Variant #0000015084 (NC_000017.10:-, TCAP(NM_003673.3):c.421C>G)

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_00010
Frequency 1/313
Variant remarks Three protein-altering variants were identified in TCAP, also known as titin-cap or

telethonin, a part of the titin complex.this proband was also known to carry a likely disease-causing lamin A/C mutation
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.421C>G - p.Pro141Ala