Variant #0000003683 (NC_000023.10:-, EMD(NM_000117.2):c.619delC)

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Hydrophobicity plots showed that the mutant emerin lacked a C-terminal hydrophobic domain that is pr
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID EMD_00054
Frequency -
Variant remarks deletion of 1 bp (C at nucleotide 672 or 673)
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     
EMD NM_000117.2 ./. 06 c.619delC - p.Arg207GlyfsX30