Variant #0000681777 (NC_000022.10:g.19126745C>T, NM_022719.2:c.749G>A (DGCR14))

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.19126745C>T
DNA change (hg38) -
Published as ESS2(NM_022719.3):c.749G>A (p.R250H)
ISCN -
DB-ID DGCR14_000001
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) 0.0001 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DGCR14 NM_022719.2 ?/. - c.749G>A r.(?) p.(Arg250His)
TSSK2 NM_053006.4 ?/. - c.*6756C>T r.(=) p.(=)


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