Variant #0001032231 (NC_000001.10:g.93299193G>A, NM_000969.3:c.165G>A (RPL5))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.93299193G>A
DNA change (hg38) -
Published as RPL5(NM_000969.5):c.165G>A (p.(Val55=))
ISCN -
DB-ID FAM69A_000017
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) 0.00556 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     
RPL5 NM_000969.3 -/. - c.165G>A r.(?) p.(=)
FAM69A NM_001006605.4 -/. - c.*9747C>T r.(=) p.(=)


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