ENST00000675931.1 FAM86C1P

Information
Transcript ID
ENST00000675931.1
Genome
hg38
Position
chr11:71,787,537-71,799,660
Strand
+
CDS length
0
Amino acid length
0
Gene symbol
FAM86C1P
Gene type
unknown
Gene description
family with sequence similarity 86 member C1, pseudogene
Gene Entrez Gene ID
55199
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 71,787,537 71,787,632
2 71,789,783 71,789,845
3 71,791,739 71,791,819
4 71,793,380 71,793,481
5 71,794,709 71,794,842
6 71,794,925 71,795,190
7 71,796,017 71,796,166
8 71,799,561 71,799,660
Other genome
Genome Chromosome Start End Links
hg19 chr11 71,498,583 71,510,706 Link
CDS sequence
Amino sequence