Variant #0000003322 (NC_000018.9:-, DSG2(NM_001943.3):c.1252_1253insATGA)

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type The 4-bp insertion in exon 9 (1253_1257insATGA)causes the addition of an amino acid residue before a
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID DSG2_00006
Frequency -
Variant remarks 1253_1257insATGA
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     
DSG2 NM_001943.3 ./. 09 c.1252_1253insATGA - p.Glu418AspfsX18