Variant #0000718494 (NC_000002.11:g.219855100T>C, NM_057093.1:c.468A>G (CRYBA2))

Chromosome 2
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.219855100T>C
DNA change (hg38) -
Published as CRYBA2(NM_057093.2):c.468A>G (p.P156=)
ISCN -
DB-ID CRYBA2_000006
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) 0.00066 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FEV NM_017521.2 -?/. - c.-5303A>G r.(?) p.(=)
CRYBA2 NM_057093.1 -?/. - c.468A>G r.(?) p.(Pro156=)


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