SEMG1 semenogelin 1

Information
Symbol
SEMG1
Type
protein-coding
Description
semenogelin 1
Entrez Gene ID
6406
Genome
hg19
Position
chr20:43,835,674-43,838,409
Genome
hg38
Position
chr20:45,207,033-45,209,768
MIM
182140 OMIM
HGNC
HGNC:10742 HGNC
Ensembl
ENSG00000124233 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
not provided 1 0
Uncertain significance 0 66
Ranking
ClinVar
0
0
0
72
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
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
SYNONYM CT103
SYNONYM SEMG
SYNONYM SGI
SYNONYM dJ172H20.2
MIM 182140 OMIM
HGNC HGNC:10742 HGNC
Ensembl ENSG00000124233 Ensembl
AllianceGenome HGNC:10742
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000372781.4 hg38 chr20 45,207,033 45,209,768 2,736
ENST00000372781.4 hg19 chr20 43,835,674 43,838,409 2,736
Genome browser