Variant #0000863813 (NC_000015.9:g.42137121C>G, NM_016642.3:c.*3693G>C (SPTBN5))

Chromosome 15
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.42137121C>G
DNA change (hg38) -
Published as JMJD7-PLA2G4B(NM_005090.3):c.1785C>G (p.T595=), PLA2G4B(NM_001114633.1):c.1092C>G (p.T364=)
ISCN -
DB-ID JMJD7_000018
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JMJD7 NM_001114632.1 -?/. - c.*7767C>G r.(=) p.(=)
PLA2G4B NM_001114633.1 -?/. - c.1092C>G r.(?) p.(Thr364=)
JMJD7-PLA2G4B NM_001198588.1 -?/. - c.1785C>G r.(?) p.(Thr595=)
SPTBN5 NM_016642.3 -?/. - c.*3693G>C r.(=) p.(=)


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