Variant #0000003684 (NC_000023.10:-, EMD(NM_000117.2):c.82+1G>T)

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type This mutation prejudices splicing of the emerin transcript.
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID EMD_00017
Frequency -
Variant remarks aberrant donor splice-site of intron 1 (G to T, +1 from 141)
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     
EMD NM_000117.2 ./. 01 c.82+1G>T - -