Variant #0000525819 (NC_000005.9:g.52402946dup, NM_176806.3:c.252dup (MOCS2))

Chromosome 5
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.52402946dup
DNA change (hg38) g.53107116dup
Published as MOCS2(NM_004531.5):c.65dup (p.(Leu23IlefsTer5)), MOCS2(NM_004531.5):c.65dupC (p.L23Ifs*5)
ISCN -
DB-ID MOCS2_000013 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MOCS2 NM_004531.4 +/. - c.65dup r.(?) p.(Leu23IlefsTer5)
MOCS2 NM_176806.3 +/. - c.252dup r.(?) p.(Ile85HisfsTer2)


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