Variant #0000283660 (NC_000005.9:g.88057003_88057006del, NC_000005.9(NM_002397.4):c.401_402+2del (MEF2C))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.88057003_88057006del |
DNA change (hg38) |
g.88761186_88761189del |
Published as |
MEF2C(NM_002397.5):c.401_402+2delGTGT |
ISCN |
- |
DB-ID |
MEF2C_000014 |
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_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-06-17 11:52:08 +02:00 (CEST) |

Variant on transcripts
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