Variant #0000912483 (NC_000006.11:g.33388110T>C, NC_000006.11(NM_006772.2):c.67+2T>C (SYNGAP1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.33388110T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID CUTA_000007
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHF1 NM_002636.4 +?/. - c.*4459T>C r.(=) p.(=)
SYNGAP1 NM_006772.2 +?/. - c.67+2T>C r.spl? p.?
CUTA NM_015921.2 +?/. - c.-2665A>G r.(?) p.(=)


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