BTN2A2 butyrophilin subfamily 2 member A2
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 24 |
| Likely benign | 0 | 26 |
| Conflicting classifications of pathogenicity | 0 | 4 |
| not provided | 26 | 0 |
| Uncertain significance | 0 | 66 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
4 |
 |
112 |
 |
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
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 | BT2.2 |
| SYNONYM | BTF2 |
| SYNONYM | BTN2.2 |
| MIM | 613591 OMIM |
| HGNC | HGNC:1137 HGNC |
| Ensembl | ENSG00000124508 Ensembl |
| AllianceGenome | HGNC:1137 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000352867.6 | hg38 | chr6 | 26,383,102 | 26,394,874 | 11,773 |
| ENST00000482536.5 | hg38 | chr6 | 26,383,126 | 26,393,007 | 9,882 |
| ENST00000432533.6 | hg38 | chr6 | 26,383,126 | 26,393,008 | 9,883 |
| ENST00000356709.9 | hg38 | chr6 | 26,383,108 | 26,394,874 | 11,767 |
| ENST00000416795.6 | hg38 | chr6 | 26,383,208 | 26,393,992 | 10,785 |
| ENST00000469230.5 | hg38 | chr6 | 26,383,096 | 26,394,874 | 11,779 |
| ENST00000469230.5 | hg19 | chr6 | 26,383,324 | 26,395,102 | 11,779 |
| ENST00000352867.6 | hg19 | chr6 | 26,383,330 | 26,395,102 | 11,773 |
| ENST00000356709.9 | hg19 | chr6 | 26,383,336 | 26,395,102 | 11,767 |
| ENST00000482536.5 | hg19 | chr6 | 26,383,354 | 26,393,235 | 9,882 |
| ENST00000432533.6 | hg19 | chr6 | 26,383,354 | 26,393,236 | 9,883 |
| ENST00000416795.6 | hg19 | chr6 | 26,383,436 | 26,394,220 | 10,785 |
Genome browser