Variant #0000809275 (NC_000020.10:g.49576685C>A, NM_003859.1:c.-1625G>T (DPM1))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49576685C>A
DNA change (hg38) -
Published as MOCS3(NM_014484.4):c.1306C>A (p.P436T)
ISCN -
DB-ID DPM1_000019
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) 0.00047 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DPM1 NM_003859.1 -?/. - c.-1625G>T r.(?) p.(=)
MOCS3 NM_014484.3 -?/. - c.1306C>A r.(?) p.(Pro436Thr)


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