rs104886257
Variant summary
Our verdict is Likely pathogenic. Variant got 9 ACMG points: 9P and 0B. PM2PM5PP3_StrongPP5
The NM_033380.3(COL4A5):c.3826G>A(p.Gly1276Ser) variant causes a missense change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. Variant has been reported in Lovd as Pathogenic (no stars). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. G1276D) has been classified as Pathogenic.
Frequency
Consequence
NM_033380.3 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Likely_pathogenic. Variant got 9 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
COL4A5 | NM_033380.3 | c.3826G>A | p.Gly1276Ser | missense_variant | 44/53 | ENST00000328300.11 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
COL4A5 | ENST00000328300.11 | c.3826G>A | p.Gly1276Ser | missense_variant | 44/53 | 1 | NM_033380.3 | ||
COL4A5 | ENST00000361603.7 | c.3808G>A | p.Gly1270Ser | missense_variant | 42/51 | 2 | P1 | ||
COL4A5 | ENST00000489230.1 | n.229G>A | non_coding_transcript_exon_variant | 3/8 | 5 | ||||
COL4A5 | ENST00000510690.2 | n.320G>A | non_coding_transcript_exon_variant | 2/11 | 4 |
Frequencies
GnomAD3 genomes ? Cov.: 23
GnomAD4 exome Cov.: 29
GnomAD4 genome ? Cov.: 23
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at