chr18-13884918-G-T
Variant summary
Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2BP4_Moderate
The NM_000529.2(MC2R):c.601C>A(p.Arg201=) variant causes a synonymous change involving the alteration of a conserved nucleotide. The variant allele was found at a frequency of 0.0000372 in 1,613,640 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.
Frequency
Consequence
NM_000529.2 synonymous
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Uncertain_significance. Variant got 0 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
MC2R | NM_000529.2 | c.601C>A | p.Arg201= | synonymous_variant | 2/2 | ENST00000327606.4 | |
MC2R | NM_001291911.1 | c.601C>A | p.Arg201= | synonymous_variant | 2/2 | ||
MC2R | XM_017025781.2 | c.601C>A | p.Arg201= | synonymous_variant | 3/3 | ||
MC2R | XM_047437537.1 | c.601C>A | p.Arg201= | synonymous_variant | 4/4 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
MC2R | ENST00000327606.4 | c.601C>A | p.Arg201= | synonymous_variant | 2/2 | 1 | NM_000529.2 | P1 |
Frequencies
GnomAD3 genomes ? AF: 0.0000132 AC: 2AN: 151758Hom.: 0 Cov.: 32
GnomAD3 exomes AF: 0.0000199 AC: 5AN: 251354Hom.: 0 AF XY: 0.0000221 AC XY: 3AN XY: 135862
GnomAD4 exome AF: 0.0000397 AC: 58AN: 1461882Hom.: 0 Cov.: 32 AF XY: 0.0000426 AC XY: 31AN XY: 727244
GnomAD4 genome ? AF: 0.0000132 AC: 2AN: 151758Hom.: 0 Cov.: 32 AF XY: 0.00 AC XY: 0AN XY: 74110
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at