All variants in the BTD gene

Information The variants shown are described using the NM_000060.2 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     
?/? 2 c.261C>T r.(?) p.(=) - VUS g.15677147C>T g.15635640C>T - - BTD_000121 - PubMed: Wiltink 2016 - - Germline - - - 0 - Jasper Saris
-?/. - c.261C>T r.(?) p.(Asn87=) - likely benign g.15677147C>T g.15635640C>T BTD(NM_001323582.1):c.201C>T (p.N67=) - BTD_000121 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Rotterdam
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