Variant #0000573246 (NC_000023.10:g.119389086A>G, NM_017938.3:c.*5639T>C (FAM70A))

Chromosome X
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.119389086A>G
DNA change (hg38) g.120255231A>G
Published as ZBTB33(NM_001184742.2):c.1816A>G (p.T606A)
ISCN -
DB-ID ZBTB33_000016
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) 6.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
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     
ZBTB33 NM_006777.3 -?/. - c.1816A>G r.(?) p.(Thr606Ala)
FAM70A NM_017938.3 -?/. - c.*5639T>C r.(=) p.(=)


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