Variant #0000513618 (NC_000002.11:g.182430149_182430157dup, NC_000002.11(NM_001030311.2):c.755+5_755+13dup (CERKL))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.182430149_182430157dup
DNA change (hg38) g.181565422_181565430dup
Published as CERKL(NM_001030311.3):c.755+5_755+13dupGTGATATAA
ISCN -
DB-ID CERKL_000047
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITGA4 NM_000885.4 -/. - c.*29895_*29903dup r.(=) p.(=)
CERKL NM_001030311.2 -/. - c.755+5_755+13dup r.spl? p.?
CERKL NM_201548.4 -/. - c.677+630_677+638dup r.(=) p.(=)


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