Variant #0000989354 (NC_000016.9:g.89629362G>C, NM_000977.3:c.548G>C (RPL13))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.89629362G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID RPL13_000019 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1597676540
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-08-01 15:37:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL13 NM_000977.3 +/. - c.548G>C r.(?) p.(Arg183Pro)


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