Variant #0000618637 (NC_000022.10:g.50312548_50312549insTTC, NM_024105.3:c.-717_-716insGAA (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.50312548_50312549insTTC
DNA change (hg38) g.49918900_49918901insTTC
Published as CRELD2(NM_001135101.1):c.129+2_129+3insTTC (p.?)
ISCN -
DB-ID ALG12_000042
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) 0.01653 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-17 15:35:04 +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.-717_-716insGAA r.(?) p.(=)
CRELD2 NM_024324.3 -?/. - c.129+2_129+3insTTC r.spl? p.?


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