Variant #0000517438 (NC_000003.11:g.114099109T>C, NM_001164342.1:c.154A>G (ZBTB20))

Chromosome 3
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.114099109T>C
DNA change (hg38) g.114380262T>C
Published as ZBTB20(NM_001164342.1):c.154A>G (p.(Thr52Ala)), ZBTB20(NM_001164342.2):c.154A>G (p.T52A)
ISCN -
DB-ID ZBTB20-AS1_000002 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) 0.0018 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
ZBTB20 NM_001164342.1 -?/. - c.154A>G r.(?) p.(Thr52Ala) -
ZBTB20-AS1 NR_038993.1 -?/. - n.979+4426T>C r.(?) - -


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