Variant #0000015092 (NC_000017.10:-, TCAP(NM_003673.3):c.226C>T)

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Blood
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID TCAP_00020
Frequency -
Variant remarks The R76C mutation in telethonin was found in a 42-year-old male diagnosed with intestinal pseudo-obstruction. There was no family history of intestinal pseudo-obstruction.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TCAP NM_003673.3 ./. 02 c.226C>T - p.Arg76Cys