ENST00000382166.2 FAM99B

Information
Transcript ID
ENST00000382166.2
Genome
hg38
Position
chr11:1,683,269-1,685,629
Strand
-
CDS length
0
Amino acid length
0
Gene symbol
FAM99B
Gene type
ncRNA
Gene description
family with sequence similarity 99 member B
Gene Entrez Gene ID
100132464
Variants

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MGeND data only
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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
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MGeND data only
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Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
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MGeND data only
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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
3 1,683,269 1,684,034
2 1,684,194 1,684,302
1 1,685,438 1,685,629
Other genome
Genome Chromosome Start End Links
hg19 chr11 1,704,499 1,706,859 Link
CDS sequence
Amino sequence