Variant #0000858937 (NC_000003.11:g.23963134C>T, NM_002948.3:c.*2142C>T (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.23963134C>T
DNA change (hg38) -
Published as RPL15(NM_001253379.1):c.*2142C>T (p.(=))
ISCN -
DB-ID NKIRAS1_000008
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) 0.00513 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL15 NM_002948.3 -?/. - c.*2142C>T r.(=) p.(=)
NKIRAS1 NM_020345.3 -?/. - c.-4999G>A r.(?) p.(=)


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