Variant #0000527624 (NC_000006.11:g.152746682C>A, NM_182961.3:c.5101G>T (SYNE1))
Chromosome |
6 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.152746682C>A |
DNA change (hg38) |
g.152425547C>A |
Published as |
SYNE1(NM_033071.3):c.5122G>T (p.(Ala1708Ser)), SYNE1(NM_182961.3):c.5101G>T (p.A1701S), SYNE1(NM_182961.4):c.5101G>T (p.A1701S) |
ISCN |
- |
DB-ID |
SYNE1_000244 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) |
0.00247 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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