LOVD - Variant listings for RB1

About this overview [Show]

Patient data (#0003433)
Patient ID #15
Phenotype bilateral rb
Mut. origin -
Tissue blood
Template DNA
tumor-genotype -
family history isolated
Reference Italy:Siena
# Reported 1
Published published
Remarks Disruption of pocket B domain and C-termus loss; mosaicism
Submitter Alessandra Renieri

Variant data
Allele Paternal (confirmed)
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
g-position g.49033971T>C
cDNA change c.2106+2T>C
Type substitution
Exon 20_in
RNA change r.2073_2106del
Protein p.(Tyr692Leufs*2)
RBWiki -
expected consequence type splice
DB-ID RB1_01248
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
?/? Paternal (confirmed) g.49033971T>C c.2106+2T>C substitution 20_in r.2073_2106del p.(Tyr692Leufs*2) - splice RB1_01248 germline

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