LOVD - Variant listings for RB1

About this overview [Show]

Patient data (#0003254)
Patient ID fam-no_19953116
Phenotype retinoblastoma
Mut. origin germline
Tissue blood
Template DNA
tumor-genotype unknown
family history isolated
Reference Dommering et al. 2014, Germany:Essen
# Reported 1
Published published
Remarks A>T, A>G reported in LOVD.
No RNA available
Predicted: alters the acceptor splice site of intron 9, leading to a skip of exon 10.
Submitter Larissa Novakovic

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Unknown
g-position -
cDNA change c.940-2A>C   (View in UCSC Genome Browser, Ensembl)
Type Substitution
Exon 09_in
RNA change -
Protein -
RBWiki -
expected consequence type splice
DB-ID RB1_01973
originated_in germline

1 entry in RB1

Path.
Allele Descending
Ascending
g-position Descending
Ascending
cDNA change Descending
Ascending
Type Descending
Ascending
Exon Descending
Ascending
RNA change Descending
Ascending
Protein Descending
Ascending
RBWiki Descending
Ascending
expected consequence type Descending
Ascending
DB-ID Descending
Ascending
originated_in Descending
Ascending
+/? Unknown - c.940-2A>C Substitution 09_in - - - splice RB1_01973 germline

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