Variant #0001026337 (NC_000013.10:g.48955416dup, NM_000321.2:c.1532dup (RB1))

Chromosome 13
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.48955416dup
DNA change (hg38) -
Published as RB1(NM_000321.3):c.1532dupA (p.D511Efs*12)
ISCN -
DB-ID LPAR6_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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RB1 NM_000321.2 +/. - c.1532dup r.(?) p.(Asp511Glufs*12)
LPAR6 NM_005767.5 +/. - c.*30109dup r.(?) p.(=)


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