Variant #0000893300 (NC_000016.9:g.89985918C>A, NM_002386.3:c.252C>A (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.89985918C>A
DNA change (hg38) -
Published as MC1R(NM_002386.3):c.252C>A (p.(Asp84Glu)), MC1R(NM_002386.4):c.252C>A (p.D84E)
ISCN -
DB-ID MC1R_000039 See all 2 reported entries
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) 0.00528 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 2022-11-01 13:41:49 +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.252C>A r.(?) p.(Asp84Glu)
TUBB3 NM_006086.3 -?/. - c.-3892C>A r.(?) p.(=)


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