Variant #0000279621 (NC_000016.9:g.89986119C>G, NM_002386.3:c.453C>G (MC1R))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.89986119C>G
DNA change (hg38) g.89919711C>G
Published as MC1R(NM_002386.4):c.453C>G (p.R151=)
ISCN -
DB-ID MC1R_000025
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00069 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MC1R NM_002386.3 ?/. - c.453C>G r.(?) p.(Arg151=)
TUBB3 NM_006086.3 ?/. - c.-3691C>G r.(?) p.(=)


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