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     
+?/. 2 c.118T>A r.(118u>a) likely pathogenic (recessive) p.(Tyr40Asn) DNA substitution (VariO:0136);transversion (VariO:0316) RNA substitution (VariO:0312);transversion (VariO:0316);missense variation (VariO:0308) amino acid substitution (VariO:0021) PH - - - - tat -> aat; 1 g.100630155A>T g.101375167A>T T250A - BTK_000058 mother is carrier; sister is carrier PubMed: Saha, B. K 1997, IDbase_AccNr: A0393 - - Germline - - - 0 - Dr. Bratin K. Saha
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