Variant #0000307712 (NC_000002.11:g.200213699_200213702del, NM_001172509.1:c.895_898del (SATB2))

Chromosome 2
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.200213699_200213702del
DNA change (hg38) g.199348976_199348979del
Published as SATB2(NM_001172509.2):c.895_898delTCTC (p.S299Pfs*8)
ISCN -
DB-ID SATB2_000024
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SATB2 NM_001172509.1 +/. - c.895_898del r.(?) p.(Ser299ProfsTer8)


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