Variant #0000723345 (NC_000011.9:g.17793324G>T, NM_001112741.1:c.683G>T (KCNC1))
Chromosome |
11 |
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.17793324G>T |
DNA change (hg38) |
- |
Published as |
KCNC1(NM_001112741.2):c.683G>T (p.(Arg228Leu)), KCNC1(NM_004976.4):c.683G>T (p.R228L) |
ISCN |
- |
DB-ID |
KCNC1_000008 See all 3 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) |
0.00031 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2021-02-08 18:36:18 +01:00 (CET) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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