Variant #0000857611 (NC_000001.10:g.7902731G>A, NC_000001.10(NM_016831.1):c.3523-1G>A (PER3))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.7902731G>A
DNA change (hg38) -
Published as PER3(NM_001289864.1):c.2590-1G>A
ISCN -
DB-ID PER3_000004
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) 8.0E-5 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 2022-05-09 15:51:19 +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     
UTS2 NM_006786.3 +?/. - c.*5095C>T r.(=) p.(=)
PER3 NM_016831.1 +?/. - c.3523-1G>A r.spl? p.?


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