Variant #0000961968 (NC_000002.11:g.233712227_233712229del, NM_002242.4:c.-71091_-71089del (KCNJ13))
Chromosome |
2 |
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.233712227_233712229del |
DNA change (hg38) |
- |
Published as |
GIGYF2(NM_001103147.1):c.3693_3695delACA (p.Q1237del), GIGYF2(NM_001103147.2):c.3693_3695delACA (p.Q1237del), GIGYF2(NM_015575.4):c.3630_3632delACA... |
ISCN |
- |
DB-ID |
GIGYF2_000042 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 |
2024-02-26 20:06:56 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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