Variant #0000285425 (NC_000015.9:g.42139863C>T, NM_016642.3:c.*951G>A (SPTBN5))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.42139863C>T
DNA change (hg38) g.41847665C>T
Published as JMJD7-PLA2G4B(NM_001198588.1):c.2657C>T (p.P886L)
ISCN -
DB-ID JMJD7-PLA2G4B_000015
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) 0.00402 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-06 10:31:16 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JMJD7 NM_001114632.1 -/. - c.*10509C>T r.(=) p.(=)
PLA2G4B NM_001114633.1 -/. - c.2151C>T r.(?) p.(Pro717=)
JMJD7-PLA2G4B NM_001198588.1 -/. - c.2657C>T r.(?) p.(Pro886Leu)
SPTBN5 NM_016642.3 -/. - c.*951G>A r.(=) p.(=)


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