TGFA transforming growth factor alpha

Information
Symbol
TGFA
Type
protein-coding
Description
transforming growth factor alpha
Entrez Gene ID
7039
Genome
hg19
Position
chr2:70,677,904-70,780,770
Genome
hg38
Position
chr2:70,450,772-70,553,638
MIM
190170 OMIM
HGNC
HGNC:11765 HGNC
Ensembl
ENSG00000163235 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 6
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
32
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 :
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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
SYNONYM TFGA
MIM 190170 OMIM
HGNC HGNC:11765 HGNC
Ensembl ENSG00000163235 Ensembl
AllianceGenome HGNC:11765
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000445399.5 hg38 chr2 70,449,319 70,553,772 104,454
ENST00000418333.6 hg38 chr2 70,450,173 70,553,826 103,654
ENST00000295400.11 hg38 chr2 70,447,284 70,553,826 106,543
ENST00000444975.5 hg38 chr2 70,450,772 70,553,638 102,867
ENST00000450929.5 hg38 chr2 70,450,656 70,553,490 102,835
ENST00000295400.11 hg19 chr2 70,674,416 70,780,958 106,543
ENST00000445399.5 hg19 chr2 70,676,451 70,780,904 104,454
ENST00000418333.6 hg19 chr2 70,677,305 70,780,958 103,654
ENST00000450929.5 hg19 chr2 70,677,788 70,780,622 102,835
ENST00000444975.5 hg19 chr2 70,677,904 70,780,770 102,867
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