ABCC10 ATP binding cassette subfamily C member 10

Information
Symbol
ABCC10
Type
protein-coding
Description
ATP binding cassette subfamily C member 10
Entrez Gene ID
89845
Genome
hg19
Position
chr6:43,395,279-43,418,165
Genome
hg38
Position
chr6:43,427,541-43,450,427
MIM
612509 OMIM
HGNC
HGNC:52 HGNC
Ensembl
ENSG00000124574 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 8
Uncertain significance 0 178
Ranking
ClinVar
0
0
0
188
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
SYNONYM EST182763
SYNONYM MRP7
SYNONYM SIMRP7
MIM 612509 OMIM
HGNC HGNC:52 HGNC
Ensembl ENSG00000124574 Ensembl
AllianceGenome HGNC:52
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000372530.9 hg38 chr6 43,427,541 43,450,427 22,887
ENST00000244533.7 hg38 chr6 43,431,751 43,450,425 18,675
ENST00000372530.9 hg19 chr6 43,395,279 43,418,165 22,887
ENST00000244533.7 hg19 chr6 43,399,489 43,418,163 18,675
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