Variant #0000926162 (NC_000016.9:g.20359630C>A, NM_003361.3:c.888G>T (UMOD))

Chromosome 16
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.20359630C>A
DNA change (hg38) -
Published as UMOD(NM_003361.3):c.888G>T (p.T296=)
ISCN -
DB-ID UMOD_000038
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 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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.987G>T r.(?) p.(Thr329=)
UMOD NM_003361.3 -?/. - c.888G>T r.(?) p.(Thr296=)


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