SERPINA7 serpin family A member 7

Information
Symbol
SERPINA7
Type
protein-coding
Description
serpin family A member 7
Entrez Gene ID
6906
Genome
hg19
Position
chrX:105,276,433-105,281,385
Genome
hg38
Position
chrX:106,032,442-106,037,394
MIM
314200 OMIM
HGNC
HGNC:11583 HGNC
Ensembl
ENSG00000123561 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 1 6
Benign 0 10
Likely benign 0 8
association 0 28
Conflicting classifications of pathogenicity 0 4
not provided 6 0
Uncertain significance 0 32
Ranking
ClinVar
0
0
6
44
34
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 TBG
SYNONYM TBGQTL
MIM 314200 OMIM
HGNC HGNC:11583 HGNC
Ensembl ENSG00000123561 Ensembl
AllianceGenome HGNC:11583
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000327674.8 hg38 chrX 106,032,442 106,037,394 4,953
ENST00000372563.2 hg38 chrX 106,032,435 106,038,727 6,293
ENST00000372563.2 hg19 chrX 105,276,426 105,282,718 6,293
ENST00000327674.8 hg19 chrX 105,276,433 105,281,385 4,953
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