Variant #0000329099 (NC_000022.10:g.50313452C>T, NM_024105.3:c.-1620G>A (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.50313452C>T
DNA change (hg38) g.49919804C>T
Published as CRELD2(NM_001135101.1):c.287C>T (p.(Ala96Val))
ISCN -
DB-ID CRELD2_000002
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) 0.016 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG12 NM_024105.3 -?/. - c.-1620G>A r.(?) p.(=)
CRELD2 NM_024324.3 -?/. - c.287C>T r.(?) p.(Ala96Val)


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