Variant #0000978072 (NC_000008.10:g.144899297_144899299del, NM_182706.4:c.-1753_-1751del (SCRIB))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.144899297_144899299del
DNA change (hg38) -
Published as PUF60(NM_001362896.2):c.1276_1278delCCT (p.P426del), PUF60(NM_078480.3):c.1165_1167del (p.(Pro389del))
ISCN -
DB-ID PUF60_000022 See all 2 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.1165_1167del r.(?) p.(Pro389del)
SCRIB NM_182706.4 -?/. - c.-1753_-1751del r.(?) p.(=)


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