Variant #0000723781 (NC_000012.11:g.100478344C>T, NM_001006947.1:c.1198G>A (UHRF1BP1L))

Chromosome 12
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.100478344C>T
DNA change (hg38) -
Published as UHRF1BP1L(NM_015054.2):c.1198G>A (p.V400I)
ISCN -
DB-ID UHRF1BP1L_000005
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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     
UHRF1BP1L NM_001006947.1 -?/. - c.1198G>A r.(?) p.(Val400Ile)


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