All variants in the SCGB1C1 gene

Information The variants shown are described using the NM_145651.2 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.*2895G>A r.(=) p.(=) - likely benign g.197345G>A - ODF3(NM_053280.4):c.41G>A (p.R14H) - ODF3_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-?/. - c.*3127G>A r.(=) p.(=) - likely benign g.197577G>A - ODF3(NM_053280.4):c.126G>A (p.T42=) - ODF3_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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