Variant #0000528723 (NC_000006.11:g.33419617_33419619dup, NM_006772.2:c.3966_3968dup (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.33419617_33419619dup
DNA change (hg38) g.33451840_33451842dup
Published as SYNGAP1(NM_006772.2):c.3964_3965insCCC (p.(Ala1322_Pro1323insPro))
ISCN -
DB-ID SYNGAP1_000135
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 2019-07-18 18:22:55 +02:00 (CEST)
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     
SYNGAP1 NM_006772.2 -?/. - c.3966_3968dup r.(?) p.(Pro1327dup)
ZBTB9 NM_152735.3 -?/. - c.-3007_-3005dup r.(?) p.(=)


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