Variant #0000523391 (NC_000004.11:g.88535850_88535867dup, NM_014208.3:c.2036_2053dup (DSPP))

Chromosome 4
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.88535850_88535867dup
DNA change (hg38) g.87614698_87614715dup
Published as DSPP(NM_014208.3):c.2018_2019insTAGCAGTGACAGCAGCAG (p.(Asp673_Ser674insSerSerAspSerSerSer)), DSPP(NM_014208.3):c.2036_2053dupGTAGCAGTGACAGCAGCA (p...)
ISCN -
DB-ID DSPP_000058 See all 3 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DSPP NM_014208.3 -/. - c.2036_2053dup r.(?) p.(Ser679_Ser684dup)


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