MYL6B myosin light chain 6B
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
26 |
![]() |
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 | MLC1SA |
MIM | 609930 OMIM |
HGNC | HGNC:29823 HGNC |
Ensembl | ENSG00000196465 Ensembl |
AllianceGenome | HGNC:29823 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000696002.1 | hg38 | chr12 | 56,153,893 | 56,157,981 | 4,089 |
ENST00000696001.1 | hg38 | chr12 | 56,152,590 | 56,157,981 | 5,392 |
ENST00000552568.5 | hg38 | chr12 | 56,152,607 | 56,157,976 | 5,370 |
ENST00000553066.5 | hg38 | chr12 | 56,152,256 | 56,157,982 | 5,727 |
ENST00000695999.1 | hg38 | chr12 | 56,152,587 | 56,157,982 | 5,396 |
ENST00000550443.5 | hg38 | chr12 | 56,152,439 | 56,157,976 | 5,538 |
ENST00000553066.5 | hg19 | chr12 | 56,546,040 | 56,551,766 | 5,727 |
ENST00000550443.5 | hg19 | chr12 | 56,546,223 | 56,551,760 | 5,538 |
ENST00000695999.1 | hg19 | chr12 | 56,546,371 | 56,551,766 | 5,396 |
ENST00000696001.1 | hg19 | chr12 | 56,546,374 | 56,551,765 | 5,392 |
ENST00000552568.5 | hg19 | chr12 | 56,546,391 | 56,551,760 | 5,370 |
ENST00000696002.1 | hg19 | chr12 | 56,547,677 | 56,551,765 | 4,089 |
Genome browser