Variant #0000554828 (NC_000015.9:g.57213234_57213235insGA, NM_207037.1:c.86_87insGA (TCF12))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57213234_57213235insGA
DNA change (hg38) g.56921036_56921037insGA
Published as TCF12(NM_207037.1):c.86_87insGA (p.P30Nfs*58)
ISCN -
DB-ID TCF12_000047
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_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 2020-07-06 15:07:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TCF12 NM_207037.1 +/. - c.86_87insGA r.(?) p.(Pro30AsnfsTer58)


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