Variant #0000003441 (NC_000006.11:-, DSP(NM_004415.2):c.1817_1846dup)

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Duplication
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID DSP_00188
Frequency -
Variant remarks The insertion occurs between the second and third nucleotides of codon 608
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     
DSP NM_004415.2 ./. 14 c.1817_1846dup - P.Arg606_Ala615dup