FAM124B family with sequence similarity 124 member B

Information
Symbol
FAM124B
Type
protein-coding
Description
family with sequence similarity 124 member B
Entrez Gene ID
79843
Genome
hg19
Position
chr2:225,243,415-225,266,824
Genome
hg38
Position
chr2:224,378,698-224,402,107
MIM
618403 OMIM
HGNC
HGNC:26224 HGNC
Ensembl
ENSG00000124019 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
48
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 :
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
TypeID
MIM 618403 OMIM
HGNC HGNC:26224 HGNC
Ensembl ENSG00000124019 Ensembl
AllianceGenome HGNC:26224
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409685.4 hg38 chr2 224,378,698 224,402,107 23,410
ENST00000389874.3 hg38 chr2 224,378,698 224,401,994 23,297
ENST00000243806.2 hg38 chr2 224,399,525 224,402,085 2,561
ENST00000389874.3 hg19 chr2 225,243,415 225,266,711 23,297
ENST00000409685.4 hg19 chr2 225,243,415 225,266,824 23,410
ENST00000243806.2 hg19 chr2 225,264,242 225,266,802 2,561
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