Variant #0000970365 (NC_000022.10:g.18901004C>T, NM_016335.4:c.1562= (PRODH))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.18901004C>T
DNA change (hg38) -
Published as PRODH(NM_016335.6):c.1562G>A (p.R521Q)
ISCN -
DB-ID PRODH_000006 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) 0.92819 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DGCR6 NM_005675.4 -/. - c.*1802C>T r.(=) p.(=)
PRODH NM_016335.4 -/. - c.1562= r.(=) p.(Gln521=)


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