CORO1C coronin 1C
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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22 |
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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
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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 |
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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 |
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MGeND data only
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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 | HCRNN4 |
MIM | 605269 OMIM |
HGNC | HGNC:2254 HGNC |
Ensembl | ENSG00000110880 Ensembl |
AllianceGenome | HGNC:2254 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000549772.5 | hg38 | chr12 | 108,647,403 | 108,703,075 | 55,673 |
ENST00000421578.6 | hg38 | chr12 | 108,647,380 | 108,696,402 | 49,023 |
ENST00000261401.8 | hg38 | chr12 | 108,645,109 | 108,731,518 | 86,410 |
ENST00000420959.6 | hg38 | chr12 | 108,645,115 | 108,702,998 | 57,884 |
ENST00000541050.5 | hg38 | chr12 | 108,646,567 | 108,730,843 | 84,277 |
ENST00000261401.8 | hg19 | chr12 | 109,038,885 | 109,125,294 | 86,410 |
ENST00000420959.6 | hg19 | chr12 | 109,038,891 | 109,096,774 | 57,884 |
ENST00000541050.5 | hg19 | chr12 | 109,040,343 | 109,124,619 | 84,277 |
ENST00000421578.6 | hg19 | chr12 | 109,041,156 | 109,090,178 | 49,023 |
ENST00000549772.5 | hg19 | chr12 | 109,041,179 | 109,096,851 | 55,673 |
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