LOVD - Variant listings for RB1

About this overview [Show]

Patient data (#0001109)
Patient ID not provided
Phenotype -
Mut. origin somatic
Tissue nd
Template DNA
tumor-genotype hemi/homozygous
family history isolated
Reference Lohmann - Essen
# Reported 1
Published unpublished
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Pathogenic
g-position g.150025C>T
cDNA change c.1723C>T
Type substitution
Exon 18_ex
RNA change -
Protein p.Gln575X
RBWiki -
expected consequence type nonsense
DB-ID RB1_00128
originated_in -

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.150025C>T c.1723C>T substitution 18_ex - p.Gln575X - nonsense RB1_00128 -

Please help to improve the quality of the data and report any error that you may find!