Variant #0000016380 (NC_000011.9:g.68549263T>C, CPT1A(NM_001876.3):c.1328T>C)

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.68549263T>C
Reference -
DB-ID CPT1A_000019
Frequency 3/53
Variant remarks -
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner ting zhang
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by ting zhang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPT1A NM_001876.3 ?/? 11 c.1328T>C r.0? Leu443Pro