Variant #0001056429 (NC_000019.9:g.3759730G>A, NM_172251.2:c.-2969G>A (MRPL54))

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.3759730G>A
DNA change (hg38) -
Published as APBA3(NM_004886.4):c.533C>T (p.(Thr178Met))
ISCN -
DB-ID APBA3_000015
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) 0.00069 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     
TJP3 NM_001267560.1 ?/. - c.*9048G>A r.(=) p.(=)
APBA3 NM_004886.3 ?/. - c.533C>T r.(?) p.(Thr178Met)
MRPL54 NM_172251.2 ?/. - c.-2969G>A r.(?) p.(=)


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