Variant #0000324009 (NC_000015.9:g.42137152G>T, NM_016642.3:c.*3662C>A (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.42137152G>T
DNA change (hg38) g.41844954G>T
Published as JMJD7-PLA2G4B(NM_001198588.1):c.1816G>T (p.(Ala606Ser))
ISCN -
DB-ID JMJD7-PLA2G4B_000007
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) 0.00019 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JMJD7 NM_001114632.1 ?/. - c.*7798G>T r.(=) p.(=)
PLA2G4B NM_001114633.1 ?/. - c.1123G>T r.(?) p.(Ala375Ser)
JMJD7-PLA2G4B NM_001198588.1 ?/. - c.1816G>T r.(?) p.(Ala606Ser)
SPTBN5 NM_016642.3 ?/. - c.*3662C>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.