Variant #0000127905 (NC_000016.9:g.89985752dup, NM_002386.3:c.86dup (MC1R))

Chromosome 16
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.89985752dup
DNA change (hg38) g.89919344dup
Published as 86insA
ISCN -
DB-ID MC1R_000004 See all 6 reported entries
Variant remarks associated with red hair, inheritance autosomal recessive
Reference PubMed: Flanagan 2000
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 20:35:05 +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.86dup r.(?) p.(Asn29Lysfs*14)


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