Variant #0000505068 (NC_000001.10:g.211280737_211280738del, NC_000001.10(NM_172362.2):c.80-7_80-6del (KCNH1))
Chromosome |
1 |
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.211280737_211280738del |
DNA change (hg38) |
g.211107395_211107396del |
Published as |
KCNH1(NM_002238.3):c.80-7_80-6del (p.(=)), KCNH1(NM_172362.2):c.80-7_80-6delTT |
ISCN |
- |
DB-ID |
KCNH1_000010 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) |
Retrieve |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-04-19 20:20:39 +02:00 (CEST) |

Variant on transcripts
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