RPL27A ribosomal protein L27a
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
6 |
![]() |
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 | L27A |
SYNONYM | uL15 |
MIM | 603637 OMIM |
HGNC | HGNC:10329 HGNC |
Ensembl | ENSG00000166441 Ensembl |
AllianceGenome | HGNC:10329 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000530913.1 | hg38 | chr11 | 8,684,259 | 8,685,848 | 1,590 |
ENST00000526562.5 | hg38 | chr11 | 8,683,201 | 8,685,848 | 2,648 |
ENST00000314138.11 | hg38 | chr11 | 8,682,792 | 8,689,872 | 7,081 |
ENST00000530022.5 | hg38 | chr11 | 8,682,810 | 8,685,848 | 3,039 |
ENST00000524496.5 | hg38 | chr11 | 8,682,789 | 8,685,847 | 3,059 |
ENST00000532359.5 | hg38 | chr11 | 8,682,792 | 8,685,848 | 3,057 |
ENST00000531978.5 | hg38 | chr11 | 8,682,788 | 8,685,415 | 2,628 |
ENST00000531978.5 | hg19 | chr11 | 8,704,335 | 8,706,962 | 2,628 |
ENST00000524496.5 | hg19 | chr11 | 8,704,336 | 8,707,394 | 3,059 |
ENST00000532359.5 | hg19 | chr11 | 8,704,339 | 8,707,395 | 3,057 |
ENST00000314138.11 | hg19 | chr11 | 8,704,339 | 8,711,419 | 7,081 |
ENST00000530022.5 | hg19 | chr11 | 8,704,357 | 8,707,395 | 3,039 |
ENST00000526562.5 | hg19 | chr11 | 8,704,748 | 8,707,395 | 2,648 |
ENST00000530913.1 | hg19 | chr11 | 8,705,806 | 8,707,395 | 1,590 |
Genome browser