Variant #0000000298 (NC_000011.9:g.2182523_2182540delinsACGAT, NM_000207.2:c.-160_-143delinsATCGT (INS))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.2182523_2182540delinsACGAT
Reference -
DB-ID INS_000001
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-29 13:36:32 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INS NM_000207.2 ?/? - c.-160_-143delinsATCGT r.(=) p.(=)