Variant #0000862290 (NC_000011.9:g.111779556C>T, NM_001885.1:c.460G>A (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.111779556C>T
DNA change (hg38) -
Published as CRYAB(NM_001289807.1):c.460G>A (p.(Gly154Ser)), CRYAB(NM_001885.2):c.460G>A (p.G154S), CRYAB(NM_001885.3):c.460G>A (p.G154S)
ISCN -
DB-ID CRYAB_000017 See all 9 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) 0.00091 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSPB2 NM_001541.3 -?/. - c.-3998C>T r.(?) p.(=)
CRYAB NM_001885.1 -?/. - c.460G>A r.(?) p.(Gly154Ser)


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