Variant #0000274449 (NC_000022.10:g.27026324C>T, CRYBA4(NM_001886.2):c.464C>T)

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.27026324C>T
DNA change (hg38) g.26630360C>T
Published as CRYBA4(NM_001886.2):c.464C>T (p.P155L)
ISCN -
DB-ID CRYBA4_000016 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) 1.0E-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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYBA4 NM_001886.2 ?/. - c.464C>T r.(?) p.(Pro155Leu)