Variant #0000553716 (NC_000015.9:g.25213097G>C, NM_022807.2:c.-276G>C (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.25213097G>C
DNA change (hg38) g.24967950G>C
Published as SNURF(NM_005678.3):c.129G>C (p.(Arg43Ser))
ISCN -
DB-ID SNRPN_000012
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) 0.00021 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 2020-03-23 16:13:27 +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.129G>C r.(?) p.(Arg43Ser) -
SNRPN NM_022807.2 ?/. - c.-276G>C r.(?) p.(=) -


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