Variant #0000557062 (NC_000016.9:g.20360508C>T, NM_003361.3:c.115G>A (UMOD))

Chromosome 16
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.20360508C>T
DNA change (hg38) g.20349186C>T
Published as UMOD(NM_001278614.1):c.214G>A (p.A72T)
ISCN -
DB-ID UMOD_000024
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UMOD NM_001278614.1 ?/. - c.214G>A r.(?) p.(Ala72Thr)
UMOD NM_003361.3 ?/. - c.115G>A r.(?) p.(Ala39Thr)


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