TCP11L2 t-complex 11 like 2

Information
Symbol
TCP11L2
Type
protein-coding
Description
t-complex 11 like 2
Entrez Gene ID
255394
Genome
hg19
Position
chr12:106,696,511-106,740,781
Genome
hg38
Position
chr12:106,302,733-106,347,003
MIM
619889 OMIM
HGNC
HGNC:28627 HGNC
Ensembl
ENSG00000166046 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
54
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
TypeID
MIM 619889 OMIM
HGNC HGNC:28627 HGNC
Ensembl ENSG00000166046 Ensembl
AllianceGenome HGNC:28627
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000299045.8 hg38 chr12 106,302,733 106,347,003 44,271
ENST00000546625.5 hg38 chr12 106,302,818 106,325,913 23,096
ENST00000547153.5 hg38 chr12 106,302,803 106,330,171 27,369
ENST00000299045.8 hg19 chr12 106,696,511 106,740,781 44,271
ENST00000547153.5 hg19 chr12 106,696,581 106,723,949 27,369
ENST00000546625.5 hg19 chr12 106,696,596 106,719,691 23,096
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