Variant #0000513619 (NC_000002.11:g.182430207A>G, NM_001030311.2:c.708T>C (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.182430207A>G
DNA change (hg38) g.181565480A>G
Published as CERKL(NM_001030311.2):c.708T>C (p.H236=)
ISCN -
DB-ID CERKL_000048
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) 0.00301 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.*29953A>G r.(=) p.(=)
CERKL NM_001030311.2 -/. - c.708T>C r.(?) p.(His236=)
CERKL NM_201548.4 -/. - c.677+578T>C r.(=) p.(=)


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