LOVD - Variant listings for RB1

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Patient data (#0000206)
Patient ID E527T
Phenotype unilateral rb
Mut. origin somatic
Tissue retinoblastoma
Template DNA
tumor-genotype heterozygous
family history isolated
Reference Lohmann et al., 1997
# Reported 1
Published published
Remarks COSMIC - COSM893

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Pathogenic
g-position g.5470C>T
cDNA change c.184C>T   (View in UCSC Genome Browser, Ensembl)
Type substitution
Exon 02_ex
RNA change -
Protein p.Gln62*
RBWiki -
expected consequence type nonsense
DB-ID RB1_00027
originated_in somatic

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 g.5470C>T c.184C>T substitution 02_ex - p.Gln62* - nonsense RB1_00027 somatic

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