Variant #0000658315 (NC_000018.9:g.13884629A>G, NM_000529.2:c.889T>C (MC2R))

Chromosome 18
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.13884629A>G
DNA change (hg38) g.13884630A>G
Published as MC2R(NM_000529.2):c.889T>C (p.(Trp297Arg)), MC2R(NM_001291911.1):c.889T>C (p.W297R)
ISCN -
DB-ID MC2R_000006 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-03-23 16:13:27 +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     
MC2R NM_000529.2 -?/. - c.889T>C r.(?) p.(Trp297Arg)


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