Variant #0000267141 (NC_000022.10:g.27021457T>C, CRYBA4(NM_001886.2):c.171T>C)

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27021457T>C
DNA change (hg38) g.26625493T>C
Published as CRYBA4(NM_001886.3):c.171T>C (p.F57=)
ISCN -
DB-ID CRYBA4_000015 See all 4 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) 0.89557 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYBA4 NM_001886.2 -/. - c.171T>C r.(?) p.(Phe57=)