Variant #0001050257 (NC_000001.10:g.151739217G>A, NM_031420.2:c.-3262C>T (MRPL9))

Chromosome 1
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.151739217G>A
DNA change (hg38) -
Published as OAZ3(NM_016178.2):c.20G>A (p.(Arg7His))
ISCN -
DB-ID MRPL9_000009
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) 1.0E-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     
TDRKH NM_006862.3 ?/. - c.*5285C>T r.(=) p.(=)
OAZ3 NM_016178.2 ?/. - c.20G>A r.(?) p.(Arg7His)
MRPL9 NM_031420.2 ?/. - c.-3262C>T r.(?) p.(=)


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