Variant #0000884624 (NC_000002.11:g.182403834G>A, NM_001030311.2:c.1601C>T (CERKL))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.182403834G>A
DNA change (hg38) -
Published as CERKL(NM_001030311.3):c.1601C>T (p.S534L)
ISCN -
DB-ID CERKL_000097 See all 3 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) 0.00085 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +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.*3580G>A r.(=) p.(=)
CERKL NM_001030311.2 ?/. - c.1601C>T r.(?) p.(Ser534Leu)
CERKL NM_201548.4 ?/. - c.1523C>T r.(?) p.(Ser508Leu)


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