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 International |
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) |

Variant on transcripts
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