Variant #0000655579 (NC_000006.11:g.33271908C>T, NM_003190.4:c.1297G>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.33271908C>T
DNA change (hg38) g.33304131C>T
Published as TAPBP(NM_003190.4):c.1297G>A (p.A433T)
ISCN -
DB-ID RGL2_000003
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) 1.0E-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 2020-03-23 16:13:27 +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     
RGL2 NM_001243738.1 -?/. - c.-5352G>A r.(?) p.(=)
TAPBP NM_003190.4 -?/. - c.1297G>A r.(?) p.(Ala433Thr)


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