rs151344495
Variant summary
Our verdict is Pathogenic. Variant got 10 ACMG points: 10P and 0B. PS1_ModeratePM1PM2PP3_Strong
The NM_000397.4(CYBB):c.1025T>A(p.Leu342Gln) 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 ClinVar as not provided (no stars). Another nucleotide change resulting in same amino acid change has been previously reported as Likely pathogenicin UniProt. Synonymous variant affecting the same amino acid position (i.e. L342L) has been classified as Likely benign.
Frequency
Consequence
NM_000397.4 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Pathogenic. Variant got 10 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
CYBB | NM_000397.4 | c.1025T>A | p.Leu342Gln | missense_variant | 9/13 | ENST00000378588.5 | |
CYBB | XM_047441855.1 | c.719T>A | p.Leu240Gln | missense_variant | 8/12 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
CYBB | ENST00000378588.5 | c.1025T>A | p.Leu342Gln | missense_variant | 9/13 | 1 | NM_000397.4 | P1 | |
CYBB | ENST00000696171.1 | c.929T>A | p.Leu310Gln | missense_variant | 8/12 | ||||
CYBB | ENST00000492288.1 | n.450T>A | non_coding_transcript_exon_variant | 4/4 | 3 | ||||
CYBB | ENST00000696170.1 | c.*534T>A | 3_prime_UTR_variant, NMD_transcript_variant | 8/12 |
Frequencies
GnomAD3 genomes ? Cov.: 22
GnomAD4 exome Cov.: 31
GnomAD4 genome ? Cov.: 22
ClinVar
Submissions by phenotype
not provided Other:1
not provided, no classification provided | literature only | UniProtKB/Swiss-Prot | - | - - |
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at