Variant #0000928755 (NC_000003.11:g.23960000dup, NM_002948.3:c.242dup (RPL15))

Chromosome 3
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.23960000dup
DNA change (hg38) -
Published as RPL15(NM_002948.5):c.242dupA (p.Y81*)
ISCN -
DB-ID NKIRAS1_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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +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.242dup r.(?) p.(Tyr81*)
NKIRAS1 NM_020345.3 +/. - c.-1865dup r.(?) p.(=)


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