Variant #0000924831 (NC_000008.10:g.144899254_144899258del, NM_182706.4:c.-1715_-1711del (SCRIB))

Chromosome 8
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.144899254_144899258del
DNA change (hg38) -
Published as PUF60(NM_078480.3):c.1203_1207delCCCCA (p.I403Gfs*42)
ISCN -
DB-ID PUF60_000039
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 2023-04-16 21:50:28 +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.1203_1207del r.(?) p.(Ile403Glyfs*42)
SCRIB NM_182706.4 +?/. - c.-1715_-1711del r.(?) p.(=)


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