Variant #0000016618 (NC_000004.11:g.159624731_159624734del, ETFDH(NM_004453.2):c.1273_1276del)

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.159624731_159624734del
Reference -
DB-ID ETFDH_000097
Frequency 2/671
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     
ETFDH NM_004453.2 +?/+? 10 c.1273_1276del r.(?) p.(Ser425Argfs*3)