Variant #0001004968 (NC_000019.9:g.49139228C>A, NM_001352.3:c.159G>T (DBP))

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.49139228C>A
DNA change (hg38) -
Published as DBP(NM_001352.3):c.159G>T (p.(Glu53Asp))
ISCN -
DB-ID CA11_000004
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) 0.00012 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CA11 NM_001217.3 ?/. - c.*2148G>T r.(=) p.(=)
DBP NM_001352.3 ?/. - c.159G>T r.(?) p.(Glu53Asp)
NTN5 NM_145807.1 ?/. - c.*25706G>T r.(=) p.(=)


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