LOVD - Variant listings for RB1

About this overview [Show]

Patient data (#0002582)
Patient ID E5516
Phenotype bilateral rb
Mut. origin germline
Tissue tumor
Template DNA
tumor-genotype heterozygous
family history isolated
Reference Germany:Essen
# Reported 1
Published -
Remarks -
Submitter Dietmar Lohmann

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
g-position g.162237C>T
cDNA change c.2359C>T   (View in UCSC Genome Browser, Ensembl)
Type substitution
Exon 23_ex
RNA change -
Protein p.Arg787X
RBWiki -
expected consequence type nonsense
DB-ID RB1_00005
originated_in somatic

2 entries 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 g.76428A>G c.1333-2A>G substitution 13_in altered splicing - - splice RB1_00227 germline
?/? Unknown g.162237C>T c.2359C>T substitution 23_ex - p.Arg787X - nonsense RB1_00005 somatic

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