Variant #0001065982 (NC_000013.10:g.49033829C>T, NM_000321.2:c.1966C>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.49033829C>T
DNA change (hg38) -
Published as RB1(NM_000321.2):c.1966C>T (p.R656W), RB1(NM_000321.3):c.1966C>T (p.R656W)
ISCN -
DB-ID RB1_000403 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) 0.00066 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RB1 NM_000321.2 -?/. - c.1966C>T r.(?) p.(Arg656Trp)
LPAR6 NM_005767.5 -?/. - c.-16614G>A r.(?) p.(=)


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