Variant #0000692842 (NC_000019.9:g.46271951_46271956dup, NM_004409.3:c.*1799_*1804dup (DMPK))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46271951_46271956dup
DNA change (hg38) -
Published as SIX5(NM_175875.4):c.156_161dupCGGGGC (p.G55_A56dup)
ISCN -
DB-ID DMPK_000054 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMPK NM_004409.3 -/. - c.*1799_*1804dup r.(=) p.(=)
SIX5 NM_175875.4 -/. - c.156_161dup r.(?) p.(Gly55_Ala56dup)


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