CCDC32 coiled-coil domain containing 32
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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8 |
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4 |
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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | C15orf57 |
SYNONYM | CFNDS |
MIM | 618941 OMIM |
HGNC | HGNC:28295 HGNC |
Ensembl | ENSG00000128891 Ensembl |
AllianceGenome | HGNC:28295 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000558750.5 | hg38 | chr15 | 40,553,942 | 40,564,980 | 11,039 |
ENST00000698443.1 | hg38 | chr15 | 40,537,585 | 40,565,054 | 27,470 |
ENST00000561011.5 | hg38 | chr15 | 40,531,341 | 40,564,992 | 33,652 |
ENST00000559911.5 | hg38 | chr15 | 40,534,900 | 40,565,011 | 30,112 |
ENST00000560305.5 | hg38 | chr15 | 40,528,683 | 40,565,011 | 36,329 |
ENST00000416810.7 | hg38 | chr15 | 40,553,099 | 40,565,042 | 11,944 |
ENST00000358005.7 | hg38 | chr15 | 40,553,099 | 40,565,052 | 11,954 |
ENST00000558113.5 | hg38 | chr15 | 40,539,229 | 40,565,011 | 25,783 |
ENST00000558871.1 | hg38 | chr15 | 40,556,621 | 40,565,042 | 8,422 |
ENST00000560305.5 | hg19 | chr15 | 40,820,882 | 40,857,210 | 36,329 |
ENST00000561011.5 | hg19 | chr15 | 40,823,540 | 40,857,191 | 33,652 |
ENST00000559911.5 | hg19 | chr15 | 40,827,099 | 40,857,210 | 30,112 |
ENST00000698443.1 | hg19 | chr15 | 40,829,784 | 40,857,253 | 27,470 |
ENST00000558113.5 | hg19 | chr15 | 40,831,428 | 40,857,210 | 25,783 |
ENST00000416810.7 | hg19 | chr15 | 40,845,298 | 40,857,241 | 11,944 |
ENST00000358005.7 | hg19 | chr15 | 40,845,298 | 40,857,251 | 11,954 |
ENST00000558750.5 | hg19 | chr15 | 40,846,141 | 40,857,179 | 11,039 |
ENST00000558871.1 | hg19 | chr15 | 40,848,820 | 40,857,241 | 8,422 |
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