Variant #0000892601 (NC_000016.9:g.20352526G>A, NM_003361.3:c.1464C>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.20352526G>A
DNA change (hg38) -
Published as UMOD(NM_001278614.1):c.1563C>T (p.G521=), UMOD(NM_003361.3):c.1464C>T (p.G488=)
ISCN -
DB-ID UMOD_000025 See all 2 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) 0.00045 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 2022-11-01 13:41:49 +01:00 (CET)
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.1563C>T r.(?) p.(Gly521=)
UMOD NM_003361.3 -?/. - c.1464C>T r.(?) p.(Gly488=)


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