chr2:227661921:C>G Detail (hg19) (IRS1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr2:227,661,921-227,661,921 |
hg38 | chr2:226,797,205-226,797,205 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_005544.2:c.1534G>C | NP_005535.1:p.Ala512Pro |
Ensemble | ENST00000305123.6:c.1534G>C | ENST00000305123.6:p.Ala512Pro |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:<0.001 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:<0.001 |
Prediction
ClinVar
Clinical Significance |
![]() |
Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
![]() |
2014-10-09 | criteria provided, single submitter | type 2 diabetes mellitus |
![]() |
Detail |
![]() |
no assertion criteria provided | not specified |
![]() |
Detail | |
![]() |
2019-05-17 | criteria provided, single submitter | IRS1-related disorder |
![]() |
Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.087 | Metabolic syndrome X | The polymorphisms PstI and MaeIII of INS, NsiI of INSR and Ala513Pro and Gly972A... | BeFree | 18716398 | Detail |
0.167 | Metabolic syndrome X | The polymorphisms PstI and MaeIII of INS, NsiI of INSR and Ala513Pro and Gly972A... | BeFree | 18716398 | Detail |
<0.001 | Metabolic syndrome X | The polymorphisms PstI and MaeIII of INS, NsiI of INSR and Ala513Pro and Gly972A... | BeFree | 18716398 | Detail |
0.044 | polycystic ovary syndrome | Abnormal glucose tolerance and insulin resistance in polycystic ovary syndrome a... | BeFree | 16603055 | Detail |
0.627 | Diabetes Mellitus, Non-Insulin-Dependent | Two mutations of the IRS-1 gene (Gly(972)Arg and Ala(513)Pro) have been describe... | BeFree | 9162610 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_005544.3(IRS1):c.1534G>C (p.Ala512Pro) AND Type 2 diabetes mellitus | ClinVar | Detail |
NM_005544.3(IRS1):c.1534G>C (p.Ala512Pro) AND not specified | ClinVar | Detail |
NM_005544.3(IRS1):c.1534G>C (p.Ala512Pro) AND IRS1-related disorder | ClinVar | Detail |
The polymorphisms PstI and MaeIII of INS, NsiI of INSR and Ala513Pro and Gly972Arg of IRS1 have been... | DisGeNET | Detail |
The polymorphisms PstI and MaeIII of INS, NsiI of INSR and Ala513Pro and Gly972Arg of IRS1 have been... | DisGeNET | Detail |
The polymorphisms PstI and MaeIII of INS, NsiI of INSR and Ala513Pro and Gly972Arg of IRS1 have been... | DisGeNET | Detail |
Abnormal glucose tolerance and insulin resistance in polycystic ovary syndrome amongst the Taiwanese... | DisGeNET | Detail |
Two mutations of the IRS-1 gene (Gly(972)Arg and Ala(513)Pro) have been described, although their ro... | 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
- rs1801276 dbSNP
- Genome
- hg19
- Position
- chr2:227,661,921-227,661,921
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- G
- 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))
- rs1801276
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.0001
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 1
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
- East Asian Chromosome Counts (ExAC)
- 8626
- 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)
- 120558
- Allele Counts in All Race (ExAC)
- 1727
- Heterozygous Counts in All Race (ExAC)
- 1687
- Homozygous Counts in All Race (ExAC)
- 20
- Allele Frequency in All Race (ExAC)
- 0.014325055160171867
Genome browser