Variant #0000973426 (NC_000001.10:g.161127064A>G, NM_001014443.2:c.-2567A>G (USP21))

Chromosome 1
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.161127064A>G
DNA change (hg38) -
Published as UFC1(NM_016406.4):c.212A>G (p.(Tyr71Cys))
ISCN -
DB-ID UFC1_000006
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 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
USP21 NM_001014443.2 ?/. - c.-2567A>G r.(?) p.(=)
UFC1 NM_016406.3 ?/. - c.212A>G r.(?) p.(Tyr71Cys)


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