Variant #0000725002 (NC_000015.9:g.25221479T>C, NM_022807.2:c.183T>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.25221479T>C
DNA change (hg38) -
Published as SNRPN(NM_022807.4):c.183T>C (p.R61=)
ISCN -
DB-ID SNRPN_000008
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) 0.00029 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
SNURF NM_005678.3 -?/. - c.*371T>C r.(=) p.(=) -
SNRPN NM_022807.2 -?/. - c.183T>C r.(?) p.(Arg61=) -


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