Variant #0000892034 (NC_000015.9:g.42116737C>T, NM_016642.3:c.*24077G>A (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.42116737C>T
DNA change (hg38) -
Published as MAPKBP1(NM_001128608.1):c.4287C>T (p.S1429=), MAPKBP1(NM_001128608.2):c.4287C>T (p.S1429=)
ISCN -
DB-ID JMJD7_000017 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) 0.00053 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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JMJD7 NM_001114632.1 -?/. - c.-3586C>T r.(?) p.(=)
PLA2G4B NM_001114633.1 -?/. - c.-14375C>T r.(?) p.(=)
JMJD7-PLA2G4B NM_001198588.1 -?/. - c.-3586C>T r.(?) p.(=)
MAPKBP1 NM_014994.2 -?/. - c.4269C>T r.(?) p.(Ser1423=)
SPTBN5 NM_016642.3 -?/. - c.*24077G>A r.(=) p.(=)


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