Variant #0000681453 (NC_000019.9:g.46270126C>A, NM_004409.3:c.*3620G>T (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.46270126C>A
DNA change (hg38) -
Published as SIX5(NM_175875.4):c.1091G>T (p.G364V, p.(Gly364Val))
ISCN -
DB-ID SIX5_000009 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) 0.00014 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.*3620G>T r.(=) p.(=)
SIX5 NM_175875.4 -?/. - c.1091G>T r.(?) p.(Gly364Val)


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