Variant #0000291924 (NC_000020.10:g.49576148G>A, NM_003859.1:c.-1088C>T (DPM1))

Chromosome 20
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.49576148G>A
DNA change (hg38) g.50959611G>A
Published as MOCS3(NM_014484.4):c.769G>A (p.A257T)
ISCN -
DB-ID MOCS3_000001
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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DPM1 NM_003859.1 +/. - c.-1088C>T r.(?) p.(=)
MOCS3 NM_014484.3 +/. - c.769G>A r.(?) p.(Ala257Thr)


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