Variant #0000724793 (NC_000014.8:g.53619494_53619495insCGCCGCCGCCGCCGCCGC, NM_001160147.1:c.336_337insGGCGGCGGCGGCGGCGGC (DDHD1))

Chromosome 14
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.53619494_53619495insCGCCGCCGCCGCCGCCGC
DNA change (hg38) -
Published as DDHD1(NM_001160148.1):c.336_337insGGCGGCGGCGGCGGCGGC (p.G112_S113insGGGGGG), DDHD1(NM_001160148.2):c.336_337insGGCGGCGGCGGCGGCGGC (p.(Gly112_Ser1...))
ISCN -
DB-ID DDHD1_000041 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) 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDHD1 NM_001160147.1 ?/. - c.336_337insGGCGGCGGCGGCGGCGGC r.(?) p.(Gly112_Ser113insGlyGlyGlyGlyGlyGly)


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