Variant #0000984144 (NC_000022.10:g.25603127G>A, NM_004076.3:c.584G>A (CRYBB3))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.25603127G>A
DNA change (hg38) -
Published as CRYBB3(NM_004076.4):c.584G>A (p.R195H), CRYBB3(NM_004076.5):c.584G>A (p.(Arg195His))
ISCN -
DB-ID CRYBB3_000019 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00016 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYBB3 NM_004076.3 ?/. - c.584G>A r.(?) p.(Arg195His)


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