4-69588571-A-T
Variant summary
Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2BP4_Strong
The NM_001105677.2(UGT2A2):c.*801T>A variant causes a 3 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
NM_001105677.2 3_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: NM_001105677.2. You can select a different transcript below to see updated ACMG assignments.
RefSeq Transcripts
| Selected | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| UGT2A2 | NM_001105677.2 | MANE Select | c.*801T>A | 3_prime_UTR | Exon 6 of 6 | NP_001099147.2 | |||
| UGT2A1 | NM_001252275.3 | MANE Select | c.*801T>A | 3_prime_UTR | Exon 7 of 7 | NP_001239204.2 | |||
| UGT2A1 | NM_001389565.1 | c.*801T>A | 3_prime_UTR | Exon 8 of 8 | NP_001376494.1 |
Ensembl Transcripts
| Selected | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| UGT2A2 | ENST00000604629.6 | TSL:1 MANE Select | c.*801T>A | 3_prime_UTR | Exon 6 of 6 | ENSP00000475028.2 | |||
| UGT2A1 | ENST00000286604.9 | TSL:1 MANE Select | c.*801T>A | 3_prime_UTR | Exon 7 of 7 | ENSP00000286604.4 | |||
| UGT2A1 | ENST00000503640.5 | TSL:1 | c.*801T>A | 3_prime_UTR | Exon 6 of 6 | ENSP00000424478.1 |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD4 exome Cov.: 0
GnomAD4 genome Cov.: 32
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at