Variant #0000502386 (NC_000001.10:g.109441561del, NM_013296.4:c.742del (GPSM2))

Chromosome 1
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.109441561del
DNA change (hg38) g.108898939del
Published as GPSM2(NM_001321039.1):c.742delC (p.G249Efs*32), GPSM2(NM_013296.5):c.742delC (p.G249Efs*32)
ISCN -
DB-ID GPSM2_000010 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 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPSM2 NM_013296.4 +/. - c.742del r.(?) p.(Gly249GlufsTer32)


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