Variant #0000558439 (NC_000016.9:g.53503894G>A, NM_005611.3:c.2042G>A (RBL2))

Chromosome 16
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.53503894G>A
DNA change (hg38) g.53469982G>A
Published as RBL2(NM_005611.4):c.2042G>A (p.R681Q)
ISCN -
DB-ID AKTIP_000006
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) 4.0E-5 View details
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBL2 NM_005611.3 ?/. - c.2042G>A r.(?) p.(Arg681Gln)
AKTIP NM_022476.2 ?/. - c.*22430C>T r.(=) p.(=)


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