Variant #0001025903 (NC_000011.9:g.111782442T>C, NM_001885.1:c.7A>G (CRYAB))

Chromosome 11
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.111782442T>C
DNA change (hg38) -
Published as CRYAB(NM_001885.2):c.7A>G (p.I3V), CRYAB(NM_001885.3):c.7A>G (p.I3V)
ISCN -
DB-ID CRYAB_000044 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-02-07 18:57:27 +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     
HSPB2 NM_001541.3 ?/. - c.-1112T>C r.(?) p.(=)
CRYAB NM_001885.1 ?/. - c.7A>G r.(?) p.(Ile3Val)


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