Variant #0001068299 (NC_000016.9:g.89986130T>C, NM_002386.3:c.464T>C (MC1R))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.89986130T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID MC1R_000007 See all 6 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1110400
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00556 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-17 10:51:02 +01:00 (CET)
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 -?/. - c.464T>C r.(?) p.(Ile155Thr)


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