Variant #0000330961 (NC_000006.11:g.33385887A>G, NM_006772.2:c.-2155A>G (SYNGAP1))

Chromosome 6
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.33385887A>G
DNA change (hg38) g.33418110A>G
Published as CUTA(NM_001014433.2):c.76T>C (p.(Ser26Pro))
ISCN -
DB-ID CUTA_000003
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) 0.00991 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
PHF1 NM_002636.4 -?/. - c.*2236A>G r.(=) p.(=)
SYNGAP1 NM_006772.2 -?/. - c.-2155A>G r.(?) p.(=)
CUTA NM_015921.2 -?/. - c.-442T>C r.(?) p.(=)


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