Variant #0000617702 (NC_000019.9:g.46271877C>G, NM_004409.3:c.*1869G>C (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.46271877C>G
DNA change (hg38) g.45768619C>G
Published as SIX5(NM_175875.4):c.226G>C (p.A76P)
ISCN -
DB-ID DMPK_000041
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.*1869G>C r.(=) p.(=)
SIX5 NM_175875.4 -?/. - c.226G>C r.(?) p.(Ala76Pro)


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