FAM221A family with sequence similarity 221 member A

Information
Symbol
FAM221A
Type
protein-coding
Description
family with sequence similarity 221 member A
Entrez Gene ID
340277
Genome
hg19
Position
chr7:23,719,818-23,742,269
Genome
hg38
Position
chr7:23,680,199-23,702,650
HGNC
HGNC:27977 HGNC
Ensembl
ENSG00000188732 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
42
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
[No Data.]
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 C7orf46
HGNC HGNC:27977 HGNC
Ensembl ENSG00000188732 Ensembl
AllianceGenome HGNC:27977
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000344962.9 hg38 chr7 23,680,199 23,702,650 22,452
ENST00000409192.7 hg38 chr7 23,680,130 23,702,174 22,045
ENST00000409994.3 hg38 chr7 23,680,184 23,702,650 22,467
ENST00000409653.5 hg38 chr7 23,680,184 23,702,167 21,984
ENST00000409192.7 hg19 chr7 23,719,749 23,741,793 22,045
ENST00000409653.5 hg19 chr7 23,719,803 23,741,786 21,984
ENST00000409994.3 hg19 chr7 23,719,803 23,742,269 22,467
ENST00000344962.9 hg19 chr7 23,719,818 23,742,269 22,452
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