chr2-233689021-C-T
Variant summary
Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2BP4_Strong
The NM_019075.4(UGT1A10):c.855+51644C>T variant causes a intron 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_019075.4 intron
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_019075.4. 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 |
|---|---|---|---|---|---|---|---|---|---|
| UGT1A10 | NM_019075.4 | MANE Select | c.855+51644C>T | intron | N/A | NP_061948.1 | |||
| UGT1A8 | NM_019076.5 | MANE Select | c.855+70459C>T | intron | N/A | NP_061949.3 | |||
| UGT1A7 | NM_019077.3 | MANE Select | c.855+6229C>T | intron | N/A | NP_061950.2 |
Ensembl Transcripts
| Selected | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| UGT1A10 | ENST00000344644.10 | TSL:1 MANE Select | c.855+51644C>T | intron | N/A | ENSP00000343838.5 | |||
| UGT1A9 | ENST00000354728.5 | TSL:1 MANE Select | c.855+16232C>T | intron | N/A | ENSP00000346768.4 | |||
| UGT1A7 | ENST00000373426.4 | TSL:1 MANE Select | c.855+6229C>T | intron | N/A | ENSP00000362525.3 |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD4 genome Cov.: 32
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at