Variant #0000930271 (NC_000014.8:g.21820878C>T, NM_020366.3:c.*1503C>T (RPGRIP1))

Chromosome 14
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.21820878C>T
DNA change (hg38) -
Published as SUPT16H(NM_007192.4):c.3098G>A (p.R1033H)
ISCN -
DB-ID SUPT16H_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) 0.00123 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited 2026-02-03 14:09:29 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUPT16H NM_007192.3 -?/. - c.3098G>A r.(?) p.(Arg1033His)
RPGRIP1 NM_020366.3 -?/. - c.*1503C>T r.(=) p.(=)


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