Variant #0000315702 (NC_000015.9:g.42166512T>C, NM_016642.3:c.4667A>G (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.42166512T>C
DNA change (hg38) g.41874314T>C
Published as SPTBN5(NM_016642.4):c.4667A>G (p.Q1556R)
ISCN -
DB-ID SPTBN5_000006
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLA2G4B NM_001114633.1 -?/. - c.*26454T>C r.(=) p.(=)
JMJD7-PLA2G4B NM_001198588.1 -?/. - c.*26624T>C r.(=) p.(=)
SPTBN5 NM_016642.3 -?/. - c.4667A>G r.(?) p.(Gln1556Arg)


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