All variants

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Effect     

Chr     

Classification method     

Clinical classification     

AscendingDNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
?/. 14 - likely benign g.106994118C>T g.106538116C>T IGHV3-48 47G>A (Gly16Asp) - chr14_005145 - PubMed: Chia 2018 - - Germline - - - - - Johan den Dunnen
?/. 14 - likely benign g.106994118C>T g.106538116C>T IGHV3-48 47G>A (Gly16Asp) - chr14_005145 - PubMed: Chia 2018 - - Germline - - - - - Johan den Dunnen
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