Variant #0000473115 (NC_000018.9:g.(58039247_58039250)insT, NM_005912.2:c.(333_336)insA (MC4R))
| Chromosome |
18 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(58039247_58039250)insT |
| DNA change (hg38) |
- |
| Published as |
ins A at codon 112 |
| ISCN |
- |
| DB-ID |
MC4R_000000 See all 10 reported entries |
| Variant remarks |
Variant Error [ESYNTAX]: This genomic variant has an error (insertion length must be 1). Please fix this entry and then remove this message. |
| Reference |
PubMed: Farooqi et al 2003 |
| 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 |
2010-10-22 15:10:09 +02:00 (CEST) |
| Date last edited |
2011-01-21 13:47:09 +01:00 (CET) |

Variant on transcripts
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