Variant #0000567773 (NC_000019.9:g.46274887T>G, NM_004409.3:c.1539A>C (DMPK))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46274887T>G
DNA change (hg38) g.45771629T>G
Published as DMPK(NM_001081563.2):c.1569A>C (p.L523=)
ISCN -
DB-ID DMPK_000027
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) 0.0001 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 09:59:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMPK NM_004409.3 -?/. - c.1539A>C r.(?) p.(Leu513=)
SIX5 NM_175875.4 -?/. - c.-2785A>C r.(?) p.(=)


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