Variant #0000557055 (NC_000016.9:g.20352490T>C, NM_003361.3:c.1500A>G (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.20352490T>C
DNA change (hg38) g.20341168T>C
Published as UMOD(NM_001278614.1):c.1599A>G (p.A533=), UMOD(NM_003361.3):c.1500A>G (p.A500=)
ISCN -
DB-ID UMOD_000018 See all 3 reported entries
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) 0.00049 View details
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 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UMOD NM_001278614.1 -?/. - c.1599A>G r.(?) p.(Ala533=)
UMOD NM_003361.3 -?/. - c.1500A>G r.(?) p.(Ala500=)


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