22-26601647-A-ATGTGGATAAACCATTCACCGTGTCGTACTAAGCTTGAGTTCTAACTAACATCAAGTAAGGATTGACTTCGAGAATTACTAGTGGTTACGAATTGTGACGGACAAGGACAGGGAGACACCAACAGAGACCCGGGAATCACTGAGGTATATTTTGTCCCTATCAGGTTCAGGGACAACCCGTCTCACCAACGGGATACAGTCGGACACACAGACTCCATCCCACCTCCCGTACGGGTCACCTGTATTCTAGGTGCGTCGAGCAAACGAGAATCAGAGGGGGGGAAACAGTTCGGACGTTTTCCAAGGTCAGTAGGACATAAGACTCGGTAAGGCTCT
Variant summary
Our verdict is Uncertain significance. Variant got 2 ACMG points: 2P and 0B. PM2
The NM_001887.4(CRYBB1):c.575+231_575+232insAGAGCCTTACCGAGTCTTATGTCCTACTGACCTTGGAAAACGTCCGAACTGTTTCCCCCCCTCTGATTCTCGTTTGCTCGACGCACCTAGAATACAGGTGACCCGTACGGGAGGTGGGATGGAGTCTGTGTGTCCGACTGTATCCCGTTGGTGAGACGGGTTGTCCCTGAACCTGATAGGGACAAAATATACCTCAGTGATTCCCGGGTCTCTGTTGGTGTCTCCCTGTCCTTGTCCGTCACAATTCGTAACCACTAGTAATTCTCGAAGTCAATCCTTACTTGATGTTAGTTAGAACTCAAGCTTAGTACGACACGGTGAATGGTTTATCCACA variant causes a intron 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 Uncertain significance (no stars).
Frequency
Consequence
NM_001887.4 intron
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Uncertain_significance. Variant got 2 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | Protein | UniProt |
---|---|---|---|---|---|---|---|---|
CRYBB1 | NM_001887.4 | c.575+231_575+232insAGAGCCTTACCGAGTCTTATGTCCTACTGACCTTGGAAAACGTCCGAACTGTTTCCCCCCCTCTGATTCTCGTTTGCTCGACGCACCTAGAATACAGGTGACCCGTACGGGAGGTGGGATGGAGTCTGTGTGTCCGACTGTATCCCGTTGGTGAGACGGGTTGTCCCTGAACCTGATAGGGACAAAATATACCTCAGTGATTCCCGGGTCTCTGTTGGTGTCTCCCTGTCCTTGTCCGTCACAATTCGTAACCACTAGTAATTCTCGAAGTCAATCCTTACTTGATGTTAGTTAGAACTCAAGCTTAGTACGACACGGTGAATGGTTTATCCACA | intron_variant | ENST00000647684.1 | NP_001878.1 | |||
CRYBA4 | XM_006724140.4 | c.-239+4564_-239+4565insTGTGGATAAACCATTCACCGTGTCGTACTAAGCTTGAGTTCTAACTAACATCAAGTAAGGATTGACTTCGAGAATTACTAGTGGTTACGAATTGTGACGGACAAGGACAGGGAGACACCAACAGAGACCCGGGAATCACTGAGGTATATTTTGTCCCTATCAGGTTCAGGGACAACCCGTCTCACCAACGGGATACAGTCGGACACACAGACTCCATCCCACCTCCCGTACGGGTCACCTGTATTCTAGGTGCGTCGAGCAAACGAGAATCAGAGGGGGGGAAACAGTTCGGACGTTTTCCAAGGTCAGTAGGACATAAGACTCGGTAAGGCTCT | intron_variant | XP_006724203.1 | ||||
CRYBB1 | XM_011529899.4 | c.575+231_575+232insAGAGCCTTACCGAGTCTTATGTCCTACTGACCTTGGAAAACGTCCGAACTGTTTCCCCCCCTCTGATTCTCGTTTGCTCGACGCACCTAGAATACAGGTGACCCGTACGGGAGGTGGGATGGAGTCTGTGTGTCCGACTGTATCCCGTTGGTGAGACGGGTTGTCCCTGAACCTGATAGGGACAAAATATACCTCAGTGATTCCCGGGTCTCTGTTGGTGTCTCCCTGTCCTTGTCCGTCACAATTCGTAACCACTAGTAATTCTCGAAGTCAATCCTTACTTGATGTTAGTTAGAACTCAAGCTTAGTACGACACGGTGAATGGTTTATCCACA | intron_variant | XP_011528201.1 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Protein | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|---|
CRYBB1 | ENST00000647684.1 | c.575+231_575+232insAGAGCCTTACCGAGTCTTATGTCCTACTGACCTTGGAAAACGTCCGAACTGTTTCCCCCCCTCTGATTCTCGTTTGCTCGACGCACCTAGAATACAGGTGACCCGTACGGGAGGTGGGATGGAGTCTGTGTGTCCGACTGTATCCCGTTGGTGAGACGGGTTGTCCCTGAACCTGATAGGGACAAAATATACCTCAGTGATTCCCGGGTCTCTGTTGGTGTCTCCCTGTCCTTGTCCGTCACAATTCGTAACCACTAGTAATTCTCGAAGTCAATCCTTACTTGATGTTAGTTAGAACTCAAGCTTAGTACGACACGGTGAATGGTTTATCCACA | intron_variant | NM_001887.4 | ENSP00000497249 | P1 | ||||
ENST00000668614.1 | n.56+4564_56+4565insTGTGGATAAACCATTCACCGTGTCGTACTAAGCTTGAGTTCTAACTAACATCAAGTAAGGATTGACTTCGAGAATTACTAGTGGTTACGAATTGTGACGGACAAGGACAGGGAGACACCAACAGAGACCCGGGAATCACTGAGGTATATTTTGTCCCTATCAGGTTCAGGGACAACCCGTCTCACCAACGGGATACAGTCGGACACACAGACTCCATCCCACCTCCCGTACGGGTCACCTGTATTCTAGGTGCGTCGAGCAAACGAGAATCAGAGGGGGGGAAACAGTTCGGACGTTTTCCAAGGTCAGTAGGACATAAGACTCGGTAAGGCTCT | intron_variant, non_coding_transcript_variant |
Frequencies
GnomAD3 genomes Cov.: 30
GnomAD4 genome Cov.: 30
ClinVar
Submissions by phenotype
Schizophrenia Uncertain:1
Uncertain significance, no assertion criteria provided | case-control | Department of Psychiatry, The University of Hong Kong | Nov 11, 2022 | - - |
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at
Publications
No publications associated with this variant yet.