chr18:58039276:C>T Detail (hg19) (MC4R)

Information

Genome

Assembly Position
hg19 chr18:58,039,276-58,039,276
hg38 chr18:60,372,043-60,372,043 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_005912.2:c.307G>A NP_005903.2:p.Val103Ile
Ensemble ENST00000299766.5:c.307G>A ENST00000299766.5:p.Val103Ile
Summary

MGeND

Clinical significance Benign
Variant entry 1
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:0.012
ToMMo:0.008
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:0.024

Prediction

ClinVar

Clinical Significance Benign
Review star
Show details
Links
Type Database ID Link
Gene MIM 155541 OMIM
HGNC 6932 HGNC
Ensembl ENSG00000166603 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv60220664 TogoVar
COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
Benign Centenarian germline MGS000068
(TMGS000140)
Kenjiro Kosaki Keio University
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Benign 2018-03-06 criteria provided, single submitter obesity germline Detail
Benign 2019-01-18 criteria provided, single submitter Monogenic diabetes unknown Detail
Benign 1999-04-01 no assertion criteria provided MELANOCORTIN 4 RECEPTOR POLYMORPHISM germline Detail
protective 1999-04-01 no assertion criteria provided OBESITY, RESISTANCE TO germline Detail
Benign no assertion criteria provided not specified germline Detail
Pathogenic 2020-05-01 no assertion criteria provided BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20 unknown Detail
Benign 2024-01-13 criteria provided, single submitter not provided germline Detail
Benign 2021-11-08 criteria provided, single submitter MC4R-related disorder germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.791 obesity Our study confirms previous findings of a meta-analysis that the relatively infr... BeFree 15805150 Detail
0.069 obesity Among the single-nucleotide polymorphisms (SNPs) previously reported to be assoc... BeFree 24518831 Detail
0.004 Cachexia Val103Ile polymorphism of the melanocortin-4 receptor gene (MC4R) in cancer cach... BeFree 18377640 Detail
0.791 obesity A low frequency of genetic variation in the coding region of MC4R was found in C... BeFree 20406574 Detail
0.791 obesity The 103Ile allele of the Val103Ile single nucleotide polymorphism (SNP) of the m... BeFree 20054160 Detail
0.006 Metabolic syndrome X Association of the MC4R V103I polymorphism with the metabolic syndrome: the KORA... BeFree 18239646 Detail
0.791 obesity Prevalence of melanocortin receptor 4 (MC4R) V103I gene variant and its associat... BeFree 22822657 Detail
0.791 obesity In humans, MC4R mutations that lead to an impaired receptor function are associa... BeFree 18377640 Detail
0.019 Obesity, Morbid The purpose of the study was to investigate the association between the MC4R V10... BeFree 18779298 Detail
0.791 obesity Association of the MC4R V103I polymorphism with obesity: a Chinese case-control ... BeFree 19696756 Detail
0.791 obesity Association of the melanocortin-4 receptor V103I polymorphism with dietary intak... BeFree 18779298 Detail
0.791 obesity The objective of this study was to examine the Val103Ile polymorphism of MC4R in... BeFree 19283510 Detail
0.002 Diabetes These results suggest that mutations including V103I in the MC4R gene are not a ... BeFree 11246450 Detail
0.791 obesity It further establishes that the association of the MC4R V103I with obesity and r... BeFree 18239646 Detail
0.791 obesity The influence of rs2229616 (MC4R) on BMI and obesity has been confirmed repeated... BeFree 24518831 Detail
0.004 diabetes mellitus These results suggest that mutations including V103I in the MC4R gene are not a ... BeFree 11246450 Detail
0.003 atherosclerosis To investigate the effects of variation in the leptin [LEP (19A>G)] and melan... BeFree 17587397 Detail
0.003 arteriosclerosis To investigate the effects of variation in the leptin [LEP (19A>G)] and melan... BeFree 17587397 Detail
<0.001 Overweight and obesity Val103Ile polymorphism of melanocortin-4 receptor is unlikely to be a major caus... BeFree 19283510 Detail
<0.001 arteriosclerosis To investigate the effects of variation in the leptin [LEP (19A&gt;G)] and melan... BeFree 17587397 Detail
0.791 obesity In the current study, we compared the eating behavior of 43 obese probands with ... BeFree 15037865 Detail
0.791 obesity The V103I polymorphism of the MC4R gene and obesity: population based studies an... BeFree 17356525 Detail
<0.001 atherosclerosis To investigate the effects of variation in the leptin [LEP (19A&gt;G)] and melan... BeFree 17587397 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_005912.3(MC4R):c.307G>A (p.Val103Ile) AND Obesity ClinVar Detail
NM_005912.3(MC4R):c.307G>A (p.Val103Ile) AND Monogenic diabetes ClinVar Detail
NM_005912.3(MC4R):c.307G>A (p.Val103Ile) AND MELANOCORTIN 4 RECEPTOR POLYMORPHISM ClinVar Detail
NM_005912.3(MC4R):c.307G>A (p.Val103Ile) AND OBESITY, RESISTANCE TO ClinVar Detail
NM_005912.3(MC4R):c.307G>A (p.Val103Ile) AND not specified ClinVar Detail
NM_005912.3(MC4R):c.307G>A (p.Val103Ile) AND BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20 ClinVar Detail
NM_005912.3(MC4R):c.307G>A (p.Val103Ile) AND not provided ClinVar Detail
NM_005912.3(MC4R):c.307G>A (p.Val103Ile) AND MC4R-related disorder ClinVar Detail
Our study confirms previous findings of a meta-analysis that the relatively infrequent G/A genotype ... DisGeNET Detail
Among the single-nucleotide polymorphisms (SNPs) previously reported to be associated with body mass... DisGeNET Detail
Val103Ile polymorphism of the melanocortin-4 receptor gene (MC4R) in cancer cachexia. DisGeNET Detail
A low frequency of genetic variation in the coding region of MC4R was found in Chilean obese childre... DisGeNET Detail
The 103Ile allele of the Val103Ile single nucleotide polymorphism (SNP) of the melanocortin-4 recept... DisGeNET Detail
Association of the MC4R V103I polymorphism with the metabolic syndrome: the KORA Study. DisGeNET Detail
Prevalence of melanocortin receptor 4 (MC4R) V103I gene variant and its association with obesity amo... DisGeNET Detail
In humans, MC4R mutations that lead to an impaired receptor function are associated with obesity; in... DisGeNET Detail
The purpose of the study was to investigate the association between the MC4R V103I polymorphism and ... DisGeNET Detail
Association of the MC4R V103I polymorphism with obesity: a Chinese case-control study and meta-analy... DisGeNET Detail
Association of the melanocortin-4 receptor V103I polymorphism with dietary intake in severely obese ... DisGeNET Detail
The objective of this study was to examine the Val103Ile polymorphism of MC4R in a population of Voj... DisGeNET Detail
These results suggest that mutations including V103I in the MC4R gene are not a major cause of obesi... DisGeNET Detail
It further establishes that the association of the MC4R V103I with obesity and related phenotypes is... DisGeNET Detail
The influence of rs2229616 (MC4R) on BMI and obesity has been confirmed repeatedly and insight into ... DisGeNET Detail
These results suggest that mutations including V103I in the MC4R gene are not a major cause of obesi... DisGeNET Detail
To investigate the effects of variation in the leptin [LEP (19A&gt;G)] and melanocortin-4 receptor [... DisGeNET Detail
To investigate the effects of variation in the leptin [LEP (19A&gt;G)] and melanocortin-4 receptor [... DisGeNET Detail
Val103Ile polymorphism of melanocortin-4 receptor is unlikely to be a major cause of overweight and ... DisGeNET Detail
To investigate the effects of variation in the leptin [LEP (19A&gt;G)] and melanocortin-4 receptor [... DisGeNET Detail
In the current study, we compared the eating behavior of 43 obese probands with functionally relevan... DisGeNET Detail
The V103I polymorphism of the MC4R gene and obesity: population based studies and meta-analysis of 2... DisGeNET Detail
To investigate the effects of variation in the leptin [LEP (19A&gt;G)] and melanocortin-4 receptor [... 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
-
dbSNP
rs2229616 dbSNP
Genome
hg19
Position
chr18:58,039,276-58,039,276
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Filtering Status (HGVD)
PASS
# of samples (HGVD)
1210
Mean of sample read depth (HGVD)
192.13
Standard deviation of sample read depth (HGVD)
81.68
Number of reference allele (HGVD)
2390
Number of alternative allele (HGVD)
30
Allele Frequency (HGVD)
0.012396694214876033
Gene Symbol (HGVD)
MC4R
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs2229616
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.0078
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
131
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
East Asian Chromosome Counts (ExAC)
8648
East Asian Allele Counts (ExAC)
204
East Asian Heterozygous Counts (ExAC)
200
East Asian Homozygous Counts (ExAC)
2
East Asian Allele Frequency (ExAC)
0.02358926919518964
Chromosome Counts in All Race (ExAC)
121398
Allele Counts in All Race (ExAC)
2116
Heterozygous Counts in All Race (ExAC)
2062
Homozygous Counts in All Race (ExAC)
27
Allele Frequency in All Race (ExAC)
0.017430270679912353
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