{{Rsnum
|rsid=6594681
|Gene=MCC
|Chromosome=5
|position=113104244
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.002296
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MCC
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 97.3 | 2.7 | 0.0
| HCB | 99.3 | 0.7 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 99.3 | 0.7 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 98.1 | 1.9 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=6594681
|allele=C
|frequency=1
|uid=1103654193136
|type=homozygous_SNP
|hugo=MCC
|ensembl gene=ENSG00000171444
|ensembl transcript=ENST00000359932
|sift=TOLERATED
|disease=Is probably involved in early stages of colorectal neoplasia in both sporadic and familial tumors.
}}

{{GET Evidence
|gene=MCC
|aa_change=Lys380Arg
|aa_change_short=K380R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6594681
|overall_frequency_n=10679
|overall_frequency_d=10756
|overall_frequency=0.992841
|n_genomes=56
|n_genomes_annotated=0
|n_haplomes=111
|n_articles=0
|n_articles_annotated=0
|nblosum100=-3
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}