Variant #0000527446 (NC_000006.11:g.152443761C>T, NM_182961.3:c.26204G>A (SYNE1))
Chromosome |
6 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.152443761C>T |
DNA change (hg38) |
g.152122626C>T |
Published as |
SYNE1(NM_182961.3):c.26204G>A (p.R8735Q), SYNE1(NM_182961.4):c.26204G>A (p.R8735Q) |
ISCN |
- |
DB-ID |
SYNE1_000908 See all 2 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) |
0.05176 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
|