Variant #0000982385 (NC_000017.10:g.27579138_27579140del, NM_005208.4:c.272_274del (CRYBA1))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.27579138_27579140del
DNA change (hg38) -
Published as CRYBA1(NM_005208.4):c.272_274delGAG (p.(Gly91del))
ISCN -
DB-ID CRYBA1_000003 See all 26 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) Retrieve
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 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYBA1 NM_005208.4 +/. - c.272_274del r.(?) p.(Gly91del)
NUFIP2 NM_020772.2 +/. - c.*12420_*12422del r.(=) p.(=)


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