Variant #0000274644 (NC_000006.11:g.33384462_33384463del, NM_006772.2:c.-3580_-3579del (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.33384462_33384463del
DNA change (hg38) g.33416685_33416686del
Published as CUTA(NM_015921.2):c.437_438delAG (p.E146Vfs*4)
ISCN -
DB-ID CUTA_000001
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-19 11:21:51 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHF1 NM_002636.4 ?/. - c.*811_*812del r.(=) p.(=)
SYNGAP1 NM_006772.2 ?/. - c.-3580_-3579del r.(?) p.(=)
CUTA NM_015921.2 ?/. - c.437_438del r.(?) p.(Glu146ValfsTer4)


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