Variant #0000297374 (NC_000022.10:g.18900750G>A, NM_016335.4:c.1741C>T (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.18900750G>A
DNA change (hg38) g.18913237G>A
Published as PRODH(NM_016335.6):c.1741C>T (p.L581=)
ISCN -
DB-ID PRODH_000002 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) 0.78378 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 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     
DGCR6 NM_005675.4 -/. - c.*1548G>A r.(=) p.(=)
PRODH NM_016335.4 -/. - c.1741C>T r.(?) p.(Leu581=)


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