Variant #0000722943 (NC_000010.10:g.79397364_79397366dup, NM_001014797.2:c.54_56dup (KCNMA1))
Chromosome |
10 |
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.79397364_79397366dup |
DNA change (hg38) |
- |
Published as |
KCNMA1(NM_001161352.1):c.54_56dupCGG (p.(Gly19dup)), KCNMA1(NM_001322830.2):c.54_56dupCGG (p.G20dup), KCNMA1(NM_002247.4):c.54_56dupCGG (p.G20dup) |
ISCN |
- |
DB-ID |
KCNMA1_000100 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) |
Retrieve |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2021-02-08 18:36:18 +01:00 (CET) |
Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|