Variant #0000982123 (NC_000016.9:g.84224988_84225009del, NM_178452.4:c.*13541_*13562del (DNAAF1))

Chromosome 16
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.84224988_84225009del
DNA change (hg38) -
Published as ADAD2(NM_001145400.2):c.152_173del (p.(Thr51Serfs*7))
ISCN -
DB-ID ADAD2_000003
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAD2 NM_001145400.1 ?/. - c.152_173del r.(?) p.(Thr51Serfs*7)
TAF1C NM_005679.3 ?/. - c.-4575_-4554del r.(?) p.(=)
ADAD2 NM_139174.3 ?/. - c.152_173del r.(?) p.(Thr51Serfs*7)
DNAAF1 NM_178452.4 ?/. - c.*13541_*13562del r.(=) p.(=)


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