Variant #0000264568 (NC_000002.11:g.182430219C>A, NM_001030311.2:c.696G>T (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.182430219C>A
DNA change (hg38) g.181565492C>A
Published as CERKL(NM_001030311.3):c.696G>T (p.L232F)
ISCN -
DB-ID CERKL_000017
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) 0.00202 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.*29965C>A r.(=) p.(=)
CERKL NM_001030311.2 -/. - c.696G>T r.(?) p.(Leu232Phe)
CERKL NM_201548.4 -/. - c.677+566G>T r.(=) p.(=)


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