chr14:52708263:C>T Detail (hg38) (PSMC6)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr14:53,174,981-53,174,981 View the variant detail on this assembly version. |
hg38 | chr14:52,708,263-52,708,263 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_002806.3:c.128-46C>T | |
Ensemble | ENST00000445930.7:c.86-46C>T | |
ENST00000612399.4:c.128-46C>T |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.164 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:0.142 |
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
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
To investigate polymorphisms of proteasomal genes PSMA6 (rs1048990 and rs2277460), PSMC6 (rs2295826 ... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs2295827 dbSNP
- Genome
- hg38
- Position
- chr14:52,708,263-52,708,263
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
- 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))
- rs2295827
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.1645
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 2757
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
- East Asian Chromosome Counts (ExAC)
- 7714
- East Asian Allele Counts (ExAC)
- 1095
- East Asian Heterozygous Counts (ExAC)
- 959
- East Asian Homozygous Counts (ExAC)
- 68
- East Asian Allele Frequency (ExAC)
- 0.1419497018408089
- Chromosome Counts in All Race (ExAC)
- 112734
- Allele Counts in All Race (ExAC)
- 11166
- Heterozygous Counts in All Race (ExAC)
- 9868
- Homozygous Counts in All Race (ExAC)
- 649
- Allele Frequency in All Race (ExAC)
- 0.09904731491830326
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