Variant #0000473565 (NC_000018.9:g.58038722A>Y, NM_005912.2:c.(861T>R) (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.58038722A>Y |
DNA change (hg38) |
- |
Published as |
Y287X |
ISCN |
- |
DB-ID |
MC4R_000000 See all 10 reported entries |
Variant remarks |
Variant Error [EMISMATCH/EUNCERTAIN]: This transcript variant has an error. Please fix this entry and then remove this message. |
Reference |
PubMed: Yeo 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 |
2011-01-19 13:14:37 +01:00 (CET) |

Variant on transcripts
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