Variant #0000274443 (NC_000011.9:g.111782430G>A, NM_001885.1:c.19C>T (CRYAB))

Chromosome 11
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.111782430G>A
DNA change (hg38) g.111911706G>A
Published as CRYAB(NM_001885.2):c.19C>T (p.H7Y), CRYAB(NM_001885.3):c.19C>T (p.H7Y)
ISCN -
DB-ID CRYAB_000043 See all 3 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSPB2 NM_001541.3 -?/. - c.-1124G>A r.(?) p.(=)
CRYAB NM_001885.1 -?/. - c.19C>T r.(?) p.(His7Tyr)


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