All transcript variants in gene BTK

BTKbase is part of the IDbases
Information The variants shown are described using the NM_000061.2 transcript reference sequence.

1 entry on 1 page. Showing entry 1.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

ClassClinical     

Protein     

VariO/DNA     

VariO/RNA     

VariO/Protein     

P-domain     

Protein level     

mRNA level     

Enzyme activity     

CpG     

Codon change     

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     
+?/. 8i_9i c.(776+?)_(840-?)del r.spl - p.? DNA deletion (VariO:0141) - - SH3 - - - - - g.(?_100615556)_(100614335_?)del - Intron 8~9 deletion - BTK_000871 Deletion of intron 8 to intron 9? PubMed: Singh 2016, IDbase_AccNr: A1611 - - Unknown - - - 0 - Qing Wang
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