Variant #0000350635 (NC_000019.9:g.46268902C>T, NM_004409.3:c.*4844G>A (DMPK))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46268902C>T
DNA change (hg38) g.45765644C>T
Published as SIX5(NM_175875.4):c.2077G>A (p.V693M), SIX5(NM_175875.5):c.2077G>A (p.V693M)
ISCN -
DB-ID SIX5_000003 See all 3 reported entries
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) 0.3189 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMPK NM_004409.3 -/. - c.*4844G>A r.(=) p.(=)
SIX5 NM_175875.4 -/. - c.2077G>A r.(?) p.(Val693Met)


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