Variant #0000614214 (NC_000012.11:g.50498404_50498405insCT, NM_005276.3:c.89_90insCT (GPD1))
| Chromosome |
12 |
| 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.50498404_50498405insCT |
| DNA change (hg38) |
g.50104621_50104622insCT |
| Published as |
GPD1(NM_001257199.1):c.89_90insCT (p.?) |
| ISCN |
- |
| DB-ID |
SMARCD1_000013 |
| 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 |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2020-07-02 15:24:08 +02:00 (CEST) |

Variant on transcripts
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