_tract_variant, intron_variant, non_coding_transcript_variant | 4 |
Frequencies
GnomAD3 genomes ? AF: 0.00972 AC: 1479AN: 152174Hom.: 9 Cov.: 33
GnomAD3 exomes AF: 0.00948 AC: 2382AN: 251302Hom.: 19 AF XY: 0.00953 AC XY: 1295AN XY: 135828
GnomAD4 exome AF: 0.0128 AC: 18679AN: 1457156Hom.: 150 Cov.: 31 AF XY: 0.0125 AC XY: 9085AN XY: 724030
GnomAD4 genome ? AF: 0.00971 AC: 1479AN: 152292Hom.: 9 Cov.: 33 AF XY: 0.00927 AC XY: 690AN XY: 74472
ClinVar
Submissions by phenotype
PIWIL1-related disorder Benign:1
Benign, criteria provided, single submitter | clinical testing | PreventionGenetics, part of Exact Sciences | Feb 25, 2019 | This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). - |
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at