All transcript variants in gene CCDC33

Information The variants shown are described using the NM_182791.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA 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     
-?/. - c.608C>T r.(?) p.(Pro203Leu) - likely benign g.74625077C>T g.74332736C>T - - CCDC33_000001 147 heterozygous; Clinindb (India) Faruq 2020, submtted - rs77396610 Germline - 147/2795 individuals - 0 - Mohammed Faruq
-?/. - c.608C>T r.(?) p.(Pro203Leu) - likely benign g.74625077C>T g.74332736C>T - - CCDC33_000001 5 homozygous; Clinindb (India) Faruq 2020, submtted - rs77396610 Germline - 5/2795 individuals - 0 - Mohammed Faruq
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