Variant #0000852099 (NC_000009.11:g.126135899_126135914dup, NM_173689.5:c.3089_3104dup (CRB2))

Chromosome 9
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.126135899_126135914dup
DNA change (hg38) -
Published as CRB2(NM_173689.5):c.3089_3104dup (p.(Gly1036Alafs*43)), CRB2(NM_173689.7):c.3089_3104dupGGCCCGGCGCGGCCCC (p.G1036Afs*43)
ISCN -
DB-ID CRB2_000003 See all 4 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRB2 NM_173689.5 +/. - c.3089_3104dup r.(?) p.(Gly1036AlafsTer43)


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