Variant #0000549529 (NC_000012.11:g.92818670del, NM_001025233.1:c.214del (CLLU1))

Chromosome 12
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.92818670del
DNA change (hg38) g.92424894del
Published as CLLU1(NM_001025233.1):c.212delT (p.(Ser72LeufsTer8))
ISCN -
DB-ID CLLU1_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-02 17:43:08 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLLU1OS NM_001025232.1 -?/. - c.53-2256del r.(=) p.(=)
CLLU1 NM_001025233.1 -?/. - c.214del r.(?) p.(Ser72LeufsTer8)


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