TDRD12 tudor domain containing 12
Information
- Symbol
- TDRD12
- Type
- protein-coding
- Description
- tudor domain containing 12
- Entrez Gene ID
- 91646
- Genome
- hg19
- Position
- chr19:33,210,673-33,320,486
- Genome
- hg38
- Position
- chr19:32,719,767-32,829,580
- HGNC
- HGNC:25044 HGNC
- Ensembl
- ENSG00000173809 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 8 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
2 |
![]() |
56 |
![]() |
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 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000639142.2 | hg38 | chr19 | 32,719,767 | 32,829,580 | 109,814 |
ENST00000444215.6 | hg38 | chr19 | 32,719,753 | 32,821,263 | 101,511 |
ENST00000647536.1 | hg38 | chr19 | 32,720,013 | 32,827,414 | 107,402 |
ENST00000421545.2 | hg38 | chr19 | 32,720,073 | 32,790,808 | 70,736 |
ENST00000444215.6 | hg19 | chr19 | 33,210,659 | 33,312,169 | 101,511 |
ENST00000639142.2 | hg19 | chr19 | 33,210,673 | 33,320,486 | 109,814 |
ENST00000647536.1 | hg19 | chr19 | 33,210,919 | 33,318,320 | 107,402 |
ENST00000421545.2 | hg19 | chr19 | 33,210,979 | 33,281,714 | 70,736 |
Genome browser