Variant #0000340122 (NC_000019.9:g.46271371C>T, NM_004409.3:c.*2375G>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.46271371C>T
DNA change (hg38) g.45768113C>T
Published as SIX5(NM_175875.4):c.732G>A (p.Q244=)
ISCN -
DB-ID SIX5_000017 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) 0.00312 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 2020-07-16 09:57:43 +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.*2375G>A r.(=) p.(=)
SIX5 NM_175875.4 -/. - c.732G>A r.(?) p.(Gln244=)


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