SERPINF2 serpin family F member 2

Information
Symbol
SERPINF2
Type
protein-coding
Description
serpin family F member 2
Entrez Gene ID
5345
Genome
hg19
Position
chr17:1,646,320-1,658,559
Genome
hg38
Position
chr17:1,743,026-1,755,265
MIM
613168 OMIM
HGNC
HGNC:9075 HGNC
Ensembl
ENSG00000167711 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 2
Benign 0 30
Likely benign 0 44
Conflicting classifications of pathogenicity 0 6
Uncertain significance 0 42
Ranking
ClinVar
0
0
10
106
4
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
SYNONYM A2AP
SYNONYM AAP
SYNONYM ALPHA-2-PI
SYNONYM API
SYNONYM PLI
SYNONYM alpha2AP
MIM 613168 OMIM
HGNC HGNC:9075 HGNC
Ensembl ENSG00000167711 Ensembl
AllianceGenome HGNC:9075
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000324015.7 hg38 chr17 1,742,836 1,755,265 12,430
ENST00000453066.6 hg38 chr17 1,742,871 1,755,265 12,395
ENST00000382061.5 hg38 chr17 1,743,026 1,755,265 12,240
ENST00000450523.6 hg38 chr17 1,742,843 1,754,642 11,800
ENST00000324015.7 hg19 chr17 1,646,130 1,658,559 12,430
ENST00000450523.6 hg19 chr17 1,646,137 1,657,936 11,800
ENST00000453066.6 hg19 chr17 1,646,165 1,658,559 12,395
ENST00000382061.5 hg19 chr17 1,646,320 1,658,559 12,240
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