Variant #0000810748 (NC_000006.11:g.33408514C>T, NM_006772.2:c.1685C>T (SYNGAP1))

Chromosome 6
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.33408514C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SYNGAP1_000010 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs397514670
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-09-17 16:37:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SYNGAP1 NM_006772.2 +/. - c.1685C>T r.(?) p.(Pro562Leu)


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