NIPSNAP2 nipsnap homolog 2

Information
Symbol
NIPSNAP2
Type
protein-coding
Description
nipsnap homolog 2
Entrez Gene ID
2631
Genome
hg19
Position
chr7:56,032,278-56,067,872
Genome
hg38
Position
chr7:55,964,585-56,000,179
MIM
603004 OMIM
HGNC
HGNC:4179 HGNC
Ensembl
ENSG00000146729 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
26
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 GBAS
MIM 603004 OMIM
HGNC HGNC:4179 HGNC
Ensembl ENSG00000146729 Ensembl
AllianceGenome HGNC:4179
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000446778.5 hg38 chr7 55,964,581 56,000,181 35,601
ENST00000322090.8 hg38 chr7 55,964,585 56,000,179 35,595
ENST00000446778.5 hg19 chr7 56,032,274 56,067,874 35,601
ENST00000322090.8 hg19 chr7 56,032,278 56,067,872 35,595
Genome browser