Variant #0001039722 (NC_000013.10:g.49039125C>A, NC_000013.10(NM_000321.2):c.2212-9C>A (RB1))

Chromosome 13
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.49039125C>A
DNA change (hg38) -
Published as RB1(NM_000321.3):c.2212-9C>A
ISCN -
DB-ID LPAR6_000031
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.2212-9C>A r.(=) p.(=)
LPAR6 NM_005767.5 -?/. - c.-21910G>T r.(?) p.(=)


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