Variant #0000534964 (NC_000008.10:g.55533894_55533895dup, RP1(NM_006269.1):c.368_369dup)

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.55533894_55533895dup
DNA change (hg38) g.54621334_54621335dup
Published as RP1(NM_006269.1):c.368_369dupGC (p.P124Afs*20), RP1(NM_006269.2):c.368_369dupGC (p.P124Afs*20)
ISCN -
DB-ID RP1_000090 See all 11 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
RP1 NM_006269.1 +/. - c.368_369dup r.(?) p.(Pro124AlafsTer20)