Variant #0000288895 (NC_000017.10:g.7906494_7906499del, NM_000180.3:c.129_134del (GUCY2D))
Chromosome |
17 |
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.7906494_7906499del |
DNA change (hg38) |
g.8003176_8003181del |
Published as |
GUCY2D(NM_000180.3):c.129_134delTCTGCT (p.(Leu44_Leu45del)), GUCY2D(NM_000180.3):c.129_134delTCTGCT (p.L44_L45del), GUCY2D(NM_000180.4):c.129_134de... |
ISCN |
- |
DB-ID |
GUCY2D_000027 See all 7 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 |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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