chr14:64269942:G>C Detail (hg38) (ESR2)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr14:64,736,660-64,736,660 View the variant detail on this assembly version. |
hg38 | chr14:64,269,942-64,269,942 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001271877.1:c.536-1031C>G | |
NM_001437.2:c.536-1031C>G | ||
NM_001040275.1:c.536-1031C>G |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.222 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:[No Data.] |
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 | HIV Infections | To investigate genetic single nucleotide polymorphisms (SNPs) in estrogen recept... | BeFree | 22011627 | Detail |
0.003 | Metabolic syndrome X | To investigate genetic single nucleotide polymorphisms (SNPs) in estrogen recept... | BeFree | 22011627 | Detail |
0.007 | Metabolic syndrome X | To investigate genetic single nucleotide polymorphisms (SNPs) in estrogen recept... | BeFree | 22011627 | Detail |
<0.001 | HIV Infections | To investigate genetic single nucleotide polymorphisms (SNPs) in estrogen recept... | BeFree | 22011627 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
To investigate genetic single nucleotide polymorphisms (SNPs) in estrogen receptor-α (ERα) (ESR1, rs... | DisGeNET | Detail |
To investigate genetic single nucleotide polymorphisms (SNPs) in estrogen receptor-α (ERα) (ESR1, rs... | DisGeNET | Detail |
To investigate genetic single nucleotide polymorphisms (SNPs) in estrogen receptor-α (ERα) (ESR1, rs... | DisGeNET | Detail |
To investigate genetic single nucleotide polymorphisms (SNPs) in estrogen receptor-α (ERα) (ESR1, rs... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs7154455 dbSNP
- Genome
- hg38
- Position
- chr14:64,269,942-64,269,942
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- C
- 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))
- rs7154455
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.2217
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 3716
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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