Variant #0000924830 (NC_000008.10:g.144894465_144894466del, NM_182706.4:c.876_877del (SCRIB))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.144894465_144894466del
DNA change (hg38) -
Published as -
ISCN -
DB-ID PUF60_000038
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
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.*4224_*4225del r.(=) p.(=)
SCRIB NM_182706.4 ?/. - c.876_877del r.(?) p.(Glu293Alafs*20)


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