Variant #0000550894 (NC_000013.10:g.49054205T>A, NM_000321.2:c.2785T>A (RB1))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.49054205T>A
DNA change (hg38) g.48480069T>A
Published as RB1(NM_000321.2):c.2785T>A (p.*929Rext*21)
ISCN -
DB-ID LPAR6_000008
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-03 17:13:10 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RB1 NM_000321.2 ?/. - c.2785T>A r.(?) p.(Ter929ArgextTer21)
LPAR6 NM_005767.5 ?/. - c.-36990A>T r.(?) p.(=)


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