18-905124-A-C
Variant summary
Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2BP4_Strong
The ENST00000579794.1(ADCYAP1):c.-263A>C variant causes a 5 prime UTR change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.
Frequency
Consequence
ENST00000579794.1 5_prime_UTR
Scores
Clinical Significance
Conservation
Publications
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ACMG classification
Our verdict: Likely_benign. The variant received -2 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: ENST00000579794.1. You can select a different transcript below to see updated ACMG assignments.
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| ADCYAP1 | TSL:1 | c.-263A>C | 5_prime_UTR | Exon 1 of 4 | ENSP00000462647.1 | P18509 | |||
| ADCYAP1 | TSL:1 MANE Select | c.-2+64A>C | intron | N/A | ENSP00000411658.3 | P18509 | |||
| ADCYAP1 | c.-263A>C | 5_prime_UTR | Exon 1 of 3 | ENSP00000631567.1 |
Frequencies
GnomAD3 genomes Cov.: 33
GnomAD4 exome Cov.: 56
GnomAD4 genome Cov.: 33
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at