Variant #0001043182 (NC_000019.9:g.55678021G>C, NM_178837.4:c.-5C>G (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.55678021G>C
DNA change (hg38) -
Published as DNAAF3(NM_001256714.1):c.-5C>G
ISCN -
DB-ID DNAAF3_000106
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) 3.0E-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 2025-05-05 21:14:00 +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     
DNAAF3 NM_001256715.1 ?/. - c.-135C>G r.(?) p.(=)
SYT5 NM_003180.2 ?/. - c.*6831C>G r.(=) p.(=)
DNAAF3 NM_178837.4 ?/. - c.-5C>G r.(?) p.(=)


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