Variant #0001056808 (NC_000019.9:g.55677710G>T, NM_178837.4:c.213C>A (DNAAF3))

Chromosome 19
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.55677710G>T
DNA change (hg38) -
Published as DNAAF3(NM_001256715.2):c.72C>A (p.(Asp24Glu))
ISCN -
DB-ID DNAAF3_000110
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) 8.0E-5 View details
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAAF3 NM_001256715.1 ?/. - c.72C>A r.(?) p.(Asp24Glu)
SYT5 NM_003180.2 ?/. - c.*7142C>A r.(=) p.(=)
DNAAF3 NM_178837.4 ?/. - c.213C>A r.(?) p.(Asp71Glu)


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