Variant #0001056337 (NC_000018.9:g.46956618C>G, NC_000018.9(NM_017653.3):c.140+7G>C (DYM))

Chromosome 18
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.46956618C>G
DNA change (hg38) -
Published as DYM(NM_001353214.3):c.140+7G>C
ISCN -
DB-ID DYM_000059
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYM NM_001353214.3 -?/. - c.140+7G>C r.(=) p.(=)
DYM NM_017653.3 -?/. - c.140+7G>C r.(=) p.(=)


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