Variant #0000978590 (NC_000009.11:g.140094948_140094958del, NM_001128228.2:c.225_235del (TPRN))

Chromosome 9
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.140094948_140094958del
DNA change (hg38) -
Published as TPRN(NM_001128228.3):c.225_235del (p.(Gly76Alafs*150)), TPRN(NM_001128228.3):c.225_235delGGGGGCGCGGC (p.G76Afs*150)
ISCN -
DB-ID TPRN_000004 See all 4 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     
TPRN NM_001128228.2 +/. - c.225_235del r.(?) p.(Gly76AlafsTer150)


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