Variant #0000553717 (NC_000015.9:g.25223336G>A, NC_000015.9(NM_022807.2):c.560-4G>A (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.25223336G>A
DNA change (hg38) g.24978189G>A
Published as SNRPN(NM_003097.3):c.560-4G>A (p.?)
ISCN -
DB-ID SNRPN_000013
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) 9.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-06 09:31:13 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
SNURF NM_005678.3 -?/. - c.*748-4G>A r.spl? p.? -
SNRPN NM_022807.2 -?/. - c.560-4G>A r.spl? p.? -


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