chr18:58039291:C>T Detail (hg19) (MC4R)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr18:58,039,291-58,039,291 |
hg38 | chr18:60,372,058-60,372,058 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_005912.2:c.292G>A | NP_005903.2:p.Gly98Arg |
Ensemble | ENST00000299766.5:c.292G>A | ENST00000299766.5:p.Gly98Arg |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:[No Data.] | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:<0.001 |
Prediction
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
<0.001 | obesity | As tested with 12 obesity-causing human MC4R variants including S58C, E61K, N62S... | BeFree | 24780838 | Detail |
<0.001 | obesity | As tested with 12 obesity-causing human MC4R variants including S58C, E61K, N62S... | BeFree | 24780838 | Detail |
0.791 | obesity | As tested with 12 obesity-causing human MC4R variants including S58C, E61K, N62S... | BeFree | 24780838 | Detail |
<0.001 | obesity | As tested with 12 obesity-causing human MC4R variants including S58C, E61K, N62S... | BeFree | 24780838 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
As tested with 12 obesity-causing human MC4R variants including S58C, E61K, N62S, I69T, P78L, C84R, ... | DisGeNET | Detail |
As tested with 12 obesity-causing human MC4R variants including S58C, E61K, N62S, I69T, P78L, C84R, ... | DisGeNET | Detail |
As tested with 12 obesity-causing human MC4R variants including S58C, E61K, N62S, I69T, P78L, C84R, ... | DisGeNET | Detail |
As tested with 12 obesity-causing human MC4R variants including S58C, E61K, N62S, I69T, P78L, C84R, ... | DisGeNET | Detail |
Overlapped Transcript Coordinates
Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
---|
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- Genome
- hg19
- Position
- chr18:58,039,291-58,039,291
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
- East Asian Chromosome Counts (ExAC)
- 8650
- East Asian Allele Counts (ExAC)
- 0
- East Asian Heterozygous Counts (ExAC)
- 0
- East Asian Homozygous Counts (ExAC)
- 0
- East Asian Allele Frequency (ExAC)
- 0.0
- Chromosome Counts in All Race (ExAC)
- 121402
- Allele Counts in All Race (ExAC)
- 1
- Heterozygous Counts in All Race (ExAC)
- 1
- Homozygous Counts in All Race (ExAC)
- 0
- Allele Frequency in All Race (ExAC)
- 8.237096588194593E-6
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