Variant #0000969298 (NC_000017.10:g.8280890G>A, NM_000987.3:c.430C>T (RPL26))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.8280890G>A
DNA change (hg38) -
Published as RPL26(NM_000987.5):c.430C>T (p.Q144*)
ISCN -
DB-ID KRBA2_000001
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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL26 NM_000987.3 ?/. - c.430C>T r.(?) p.(Gln144*)
KRBA2 NM_213597.2 ?/. - c.-6038C>T r.(?) p.(=)


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