INHA inhibin subunit alpha

Information
Symbol
INHA
Type
protein-coding
Description
inhibin subunit alpha
Entrez Gene ID
3623
Genome
hg19
Position
chr2:220,437,032-220,440,433
Genome
hg38
Position
chr2:219,572,310-219,575,711
MIM
147380 OMIM
HGNC
HGNC:6065 HGNC
Ensembl
ENSG00000123999 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 20
not provided 5 0
Uncertain significance 0 38
Ranking
ClinVar
0
0
4
58
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 147380 OMIM
HGNC HGNC:6065 HGNC
Ensembl ENSG00000123999 Ensembl
AllianceGenome HGNC:6065
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000243786.3 hg38 chr2 219,572,310 219,575,711 3,402
ENST00000243786.3 hg19 chr2 220,437,032 220,440,433 3,402
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