SEC61G SEC61 translocon subunit gamma

Information
Symbol
SEC61G
Type
protein-coding
Description
SEC61 translocon subunit gamma
Entrez Gene ID
23480
Genome
hg19
Position
chr7:54,819,946-54,827,667
Genome
hg38
Position
chr7:54,752,253-54,759,974
MIM
609215 OMIM
HGNC
HGNC:18277 HGNC
Ensembl
ENSG00000132432 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
Uncertain significance 0 2
Ranking
ClinVar
0
0
0
2
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 :
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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 SSS1
MIM 609215 OMIM
HGNC HGNC:18277 HGNC
Ensembl ENSG00000132432 Ensembl
AllianceGenome HGNC:18277
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000352861.9 hg38 chr7 54,752,253 54,759,211 6,959
ENST00000415949.5 hg38 chr7 54,752,253 54,759,974 7,722
ENST00000450622.1 hg38 chr7 54,752,257 54,759,182 6,926
ENST00000395535.7 hg38 chr7 54,752,250 54,759,246 6,997
ENST00000395535.7 hg19 chr7 54,819,943 54,826,939 6,997
ENST00000352861.9 hg19 chr7 54,819,946 54,826,904 6,959
ENST00000415949.5 hg19 chr7 54,819,946 54,827,667 7,722
ENST00000450622.1 hg19 chr7 54,819,950 54,826,875 6,926
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