Variant #0000567770 (NC_000019.9:g.46273821G>C, NM_004409.3:c.1815C>G (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.46273821G>C
DNA change (hg38) g.45770563G>C
Published as DMPK(NM_001081560.1):c.1800C>G (p.(=))
ISCN -
DB-ID DMPK_000024
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 09:59:12 +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.1815C>G r.(?) p.(Gly605=)
SIX5 NM_175875.4 -?/. - c.-1719C>G r.(?) p.(=)


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