Variant #0000127906 (NC_000016.9:g.89985844G>T, NM_002386.3:c.178G>T (MC1R))
| Chromosome |
16 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.89985844G>T |
| DNA change (hg38) |
g.89919436G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MC1R_000013 See all 6 reported entries |
| Variant remarks |
associated with red hair, partially penetrant autosomal recessive allele |
| Reference |
PubMed: Flanagan 2000 |
| ClinVar ID |
- |
| dbSNP ID |
rs1805005 |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.08493 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2016-07-31 20:40:30 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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