Variant #0000690025 (NC_000007.13:g.50611663G>T, NM_000790.3:c.121C>A (DDC))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.50611663G>T
DNA change (hg38) -
Published as DDC(NM_000790.3):c.121C>A (p.(Leu41Met)), DDC(NM_001082971.1):c.121C>A (p.L41M)
ISCN -
DB-ID DDC_000034 See all 2 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) 0.00011 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDC NM_000790.3 ?/. - c.121C>A r.(?) p.(Leu41Met)


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