Variant #0000547830 (NC_000012.11:g.32777902T>C, NC_000012.11(NM_139241.2):c.1543-8T>C (FGD4))
| Chromosome |
12 |
| 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.32777902T>C |
| DNA change (hg38) |
g.32624968T>C |
| Published as |
FGD4(NM_001304484.2):c.511-8T>C, FGD4(NM_139241.3):c.1543-8T>C |
| ISCN |
- |
| DB-ID |
FGD4_000050 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) |
0.00353 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-07-07 10:10:56 +02:00 (CEST) |

Variant on transcripts
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