Variant #0001043697 (NC_000022.10:g.19132135A>C, NM_022719.2:c.19T>G (DGCR14))

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.19132135A>C
DNA change (hg38) -
Published as ESS2(NM_022719.3):c.19T>G (p.(Ser7Ala))
ISCN -
DB-ID DGCR14_000003
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) 0.00171 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GSC2 NM_005315.1 -?/. - c.*4369T>G r.(=) p.(=)
DGCR14 NM_022719.2 -?/. - c.19T>G r.(?) p.(Ser7Ala)
TSSK2 NM_053006.4 -?/. - c.*12146A>C r.(=) p.(=)


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