Variant #0000676413 (NC_000002.11:g.182521707C>T, NM_001030311.2:c.27G>A (CERKL))

Chromosome 2
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.182521707C>T
DNA change (hg38) -
Published as CERKL(NM_001030311.2):c.27G>A (p.R9=), CERKL(NM_001030311.3):c.27G>A (p.R9=)
ISCN -
DB-ID CERKL_000053 See all 2 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) 0.00153 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 2020-08-06 14:59:34 +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.*121453C>T r.(=) p.(=)
CERKL NM_001030311.2 -?/. - c.27G>A r.(?) p.(Arg9=)
CERKL NM_201548.4 -?/. - c.27G>A r.(?) p.(Arg9=)


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