Variant #0001000838 (NC_000014.8:g.21822563C>T, NM_020366.3:c.*3188C>T (RPGRIP1))

Chromosome 14
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.21822563C>T
DNA change (hg38) -
Published as SUPT16H(NM_007192.3):c.2790+7G>A (p.?)
ISCN -
DB-ID SUPT16H_000033
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2026-02-03 14:10:31 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUPT16H NM_007192.3 ?/. - c.2790+7G>A r.(=) p.(=)
RPGRIP1 NM_020366.3 ?/. - c.*3188C>T r.(=) p.(=)


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