Variant #0000622433 (NC_000010.10:g.79397284_79397286dup, NM_001014797.2:c.135_137dup (KCNMA1))
| Chromosome |
10 |
| 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.79397284_79397286dup |
| DNA change (hg38) |
g.77637526_77637528dup |
| Published as |
KCNMA1(NM_001014797.3):c.135_137dupCTC (p.S60dup), KCNMA1(NM_001322830.2):c.135_137dupCTC (p.S60dup) |
| ISCN |
- |
| DB-ID |
KCNMA1_000092 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_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2019-12-06 12:43:26 +01:00 (CET) |
| Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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