Variant #0001040229 (NC_000015.9:g.25149204G>C, NC_000015.9(NM_022807.2):c.-504-15954G>C (SNRPN))

Chromosome 15
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.25149204G>C
DNA change (hg38) -
Published as SNRPN(NM_001349454.2):c.-727-8306G>C
ISCN -
DB-ID SNRPN_000030
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 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     

Haplotype     
SNURF NM_005678.3 -?/. - c.-50992G>C r.(?) p.(=) -
SNRPN NM_022807.2 -?/. - c.-504-15954G>C r.(=) p.(=) -


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