Variant #0000297578 (NC_000013.10:g.49051481T>A, NC_000013.10(NM_000321.2):c.2664-10T>A (RB1))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49051481T>A
DNA change (hg38) g.48477345T>A
Published as RB1(NM_000321.3):c.2664-10T>A
ISCN -
DB-ID RB1_002135
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) 0.23802 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 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.2664-10T>A r.(=) p.(=)
LPAR6 NM_005767.5 -/. - c.-34266A>T r.(?) p.(=)


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