ENST00000505109.2 LOC102724637

Information
Transcript ID
ENST00000505109.2
Genome
hg38
Position
chr5:89,900,664-89,990,883
Strand
+
CDS length
0
Amino acid length
0
Gene symbol
LOC102724637
Gene type
ncRNA
Gene description
uncharacterized LOC102724637
Gene Entrez Gene ID
102724637
Variants

Display target variant


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
Exon
Exon number Start Stop
1 89,900,664 89,901,201
2 89,904,863 89,904,908
3 89,937,945 89,938,116
4 89,940,581 89,940,763
5 89,944,873 89,944,985
6 89,949,834 89,949,912
7 89,950,309 89,950,415
8 89,975,989 89,976,019
9 89,990,550 89,990,883
Other genome
Genome Chromosome Start End Links
hg19 chr5 89,196,481 89,286,700 Link
CDS sequence
Amino sequence