Variant #0000951432 (NC_000020.10:g.411155G>A, NM_031229.2:c.*81G>A (RBCK1))

Chromosome 20
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.411155G>A
DNA change (hg38) -
Published as RBCK1(NM_001323956.1):c.*81G>A (p.(=))
ISCN -
DB-ID RBCK1_000045
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBCK1 NM_031229.2 -?/. - c.*81G>A r.(=) p.(=)
TBC1D20 NM_144628.2 -?/. - c.*8075C>T r.(=) p.(=)


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