Variant #0000256244 (NC_000022.10:g.18909902A>T, NM_016335.4:c.865T>A (PRODH))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.18909902A>T
DNA change (hg38) g.18922389A>T
Published as PRODH(NM_016335.4):c.865T>A (p.L289M), PRODH(NM_016335.6):c.865T>A (p.L289M)
ISCN -
DB-ID PRODH_000019 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) 0.00357 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRODH NM_016335.4 ?/. - c.865T>A r.(?) p.(Leu289Met)


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