Variant #0000658909 (NC_000022.10:g.25597435C>T, NM_004076.3:c.72C>T (CRYBB3))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.25597435C>T
DNA change (hg38) g.25201468C>T
Published as CRYBB3(NM_004076.4):c.72C>T (p.Y24=)
ISCN -
DB-ID KIAA1671_000005
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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA1671 NM_001145206.1 -?/. - c.*9067C>T r.(=) p.(=)
CRYBB3 NM_004076.3 -?/. - c.72C>T r.(?) p.(Tyr24=)


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