Variant #0000888194 (NC_000008.10:g.144900161del, NM_182706.4:c.-2619del (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.144900161del
DNA change (hg38) -
Published as PUF60(NM_001362896.2):c.799delG (p.V267Wfs*58)
ISCN -
DB-ID PUF60_000034
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PUF60 NM_078480.2 +/. - c.688del r.(?) p.(Val230Trpfs*58)
SCRIB NM_182706.4 +/. - c.-2619del r.(?) p.(=)


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