Variant #0000808954 (NC_000019.9:g.46285494G>A, NM_004409.3:c.117C>T (DMPK))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.46285494G>A
DNA change (hg38) -
Published as DMPK(NM_001288764.2):c.136C>T (p.R46*)
ISCN -
DB-ID DMPK_000065
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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +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.117C>T r.(?) p.(Ser39=)
DMWD NM_004943.1 ?/. - c.*2007C>T r.(=) p.(=)


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