Variant #0000727451 (NC_000019.9:g.46281385C>T, NM_004409.3:c.675G>A (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.46281385C>T
DNA change (hg38) -
Published as DMPK(NM_001081563.2):c.705G>A (p.T235=)
ISCN -
DB-ID DMPK_000061
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) 0.00041 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 2021-02-08 18:36:18 +01:00 (CET)
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.675G>A r.(?) p.(Thr225=)
DMWD NM_004943.1 -?/. - c.*6116G>A r.(=) p.(=)


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