Variant #0000800214 (NC_000002.11:g.182468729G>T, NM_001030311.2:c.316C>A (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.182468729G>T
DNA change (hg38) -
Published as CERKL(NM_001030311.3):c.316C>A (p.R106S)
ISCN -
DB-ID CERKL_000068 See all 6 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) 5.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-09-17 14:40:49 +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.*68475G>T r.(=) p.(=)
CERKL NM_001030311.2 ?/. - c.316C>A r.(?) p.(Arg106Ser)
CERKL NM_201548.4 ?/. - c.316C>A r.(?) p.(Arg106Ser)


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