chr2-233682323-AT-GG
Variant summary
Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2BP6_Moderate
The NM_019077.3(UGT1A7):c.386_387delinsGG(p.Asn129Arg) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Likely benign (★). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. N129K) has been classified as Benign.
Frequency
Consequence
NM_019077.3 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Uncertain_significance. Variant got 0 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
UGT1A7 | NM_019077.3 | c.386_387delinsGG | p.Asn129Arg | missense_variant | 1/5 | ENST00000373426.4 | |
UGT1A10 | NM_019075.4 | c.855+44946_855+44947delinsGG | intron_variant | ENST00000344644.10 | |||
UGT1A8 | NM_019076.5 | c.855+63761_855+63762delinsGG | intron_variant | ENST00000373450.5 | |||
UGT1A9 | NM_021027.3 | c.855+9534_855+9535delinsGG | intron_variant | ENST00000354728.5 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
UGT1A7 | ENST00000373426.4 | c.386_387delinsGG | p.Asn129Arg | missense_variant | 1/5 | 1 | NM_019077.3 | P1 | |
UGT1A10 | ENST00000344644.10 | c.855+44946_855+44947delinsGG | intron_variant | 1 | NM_019075.4 | P1 | |||
UGT1A9 | ENST00000354728.5 | c.855+9534_855+9535delinsGG | intron_variant | 1 | NM_021027.3 | P1 | |||
UGT1A8 | ENST00000373450.5 | c.855+63761_855+63762delinsGG | intron_variant | 1 | NM_019076.5 | P1 |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD4 genome Cov.: 32
ClinVar
Submissions by phenotype
not provided Benign:1
Likely benign, criteria provided, single submitter | clinical testing | ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories | Nov 30, 2023 | - - |
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at
Publications
No publications associated with this variant yet.