Variant #0000330959 (NC_000006.11:g.33263192C>T, NM_003190.4:c.*6345G>A (TAPBP))

Chromosome 6
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.33263192C>T
DNA change (hg38) g.33295415C>T
Published as RGL2(NM_001243738.1):c.782G>A (p.(Arg261Gln))
ISCN -
DB-ID RGL2_000001
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RGL2 NM_001243738.1 -?/. - c.782G>A r.(?) p.(Arg261Gln)
TAPBP NM_003190.4 -?/. - c.*6345G>A r.(=) p.(=)
PFDN6 NM_014260.3 -?/. - c.*4570C>T r.(=) p.(=)


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