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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-07-31 20:40:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MC1R NM_002386.3 +?/+? 1 c.178G>T r.(?) p.(Val60Leu)


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