Variant #0000472752 (NC_000018.9:g.58040287T>A, NM_005912.2:c.-705A>T (MC4R))
| Chromosome |
18 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Probably does not affect function |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.58040287T>A |
| DNA change (hg38) |
g.60373054T>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MC4R_000006 See all 3 reported entries |
| Variant remarks |
The variant c.-705A>T is located in a putative cAMP responsive element according to an in silico analysis of Lubrano-Berthelier [2003]. We studied the effect of the c.-705A>T variant on promoter activity using a luciferase reporter gene assay. No significant difference between the wildtype and mutant promoter basal activity was observed. |
| Reference |
unpublished data van den Berg et al |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Linda van den Berg |
| Database submission license |
No license selected |
| Created by |
Linda van den Berg |
| Date created |
2011-01-21 16:34:53 +01:00 (CET) |
| Date last edited |
2019-12-04 12:41:11 +01:00 (CET) |

Variant on transcripts
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