Variant #0001039723 (NC_000013.10:g.49047493C>G, NC_000013.10(NM_000321.2):c.2490-3C>G (RB1))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49047493C>G
DNA change (hg38) -
Published as RB1(NM_000321.3):c.2490-3C>G
ISCN -
DB-ID LPAR6_000032
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 2025-05-05 21:14:00 +02:00 (CEST)
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.2490-3C>G r.spl? p.?
LPAR6 NM_005767.5 +?/. - c.-30278G>C r.(?) p.(=)


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