Variant #0000330960 (NC_000006.11:g.33384689G>A, NM_006772.2:c.-3353G>A (SYNGAP1))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.33384689G>A
DNA change (hg38) g.33416912G>A
Published as CUTA(NM_001014433.2):c.470+8C>T (p.(=))
ISCN -
DB-ID CUTA_000002
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHF1 NM_002636.4 ?/. - c.*1038G>A r.(=) p.(=)
SYNGAP1 NM_006772.2 ?/. - c.-3353G>A r.(?) p.(=)
CUTA NM_015921.2 ?/. - c.344+8C>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.