Variant #0000316214 (NC_000006.11:g.33271606C>G, NC_000006.11(NM_003190.4):c.1335+126G>C (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.33271606C>G
DNA change (hg38) g.33303829C>G
Published as TAPBP(NM_172208.2):c.1461G>C (p.W487C)
ISCN -
DB-ID TAPBP_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) 0.00249 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 2018-01-15 20:58:59 +01:00 (CET)
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     
RGL2 NM_001243738.1 -?/. - c.-5050G>C r.(?) p.(=)
TAPBP NM_003190.4 -?/. - c.1335+126G>C r.(=) p.(=)


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