Variant #0000808949 (NC_000019.9:g.46270033A>G, NM_004409.3:c.*3713T>C (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.46270033A>G
DNA change (hg38) -
Published as SIX5(NM_175875.4):c.1184T>C (p.L395P)
ISCN -
DB-ID DMPK_000062
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMPK NM_004409.3 ?/. - c.*3713T>C r.(=) p.(=)
SIX5 NM_175875.4 ?/. - c.1184T>C r.(?) p.(Leu395Pro)


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