Variant #0000533936 (NC_000008.10:g.144900218_144900236del, NM_182706.4:c.-2688_-2670del (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.144900218_144900236del
DNA change (hg38) g.143818048_143818066del
Published as PUF60(NM_001136033.3):c.490_508delAACATAGGGCAGGCCCAGC (p.N164Pfs*3)
ISCN -
DB-ID PUF60_000017
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PUF60 NM_078480.2 +/. - c.619_637del r.(?) p.(Asn207ProfsTer3)
SCRIB NM_182706.4 +/. - c.-2688_-2670del r.(?) p.(=)


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