Variant #0000996993 (NC_000008.10:g.144900433dup, NM_182706.4:c.-2891dup (SCRIB))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.144900433dup
DNA change (hg38) -
Published as PUF60(NM_078480.3):c.533dupA (p.V179Gfs*42)
ISCN -
DB-ID PUF60_000055
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-08-28 13:16:32 +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     
PUF60 NM_078480.2 +/. - c.533dup r.(?) p.(Val179Glyfs*42)
SCRIB NM_182706.4 +/. - c.-2891dup r.(?) p.(=)


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