MYL12B myosin light chain 12B
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 2 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
2 |
 |
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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| 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 | |||||||||||
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| 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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | MLC-B |
| SYNONYM | MRLC2 |
| MIM | 609211 OMIM |
| HGNC | HGNC:29827 HGNC |
| Ensembl | ENSG00000118680 Ensembl |
| AllianceGenome | HGNC:29827 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000648965.1 | hg38 | chr18 | 3,261,479 | 3,278,431 | 16,953 |
| ENST00000400175.9 | hg38 | chr18 | 3,262,613 | 3,278,284 | 15,672 |
| ENST00000237500.10 | hg38 | chr18 | 3,262,133 | 3,278,461 | 16,329 |
| ENST00000581193.5 | hg38 | chr18 | 3,262,417 | 3,278,284 | 15,868 |
| ENST00000584539.1 | hg38 | chr18 | 3,262,956 | 3,278,284 | 15,329 |
| ENST00000648965.1 | hg19 | chr18 | 3,261,477 | 3,278,429 | 16,953 |
| ENST00000237500.10 | hg19 | chr18 | 3,262,131 | 3,278,459 | 16,329 |
| ENST00000581193.5 | hg19 | chr18 | 3,262,415 | 3,278,282 | 15,868 |
| ENST00000400175.9 | hg19 | chr18 | 3,262,611 | 3,278,282 | 15,672 |
| ENST00000584539.1 | hg19 | chr18 | 3,262,954 | 3,278,282 | 15,329 |
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