Variant #0000321947 (NC_000011.9:g.2683246C>A, NM_000218.2:c.1449C>A (KCNQ1))
Chromosome |
11 |
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.2683246C>A |
DNA change (hg38) |
g.2662016C>A |
Published as |
KCNQ1(NM_000218.2):c.1449C>A (p.(Asn483Lys)), KCNQ1(NM_000218.3):c.1449C>A (p.N483K), KCNQ1OT1(NR_002728.3):n.37983G>T |
ISCN |
- |
DB-ID |
KCNQ1OT1_000002 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 |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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