Variant #0000328855 (NC_000022.10:g.18897756C>G, NM_016335.4:c.*2932G>C (PRODH))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.18897756C>G
DNA change (hg38) g.18910243C>G
Published as DGCR6(NM_005675.4):c.343C>G (p.(Leu115Val))
ISCN -
DB-ID DGCR6_000016
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) 0.00411 View details
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 2020-03-23 16:13:27 +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.343C>G r.(?) p.(Leu115Val)
PRODH NM_016335.4 -?/. - c.*2932G>C r.(=) p.(=)


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