Variant #0000328857 (NC_000022.10:g.18897771C>T, NM_016335.4:c.*2917G>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.18897771C>T
DNA change (hg38) g.18910258C>T
Published as DGCR6(NM_005675.4):c.358C>T (p.(Gln120Ter))
ISCN -
DB-ID DGCR6_000018
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-17 10:25:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DGCR6 NM_005675.4 ?/. - c.358C>T r.(?) p.(Gln120Ter)
PRODH NM_016335.4 ?/. - c.*2917G>A r.(=) p.(=)


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