9-32972742-C-T
Variant summary
Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_StrongBP6_Very_StrongBS1BS2
The NM_001195248.2(APTX):c.*756G>A variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00212 in 454,068 control chromosomes in the GnomAD database, including 6 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).
Frequency
Consequence
NM_001195248.2 3_prime_UTR
Scores
Clinical Significance
Conservation
Genome browser will be placed here
ACMG classification
Verdict is Benign. Variant got -20 ACMG points.
Transcripts
RefSeq
Ensembl
Frequencies
GnomAD3 genomes AF: 0.00511 AC: 778AN: 152174Hom.: 5 Cov.: 32
GnomAD3 exomes AF: 0.000974 AC: 127AN: 130420Hom.: 0 AF XY: 0.000843 AC XY: 60AN XY: 71188
GnomAD4 exome AF: 0.000616 AC: 186AN: 301776Hom.: 1 Cov.: 0 AF XY: 0.000448 AC XY: 77AN XY: 171982
GnomAD4 genome AF: 0.00511 AC: 778AN: 152292Hom.: 5 Cov.: 32 AF XY: 0.00500 AC XY: 372AN XY: 74472
ClinVar
Submissions by phenotype
Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia Benign:1
This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease. -
not provided Benign:1
- -
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at