Variant #0000681921 (NC_000022.10:g.50312428C>G, NM_024105.3:c.-596G>C (ALG12))

Chromosome 22
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.50312428C>G
DNA change (hg38) -
Published as CRELD2(NM_001135101.2):c.11C>G (p.P4R)
ISCN -
DB-ID ALG12_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) Retrieve
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 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG12 NM_024105.3 -?/. - c.-596G>C r.(?) p.(=)
CRELD2 NM_024324.3 -?/. - c.11C>G r.(?) p.(Pro4Arg)


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