Variant #0000530966 (NC_000007.13:g.139480536del, NM_001061.4:c.-48651del (TBXAS1))

Chromosome 7
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.139480536del
DNA change (hg38) g.139780737del
Published as TBXAS1(NM_001130966.2):c.-314-3del (p.(=))
ISCN -
DB-ID HIPK2_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) Retrieve
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 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     
TBXAS1 NM_001061.4 -?/. - c.-48651del r.(?) p.(=)
HIPK2 NM_022740.4 -?/. - c.-3113del r.(?) p.(=)


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