LAYN layilin
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
54 |
![]() |
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 |
---|---|
MIM | 618843 OMIM |
HGNC | HGNC:29471 HGNC |
Ensembl | ENSG00000204381 Ensembl |
AllianceGenome | HGNC:29471 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000436913.6 | hg38 | chr11 | 111,540,508 | 111,561,745 | 21,238 |
ENST00000375614.7 | hg38 | chr11 | 111,540,720 | 111,561,745 | 21,026 |
ENST00000375615.7 | hg38 | chr11 | 111,540,659 | 111,560,960 | 20,302 |
ENST00000525126.5 | hg38 | chr11 | 111,540,709 | 111,560,933 | 20,225 |
ENST00000533265.5 | hg38 | chr11 | 111,540,730 | 111,560,918 | 20,189 |
ENST00000436913.6 | hg19 | chr11 | 111,411,233 | 111,432,470 | 21,238 |
ENST00000375615.7 | hg19 | chr11 | 111,411,384 | 111,431,685 | 20,302 |
ENST00000525126.5 | hg19 | chr11 | 111,411,434 | 111,431,658 | 20,225 |
ENST00000375614.7 | hg19 | chr11 | 111,411,445 | 111,432,470 | 21,026 |
ENST00000533265.5 | hg19 | chr11 | 111,411,455 | 111,431,643 | 20,189 |
Genome browser