Variant #0001040337 (NC_000015.9:g.42147078dup, NM_016642.3:c.9520dup (SPTBN5))

Chromosome 15
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.42147078dup
DNA change (hg38) -
Published as SPTBN5(NM_016642.4):c.9520dupC (p.R3174Pfs*18)
ISCN -
DB-ID SPTBN5_000001 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +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     
PLA2G4B NM_001114633.1 ?/. - c.*7020dup r.(?) p.(=)
JMJD7-PLA2G4B NM_001198588.1 ?/. - c.*7190dup r.(?) p.(=)
SPTBN5 NM_016642.3 ?/. - c.9520dup r.(?) p.(Arg3174Profs*18)


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