Variant #0000975726 (NC_000003.11:g.23963134del, NM_002948.3:c.*2142del (RPL15))

Chromosome 3
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.23963134del
DNA change (hg38) -
Published as RPL15(NM_001253384.2):c.406del (p.(Arg136Glyfs*57))
ISCN -
DB-ID NKIRAS1_000011
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) 0.00011 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     
RPL15 NM_002948.3 -?/. - c.*2142del r.(?) p.(=)
NKIRAS1 NM_020345.3 -?/. - c.-4999del r.(?) p.(=)


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