Variant #0000299263 (NC_000013.10:g.48878090C>T, NM_000321.2:c.42C>T (RB1))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48878090C>T
DNA change (hg38) g.48303954C>T
Published as RB1(NM_000321.2):c.42C>T (p.A14=), RB1(NM_000321.3):c.42C>T (p.A14=)
ISCN -
DB-ID RB1_000023 See all 3 reported entries
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) 0.00147 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RB1 NM_000321.2 -?/. - c.42C>T r.(?) p.(Ala14=)
LPAR6 NM_005767.5 -?/. - c.*107435G>A r.(=) p.(=)


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