chr11:11989899:T>C Detail (hg19) (DKK3)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr11:11,989,899-11,989,899 |
hg38 | chr11:11,968,352-11,968,352 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001330220.1:c.528+43A>G | |
NM_001018057.1:c.528+43A>G | ||
NM_015881.5:c.528+43A>G |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.720 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:0.723 |
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 |
---|---|---|---|---|---|
0.003 | renal cell carcinoma | including Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs170... | BeFree | 19562778 | Detail |
0.003 | renal cell carcinoma | including Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs170... | BeFree | 19562778 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
including Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, an... | DisGeNET | Detail |
including Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, an... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs2291599 dbSNP
- Genome
- hg19
- Position
- chr11:11,989,899-11,989,899
- Variant Type
- snv
- Reference Allele
- T
- 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))
- rs2291599
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.7195
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 12058
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16758
- East Asian Chromosome Counts (ExAC)
- 8366
- East Asian Allele Counts (ExAC)
- 6045
- East Asian Heterozygous Counts (ExAC)
- 1735
- East Asian Homozygous Counts (ExAC)
- 2155
- East Asian Allele Frequency (ExAC)
- 0.7225675352617739
- Chromosome Counts in All Race (ExAC)
- 115082
- Allele Counts in All Race (ExAC)
- 95524
- Heterozygous Counts in All Race (ExAC)
- 15718
- Homozygous Counts in All Race (ExAC)
- 39903
- Allele Frequency in All Race (ExAC)
- 0.8300516153699101
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