Variant #0000656359 (NC_000009.11:g.3829302C>G, NC_000009.11(NM_152629.3):c.2191+8G>C (GLIS3))
| Chromosome |
9 |
| 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.3829302C>G |
| DNA change (hg38) |
g.3829302C>G |
| Published as |
GLIS3(NM_001042413.1):c.2656+8G>C (p.(=)), GLIS3(NM_001042413.2):c.2656+8G>C |
| ISCN |
- |
| DB-ID |
GLIS3_000046 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_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2022-05-09 15:24:52 +02:00 (CEST) |

Variant on transcripts
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