Variant #0001046488 (NC_000015.9:g.25200203G>A, NC_000015.9(NM_022807.2):c.-390-7058G>A (SNRPN))

Chromosome 15
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.25200203G>A
DNA change (hg38) -
Published as SNRPN(NM_003097.6):c.-397G>A
ISCN -
DB-ID SNRPN_000034
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
SNURF NM_005678.3 ?/. - c.8G>A r.(?) p.(Arg3Gln) -
SNRPN NM_022807.2 ?/. - c.-390-7058G>A r.(=) p.(=) -


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