Variant #0000570738 (NC_000021.8:g.44589243C>T, NM_000394.2:c.34C>T (CRYAA))

Chromosome 21
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.44589243C>T
DNA change (hg38) g.43169133C>T
Published as CRYAA(NM_000394.2):c.34C>T (p.(Arg12Cys)), CRYAA(NM_000394.4):c.34C>T (p.R12C)
ISCN -
DB-ID CRYAA_000002 See all 18 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +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     
CRYAA NM_000394.2 +/. - c.34C>T r.(?) p.(Arg12Cys)


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