Variant #0000720764 (NC_000006.11:g.152768726T>G, NM_182961.3:c.3536A>C (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.152768726T>G |
DNA change (hg38) |
- |
Published as |
SYNE1(NM_033071.3):c.3557A>C (p.(Glu1186Ala)), SYNE1(NM_033071.5):c.3557A>C (p.E1186A), SYNE1(NM_182961.3):c.3536A>C (p.E1179A), SYNE1(NM_182961.4)... |
ISCN |
- |
DB-ID |
SYNE1_000811 See all 10 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) |
0.00066 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2021-02-08 18:36:18 +01:00 (CET) |
Date last edited |
2024-10-29 21:08:56 +01:00 (CET) |

Variant on transcripts
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