Variant #0000693101 (NC_000022.10:g.18905934A>G, NM_016335.4:c.1322T>C (PRODH))

Chromosome 22
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.18905934A>G
DNA change (hg38) -
Published as PRODH(NM_016335.4):c.1322T>C (p.L441P), PRODH(NM_016335.5):c.1322T>C (p.L441P), PRODH(NM_016335.6):c.1322T>C (p.(Leu441Pro), p.L441P)
ISCN -
DB-ID PRODH_000012 See all 6 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) 0.00521 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRODH NM_016335.4 +/. - c.1322T>C r.(?) p.(Leu441Pro)


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