Variant #0000677796 (NC_000006.11:g.50791606_50791609dup, NC_000006.11(NM_003221.3):c.540+28_540+31dup (TFAP2B))

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.50791606_50791609dup
DNA change (hg38) -
Published as TFAP2B(NM_003221.3):c.540+7_540+10dup (p.(=)), TFAP2B(NM_003221.4):c.540+28_540+31dupCAAA
ISCN -
DB-ID TFAP2B_000001 See all 2 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TFAP2B NM_003221.3 -?/. - c.540+28_540+31dup r.(=) p.(=)


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