Variant #0000015081 (NC_000017.10:-, TCAP(NM_003673.3):c.316C>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_00007
Frequency -
Variant remarks however, only the two individuals who were double-heterozygous

for the p.Arg145Trp mutation as well as a TCAP mutation were

clinically affected.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TCAP NM_003673.3 ./. 02 c.316C>T - p.Arg106Cys