Variant #0000623591 (NC_000016.9:g.89986122C>A, NM_002386.3:c.456C>A (MC1R))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.89986122C>A
DNA change (hg38) g.89919714C>A
Published as MC1R(NM_002386.3):c.456C>A (p.Y152*)
ISCN -
DB-ID MC1R_000050
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) 0.00081 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-10 18:02:43 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MC1R NM_002386.3 +/. - c.456C>A r.(?) p.(Tyr152Ter)
TUBB3 NM_006086.3 +/. - c.-3688C>A r.(?) p.(=)


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