Variant #0000308916 (NC_000006.11:g.152806014C>T, NM_182961.3:c.1141G>A (SYNE1))
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.152806014C>T |
DNA change (hg38) |
g.152484879C>T |
Published as |
SYNE1(NM_033071.5):c.1162G>A (p.D388N), SYNE1(NM_182961.3):c.1141G>A (p.D381N), SYNE1(NM_182961.4):c.1141G>A (p.D381N) |
ISCN |
- |
DB-ID |
SYNE1_000290 See all 12 reported entries |
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) |
0.00128 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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