TSACC TSSK6 activating cochaperone
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
12 |
![]() |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | C1orf182 |
SYNONYM | SIP |
SYNONYM | SSTK-IP |
MIM | 619679 OMIM |
HGNC | HGNC:30636 HGNC |
Ensembl | ENSG00000163467 Ensembl |
AllianceGenome | HGNC:30636 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000470342.5 | hg38 | chr1 | 156,338,507 | 156,346,993 | 8,487 |
ENST00000466306.5 | hg38 | chr1 | 156,338,788 | 156,346,992 | 8,205 |
ENST00000368254.6 | hg38 | chr1 | 156,338,526 | 156,346,995 | 8,470 |
ENST00000368255.7 | hg38 | chr1 | 156,337,314 | 156,346,995 | 9,682 |
ENST00000368252.5 | hg38 | chr1 | 156,338,694 | 156,346,995 | 8,302 |
ENST00000368253.6 | hg38 | chr1 | 156,338,503 | 156,346,990 | 8,488 |
ENST00000368251.1 | hg38 | chr1 | 156,338,902 | 156,346,995 | 8,094 |
ENST00000481479.5 | hg38 | chr1 | 156,338,628 | 156,346,995 | 8,368 |
ENST00000368255.7 | hg19 | chr1 | 156,307,105 | 156,316,786 | 9,682 |
ENST00000368253.6 | hg19 | chr1 | 156,308,294 | 156,316,781 | 8,488 |
ENST00000470342.5 | hg19 | chr1 | 156,308,298 | 156,316,784 | 8,487 |
ENST00000368254.6 | hg19 | chr1 | 156,308,317 | 156,316,786 | 8,470 |
ENST00000481479.5 | hg19 | chr1 | 156,308,419 | 156,316,786 | 8,368 |
ENST00000368252.5 | hg19 | chr1 | 156,308,485 | 156,316,786 | 8,302 |
ENST00000466306.5 | hg19 | chr1 | 156,308,579 | 156,316,783 | 8,205 |
ENST00000368251.1 | hg19 | chr1 | 156,308,693 | 156,316,786 | 8,094 |
Genome browser