Variant #0000963271 (NC_000004.11:g.88583939dup, NM_004407.3:c.1009dup (DMP1))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.88583939dup
DNA change (hg38) -
Published as DMP1(NM_004407.3):c.1009dupA (p.(Ser337fs)), DMP1(NM_004407.4):c.1009dupA (p.S337Kfs*3)
ISCN -
DB-ID DMP1_000020 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMP1 NM_004407.3 +/. - c.1009dup r.(?) p.(Ser337Lysfs*3)


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