Variant #0001002009 (NC_000016.9:g.20359959G>A, NM_003361.3:c.664C>T (UMOD))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.20359959G>A
DNA change (hg38) -
Published as UMOD(NM_003361.3):c.664C>T (p.R222C)
ISCN -
DB-ID UMOD_000046
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-08-28 13:16:32 +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     
UMOD NM_001278614.1 +?/. - c.763C>T r.(?) p.(Arg255Cys)
UMOD NM_003361.3 +?/. - c.664C>T r.(?) p.(Arg222Cys)


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