Variant #0000515130 (NC_000002.11:g.233712226_233712227insGC, NM_002242.4:c.-71088_-71087insCG (KCNJ13))
| Chromosome |
2 |
| 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.233712226_233712227insGC |
| DNA change (hg38) |
g.232847516_232847517insGC |
| Published as |
GIGYF2(NM_015575.3):c.3629_3630insGC (p.Q1211Hfs*25), GIGYF2(NM_015575.4):c.3629_3630insGC (p.Q1211Hfs*25) |
| ISCN |
- |
| DB-ID |
GIGYF2_000040 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_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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