Variant #0000614658 (NC_000013.10:g.49050881_49050885dup, NM_000321.2:c.2565_2569dup (RB1))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49050881_49050885dup
DNA change (hg38) g.48476745_48476749dup
Published as RB1(NM_000321.2):c.2564_2565insCGACC (p.(Arg857ProfsTer18))
ISCN -
DB-ID LPAR6_000011
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-03 17:12:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RB1 NM_000321.2 +?/. - c.2565_2569dup r.(?) p.(Arg857ProfsTer18)
LPAR6 NM_005767.5 +?/. - c.-33670_-33666dup r.(?) p.(=)


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