Variant #0000865035 (NC_000016.9:g.89985845T>C, NM_002386.3:c.179T>C (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.89985845T>C
DNA change (hg38) -
Published as MC1R(NM_002386.3):c.179T>C (p.V60A)
ISCN -
DB-ID MC1R_000052
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MC1R NM_002386.3 ?/. - c.179T>C r.(?) p.(Val60Ala)
TUBB3 NM_006086.3 ?/. - c.-3965T>C r.(?) p.(=)


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