CD300A CD300a molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
36 |
![]() |
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 |
Type | ID |
---|---|
SYNONYM | CLM-8 |
SYNONYM | CMRF-35-H9 |
SYNONYM | CMRF-35H |
SYNONYM | CMRF35-H |
SYNONYM | CMRF35-H9 |
SYNONYM | CMRF35H |
SYNONYM | CMRF35H9 |
SYNONYM | IGSF12 |
SYNONYM | IRC1 |
SYNONYM | IRC1/IRC2 |
SYNONYM | IRC2 |
SYNONYM | IRp60 |
MIM | 606790 OMIM |
HGNC | HGNC:19319 HGNC |
Ensembl | ENSG00000167851 Ensembl |
AllianceGenome | HGNC:19319 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000360141.8 | hg38 | chr17 | 74,466,634 | 74,484,794 | 18,161 |
ENST00000361933.7 | hg38 | chr17 | 74,466,675 | 74,484,167 | 17,493 |
ENST00000577511.1 | hg38 | chr17 | 74,466,862 | 74,484,296 | 17,435 |
ENST00000648095.1 | hg38 | chr17 | 74,466,399 | 74,484,794 | 18,396 |
ENST00000310828.9 | hg38 | chr17 | 74,466,675 | 74,484,167 | 17,493 |
ENST00000392625.7 | hg38 | chr17 | 74,466,658 | 74,484,790 | 18,133 |
ENST00000648095.1 | hg19 | chr17 | 72,462,538 | 72,480,933 | 18,396 |
ENST00000360141.8 | hg19 | chr17 | 72,462,773 | 72,480,933 | 18,161 |
ENST00000392625.7 | hg19 | chr17 | 72,462,797 | 72,480,929 | 18,133 |
ENST00000310828.9 | hg19 | chr17 | 72,462,814 | 72,480,306 | 17,493 |
ENST00000361933.7 | hg19 | chr17 | 72,462,814 | 72,480,306 | 17,493 |
ENST00000577511.1 | hg19 | chr17 | 72,463,001 | 72,480,435 | 17,435 |
Genome browser