Variant #0000981675 (NC_000016.9:g.1997309C>T, NM_005061.2:c.574G>A (RPL3L))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1997309C>T
DNA change (hg38) -
Published as RPL3L(NM_005061.3):c.574G>A (p.(Glu192Lys))
ISCN -
DB-ID RPL3L_000002
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) 0.00036 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 2024-04-19 20:27:30 +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     
RPL3L NM_005061.2 -?/. - c.574G>A r.(?) p.(Glu192Lys)
MSRB1 NM_016332.2 -?/. - c.-4152G>A r.(?) p.(=)


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